Abstract Code |
Title |
Authors |
Affiliations |
Category |
P1-1 |
Evaluation of Glucose Metabolism and Cardiovascular Risk Factors and Hyperandrogenemia in Prepubertal Girls with Premature Pubarche |
Digdem Bezen, Filiz Tutunculer, Emine Dilek, Didem Ag Seleci, Hakan Erbas |
|
Adrenals and HPA Axis |
P1-10 |
Use of a Cord Blood F-Dex Monocyte Binding Assay to Study the Glucocorticoid Receptor in Neonates |
Arun Kashyap, Javier Aisenberg, Steven Ghanny |
|
Adrenals and HPA Axis |
P1-100 |
Atypical features in patients with Leprechaunism suggesting a wide clinical spectrum of disease |
Harshini Katugampola, Nicola Improda, Pratik Shah, Hannah Gordon, Rakesh Amin, Catherine J Peters, Robert K Semple, Mehul T Dattani |
|
Diabetes and Insulin |
P1-101 |
Does Type 1 childhood diabetes start in utero? |
Zvi Laron, Christiane Hampe, Lester Shulman |
|
Diabetes and Insulin |
P1-102 |
The role of HNF1B in human pancreas development and diabetes |
Ranna El Khairi, Andrew Hattersley, Ludovic Vallier |
|
Diabetes and Insulin |
P1-103 |
Molecular Characterization of a Novel Non-Stop KCNJ11 Mutation Associated with a Dual Focal and Diffuse Hyperinsulinaemic Hypoglycaemia Phenotype |
Ved Bhushan Arya, Qadeer Aziz, Sarah E. Flanagan, Sian Ellard, Andrew Tinker, Khalid Hussain |
|
Hypoglycaemia |
P1-104 |
Diazoxide Responsive Congenital Hyperinsulinism in a Patient with Dual Genetic Aetiology (HNF4A and ABCC8 mutation) |
Dinesh Giri, Sarah E. Flanagan, Julie Park, Sian Ellard, Mo Didi, Senthil Sennaippan |
|
Hypoglycaemia |
P1-105 |
Fluoxetine induced Hypoglycemia in a patient with Congenital Hyperinsulinism on Lanreotide Therapy |
Dinesh Giri, Zoe Yung, Kelly Stirrup, Mo Didi, Senthil Seniappan |
|
Hypoglycaemia |
P1-106 |
Influence of nocturnal glycemia on ventricular repolarization and heart rate variability in prepubertal children with type 1 diabetes. |
Marie-Béatrice Saade, Aurélien Pecquet, Patrick Pladys, Alain Beuchée, Fabienne Pelé, Sylvie Nivot, Marc de Kerdanet |
|
Hypoglycaemia |
P1-107 |
CHANGES IN SERUM PROTEIN EXPRESSION IN SMALL-FOR-GESTATIONAL-AGE NEWBORN INFANTS AT DIFFERENT GESTATIONAL AGES |
Ramón Cañete, María Dolores Ruiz-González, María Dolores Cañete, José Luis Gómez-Chaparro, Nieves Abril-Díaz, Juan Luis López-Barea |
|
Perinatal and Neonatal Endocrinology |
P1-108 |
Liver ER stress and Intrauterine growth retardation in rats |
Annalisa Deodati, Josepmaria Argemi, Antonella Puglianiello, Daniela Germani, Roberto Ferrero, Tomas Aragon, Stefano Cianfarani |
|
Perinatal and Neonatal Endocrinology |
P1-109 |
Continuous subcutaneous infusion of recombinant LH and FSH during early infancy promotes testicular descent in congenital hypogonadotropic hypogonadism. |
Anne Sophie LAMBERT, Philippe Lucchini, Claire Bouvattier, Pierre Bougnères |
|
Perinatal and Neonatal Endocrinology |
P1-11 |
Steroid 11β-Hydroxylase Deficient Congenital Adrenal Hyperplasia with a Reversible Cardiomyopathy Caused by a Novel CYP11B1 Mutation: Report of Three Cases |
Mohammad Ahmad Awwad Alqahtani, Ayed A Shati, Minjing Zou, Ali M Alsuheel, Abdullah A Alhayani, Saleh M Al-Qahtani, Hessa M Gilban, Brain F Meyer, Yufei Shi |
|
Adrenals and HPA Axis |
P1-110 |
Neonatal screening program for Central Congenital Hypothyroidism |
Debora Braslavsky, Laura Prieto, Ana Keselman, Laura Gruñeiro de Papendieck, Rosa Enacan, Virginia Mendez, Ignacio Bergadá, Ana Chiesa |
|
Perinatal and Neonatal Endocrinology |
P1-111 |
Serum Neurokinin B level can be used to differentiate central precocious puberty from premature thelarche. |
Mesut Parlak, Doga Turkkahraman, Hamit Yasar Ellidag, Ayse Eda Parlak |
|
Puberty and Neuroendocrinology |
P1-112 |
Etiological spectrum and clinical characteristics of 129 children with gonadotropin independent precocious puberty: A nationwide cohort study |
Zeynep Atay, Ediz Yeşilkaya, Senay Savas Erdeve, Leyla Akin, Erdal Eren, Esra Döger, Zehra Aycan, Zehra Yavaş Abali, Ayşehan Akinci, Zeynep Şiklar, Samim Özen, Cengiz Kara, Meltem Tayfun, Filiz Tutunculer, Gülcan Seymen Karabulut, Gülay Karagüzel, Halil Sağlam, Aysun Bideci, Selim Kurtoğlu, Abdullah Bereket, Serap Turan, Erkan Sari, Semra Çetinkaya, Tülay Güran, Turkish Peropheral Puberty Research Group |
|
Puberty and Neuroendocrinology |
P1-113 |
Relevance of astrocytic signals for GnRH-neuronal function |
Johanna Ernst, Hanna Moeller, Manuel Pfeifer, Sabine Heger |
|
Puberty and Neuroendocrinology |
P1-114 |
Screening of mutations in idiopathic hypogonadotropic hypogonadism using a targeted next-generation sequencing approach |
Anna Kolodkina, Maria Kareva, Natalia Kalinchenko, Nadezhda Raygorodskaya, Oleg Malievsky, Olga Fidelina, Evgeny Vasilyev, Vasily Petrov, Maria Naumova, Anatoly Tiulpakov |
|
Puberty and Neuroendocrinology |
P1-115 |
Clinical guidance on 17β-Estradiol and LH serum levels in girls with Premature Thelarche based on clinical outcome of 129 girls aged up to 4 year with premature thelarche in West Sweden. |
Martin Österbrand, Kerstin Alvin, Hans Fors, Ensio Norjavaara |
|
Puberty and Neuroendocrinology |
P1-116 |
FSHB/FSHR genetic variants alter serum FSH levels and prepubertal ovarian follicular growth in healthy girls |
Alexander S. Busch, Casper P. Hagen, Kristian Almstrup, Katharina M. Main, Anders Juul |
|
Puberty and Neuroendocrinology |
P1-117 |
Transient breast budding in healthy girls is a frequent phenomenon: Description of pubertal progression and associations to gonadotropins, estradiol and FSHB/FSHR genetic polymorphisms |
Marie Lindhardt Johansen, Casper P. Hagen, Mikkel G. Mieritz, Jørgen Holm Petersen, Anders Juul |
|
Puberty and Neuroendocrinology |
P1-118 |
Specific hypothalamic activation pattern by mGlu5 receptor blockade in vivo during pubertal development in female mice |
Ioana Inta, Roberto de Angelis, Katja Lankisch, Christof Dormann, Natascha Pfeiffer, Ulrich Boehm, Peter Gass, Markus Bettendorf |
|
Puberty and Neuroendocrinology |
P1-119 |
Lipid profiles in gender dysphoric adolescents treated with GnRH agonists alone and in combination with cross-sex hormones |
Sebastian Schagen, Henriette Delemarre-van de Waal, Sabine Hannema |
|
Puberty and Neuroendocrinology |
P1-12 |
GENETIC DIAGNOSIS USING WHOLE EXOME ANALYSIS IN TWO CASES WITH MALIGN INFANTILE OSTEOPETROSIS |
Korcan Demir, Özlem Nalbantoğlu, Kadri Karaer, Hüseyin Anıl Korkmaz, Melek Yıldız, Selma Tunç, Behzat Özkan |
|
Bone, Growth Plate and Mineral Metabolism |
P1-120 |
A novel LHX4 mutation is associated with hypogonadotropic hypogonadism, not combined pituitary hormone deficiency |
Masaki Takagi, Takashi Daitsu, Chikahiko Numakura, Takeshi Sato, Satoshi Narumi, Tomonobu Hasegawa |
|
Puberty and Neuroendocrinology |
P1-121 |
A missense mutation in MKRN3 in a Danish girl with central precocious puberty and her brother with early puberty |
Johanna Känsäkoski, Taneli Raivio, Anders Juul, Johanna Tommiska |
|
Puberty and Neuroendocrinology |
P1-122 |
Congenital hypothyroidism in twin couples and triplets |
Antonella Olivieri, Giovanna Weber, Alessandra Cassio, Pietro Costa, Francesca Calaciura, Emanuela Medda, Maria Cristina Vigone, Tiziana De Filippis, Giulia Gelmini, Federica Marelli, Valeria Di Russo, Luca Persani |
|
Thyroid |
P1-123 |
Th17 cells in children with Graves’ disease during methimazole treatment |
Maria Klatka, Ewelina Grywalska, Jacek Rolinski |
|
Thyroid |
P1-124 |
Thyrocytes are particularly well protected against oxidative stress induced by H2O2 |
Chiraz Ghaddhab, Emmanuel Van Den Eeckhaute, Olivier Hancisse, Natacha Driessens, Jacques-Emile Dumont, Françoise Miot, Bernard Corvilain |
|
Thyroid |
P1-125 |
Thyrocyte is particularly well protected against oxidative stress induced by H2O2 |
Chiraz Ghaddhab, Emmanuel Van Den Eeckhaute, Olivier Hancisse, Natacha Driessens, Soetkin Versteyhe, Françoise Miot, Jacques-Emile Dumont, Bernard Corvilain |
|
Thyroid |
P1-126 |
Characteristics and Outcome of Neonates with Congenital Hypothyroidism Born after In Vitro Fertilisation (IVF) |
Vassiliki Giogli, Christina Kanaka-Gantenbein, Jessica-Debora Arditi, Dimitris Platis, George Chouliaras, Chrysoula Kourkouti, Ioanna Kosteria, Anna Gika, Alexandra Iliadi, George Chrousos, Panagiotis Girginoudis, Antonis Voutetakis |
|
Thyroid |
P1-127 |
Transient vs. Permanent Congenital Hypothyroidism: The Use of Baseline Characteristics and Long-term Data Can Help Formulate a Practical Prognostic Algorithm |
Vassiliki Giogli, Christina Kanaka-Gantenbein, George Chouliaras, Jessica-Debora Arditi, Anna Gika, Alexandra Iliadi, Dimitris Platis, Eleni Magdalini Kyritsi, Petros Karkalousos, George-Albert Karikas, Chrysanthi Mengreli, George Chrousos, Panagiotis Girginoudis, Antonis Voutetakis |
|
Thyroid |
P1-128 |
Diverse Genotypes and Phenotypes of Three Novel Thyroid Hormone Receptor Alpha Mutations |
Korcan Demir, Anja van Gucht, Muammer Büyükinan, Gönül Catli, Yavuz Ayhan, Veysel Nijat Bas, Bumin Nuri Dündar, Behzat Ozkan, Marcel E. Meima, W. Edward Visser, Robin P. Peeters, Theo J. Visser |
|
Thyroid |
P1-129 |
Intelligence and behaviour in children and adolescents with Hashimoto´s thyroiditis |
Claudia Boettcher, Burkhard Brosig, Henriette Windhaus, Stefan A. Wudy, Andreas Hahn |
|
Thyroid |
P1-13 |
Osteogenesis imperfecta - a pilot trial on treatment with the RANKL-antibody Denosumab |
Heike Hoyer-Kuhn, Christian Netzer, Barbara Hero, Eckhard Schoenau, Oliver Semler |
|
Bone, Growth Plate and Mineral Metabolism |
P1-130 |
Brain-lung-thyroid syndrome - update on the clinical spectrum of a heterogeneous disorder |
Nina Lenherr, Jean-Marc Vuissoz, Karl Heinimann, Gabor Szinnai |
|
Thyroid |
P1-131 |
