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Showing page 1 of results 1 - 10 of about 1000 matches for "wayte-a"

100% match
16 hit(s)
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37kb

A Nation-Wide Questionnaire Survey Targeting Japanese Pediatric Endocrinologists Regarding Transitional Care in Pediatric and Adolescent Cancer Patients | ESPE2019
Yoko Miyoshi; Tohru Yorifuji; Susumu Yokoya; Keisuke Nagasaki; Masanobu Kawai; Hiroyuki Ishiguro; Satoshi Okada; Junko Kanno; No
http://abstracts.eurospe.org/hrp/0092/hrp0092P1-243
Published: 2019-08-22

91% match
20 hit(s)
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46XY, DSD with Hemolytic Uremic Syndrome as the Primary Manifestation——Denys–Drash Syndrome Caused by WT1 Gene Mutation | ESPE2019
jun zhang; song guo; qiuli chen; huamei ma; yanhong li; hongshan chen; minlian du; cheng; minyi ye
http://abstracts.eurospe.org/hrp/0092/hrp0092P3-241
Published: 2019-08-22

91% match
18 hit(s)
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The Encephalopathy as Complication of Hashimoto Thyroiditis in Children: A Wide Variety of Clinical Manifestations | ESPE2019
Paola Chiarello; Valentina Talarico; Maria Concetta Galati; Giuseppe Raiola
http://abstracts.eurospe.org/hrp/0092/hrp0092P2-300
Published: 2019-08-22

51% match
26 hit(s)
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Large Spectrum of DSD Phenotype Caused by Pathogenic Variants in Wilms Tumor Suppressor Gene 1 | ESPE2019
Maria Tereza Martins Ferrari; Sorahia Domenice; Berenice Bilharino Mendonça; Daniela Rodrigues Moraes; Rafael Loch Batista; Nat
http://abstracts.eurospe.org/hrp/0092/hrp0092P1-270
Published: 2019-08-22

39% match
14 hit(s)
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Novel Heterozygous Mutation in Wilms Tumor 1 Gene in Patient with Mixed Gonadal Dysgenesis | ESPE2019
Heba Hassan; Mona Essawi; Mona Mekkawy; Alaa Kamel; Inas Mazen
http://abstracts.eurospe.org/hrp/0092/hrp0092P3-230
Published: 2019-08-22

32% match
12 hit(s)
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A Rare case of Neonatal Hypocalciuric Hypercalcemia Complicated with Arrhythmia | ESPE2019
Yuto Arai; Ryo Okumura; Soichiro Wada; Keiji Haseyama; Shuji Sai
http://abstracts.eurospe.org/hrp/0092/hrp0092P2-30
Published: 2019-08-22

31% match
12 hit(s)
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A Female Infant with Severe Salt-Wasting due to Aldosterone Synthase Deficiency, Initially Mimicking Adrenal Insufficiency | ESPE2019
Simone Krull; Clemens Kamrath; Egbert Schulze; Sofia Giatropoulou; Stefan Wudy
http://abstracts.eurospe.org/hrp/0092/hrp0092P3-4
Published: 2019-08-22

31% match
12 hit(s)
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New Mutation of the PDX-1 Gene Causes MODY Type 4 Diabetes in a 17 year old girl with Good Response to Oral Antidiabetics | ESPE2019
Sofia Giatropoulou; Clemens Kamrath; Simone Krull; Stefan Wudy
http://abstracts.eurospe.org/hrp/0092/hrp0092P2-66
Published: 2019-08-22

31% match
12 hit(s)
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Height in Infants Aged 1 Year with Classic Congenital Adrenal Hyperplasia is Related to their Urinary Steroid Metabolome | ESPE2019
Clemens Kamrath; Clemens Friedrich; Michaela F. Hartmann; Stefan A. Wudy
http://abstracts.eurospe.org/hrp/0092/hrp0092P1-301
Published: 2019-08-22

31% match
12 hit(s)
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Individual Patterns of Objectively Measured Adherence to Growth Hormone Treatment and its Effect on Growth in Prepubertal Children with Growth Hormone Deficiency | ESPE2019
Dommelen Paula van; Jan M Wit; Ekaterina Koledova
http://abstracts.eurospe.org/hrp/0092/hrp0092P1-221
Published: 2019-08-22

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