Increased Detection Rate of Paired Box Domain Gene Mutations by Application of Multiplex Ligation-Dependent Probe Amplification Analysis in Patients with Primary Congenital Hypothyroidism and Thyroid Dysgenesis |
Malgorzata Kumorowicz-Czoch, Pia Hermanns, Anna Madetko-Talowska, Joahim Pohlenz |
|
Thyroid |
P1-132 |
A severe hyperthyroidism in an infant revealed a familial nonautoimmune hyperthyroidism with novel heterozygous thyrotropin receptor gene mutation. |
Isabelle OLIVER PETIT, Frédérique SAVAGNER, Thomas EDOUARD, Philippe CARON |
|
Thyroid |
P1-133 |
Improved determination of total serum estrogenic bioactivity: characterization of estrogenic activity modulators. |
Paris Françoise, Grimaldi Marina, Sultan Charles, Balaguer Patrick |
|
Gonads and Gynaecology |
P1-134 |
Co-existing variants of FOXE1 and BMP15 genes in young females with primary ovarian insufficiency (POI): Evidence of digenic inheritance. |
NIKOLAOS SETTAS, LINA MICHALA, EFTHIMIOS DELIGEOROGLOU, DIONISIOS CHRYSIS, ANDREAS PAMPANOS, ELENI THEOCHARI, OLYMPIA VALLA, CHRISTALENA SOFOCLEOUS, KITSIOU SOFIA, HELEN FRYSSIRA, EMMANUEL KANAVAKIS, CATHERINE DACOU-VOUTETAKIS, GEORGE P CHROUSOS, ANTONIS VOUTETAKIS |
|
Gonads and Gynaecology |
P1-135 |
Sex hormones and gonadal size in pubertal girls born small or appropriate for gestational age |
Indre Petraitiene, Rasa Verkauskiene, Kristina Jariene, Astra Vitkauskiene |
|
Gonads and Gynaecology |
P1-136 |
The Eap1 promoter is differentially methylated at the onset of puberty in normal weight and obese female rats |
Hanna Moeller, Sabine Heger |
|
Puberty and Neuroendocrinology |
P1-137 |
Normalization of puberty and adult height in girls with Turner syndrome, randomized trials versus age and dose at GH-start |
Berit Kriström, Carina Ankarberg-Lindgren, Marie-Louise Barrenäs, Karlolof Nilsson, Kerstin Albertsson-Wikland |
|
Turner Syndrome |
P1-138 |
Weight gain in Turner Syndrome: Association to puberty induction? |
Thomas Reinehr, Anders Lindberg, Christina Toschke, Jose Cara, Dionisios Chrysis, Cecila Camacho-Hübner |
|
Turner Syndrome |
P1-139 |
A study of arterial stiffness in Turner syndrome patients using cardio-ankle vascular index |
Hae Woon Jung, Hwa Young Kim, Gyung Min Lee, So Youn Kim, Kyung A Jeong, Keun Hee Choi, Jieun Lee, Young Ah Lee, Choong Ho Shin, Sei Won Yang |
|
Turner Syndrome |
P1-14 |
No secular trend in vitamin D levels over the past 30 years in Swedish children |
Björn Andersson, Kerstin Albertsson-Wikland, Diana Swolin-Eide, Per Magnusson |
|
Bone, Growth Plate and Mineral Metabolism |
P1-140 |
Impaired motor function in Turner syndrome: what is the relationship to performal intelligence scores? |
Betül Taskin, Chris Verhaak, Marlou Essink, Marlies Kempers, Anja Vinck, Ria Nijhuis-van der Sanden, Janiëlle van Alfen-van der Velden |
|
Turner Syndrome |
P1-141 |
Adult height after growth hormone treatment and its association with X chromosome dosage in Turner Syndrome: a cross-sectional database analysis of the French national rare disease network. |
Elodie Fiot, Delphine Zenaty, Priscilla Boizeau, Jérémie Haignere, Sophie Dos Santos, Juliane Léger, French Turner Syndrome Study Group . |
|
Turner Syndrome |
P1-142 |
Fracture incidence is not associated with the 6-year development of trabecular BMD in paediatric Turner syndrome patients |
Ondrej Soucek, Zdenek Sumnik, Marta Snajderova, Stanislava Kolouskova, Jan Lebl |
|
Turner Syndrome |
P1-143 |
Is Aortic Stiffness Increased in Young Turner Syndrome Patients? |
Danya Fox, Kristopher Kang, Laura Stewart, Janis Dionne, James Potts, George Sandor |
|
Turner Syndrome |
P1-144 |
Primary Adrenal Insufficiency in children
without congenital adrenal hyperplasia:
Molecular and clinical characterization of a nationwide cohort |
Tulay Guran, Federica Buonocore, Nurcin Saka, Mehmet Nuri Ozbek, Zehra Aycan, Abdullah Bereket, Firdevs Bas, Sukran Darcan, Aysun Bideci, Serap Turan, Ayla Guven, Omer Tarim, Sebahat Yilmaz Agladioglu, Zeynep Atay, Samim Ozen, Korcan Demir, Aysehan Akinci, Banu Kucukemre Aydin, Muammer Buyukinan, Bilgin Yuksel, Metin Yildiz, Teoman Akcay, Cengiz Kara, Tolga Ozgen, Gonul Catli, Emregul Isik, Semih Bolu, Bayram Ozhan, Fatih Gurbuz, Ahmet Ucar, Huseyin Demirbilek, Zehra Yavas Abali, Esra Doger, Erdal Eren, Merih Berberoglu, Bulent Hacihamdioglu, John C. Achermann |
|
Adrenals and HPA Axis |
P1-145 |
Clinical follow-up of the first SF-1 deficient female patient |
Karine Gerster, Anna Biason-Lauber, Eugen J. Schoenle |
|
Adrenals and HPA Axis |
P1-146 |
Salt sensitivity of blood pressure at age 7-8 years in preterm born children. |
Charlotte A. Ruys, Harrie N. Lafeber, Joost Rotteveel, Martijn J.J. Finken |
|
Miscellaneous |
P1-147 |
A new LC-MS/MS assay for the analysis of sulfated steroids in human serum: quantification of cholesterol sulfate, pregnenolone sulfate, 17-hydroxypregnenolone sulfate and androgen sulfates |
Alberto Sánchez-Guijo, Vinzenz Oji, Michaela F. Hartmann, Heiko Traupe, Stefan A. Wudy |
|
Miscellaneous |
P1-148 |
The analysis of occurrence the zinc transporter antibodies ZnT8 in children with Graves’ disease and Hashimoto’s thyroiditis. |
Artur Bossowski, Hanna Borysewicz-Sanczyk, Anna Bossowska, Mieczyslaw Szalecki, Anna Kucharska, Beata Pyrzak, Mieczyslaw Walczak, Elzbieta Petriczko, Katarzyna Ziora, Maria Del Pilar Larosa, Shu Chen, Michael Powell, Jadwiga Furmaniak, Bernard Rees Smith |
|
Autoimmune Endocrine Disease |
P1-149 |
Recombinant Parathyroid Hormone (1-34) replacement treatment of Hypoparathyroidism in the alfacalcidol-resistant patient with severe Autoimmune Polyendocrinopathy Syndrome type 1 |
Leila Sozaeva, Elizaveta Orlova, Maria Kareva |
|
Autoimmune Endocrine Disease |
P1-15 |
Lithium chloride prevents glucocorticoid-induced growth failure in cultured fetal rat metatarsal bones |
Ondrej Soucek, Farasat Zaman, Lars Sävendahl |
|
Bone, Growth Plate and Mineral Metabolism |
P1-150 |
Severe immunodysregulation phenotypes including infancy-onset type 1 diabetes mellitus in two siblings with a homozygous mutation in the LPS-responsive beige-like anchor (LRBA) gene |
Felix Schreiner, Michaela Plamper, Gesche Düker, Stefan Schoenberger, Janine Altmueller, Alina Hilger, Heiko Reutter, Joachim Woelfle |
|
Autoimmune Endocrine Disease |
P1-151 |
A case of autoimmune polyglandular syndrome type I presenting as progressive generalized lipodystrophy in a 15-month-old child. |
Ekaterina Sorkina, Elena Frolova, Dina Rusinova, Svetlana Polyakova, Evgeny Vasilyev, Vasily Petrov, Anatoly Tiulpakov |
|
Autoimmune Endocrine Disease |
P1-152 |
Noonan syndrome-causing SHP2 mutant inhibits murine growth plate chondrogenesis and bone development: role of Ras/MAPK hyperactivation |
Armelle Yart, Mylène Tajan, Florence Capilla, Nicolas Beton, Jean-Luc Davignon, Maithé Tauber, Jean-Pierre Salles, Thomas Edouard |
|
Bone, Growth Plate and Mineral Metabolism |
P1-153 |
Relationship between Vitamin D and Brainstem Auditory Evoked Potentials (BAEPs) |
Murat Doğan, İlyas Aydın, Keziban Aslı Bala, Sultan Kaba, Özlem Gülpınar |
|
Bone, Growth Plate and Mineral Metabolism |
P1-154 |
Novel Compound Heterozygous BMP1 variants associated with Osteogenesis Imperfecta |
Aram Yang, Rimm Huh, Jinsup Kim, Sung Yoon Cho, Dong-Kyu Jin |
|
Bone, Growth Plate and Mineral Metabolism |
P1-155 |
Prospective Cognitive Assessment in Children with Craniopharyngioma Identifies Dysfunction at Diagnosis, After Conservative Surgery and Before Adjuvant Radiation. |
Penelope Rodriguez-Cabrera, Adam Kuczynski, Maria Michaelidou, Laura Losa, Helen Spoudeas |
|
Endocrine Oncology |
P1-156 |
CUSHING SYNDROME DUE TO ADRENOCORTICAL CARCINOMA IN A 3 MONTH OLD INFANT WITH A LARGE INTERSTITIAL DELETION OF CHROMOSOME 5Q INCLUDING THE APC GENE |
Halit Ilker Akkurt, Esther Schulz, Konrad Reinshagen, Inga Vater, Almuth Caliebe, Jessika Johannsen |
|
Endocrine Oncology |
P1-157 |
How do Adolescent Minors Banking Sperm Before Cancer Therapy Subsequently Use the Fertility Service? A Post Banking Re-evaluation. |
James Pigot, Maria Michaelidou, Elizabeth Williamson, Alison Webb, Hoong-Wei Gan, Helen Spoudeas |
|
Endocrine Oncology |
P1-158 |
The Expression of Related Neuroendocrine Factors with Puberty Onset in Rat at Different Developmental Stages |
Mo Kyung Jung, Ki Eun Kim, Ah Reum Kwon, Hyun Wook Hyun Wook, Duk Hee Kim, Ho-Seong Kim |
|
Pituitary |
P1-159 |
FOXL2 gene and combined pituitary hormone deficiency: a possible link |
Sarah Castets, Alexandru Saveanu, Christine Raybaud, Delphine Mallet, Florence Roucher, Yves Morel, Thierry Brue, Rachel Reynaud, Marc Nicolino |
|
Pituitary |
P1-16 |
Diverse presentations of hypophosphatasia in pediatric patients: a review of the case literature |
Eileen K Sawyer, Karen Anderson |
|
Bone, Growth Plate and Mineral Metabolism |
P1-160 |
Septo-optic dysplasia (SOD) associated with Koolen-de Vries syndrome (KDVS): a case report |
Ani Aroyo, Iva Stoeva, Gergana Stancheva, Reni Koleva, Radka Kaneva |
|
Pituitary |
P1-161 |
Screening of IGSF1 in patients with Central Hypothyroidism and GH deficiency, participating in the Dutch HYPOPIT study |
Melitza Elizabeth, Robin Peeters, Theo Visser, Anita Hokken-Koelega, Laura de Graaff |
|
Pituitary |
P1-162 |
Congenital Hypothyroidism: Reduction in the Female to Male Ratio Following the Decrease of the TSH Cut-off Point Used for Neonatal Screening |
Antonis Voutetakis, Vassiliki Giogli, Dimitris Platis, Anna Gika, Alexandra Iliadi, Chrysanthi Mengreli, George Chrousos, Christina Kanaka-Gantenbein, Panagiotis Girginoudis |
|
Thyroid |
P1-163 |
Pediatric Thyroid Nodule Score (PTNS): Derivation and Validation of a Predictive Score for Thyroid Nodule Assessment in Children |
Danielle van der Kaay, Jonathan Wasserman, Nadia Akseer, Michael Roskies, Frederique la Liberte, Lily Nguyen, Pramod Puligandla |
|
Thyroid |
P1-164 |
Practical application of elastography in the diagnosis of thyroid nodules in children. |
Hanna Borysewicz-Sanczyk, Beata Sawicka, Janusz Dzieciol, Katarzyna Drzewek, Magdalena Oleksinska, Klaudyna Noiszewska, Artur Bossowski |
|
Thyroid |
P1-165 |
Higher urinary iodine levels iodine correlates with lower systolic blood pressure in Chilean schoolchildren |
Francisca Grob, Alejandro Martínez-Aguayo, María Clara Ateaga, Carolina Loureiro, Diego Carrillo, Caroline Hill, Carmen Campino, Carolina Mendoza, Clarita Ferrada, Rodrigo Bancalari, Constanza Pinochet, Cristian Carvajal, Marlene Aglony, Carolina Valdivia, Andrea Vecchiola, Carmen Carrasco, René Baudrand, Cristobal Fuentes, Hernán García, Carlos Fardella |
|
Miscellaneous |
P1-17 |
Humanin prevents undesired apoptosis of chondrocytes without interfering with the anti-inflammatory effect of Dexamethasone in a model of arthritis |
Bettina Sederquist, Cecilia Aulin, Farasat Zaman, Lars Sävendahl |
|
Bone, Growth Plate and Mineral Metabolism |
P1-18 |
RESPONSE TO VITAMIN D REPLACEMENT IS DETERMINED BY BODY SURFACE AREA IN CHILDREN WITH VITAMIN D DEFICIENCY |
In Hyuk Chung, Yu Sun Kang, Eun-Gyong Yoo |
|
Bone, Growth Plate and Mineral Metabolism |
P1-19 |
Bone-Muscle Unit Assessment With pQCT In Children With Inflammatory Bowel Disease Following Treatment With Infliximab |
Mabrouka Altowati, UMM-IE-SALMA Malik, Sheila Shepherd, Paraic Mcgrogan, Richard Russell, Faisal Ahmed, S. C. Wong |
|
Bone, Growth Plate and Mineral Metabolism |
P1-2 |
ONTOGENY OF THE SYNCHRONIZATION BETWEEN ADRENAL CLOCK GENES, ADRENAL STEROIDOGENESIS-RELATED GENES AND THE CIRCADIAN RHYTHM OF THE HPA AXIS IN RATS |
Silvia Ruiz, Clarissa Martins, Margaret Castro, Sonir Antonini, Edson Martinez, Ayrton Moreira |
|
Adrenals and HPA Axis |
P1-20 |
24 hydroxylase polymorphism as a possible contributor to the increased 1, 25(OH)2D in African Americans |
Thomas O Carpenter, David EC Cole, Laleh Ardeshirpour, Shadab Salehpour |
|
Bone, Growth Plate and Mineral Metabolism |
P1-21 |
Effects of inorganic phosphate and FGF23 on C2C12 myoblast cells |
Adalbert Raimann, Alexander Dangl, Susanne Greber-Platzer, Monika Egerbacher, Gabriele Haeusler |
|
Bone, Growth Plate and Mineral Metabolism |
P1-22 |
EVALUATION OF BONE MINERAL DENSITY AND MICROARCHITECTURAL PARAMETERS BY DXA AND HR-pQCT IN 36 X-LINKED HYPOPHOSPHATEMIC RICKETS PATIENTS FROM A SINGLE-CENTER STUDY |
Guido de Paula Colares Neto, Rosa Maria Rodrigues Pereira, Jackeline Couto Alvarenga, Liliam Takayama, Mariana Ferreira de Assis Funari, Regina Matsunaga Martin |
|
Bone, Growth Plate and Mineral Metabolism |
P1-23 |
Safety and efficacy of treatment with long-acting lanreotide autogel® in early infancy in patients with congenital hyperinsulinism |
Heike Corda, Thomas Meissner, Sebastian Kummer, Alena Welters, Norbert Teig |
|
Diabetes and Insulin |
P1-24 |
The influence of miR-125b in pancreatic β-cell apoptosis |
Bei Han, Ziyang Zhu, Wei Gu, Shining Ni, Ruixue Yang, Xing Shi, Xuewen Yuan, Wentao Gao |
|
Diabetes and Insulin |
P1-25 |
Lower Bone Mineral Density in type 1 Diabetes Mellitus (T1DM) is probably associated with Wnt/β-catenin pathway downregulation through increased Dickkopf-1 levels |
Kyriaki Karavanaki, Charalampos Tsentidis, Lydia Kossiva, Antonios Marmarinos, Artemis Doulgeraki, Dimitrios Gourgiotis |
|
Diabetes and Insulin |
P1-26 |
Human Placenta-Derived Mesenchymal Stem Cells: a novel protocol for pancreatic differentiation. |
Viviana Dora Patianna, Bernard Okere, Barbara Predieri, Patrizia Bruzzi, Lorenzo Iughetti |
|
Diabetes and Insulin |
P1-27 |
Activation of insulin signaling in gastrocnemius after central leptin infusion is associated with an increase in proliferation and muscle fiber size |
Vicente Barrios, Emma Burgos-Ramos, Sandra Canelles, Amaia Rodríguez, Javier Gómez-Ambrosi, Julie A. Chowen, Gema Frühbeck, Jesús Argente |
|
Diabetes and Insulin |
P1-28 |
Clinical characterisation of a novel RFX6 mutation- a rare cause of neonatal diabetes syndrome |
Moira Cheung, Simon Chapman, Katie Hunt, Erin Makin, Ann Hickey, Jonathan Hind, Sian Ellard, Charles Buchanan, Ritika Kapoor |
|
Diabetes and Insulin |
P1-29 |
Is reduced heart rate variability associated with arterial stiffness in youth with childhood-onset type 1 diabetes mellitus? |
Hwa Young Kim, Hae Woon Jung, Gyung Min Lee, So Youn Kim, Kyung A Jeong, Keun Hee Choi, Jieun Lee, Young Ah Lee, Choong Ho Shin, Sei Won Yang |
|
Diabetes and Insulin |
P1-3 |
Are heterozygous carriers of CYP21A2 less vulnerable to psychological stress? |
Anna Nordenström, Agnieszka Butwicka, Henrik Falhammar, Angelica Lindén Hirschberg, Catharina Almqvist, Agneta Nordenskjöld, Louise Frisén |
|
Adrenals and HPA Axis |
P1-30 |
A NOVEL MUTATION IN THE ABCC8 GENE CAUSING A VARIABLE PHENOTYPE OF IMPAIRED GLUCOSE METABOLISM IN THE SAME FAMILY |
Evelina Maines, Khalid Hussain, Sarah E. Flanagan, Sian Ellard, Claudia Piona, Grazia Grazia Morandi, Sarah Dal Ben, Paolo Cavarzere, Franco Franco Antoniazzi, Rossella Gaudino |
|
Diabetes and Insulin |
P1-31 |
Type 1 Diabetes Onset: a story of innate and adaptive immune cells? |
Ana Laura Fitas, Catarina Martins, Anabela Alonso, Glória Nunes, Rosa Pina, Daniela Amaral, Sigurd Lenzen, Lurdes Lopes, Luis Miguel Borrego, Catarina Limbert |
|
Diabetes and Insulin |
P1-32 |
Etiological diagnosis of diabetes in Italian diabetic children and adolescents |
Maurizio Delvecchio, Giuseppina Salzano, Enza Mozzillo, Giulio Frontino, Ippolita Patrizia Patera, Sonia Toni, Ivana Rabbone, Valentino Cherubini, Stefano Tumini, Giuseppe D'Annunzio, Lorenzo Iughetti, Giulio Maltoni, Vittoria Cauvin, Marco Marigliano, Fabrizio Barbetti |
|
Diabetes and Insulin |
P1-33 |
Improved genetic testing for monogenic diabetes in the Swiss population by targeted next generation sequencing |
Mirjam Dirlewanger, Jean-Louis Blouin, Philippe Klee, Montserrat Castellsague-Perolini, Céline Girardin, Federico Santoni, Valérie Schwitzgebel |
|
Diabetes and Insulin |
P1-34 |
Low bone mineral density is associated to poor glycemic control and increased dickkopf-1 (DKK-1) serum levels in children and adolescents with type 1 diabetes |
Maria Felicia Faienza, Maurizio Delvecchio, Anna Fusillo, Antonella Lonero, Clara Zecchino, Angelo Acquafredda, Laura Piacente, Maria Grano, Luciano Cavallo, Giacomina Brunetti |
|
Diabetes and Insulin |
P1-35 |
Effect of 6 months therapy with Metreleptin in an African American boy with Congenital generalized lipodystrophy. |
Svetlana Ten, Amrit Bhangoo, Divya Khurana, Mark Flyer, Abhimanyu Garg |
|
Diabetes and Insulin |
P1-36 |
Somatic paternal UPD on chromosome 11p15 in focal form of congenital hyperinsulinism (CHI) causes monoallelic expression of mutant ABCC8 and KCNJ11 |
Ina Dallmann, Silke Vogelgesang, Winfried Barthlen, Emine Varol, Wolfgang Mohnike, Susann Empting, Klaus Mohnike, Martin Zenker, Ilse Wieland |
|
Diabetes and Insulin |
P1-37 |
Hyperthyroidism in 276 Children and Adolescents with Type 1 Diabetes from Germany and Austria |
Axel Dost, Tilman R. Rohrer, Elke Fröhlich-Reiterer, Esther Bollow, Beate Karges, Andreas Böckmann, Johannes Hamann, Reinhard W. Holl |
|
Diabetes and Insulin |
P1-38 |
METABOLIC SYNDROME FREQUENCY IN LONGITUDINALLY FOLLOWED CHILDREN WITH PREMATURE ADRENARCHE DURING PUBERTAL AGES |
Gamze Kaya, Sükran Poyrazoglu, Oguz Bulent Erol, Seha Saygili, Mine Sükür, Firdevs Bas, Ruveyde Bundak, Feyza Darendeliler |
|
Diabetes and Insulin |
P1-39 |
EVALUATION OF ABILITY OF URINARY PODOCALYXIN, NEPHRIN AND LIVER TYPE FATTY ACID BINDING PROTEIN FOR EARLY DIAGNOSIS IN RENAL INJURY IN ADOLESCENTS WITH TYPE 1 DIABETES |
seniha kiremitci yilmaz, fatma taneli, arzu oran, gülgün yilmaz ovali, betül ersoy |
|
Diabetes and Insulin |
P1-4 |
Effect of CYP17A1 inhibitors orteronel and galeterone on adrenal androgen biosynthesis. |
Sameer S. Udhane, Amit V. Pandey |
|
Adrenals and HPA Axis |
P1-40 |
Efficacy and safety of a fixed combination of insulin degludec/ insulin aspart in children and adolescents with type 1 diabetes |
Tadej Battelino, Larry Deeb, Panagiota Diamantopoulou Reiter, Tina Maria Greve, Georgeanna Klingensmith, Miriana Kocova, Margarita Kovarenko, Naim Shehadeh |
|
Diabetes and Insulin |
P1-41 |
Current care and outcomes for children and young people with diabetes in England and Wales: Results from the National Paediatric Diabetes Audit |
Naomi Holman, Fiona Campbell, Justin Warner |
|
Diabetes and Insulin |
P1-42 |
Dynamics perceptions of their own health in the process of learning self-control adolescents with type 1 diabetes mellitus |
Olena Budreiko, Olena Kirilova, Sergey Tsylyuryk, Svitlana Chumak |
|
Diabetes and Insulin |
P1-43 |
Evaluation of median nerve in children with type1 diabetes using ultrasonographic imaging and
electrophysiology |
Nancy Elbarbary, Abeer Maghawry, Rana ElHilaly, Rania Refaat |
|
Diabetes and Insulin |
P1-44 |
Is metabolic control affected by military service in young adults with type 1 diabetes? |
Avivit Brener, Eran Mel, Shlomit Shalitin, Liora Lazar, Liat de Vries, Ariel Tenebaum, Tal Oron, Moshe Philip, Yael Lebenthal |
|
Diabetes and Insulin |
P1-45 |
IMMUNE/INFLAMMATORY PROFILE IN CHILDREN WITH TYPE 1 DIABETES MELLITUS AND CELIAC DISEASE AND/OR AUTOIMMUNE THYROIDITIS |
Valentina Fattorusso, Mario Galgani, Enza Mozzillo, Marianna Santopaolo, Rosa Nugnes, Giuseppe Matarese, Adriana Franzese |
|
Autoimmune Endocrine Disease |
P1-46 |
Trends in insulin therapy in 50,861 children and adolescents with type 1 diabetes from Austria and Germany between 2000 and 2014 |
Barbara Bohn, Susanna Wiegand, Sebastian Kummer, Ulrike Menzel, Olga Kordonouri, Claudia Böttcher, Elke Fröhlich-Reiterer, Reinhard W. Holl |
|
Diabetes and Insulin |
P1-47 |
RELATIVE HYPOALDOSTERONISM IN A PATIENT WITH WOLCOTT-RALLISON SYNDROME |
Ahmet Ucar, Yusuf Aydemir, Ayse Dogan, Ebru Tuncez |
|
Diabetes and Insulin |
P1-48 |
Structured Education Programmes for Children with Type 1 Diabetes – A Systematic Review |
Anbezhil Subbarayan |
|
Diabetes and Insulin |
P1-49 |
Can hypothalamic obesity be treated with stimulants? -Follow up |
Friederike Denzer, Belinda Lennerz, Heike Vollbach, Christian Denzer, Martin Wabitsch |
|
Fat Metabolism, Obesity |
P1-5 |
Genetic heterogeneity in triple A syndrome – discrimination of the classic syndrome from two triple A-like syndromes |
Angela Huebner, Felix Reschke, Ingo Kurth, Susann Kutzner, Eda Utine, Filiz Hazan, Dana Landgraf, Christian A. Hübner, Katrin Koehler |
|
Adrenals and HPA Axis |
P1-50 |
A feasibility study of intra-gastric balloons (supported by a lifestyle programme) for the treatment of severe adolescent obesity - the (BOB) Study. |
Pooja Sachdev, Lindesy Reece, Rob Copeland, Mike Thomson, Anuja Natarajan, Jerry Wales, Neil Wright |
|
Fat Metabolism, Obesity |
P1-51 |
Distribution of obesity indices among European preschool children and associated risk factors: the ToyBox-study |
Sonya Galcheva, Mina Lateva, Violeta Iotova, Ilse De Bourdeaudhuij, Greet Cardon, Odysseas Androutsos, Zbigniew Kulaga, Piotr Socha, Luis Moreno, Berthold Koletzko, Yannis Manios, ToyBox-study Group |
|
Fat Metabolism, Obesity |
P1-52 |
A Randomized Trial of the Effects of Perinatal Education of Overweight Pregnant Women to Prevent Childhood Overweight: the ETOIG study. |
Sophie PARAT, Emmanuel COSSON, Amandine BAPTISTE, Marie-Therese TAUBER, Paul VALENSI, Anne-Marie BERTRAND, Myriam DABBAS, Caroline ELIE, Françoise LORENZINI, Veronique NEGRE |
|
Fat Metabolism, Obesity |
P1-53 |
Perypheral neuroblastic tumors and ROHHADNET syndrome (Rapid-onset Obesity with Hypothalamic dysfunction, Hypoventilation, Autonomic Dysregulation and NEural Tumor) |
Flavia Napoli, Ramona Tallone, Annalisa Calcagno, Stefania Sorrentino, Anna Allegri, Natascia Di Iorgi, Mohamad Maghnie |
|
Fat Metabolism, Obesity |
P1-54 |
“bestPWS EU”: A Phase 3 study in adolescent and adult patients with PWS in Europe |
Maithe Tauber, Terri Kim, Nerissa Kreher, Dennis Kim, Berthold Hauffa |
|
Fat Metabolism, Obesity |
P1-55 |
Intrauterine growth restriction is associated with greater severity in childhood obesity-associated metabolic impairment and poorer adult height prediction |
Rocío González-Leal, Julián Martínez-Villanueva, Jesús Argente, Gabriel Á. Martos-Moreno |
|
Fat Metabolism, Obesity |
P1-56 |
Immunohistochemical detection of estrogen α and androgen receptors in genital tissues in girls with congenital adrenal hyperplasia |
Irina Kopylova, Elizaveta Orlova, Veronika Sysoeva, Tatyana Glybina, Mariia Kareva |
|
Gonads and Gynaecology |
P1-57 |
Attitudes of parents of Klinefelter boys and Flemish pediatricians towards neonatal screening and fertility preservation techniques in Klinefelter syndrome. |
Inge Gies, Herman Tournaye, Jean De Schepper |
|
Gonads and Gynaecology |
P1-58 |
Long-Term Endocrine Outcome In Men With Partial Androgen Insensitivity Syndrome |
Angela K Lucas-Herald, S Faisal Ahmed, Silvano Bertelloni, Anders Juul, Jillian Bryce, Jipu Jiang, Martina Rodie, Marie L Johansen, Olaf Hiort, Paul-Martin Holterhus, Martine Cools, An Desloovere, Naomi Weintrob, Sabine E Hannema, Tulay Guran, Feyzad Darendeliler, Anna Nordenstrom, Ieuan Hughes |
|
Sex Differentiation |
P1-59 |
Novel Genetic Associations In Children With Disorders Of Sex Development (DSD) And Neurodevelopment Disorders – Insights From The Deciphering Developmental Disorders (DDD) Study |
Gabriella Gazdagh, DDD Study, Edward S. Tobias, S. Faisal Ahmed, Ruth McGowan |
|
Sex Differentiation |
P1-6 |
Genetic diagnosis of congenital primary adrenal insufficiency by Massive Parallel Sequencing (MPS). |
Florence Roucher Boulez, Delphine Mallet Motak, Mad-Helenie Guerrin Elsensohn, Claire Bardel, Pascal Roy, Yves Morel |
|
Adrenals and HPA Axis |
P1-60 |
Insight into the Human Ovarian Sex Development Networks |
Leila Bouazzi, Mariangela Franco, Wassim Eid, Monika Meyer-Böni, Patrick Sproll, Alexander Maret, Anna Lauber-Biason |
|
Sex Differentiation |
P1-61 |
Current Models Of Practice & Professional Development Of Clinicians In DSD Centres – Results From An International Survey Of Specialist Care For DSD. |
Andreas Kyriakou, Arianne B Dessens, Jillian Bryce, Ira Haraldsen, Violeta Iotova, Anders Juul, Maciej Krawczynski, Agneta Nordenskjöld, Marta Rozas, Caroline Sanders, Olaf Hiort, S Faisal Ahmed |
|
Sex Differentiation |
P1-62 |
Prediction of germ cell cancer occurrence in postpubertal individuals with androgen insensitivity based on pathological findings and cancer predisposition SNPs |
Martine Cools, Katja P Wolffenbuttel, Jana Kaprova, Berenice B Mendonca, Sten LS Drop, Remko Hersmus, Hans Stoop, Ad JM Gillis, Elaine MF Costa, Soraiah Domenice, Lutsz Wunsch, Charmian Quigley, Wiebke Arlt, Guy T'Sjoen, Leendert HJ Looijenga |
|
Sex Differentiation |
P1-63 |
Gender identity prediction in adulthood by HTP test (House-Tree-Family) in 46, XY DSD patients |
Rafael Loch Batista, Marlene Inacio, Ari Oliveira Jr, Vinicius N Brito, Elaine M F Costa, Sorahia Domenice, Berenice B Mendonça |
|
Sex Differentiation |
P1-64 |
MAMLD1 mutations seem not sufficient to explain a 46,XY DSD phenotype. What else? |
Núria Camats, Mónica Fernández-Cancio, Laura Audí, Primus E Mullis, Francisca Moreno, Isabel González Casado, Juan Pedro López-Siguero, Raquel Corripio, José Antonio Bermúdez de la Vega, José Antonio Blanco, Christa E Flück |
|
Sex Differentiation |
P1-65 |
Subcutaneous continuous administration of recombinant human luteinizing and follicle-stimulating hormones is an effective treatment for micropenis during the mini-puberty |
Athanasia Stoupa, Dinane Samara-Boustani, Isabelle Flechtner, Graziella Pinto, Isabelle Jourdon, Kathleen Laborde, Didier Chevenne, Anne-Elodie Millischer-Bellaiche, Michel Polak, Jacques Beltrand |
|
Sex Differentiation |
P1-66 |
46,XX ovotesticular DSD in the absence of SRY gene associated to SOX3 duplication |
Romina P. Grinspon, Julián Nevado, María de los Angeles Mori Alvarez, Rodolfo A. Rey, Graciela del Rey, Ana Chiesa |
|
Sex Differentiation |
P1-67 |
miR-146a-mediated suppression of the inflammatory response in human adipocytes |
Julian Roos, Eveliina Enlund, Daniel Tews, Jan-Bernd Funcke, Verena Zoller, Klaus-Michael Debatin, Martin Wabitsch, Pamela Fischer-Posovszky |
|
Fat Metabolism, Obesity |
P1-68 |
Leptin resistance alteration after modulation of dopamine system funcional activity in rat's diet-induced obesity |
Liudmila Viazava, Angzhalika Solntsva, Alexander Sukalo, Alena Dashkevich, Julia Stukach |
|
Fat Metabolism, Obesity |
P1-7 |
Carriers of 21- Hydroxylase Deficiency Demonstrate Increased Psychological Vulnerability to Stress |
Georgia Koltsida, Ioanna Farakla, Aikaterini Papanikolaou, Gerasimos Kolaitis, Emilia Mantzou, Evangelia Charmandari |
|
Adrenals and HPA Axis |
P1-70 |
Outcome of Adolescents Undergoing Bariatric Surgery – One Year Follow-up |
Michal Ben-Ami, Maayan Bacher, Irena Vusiker, Reut Pink, Daniel Stein, Benjamin Vagner, Gal Raz-Dubnov, Danny Yardeni, Orit PInhas-Hamiel |
|
Fat Metabolism, Obesity |
P1-71 |
Identifying critical periods for maintaining weight loss in obese children |
Amanda Peacock, Talat Mushtaq, Erin Alexander, Helen Truby, Darren Greenwood, Vince Russo, Steven Yau, George Werther, Matthew Sabin |
|
Fat Metabolism, Obesity |
P1-72 |
Use of topiramate in severe hyperphagia associated to neuropsychiatric features in a boy with congenital proopiomelanocortin deficiency (POMC) |
Romana Marini, Sara Ciccone, Paolo Alfieri, Stefania Pedicelli, Marco Cappa |
|
Fat Metabolism, Obesity |
P1-73 |
CIRCULATING miR146a AND 486-5p ARE ALTERED IN OBESE CHILDREN WITH AND WITHOUT NON-ALCOHOLIC FATTY LIVER DISEASE (NAFLD) AND CORRELATE WITH ABDOMINAL FAT AND BMI. |
Luisa Montanini, Viviana D. Patianna, Chiara Sartori, Barbara Predieri, Patrizia Bruzzi, Pietro Lazzeroni, Silvia Merli, Paolo Bergamaschi, Sergio Bernasconi, Lorenzo Iughetti, Maria Elisabeth Street |
|
Fat Metabolism, Obesity |
P1-74 |
Erythropoietin activates heat production and lipolysis on brown adipose tissue and consequently reduces obesity in dietary-induced obese mice |
Kazuki Kodo, Hisakazu Nakajima, Satoru Sugimoto, Ikuyo Itoh, Shota Fukuhara, Shigehara keiichi, Taichiro Nishikawa, Jun Mori, Kitaro Kosaka, Hajime Hosoi |
|
Fat Metabolism, Obesity |
P1-75 |
Ghrelin and brain-derived neurotrophic factor in children with Prader-Willi syndrome. |
Elena Bogova, Natalya Volevodz, Valentina Peterkova |
|
Fat Metabolism, Obesity |
P1-76 |
Endothelial Progenitor Cells in Obese Non-diabetic Children and Adolescents: Relations to Some Metabolic Parameters, Echocardiographic Parameters and Tissue Doppler Imaging |
Alaa Ahmed, Omneya Youssef, Botheina Thabet |
|
Fat Metabolism, Obesity |
P1-77 |
Evaluation of adiponectin concentrations in obese children and its correlation with lipid and carbohydrate parameters |
Malgorzata Ruminska, Anna Majcher, Beata Pyrzak |
|
Fat Metabolism, Obesity |
P1-78 |
Influence of Genetic Variation on the Response to Recombinant Human Growth Hormone (GH) Treatment in Children with GH Deficiency: An Analysis of 13 Single Nucleotide Polymorphisms and the GH Receptor Exon 3 Deletion |
Anna-Maria Jung, Paul Francois Hoffmann, Dominik Monz, Christina Lissewski, Denny Schanze, Martin Zenker, Tilman Robert Rohrer |
|
GH and IGF Treatment |
P1-79 |
Decrease of jumping power in adolescents with severe GHD (sGHD) after stop of GH-therapy |
Roland Schweizer, Julian Ziegler, Gerhard Binder |
|
GH and IGF Treatment |
P1-8 |
CORTISOL – CORTISONE RATIO AND METALLOPROTEINASE-9 EMERGING AS RISK FACTORS ASSOCIATED WITH PEDIATRICS HIPERTENSION |
Alejandro Martinez-Aguayo, Carmen Campino, Rene Baudrand, Cristian Carvajal, Constanza Pinochet, Hernan Garcia, Rodrigo Bancalari, Alejandra Tapia, Lorena Garcia, Carolina Loureiro, Carolina Mendoza, Andrea Vecchiola, Carolina Valdivia, Cristobal Fuente, Carlos Lagos, Francisca Grob, Sandra Solari, Fidel Allende, Alexis Kalergis, Carlos Fardella |
|
Adrenals and HPA Axis |
P1-80 |
GOOD CLINICAL RESPONSE TO GROWTH HORMONE THERAPY IN A BOY WITH A COMBINATION OF FAMILIAR SHORT STATURE CAUSED BY NOVEL p.Val478Serfs*14 MUTATION IN ACAN GENE AND ISOLATED GROWTH HORMONE DEFICIENCY |
Stepanka Pruhova, Lenka Dusatkova, Petra Dusatkova, Dana Zemkova, Jan Lebl |
|
GH and IGF Treatment |
P1-81 |
The growth response to growth hormone treatment is greater in patients with SHOX enhancer deletions compared to SHOX defects. |
Stephany Donze, Caroline Meijer, Sarina Kant, Gladys Zandwijken, Annemieke van der Hout, Resie van Spaendonk, Ans van den Ouweland, Jan Maarten Wit, Monique Losekoot, Wilma Oostdijk |
|
GH and IGF Treatment |
P1-82 |
Assessment of Primary Cancers in Growth Hormone (GH)–Treated Paediatric Patients Compared with General Population Registries: An Epidemiological Analysis of a Large, Multinational, Prospective Observational Study |
Christopher Child, Alan Zimmermann, Nan Jia, Leslie Robison, Jürgen Brämswig, Werner Blum |
|
GH and IGF Treatment |
P1-83 |
Genetic markers contribute to the Prediction of response to GH in severe but not mild GH deficiency |
Adam Stevens, Philip Murray, Jerome Wojcik, John Raelson, Ekaterina Koledova, Pierre Chatelain, Peter Clayton |
|
GH and IGF Treatment |
P1-84 |
Disease and Treatment Burden In Children And Adolescents with Growth Hormone Deficiency (GHD) |
Meryl Brod, Lise Højbjerre, Suzanne Alolga, Alise Nacson, Lars Nordholm, Michael Højby Rassmussen |
|
GH and IGF Treatment |
P1-85 |
EFFECTS OF GROWTH HORMONE TREATMENT ON IMMUNITY |
Ramón Cañete, María Dolores Caballero, Rocío Aguado, Manuel Santamaría |
|
GH and IGF Treatment |
P1-86 |
The growth hormone treatment results in the increase of irisin concentration in plasma |
Beata Wikiera, Katarzyna Pukajlo, Lukasz Laczmanski, Natalia Sloka, Aleksander Basiak, Anna Noczynska, Marek Bolanowski, Jacek Daroszewski |
|
GH and IGF Treatment |
P1-87 |
A novel OTX2 gene mutation in a child with growth hormone deficiency |
Antonella Lonero, Maurizio Delvecchio, Paola Primignani, Roberto Caputo, Fabrizia De Palma, Vincenza Luce, Maria Felicia Faienza, Luciano Cavallo |
|
GH and IGF Treatment |
P1-88 |
The dose dependent effect of growth hormone therapy in patients with IGF-1 receptor haploinsufficiency due to heterozygous deletion |
Haruo Mizuno, Kohei Aoyama, Tatsushi Tanaka, Shinji Saitoh |
|
GH and IGF Treatment |
P1-89 |
Royal Jelly supplementation induces the growth plate development and increases plasma growth hormone and estradiol levels in prepubertal rats |
Murat Sever, Ozgur Pirgon, Metin Ciris, Bunyamin Aydin |
|
Growth |
P1-9 |
Founder Effect and the Clinical and Molecular Characteristics in a Cohort of Classical and Non-Classical Congenital Lipoid Adrenal Hyperplasia (CLAH) due to StAR Mutations |
Abdulsalam Abu-Libdeh, Ariella Weinberg Shokrun, Ephrat Levy-Lahad, Osnat Admoni, Yardena Tenenbaum-Rakover, David Zangen |
|
Adrenals and HPA Axis |
P1-90 |
Silver-Russell syndrome without body asymmetry in three patients with duplications of maternally derived chromosome 11p15 involving CDKN1C |
Shinichi Nakashima, Fumiko Kato, Tomoki Kosho, Keisuke Nagasaki, Toru Kikuchi, Masayo Kagami, Maki Fukami, Tsutomu Ogata |
|
Growth |
P1-91 |
Mutation in RTTN, a regulator of ciliary function, causes a complex syndrome characterized by severe congenital microcephaly, lissencephaly and profound growth failure in two siblings |
Anna Grandone, Vincenzo Nigro, Annalaura Torella, Adalgisa Festa, Caterina Luongo, Pierluigi Marzuillo, Ruggero Coppola, Emanuele Miraglia del Giudice, Laura Perrone |
|
Growth |
P1-92 |
Chronic Effects of Bisphenol A administration on Growth Hormone Activity |
Mohammed AL-Masroori, Mohammed Hebais, Amnah AL-Araimi, Fahad Zadjali |
|
Growth |
P1-93 |
Severe IGF-I deficiency and multi-organ autoimmune disease associated with novel germline STAT3 mutations. |
Paula Scaglia, Ana Keselman, Mariana Gutiérrez, Sabina Domené, Miguel Blanco, Nora Sanguinetti, Liliana Bezrodnik, Daniela Di Giovanni, María Soledad Caldirola, Lucia Martucci, Liliana Karabatas, Ashish Kumar, Nana-Hawa Jones, Vivian Hwa, Santiago Revale, Martín Vázquez, Héctor Jasper, Horacio Domené |
|
Growth |
P1-95 |
Various imprinting disorders underlying Silver-Russell Syndrome-compatible phenotype |
Masayo Kagami, Keiko Matsubara, Shinichiro Sano, Akie Nakamura, Seiji Mizuno, Naoki Hamajima, Atsuhiro Yanagisawa, Miyuki Hashimoto, Akira Yukote, Maki Fukami, Tsutomu Ogata |
|
Growth |
P1-96 |
Ligase IV deficiency syndrome as a cause of microcephalic primordial dwarfism in dizygotic twins |
Céline Girardin, Emmanuelle Ranza, Philippe Klee, Mirjam Dirlewanger, Marianne Caflisch, Armand Bottani, Valérie Schwitzgebel |
|
Growth |
P1-97 |
HIGH FREQUENCY OF HYPOMORPHIC ALLELIC HAPLOTYPES OF THE GH1 PROXIMAL PROMOTER IN PATIENTS WITH PROPORTIONAL UNDERGROWTH AND ISOLATED GH DEFICIENCY |
Angel Campos-Barros, Ana Gómez-Núñez, Olga Zurita-Múñoz, Elena Gallego-Gómez, Jaime Cruz-Rojo, Lucía Garzón, Cristina Luzuriaga-Tomás, Isolina Riaño-Galán, Carolina Bezanilla-López, José María Donate-Legaz, Mercedes Marbán-Calzón, Sara Rupérez, Florinda Hermoso, Emma Lara-Orejas, Mª Victoria Borrás-Pérez, Jose Manuel Rius-Peris, Beatriz García-Cuartero, Isabel González-Casado |
|
Growth |
P1-98 |
Growth Hormone Excess in McCune-Albright Syndrome |
Daniele Tessaris, Alison M. Boyce, Patrizia Matarazzo, Roberto Lala, Michael T. Collins |
|
Pituitary |
P1-99 |
Growth hormone hypersecretion in children with NF1 and optic pathway gliomas |
Stefania Pedicelli, Paola Cambiaso, Marina Macchiaiolo, Stefania Galassi, Angela Mastronuzzi, Francesca Del Bufalo, Graziamaria Ubertini, Marco Cappa |
|
Pituitary |
P2-166 |
Late diagnosis of adrenal insufficiency caused by novel compound heterozygous mutations in POMC. |
Elena Frolova, Irina Shirokova, Svetlana Karpova, Anna Kolodkina, Nina Makretskaya, Anatoly Tiulpakov |
|
Adrenals and HPA Axis |
P2-167 |
Hyponatraemia secondary to exudative eczema |
Irene Pilar Fernandez Viseras, Michal Ajzensztejn |
|
Adrenals and HPA Axis |
P2-168 |
The Natural Mutant Receptor hGRαT556I Causes Primary Generalized Glucocorticoid Resistance Through Decreased Affinity for the Ligand and Impaired Interaction with the GRIP1 Coactivator |
Nicolas C. Nicolaides, Eirini Skyrla, Dimitrios Vlachakis, Anna-Maria G. Psarra, Amalia Sertedaki, Sophia Kossida, Evangelia Charmandari |
|
Adrenals and HPA Axis |
P2-169 |
References values under Synacthen® test for 6 steroids in serum by LC-MS/MS |
marie Souillot, ingrid Plotton, chantal Rigaud, veronique Tardy, severine Ruet, yves Morel |
|
Adrenals and HPA Axis |
P2-170 |
Usefulness of salivary cortisol levels in secondary adrenal insufficiency in pediatric population |
Raquel Corripio, Jacobo Pérez, Ariadna Borràs, Laura Capdevila, Judith Sánchez, Josefa Rivera |
|
Adrenals and HPA Axis |
P2-171 |
Acute adrenal failure in a term newborn with congenital cytomegalovirus infection: case description and review of the literature |
Lucia Marseglia, Tommaso Alterio, Lauretta Manti, Tommaso Aversa, Maria Rosa Calafiore, Eloisa Gitto, Malgorzata Wasniewska |
|
Adrenals and HPA Axis |
P2-172 |
Resveratrol disrupts steroidogenesis in human fetal adrenals |
Iuliia Savchuk, Olle Söder, Konstantin Svechnikov |
|
Adrenals and HPA Axis |
P2-173 |
Normal Ranges of Basal and Glucagon-Stimulated Free Cortisol in Children |
Anita Schachter Davidov, Ori Eyal, Anat Becker Anat, Asaf Oren, Naftali Stern, Rona Limor, Naomi Weintrob |
|
Adrenals and HPA Axis |
P2-174 |
CLINICAL, BIOCHEMICAL AND MOLECULAR CHARACTERISTICS OF THE PATIENTS WITH NONCLASSICAL CONGENITAL ADRENAL HYPERPLASIA DUE TO 21-HYDROXYLASE DEFICIENCY IN CROATIA |
Miroslav Dumic, Nevena Krnic, Vesna Kusec, Zorana Grubic, Katarina Stingl, Tony Yuen, Katja Dumic Kubat, Veselin Skrabic, Maria I. New |
|
Adrenals and HPA Axis |
P2-175 |
Abnormal circadian blood pressure profile in patients with congenital adrenal hyperplasia without overt hypertension |
Dominika Janus, Malgorzata Wojcik, Katarzyna Tyrawa, Jerzy Starzyk |
|
Adrenals and HPA Axis |
P2-176 |
Triple A syndrome - the second most common cause of chronic adrenal insufficiency in North Africa? |
Kahina Mohammedi, Asmahane Ladjouze, Ammar Tebaibia, Leila Kedji, Abdelmajid Maoudj, Karima Berkouk, Manoubia Bensmina, Souhila Amoura, Mohamed El Amine Boudjella, Abdennour Laraba |
|
Adrenals and HPA Axis |
P2-177 |
Analysis the relationship between clinical characteristics and genotype of six cases of Bartter syndrome and Gitelman syndrome in children |
zhang jun, chen qiuli, guo song, yang ping, ma huamei, li yanhong, du minlian |
|
Miscellaneous |
P2-178 |
Genotypic heterogeneity and clinical phenotype in two patients with triple A syndrome (AAAS). |
Antonella Meloni, Maria Rosaria Casini, Roberta Mazzitti, Riccardo Congia, Maria Cristina Rosatelli, Marco Bonomi |
|
Miscellaneous |
P2-179 |
Primary adrenal insufficiency: About a pediatric series |
imen nardine, nora soumeya fedala, boubker derghoum, leyla ahmed ali, ali el mahdi haddam, djamila meskine, farida chentli |
|
Adrenals and HPA Axis |
P2-180 |
High-dose Hook Effect in 17- Hydroxyprogesterone Assay in 21-hydroxylase deficiency |
Mesut Parlak, Doga Turkkahraman, Ayse Eda Parlak, Hamit Yasar Ellidag |
|
Adrenals and HPA Axis |
P2-181 |
Baseline cortisol concentrations predict positively and negatively anti- and pro- oxidation, respectively that are measured following an acute aerobic exercise bout in pre- and early pubertal normal-weight and obese boys. |
George Paltoglou, Maria Papagianni, Ioannis G. Fatouros, Aimilia Mantzou, Athanasios Jamurtas, Alexandra Avloniti, Charikleia Stefanaki, Christina Kanaka-Gantenbein, George P. Chrousos, George Mastorakos |
|
Adrenals and HPA Axis |
P2-182 |
Insulin sensitivity and adipocytokynes in children with Classical Congenital Adrenal Hyperplasia |
Nicola Improda, Manuela Cerbone, Andrea Esposito, Flavia Barbieri, Raffaella Di Mase, Donatella Capalbo, Mariacarolina Salerno |
|
Adrenals and HPA Axis |
P2-183 |
24-hour urinary free cortisol as a screening test for Cushing’s syndrome in children. |
Lucy Shapiro, Shezan Elahi, Joe Baliey, Les Perry, Lee Martin, Ashley Grossman, Scott Akker, John Monson, William Drake, Martin Savage, Helen Storr |
|
Adrenals and HPA Axis |
P2-184 |
Familial Hyporeninemic Hyperkalemia and Hypertension (Pseudohypoaldosteronism Type II) in Infancy and Childhood. |
Aaron Hanukoglu, Shira London, Rafael Halevi, Yardena Tenenbaum-Rakover |
|
Adrenals and HPA Axis |
P2-185 |
Severe craniosynostosis syndrome associated to salt wasting congenital adrenal hyperplasia |
Luciana Amorim Beltrão, Elisa Cordeiro Apolinario, Liana Capelo Costa, Yve Lozovei, Simone Martins Castro, Rafael Fabiano Machado Rosa, Cristiane Kopacek |
|
Adrenals and HPA Axis |
P2-186 |
TESTICULAR ADRENAL CELL REST TUMORS ARE NOT ASSOCIATED WITH 21 HYDROXYLASE MUTATIONS OR THERAPY COMPLIANCE IN BOYS WITH CLASSIC FORM OF CAH |
Mirjana Kocova, Vesna Janevska, Violeta Anastasovska, Elena Sukarova-Angelovska |
|
Adrenals and HPA Axis |
P2-187 |
A large family with a novel mutation in the SCNN1A gene causing a mild and transient form of autosomal recessive Pseudohypoaldosteronism type 1 (PHA1) |
Alexandra Efthymiadou, Amalia Sertedaki, George Chrousos, Dionisios Chrysis |
|
Adrenals and HPA Axis |
P2-188 |
Phosphoglucomutase -1 deficiency presented as adrenal insufficiency |
Neta Loewenthal, Ruti Parvari, Alon Haim, Judy Tavashi, Eli Hetshkovits |
|
Adrenals and HPA Axis |
P2-189 |
The etiological spectrum of congenital adrenal hyperplasia based on molecular genetic analyses |
Jin-Ho Choi, Ja Hye Kim, Eungu Kang, Ja Hyang Cho, Gu-Hwan Kim, Han-Wook Yoo |
|
Adrenals and HPA Axis |
P2-190 |
Higher serum DHEAS concentration is associated with lower plasma LDL cholesterol concentration in children |
Aino Mäntyselkä, Jarmo Jääskeläinen, Virpi Lindi, Timo Lakka |
|
Adrenals and HPA Axis |
P2-191 |
Central adrenal insufficiency is not a common feature in CHARGE syndrome |
Gianni Bocca, Monica Wong, Conny van Ravenswaaij-Arts |
|
Adrenals and HPA Axis |
P2-192 |
Baseline adrenal function by measurement of long term cortisol levels in scalp hair of asthmatic children using inhaled corticosteroids equals healthy controls. |
Maria Smit, Ed van Leer, Gerard Noppe, Yolanda de Rijke, Jurriaan Hoekx, Erica van den Akker |
|
Adrenals and HPA Axis |
P2-193 |
Adrenal function in children born small for gestational age |
Indre Petraitiene, Rasa Verkauskiene |
|
Adrenals and HPA Axis |
P2-194 |
Cushing's syndrome in children and adolescents : About a pediatric serie |
aicha houatia, soumeya nora fedala, ali el mahdi haddam, djamila meskine, farida chentli |
|
Adrenals and HPA Axis |
P2-195 |
Serum cortisol and cortisone ratio as sensitive tool to identify subjects with severe or partial 11β-hydroxysteroid dehydrogenase type 2 deficiency |
Cristian Carvajal, Virginia Iturrieta, Carmen Campino, Carolina Valdivia, Jaime Lizama, Fidel Allende, Sandra Solari, René Baudrand, Carlos Lagos, Andrea Vecchiola, Alejandro Martínez-Aguayo, Hernán García, Carlos Fardella |
|
Adrenals and HPA Axis |
P2-196 |
The role of de Nurse practitioner in optimizing care for Children with Congenital Adrenal Hyperplasia |
Viviane van de Crommert, Janiëlle van Alfen-van der Velden, Annelieke van der Linde, Kees Noordam, Hedi Claahsen-van der Grinten |
|
Adrenals and HPA Axis |
P2-197 |
Evaluation of medical treatment in the first 2 years of life with a new Dutch national longitudinal registry for children with congenital adrenal hyperplasia (CAH) |
Annelieke van der Linde, Erica van den Akker, Willy Bakker- van Waarde, Sabine Hannema, Gea Hoorweg-Nijman, Hetty van de Kamp, Daniel Klink, Roelof Odink, Saartje Straetemans, Paul van Trotsenburg, Paul Verkerk, Hedi Claahsen-van der Grinten |
|
Adrenals and HPA Axis |
P2-198 |
Incidence of nonclassical 21-hydroxylase deficiency in Russian population as estimated by the carrier frequency of V281L mutation |
Tatiana Anosova, Anatoly Tiulpakov |
|
Adrenals and HPA Axis |
P2-199 |
CARDIO-METABOLIC RISK FACTORS IN CHILDREN AND ADOLESCENTS WITH CLASSICAL 21-HYDROXYLASE DEFICIENCY |
Kansuda Ariyawatkul, Supatporn Tepmongkol, Taninee Sahakitrungruang |
|
Adrenals and HPA Axis |
P2-200 |
A novel mutation (c.delG209) in the proopiomelanocortin (POMC) gene in a child with early-onset obesity |
Semra Cetinkaya, Tulay Guran, Erdal Kurnaz, Meliksah Keskin, Elif Sagsak, Senay Savas Erdeve, Federica Buonocore, Zehra Aycan |
|
Adrenals and HPA Axis |
P2-201 |
IMPROVED LINEAR GROWTH IN PATIENTS WITH CLASSICAL CONGENITAL ADRENAL HYPERPLASIA. |
Silvia Roma, Carla Bizzarri, Giuseppe Scirè, Gian Luigi Spadoni, Marco Cappa, Chiara Maggioli |
|
Adrenals and HPA Axis |
P2-202 |
Autoimmune polyglandular syndrome type 1 in Russia: clinical experience in 112 patients. |
Elizaveta Orlova, Leila Sozaeva, Maria Kareva, Bergithe E. Oftedal, Lars Breivik, Per M. Knappskog, Ekaterina Zakharova, Eystein S. Husebye, Valentina Peterkova |
|
Autoimmune Endocrine Disease |
P2-203 |
Autoimmune encephalitis - a newly recognised clinical manifestation of autoimmune polyendocrine syndrome type 1? |
Juliana Ferenczova, Veronika Vargova, David Krysl, Erika Banoova, Eva Sadova |
|
Autoimmune Endocrine Disease |
P2-204 |
Children With Coeliac Disease On Gluten Free Diet Have Normal Bone Mass, Geometry And Muscle Mass |
M Mackinder, S C Wong, M Tsiountsioura, S Shepherd, E Buchanan, C Edwards, S F Ahmed, K Gerasimidis |
|
Bone, Growth Plate and Mineral Metabolism |
P2-205 |
Mechanism of bone disease in Prader-Willi syndrome |
Maria Felicia Faienza, Giacomina Brunetti, Graziano Grugni, Antonino Crinò, Sarah Bocchini, Angela Oranger, Isabella Gigante, Laura Piacente, Annamaria Ventura, Silvia Colucci, Maria Grano, Luciano Cavallo, Maurizio Delvecchio |
|
Bone, Growth Plate and Mineral Metabolism |
P2-206 |
Hereditary vitamin D-resistant rickets (HVDRR): Report of four cases with successful use of intermittent intravenous calcium via peripheral route |
Saygin Abali, Mayuko Tamura, Zeynep Atay, Pinar Isguven, Tulay Guran, Belma Haliloglu, Serpil Bas, Tsuyoshi Isojima, Serap Turan, Sachiko Kitanaka, Abdullah Bereket |
|
Bone, Growth Plate and Mineral Metabolism |
P2-207 |
A novel PRKAR1A gene mutation with mild brachydactyly |
Hiroko Yagi, Masaki Takagi, Toshikastu Mistui, Tomonobu Hasegawa, Yukihiro Hasegawa |
|
Bone, Growth Plate and Mineral Metabolism |
P2-208 |
Bone mineral density in children and adolescents with vertical HIV infection. |
Deisi Maria Vargas, Daniela Oliveira Prust, Jose Carlos Galvão |
|
Bone, Growth Plate and Mineral Metabolism |
P2-209 |
Sclerostin and its associations with energy metabolism in children and adolescents |
Anna Wedrychowicz, Jerzy Starzyk |
|
Bone, Growth Plate and Mineral Metabolism |
P2-210 |
Genetic and epigenetic alterations at the GNAS locus and clinical consequences in Pseudohypoparathyroidism: a new healthcare pathway |
Federica Giachero, Francesca M. Elli, Marta Baricco, Patrizia Matarazzo, Giovanna Mantovani, Luisa de Sanctis |
|
Bone, Growth Plate and Mineral Metabolism |
P2-211 |
Fibrous cortical defects and non-ossifying fibromas in patients with precocious puberty |
Bang Won Lee, Kyung-Sue Shin |
|
Bone, Growth Plate and Mineral Metabolism |
P2-212 |
The effect of high dose oral 17ß estradiol on bone mineralization and body composition in young women with Turner syndrome - a 5 year randomized controlled clinical trial |
Line Cleemann, Kirsten Holm, Hanne Kobbernagel, Bent Kristensen, Sven Olaf Skouby, Andreas Emil Kryger Jensen, Claus Gravholt |
|
Bone, Growth Plate and Mineral Metabolism |
P2-213 |
Comparison of cost benefits and efficacy of Zoledronic acid and Pamidronate in the treatment of Osteogenesis Imperfecta in children. |
Vrinda Saraff, Jaskiran Sahota, Nicola Crabtree, Nick Shaw, Wolfgang Högler |
|
Bone, Growth Plate and Mineral Metabolism |
P2-214 |
TmP/GFR is a useful marker in making a clinical diagnosis of X-linked hypophosphatemic rickets caused by the PHEX gene mutation |
Ryojun Takeda, Kentaro Miyai, Masaki Takagi, Masahiro Goto, Daisuke Ariyasu, Masako Izawa, Junko Igaki, Eri Suzuki, Yoshie Nakamura, Yukihiro Hasegawa |
|
Bone, Growth Plate and Mineral Metabolism |
P2-215 |
Whole body vibration training improves physical function and increases bone and muscle mass in youngsters with mild cerebral palsy |
Silmara Gusso, Patricia Colle, Jose G B Derraik, Janene Biggs, Craig Munns, Wayne Cutfield, Paul Hofman |
|
Bone, Growth Plate and Mineral Metabolism |
P2-216 |
A CASE WITH ACRODYSOSTOSIS AND HORMONE RESISTANCE |
Selma Tunç, Korcan Demir, Filiz Hazan, Özgür Kırbıyık, Eren Soyaltın, Özlem Nalbantoğlu, Melek Yıldız, Hüseyin Anıl Korkmaz, Behzat Özkan |
|
Miscellaneous |
P2-217 |
The spectrum of molecular defects in 64 patients with hypophosphatemic rickets identified by targeted next-generation sequencing. |
Kristina Kulikova, Anna Kolodkina, Evgeny Vasilyev, Vasily Petrov, Fedor Gofman, Anatoly Horkin, Vladimir Kenis, Michael Petrov, Anatoly Tiulpakov |
|
Bone, Growth Plate and Mineral Metabolism |
P2-218 |
NEPHROCALCINOSIS AND NEPHROLITHIASIS IN 36 X-LINKED HYPOPHOSPHATEMIC RICKETS PATIENTS: DIAGNOSTIC IMAGING AND EVALUATION OF RISK FACTORS IN A SINGLE-CENTER STUDY |
Guido de Paula Colares Neto, Fernando Ide Yamauchi, Ronaldo Hueb Baroni, Igor Fontenele, Andrea Cavalanti Gomes, Maria Cristina Chammas, Regina Matsunaga |
|
Bone, Growth Plate and Mineral Metabolism |
P2-219 |
Early increase of the bone formation marker PINP is in a higher degree related to growth response compared to bone mineralization in GH treated prepubertal children |
Ralph Decker, Björn Andersson, Diana Swolin-Eide, Per Magnusson, Berit Kriström, Kerstin Albertsson-Wikland |
|
Bone, Growth Plate and Mineral Metabolism |
P2-220 |
Genotype and phenotype characteristics in 22 patients with Vitamin D Dependent Rickets
Type I (VDDR1) |
Sophia Tahir, Huseyin Demirbilek, Mehmet Nuri Ozbek, Riza Taner Baran, Sibel Tanriverdi, Khalid Hussain |
|
Bone, Growth Plate and Mineral Metabolism |
P2-221 |
Evidence of a link between resting energy expenditure and bone remodelling, glucose homeostasis and adipokine variations in adolescent girls with anorexia nervosa |
Laurent Maimoun, Sebastien Guillaume, Patrick Lefbvre, Pascal Philibert, Helena Bertet, Marie-Christine Picot, Laura Gaspari, Françoise Paris, Maude Sennec, Anne-Marie Dupuys, Philippe Courtet, Eric Thomas, Denis Mariano-Goulart, Jacques Bringer, Eric Renard, Charles Sultan |
|
Bone, Growth Plate and Mineral Metabolism |
P2-222 |
Bone density, HIV infection and antiretroviral treatment: a 10-year follow-up in young patients |
Stefano Mora, Katia Maruca, Alessandro Ambrosi, Maria Puzzovio, Paola Erba, Pilar Nannini, Annarita Benincaso, Silvia Capelli, Vania Giacomet |
|
Bone, Growth Plate and Mineral Metabolism |
P2-223 |
Refractory Hypercalcaemia of Malignancy: Responsiveness to Denosumab and Zoledronate |
Dinesh Giri, Renuka Ramakrishnan, James Hayden, Lynda Brook, Urmi Das, M.Zulf Mughal, Peter Selby, Poonam Dharmaraj, Senthil Senniappan |
|
Bone, Growth Plate and Mineral Metabolism |
P2-224 |
Fractures In Boys With Duchenne Muscular Dystrophy And Their Relationship To Age |
Shuko Joseph, Marina Di Marco, Iain Horrocks, S Faisal Ahmed, S C Wong |
|
Bone, Growth Plate and Mineral Metabolism |
P2-225 |
Early Detection of Increased Bone Turnover among Children and Adolescents with Type 1 Diabetes Mellitus |
Amina Abdel Wahab, Sonia El Sharkawy, Fadia Attia, Mona Amin |
|
Bone, Growth Plate and Mineral Metabolism |
P2-226 |
Association between oxidative stress and bone turnover markers in the obese children |
Pawel Matusik, Magdalena Olszanecka-Glinianowicz, Jerzy Chudek, Ewa Malecka-Tendera |
|
Bone, Growth Plate and Mineral Metabolism |
P2-227 |
Longitudinal bone development in patients with classical congenital adrenal hyperplasia: data using peripheral quantitative computed tomography |
Susanne Bechtold, Leyla Duman, Claudia Weissenbacher, Julia Roeb, Robert Dalla Pozza, Heinrich Schmidt |
|
Bone, Growth Plate and Mineral Metabolism |
P2-228 |
Online Survey to Characterize the Burden of Illness in Children with X-linked Hypophosphatemia (XLH) |
Agnes Linglart MD, PhD, Melita Dvorak-Ewell, PhD, Ayla Marshall, Javier San Martin, MD, Alison Skrinar, PhD |
|
Bone, Growth Plate and Mineral Metabolism |
P2-229 |
Comparison of the response to bisphosphonate treatment between acute lymphoblastic leukaemia and osteogenesis imperfecta type I |
Suma Uday, Anitha Kumaran, Nimasari Ginige, Sophia Sakka, Vrinda Saraff, J Sahota, Nicola Crabtree, Nick Shaw, Wolfgang Högler |
|
Bone, Growth Plate and Mineral Metabolism |
P2-230 |
The relationship between serum 25-hydroxyvitamin D and parathyroid hormone in children |
Hae Soon Kim, Jung In Kang, Ye Jin Han |
|
Bone, Growth Plate and Mineral Metabolism |
P2-231 |
Cinacalcet treatment in girls with hereditary vitamin D resistant rickets |
Erkan Sari, Firat Ozkececi, Onur Akin, Ahmet Bolat, Ediz Yesilkaya |
|
Bone, Growth Plate and Mineral Metabolism |
P2-232 |
Regulation of bone growth via ligand-specific activation of estrogen receptor alpha |
Maryam Iravani, Marie Lagerquist, Claes Ohlsson, Lars Savendahl |
|
Bone, Growth Plate and Mineral Metabolism |
P2-233 |
Teriparatide (rhPTH) therapy in a boy with Hypoparathyroidism-Deafness-Renal dysplasia (HDR) syndrome due to GATA3 mutation |
Dinesh Giri, Senthil Senniappan, Poonam Dharmaraj, Lynne Hatchard, Renuka Ramakrishnan |
|
Bone, Growth Plate and Mineral Metabolism |
P2-234 |
Variable degree of hormonal resistance in patients with Progressive Osseous Heteroplasia |
Kentaro Miyai, Noriko Nishina, Masaki Takagi, Masahiro Goto, Yukihiro Hasegawa |
|
Bone, Growth Plate and Mineral Metabolism |
P2-235 |
Assessment of foramen magnum in early infancy is efficient for patients with achondroplasia |
Chisumi Sogi, Miki Kamimura, Akiko Hakoda, Junko Kanno, Ikuma Fujiwara, Shigeo Kure |
|
Bone, Growth Plate and Mineral Metabolism |
P2-236 |
Body composition measures on different DEXA scanners are not the same |
Udo Meinhardt, Fabienne Witassek, Christiane Fritz, Urs Eiholzer |
|
Bone, Growth Plate and Mineral Metabolism |
P2-237 |
Intrauterine growth restriction, gestational age, steroidal prophylaxis and breastfeeding influence bone mass in prepubertal children |
Annalisa Calcagno, Giovanna Pala, Anna Elsa Maria Allegri, Flavia Napoli, Nadia Fratangeli, Maria Grazia Calevo, Mohamad Maghnie, Natascia Di Iorgi |
|
Bone, Growth Plate and Mineral Metabolism |
P2-238 |
Can vitamin D deficiency cause prolongation in visual evoked potentials? |
Murat Doğan, İlyas Aydin, Sultan Kaba, Keziban Aslı Bala, Özlem Gülpınar |
|
Bone, Growth Plate and Mineral Metabolism |
P2-239 |
Novel CYP27B1 Gene Mutations in Children with Vitamin D-Dependent Rickets Type 1A |
Korcan Demir, Walaa E Kattan, Minjing Zou, Erdem Durmaz, Huda BinEssa, Ozlem Nalbantoglu, Roua A.Al-Rijjal, Brian Meyer, Behzat Ozkan, Yufei Shi |
|
Bone, Growth Plate and Mineral Metabolism |
P2-240 |
Size-corrected bone mineral density is not affected by haematopoietic stem cell transplantation and total body irradiation (HSCT/TBI) in leukaemia survivors |
Christina Wei, Ruth Elson, Rachel Cox, Karin Bradley, John Barton, Michael Stevens, Elizabeth Crowne |
|
Bone, Growth Plate and Mineral Metabolism |
P2-241 |
Quantitative Sonometeric Bone Age (SBA) as a Function of Height and BMI |
Alina German, Nira Koren-Morag, Shmuel Levin, Ze'ev Hochberg |
|
Bone, Growth Plate and Mineral Metabolism |
P2-242 |
THE ASSOCIATION OF ATTENTION DEFICIT HYPERACTIVITY DISORDER (ADHD) AND AUTISM SPECTRUM DISORDERS (ASD) WITH THE MEAN PLATELET VOLUME (MPV) AND VITAMIN D |
Keziban Aslı Bala, Murat Doğan, Tuba Mutluer, Sultan Kaba, Oktay Aslan, Nihat Demir, Lokman Üstyol |
|
Miscellaneous |
P2-243 |
Dyslipidemia in Children with Diabetes |
Pei Kwee Lim, Rashida Vasanwala, Tuck Seng Cheng, Ngee Lek, Yuen Ching Angela Hui, Soo Ting Lim, Fabian Yap |
|
Diabetes and Insulin |
P2-244 |
Diabetes mellitus and hypoparathyroidism in a girl with mitochondrial disease |
Gonul Buyukyilmaz, Nazli Gonc, Goknur Haliloglu, Beril Talim, Alev Ozon, Ayfer Alikasifoglu, Nurgun Kandemir |
|
Diabetes and Insulin |
P2-245 |
Association of ghrelin levels and insulin resistance in small for gestational age rats |
wangkai liu, zhenyu shen, minlian du, siqi zhuang, huamei ma |
|
Diabetes and Insulin |
P2-246 |
Protective Effects of Combined Intervention with Adenovirus Vector Mediated IL-10 and IGF-1 Genes on Endogenous Islet β Cells in Nonobese Diabetes Mice with Onset of Type 1 Diabetes Mellitus |
Tang Li |
|
Diabetes and Insulin |
P2-247 |
A case of Donohue Syndrome : New Genetic Mutation and added phenotypic characteristics |
Fawzia Alyafei, Mahmoud Zyoid, , Ashraf Soliman, Anas Abdulkayoum, Rawia Jarir, Bader Kurdi, Laila Mahmoud |
|
Diabetes and Insulin |
P2-248 |
Genetic analysis and follow-up of 23 neonatal diabetes mellitus patients in China |
Cao bingyan, Gong chunxiu, Wu di, Lu chaoxia, Liu Fang, Liu Xiaojing, Zhang Ying-xian, Gu Yi, Qi Zhan, Li Xiaoqiao, Liu Min, Li Wenjing, Su Chang, Liang Xuejun, Feng Mei |
|
Diabetes and Insulin |
P2-249 |
Level of knowledge about type I diabetes mellitus among nurses employed at endocrinological dispensaries |
Akmaral Tashmanova |
|
Diabetes and Insulin |
P2-250 |
Recombinant human insulin-like growth factor-1 treatment in patients with insulin receptor mutations resulting in Donohue syndrome: a 10-year experience in a tertiary centre. |
Nicola Improda, Harshini Katugampola, Pratik Shah, Hannah Gordon, Rakesh Amin, Catherine J Peters, Robert K Semple, Mehul T Dattani |
|
Diabetes and Insulin |
P2-251 |
Sick day rule: Survey of parents of children with Type 1 diabetes (experience and Knowledge) |
Juliana Chizomam Agwu, S May Ng, J DREW, J EDGE, M KERSHAW, N WRIGHT, C GARDNER |
|
Diabetes and Insulin |
P2-252 |
Brachial Flow Mediated Dilation and its Relation to Osteoprotegerin in Type 1 Diabetes Mellitus |
Eman Sherief, Omneyia Youssef, Karim Abd El-Tawab, Hoda Ez-elarab, Moaz Ibrahim, Nermine Amr |
|
Diabetes and Insulin |
P2-253 |
Value of the intrarenal arterial resistivity indices and different renal biomarkers for early identification of diabetic nephropathy in type 1 diabetic patients. |
Ahmed Battah, Soha Abd El Dayem, Abo El Magd El Bohy, Amal El Shohaby, Nagwa Abd Allah |
|
Diabetes and Insulin |
P2-254 |
Can we rely on finger stick haemoglobin A1c?
Comparison of levels assayed by DCA 2000 with IFCC reference method in a pediatric cohort |
Gianluca Tornese, Nadia Milic, Laura Spetti, Daniela Gembrini, Carmen Loganes, Maria Chiara Pellegrin, Lucia Radillo, Oriano Radillo, Elena Faleschini, Alessandro Ventura |
|
Diabetes and Insulin |
P2-255 |
Significant impact of nocturnal melatonin secretion on obesity-related metabolic disorders in children and adolescents |
Johanna Overberg, Peter Kühnen, Andrea Ernert, Heiko Krude, Susanna Wiegand |
|
Diabetes and Insulin |
P2-256 |
Exposure to phthalates and phenols in relation to gestational blood glucose homeostasis |
Benjamin G. Fisher, Hanne Frederiksen, Anna-Maria Andersson, Anders Juul, A Thankamony, Kenneth K. Ong, David B. Dunger, Ieuan A. Hughes |
|
Diabetes and Insulin |
P2-257 |
Developing a targeted, mobile-health technology (e-book) to promote self-care during diabetes transition |
Andrew Dwyer, Samaita Unal, Severine Emmanouilidis, Marie-Paule Aquarone-Vaucher, Silvia Pichard, Teresa Gyuriga, Joelle Korpes, Francois Jornayvaz, Elena Gonzalez-Rodriguez, Eglantine Elowe-Gruau, Sophie Stoppa, Anne Zanchi-Delacretaz, Jardena Puder, Francesca Amati, Therese Bouthors, Franziska Phan-Hug, Nelly Pitteloud, Michael Hauschild |
|
Diabetes and Insulin |
P2-258 |
CARDIAC AUTONOMIC NEUROPATHY IS HIGHLY PREDICTIVE FOR SURVIVAL IN CHILDREN WITH MAURIAC SYNDROME |
Margarita Arshinkova, Olga Slavcheva, Maia Konstantinova |
|
Diabetes and Insulin |
P2-259 |
Predictors of Cystic Fibrosis-Related Diabetes (CFRD) in Patients with CF and Pancreatic Insufficiency |
Joseph Meyerovitch, Rony Be'eri Berkowiz, Meir Mei-Zahav, Hannah Blau, Huda Mussaffi-Georgy |
|
Diabetes and Insulin |
P2-260 |
Adherence to diabetes care in children and adolescents with Type 1 Diabetes Mellitus in Spain: Results from the CHRYSTAL Study. |
Juan Pedro López Siguero, Luis Alberto Vázquez, Renata Villoro, Dingfeng Jiang, María Merino, Jesús Reviriego, Magaly Perez-Nieves |
|
Diabetes and Insulin |
P2-261 |
Gaining from patient experience on a local level: The introduction of annual questionnaires for children and teenagers with diabetes |
Emily Cottrell, Manju Chandwani, Frances Hanson, James Wong |
|
Diabetes and Insulin |
P2-262 |
Factitious administration of analogue insulin to a 2 year old child |
Nehal Thanawala, Sarah Cheney, Gwen Wark, Mario Thevis, A Thomas, V Tziaferi, James Greening |
|
Diabetes and Insulin |
P2-263 |
Insulin Sensitivity in Adolescents with Gender Dysphoria during Puberty Suppressing Therapy with GnRH Agonists |
Sebastian Schagen, Henriette Delemarre-van de Waal, Sabine Hannema |
|
Diabetes and Insulin |
P2-264 |
Ethnic variation in the correlation of waist circumference to daily insulin requirement in children with type 1 diabetes |
Suma Uday, Shaun Gorman, Richard Feltbower, Mathew Mathai |
|
Diabetes and Insulin |
P2-265 |
IMPORTANCE OF THROMBOCYTE VOLUME PARAMETERS IN TYPE I DIABETES MELLITUS PATIENTS WITH AND WITHOUT CLINICAL FINDINGS OF DIABETIC KETOACIDOSIS |
Dogus Vuralli, Hatice Tatar Aksoy, Arzu Yilmaz, Ozlem Engiz, Yildiz Bilge Dallar |
|
Diabetes and Insulin |
P2-266 |
Increased Arterial Wall Stiffness in Children with Type 1 Diabetes and Poor Metabolic Control: An Early Marker of Vascular Complications? |
Barbora Obermannova, Lenka Petruzelkova, Terezie Sulakova, Zdenek Sumnik |
|
Diabetes and Insulin |
P2-267 |
Glycaemic dysregulation in transfusion dependent thalassaemia patient in a children’s hospital |
SONG HAI LIM, WILKINS LIM, THIAN LIAN SOO |
|
Diabetes and Insulin |
P2-268 |
MODY-GCK and MODY-HNF1A in children and adolescents in Russian population |
Elena Sechko, Lubov Zilberman, Olga Ivanova, Tamara Kuraeva, Valentina Peterkova |
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Diabetes and Insulin |
P2-269 |
Clinical and hormonal profile in Mini-puberty of daughters born after pregnancies with diabetes: preliminary report |
Joel Riquelme, Daniela Martínez, Teresa Sir-Petermann, Claudio Villarroel, Ethel Codner |
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Diabetes and Insulin |
P2-270 |
Growth and Endocrinopathy in Wolfram Syndrome: the experience of a nationally commissioned specialist clinic. |
Melanie Kershaw, Susan Gleeson, Denise Williams, Rajat Gupta, John Ainsworth, Archana Kulkarni, Liam McCarthy, Lesley MacPherson, Rachel Bates, Marie McGee, Timothy G Barrett |
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Diabetes and Insulin |
P2-271 |
Evaluation of a Novel Tool to Adjust Insulin Boluses based on Continuous Glucose Monitoring Trend Arrows and Insulin Sensitivity (Trend Arrow Adjustment Tool©) in Children and Youth with Type 1 Diabetes using Insulin Pump Therapy |
Emmeline Heffernan, Margaret Lawson, Brenda Bradley, Jennilea Courtney, Christine Richardson |
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Diabetes and Insulin |
P2-272 |
Circulating GLP-1 in infants born small-for-gestational-age: breast-feeding versus formula-feeding |
Marta Díaz, Judit Bassols, Giorgia Sebastiani, Abel López-Bermejo, Lourdes Ibáñez, Francis de Zegher |
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Diabetes and Insulin |
P2-273 |
Utility of estimated glucose disposal rate and fat mass percentage for predicting metabolic syndrome in children and adolescents with type 1 diabetes |
Ozlem Koken, Cengiz Kara, Gulay Can Yilmaz, Murat Aydin |
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Diabetes and Insulin |
P2-274 |
Friedreich’s Ataxia presenting with Diabetes Mellitus in an adolescent |
Serpil Bas, Saygin Abali, Zeynep Atay, Ziya Gurbanov, Dilsad Turkdogan, Serap Turan, Abdullah Bereket |
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Diabetes and Insulin |
P2-275 |
DO PANCREATIC FUNCTIONS PREDICT CARDIAC AND LIVER IRON LOADING IN TRANSFUSION-DEPENDENT BETA THALASSEMIA MAJOR PATIENTS USING CARDIOVASCULAR AND LIVER T2-STAR (T2*)MAGNETIC RESONANCE ? |
Galila Mokhtar, Wafaa Ibrahim, Nancy Elbarbary, Randa Matter, Ahmed Ibrahim, Safa Sayed |
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Diabetes and Insulin |
P2-276 |
Determinants of outcome of children with type 1 diabetes in Cameroon. |
Loveline Niba, Benedikt Aulinger, Wilfred Mbacham, Klaus Parhofer |
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Diabetes and Insulin |
P2-277 |
Psychosocial Screening in children with Type 1 Diabetes in Ireland |
Elena Hennessy, Patricia Gallagher, Triona Butler, Norma O’Toole, Susan M O’Connell, Stephen MP O’Riordan |
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Diabetes and Insulin |
P2-278 |
Neonatal Diabetes –Experience from a single center in Sri Lanka |
Navoda Atapattu, Vasundara Vithanage, Kirikankanange Shamya Harshini de Silva, Daham Haresha de Silva, Mala Mangalika Jayathilaka, Andrew T Hattersley, Sian Ellard, Sarah E. Flanagan, J.A.L Houghton, Khalid Hussain |
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Diabetes and Insulin |
P2-279 |
Dive: a serious game for diabetes therapeutic education in children |
Cecile Godot, Nadine Lepage, Isabelle Jourdon, Marie-Eve Schmidt, Pierre Maccini, Michel Polak, Jacques Beltrand |
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Diabetes and Insulin |
P2-280 |
GLUCOSE AND INSULIN RESPONSE AT STANDARD ORAL GLUCOSE LOAD AND FOLLOWED SUBMAXIMAL TREADMILL TEST IN OBESE ADOLESCENTS |
Tetyana Chaychenko, Olena Rybka |
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Diabetes and Insulin |
P2-281 |
Insulin Dynamics and Biochemical Markers for Predicting Impaired Glucose Tolerance in Thai Obese Youth |
Sirapassorn Tirabanchasak, Sukumarn Siripunthana, Vichit Supornsilchai, Suttipong Wacharasindhu, Taninee Sahakitrungruang |
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Diabetes and Insulin |
P2-282 |
Total-Body Irradiation is a major risk factor for young adult onset diabetes mellitus and hyperlipidemia in childhood cancer survivors after hematopoietic stem cell transplantation. |
Ryuichi Nakagawa, Atsumi Tsuji, Yuki Aoki, Keisuke Nakajima, Akito Sutani, Yuichi Miyakawa, Kei Takasawa, Daisuke Tomizawa, Masatoshi Takagi, Kenichi Kashimada, Tomohiro Morio |
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Diabetes and Insulin |
P2-283 |
Variables in Diabetic Children and Adolescents associated with High, Acceptable and Low range of Glycosylated Haemoglobin (HbA1c) in a DGH setting – An Analysis |
Karthi Manoharan, Sharon Lim |
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Diabetes and Insulin |
P2-284 |
In-patient care for children with type 1 diabetes- a regional audit in the Yorkshire and Humber region in the north of England. |
Suma Uday, Nadia Amin, Fiona Campbell, James Yong |
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Diabetes and Insulin |
P2-285 |
Implementation of Effective Transition from Paediatric to Adult Diabetes Care: Epidemiological and clinical characteristics. A pioneering experience in North Africa. |
ESSADDAM Leïla, TURKI Zinet, FITOURI Zohra, BEN SLAMA Claude, MATOUSSI Nadia, BEN BECHER Saayda |
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Diabetes and Insulin |
P2-286 |
Assessment of Ventricular Function by Tissue Doppler Echocardiography in Children and Adolescents with Type 1 Diabetes Mellitus |
Shereen Abdelghaffar, Nermeen Salah, Mona Attia, Mona Hafez, Mona Mamdouh, Abeer Atef, Fatma Elmougy, Sahar Abdelaty, Amany Ibrahim, Hend Mehawed, Noha Musa, Noha Arafa, Marwa Farouk, Mohamed Ismail, Faten Abdelaziz, Aya Fattouh, Eman Hussein, Isis Ghali |
|
Diabetes and Insulin |
P2-287 |
Incidence of Type 1 Diabetes among Korean Children and Adolescents in 2012-2013: Analysis of Data from the Nationwide Registry of Korea |
Jae Hyun Kim, Young Ah Lee, Sei Won Yang, Choong Ho Shin |
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Diabetes and Insulin |
P2-288 |
Functional condition of the kidneys (K/DOQI , 2002) by ACE gene I/D polymorphism in children and adolescents with type I diabetes mellitus |
Gulnara Rakhimova, Akida Sadikova, Nasiba Alimova |
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Diabetes and Insulin |
P2-289 |
LONGITUDINAL STUDY OF IRISH CHILDREN AND ADOLESCENTS ON CONTINUOUS SUBCUTANEOUS INSULIN INFUSION (CSII) |
Mary-Ellen Bohane, Niamh McGrath, Aoife Carroll, Dympna Devenney, Ciara McDonnell, Nuala Murphy |
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Diabetes and Insulin |
P2-290 |
C peptide variation after the diagnosis of type 1 diabetes in pediatric age |
Joana Correia, Catarina Mendes, Marina Pinheiro, Clara Preto, Helena Cardoso, Maria João Oliveira, Teresa Borges |
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Diabetes and Insulin |
P2-291 |
Metformin Utilizat |