ESPE Abstracts Search

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Severe 5 Alpha Reductase 2 Deficiency with Aphallia is Caused by p.Y91H SRD5A2 Mutation and is Responsive to Dihydrotestosterone Administration During Childhood | ESPE2016
Adi Auerbach; Shokrun Ariella Weinberg; Najwa Abdelhak; Eran Lavi; Guy Hidas; Yehezkel Landau; Ephrat Levy-Lahad; David Zangen
http://abstracts.eurospe.org/hrp/0086/hrp0086p1-p349.htm
Published: 2016-08-19

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NKX2-2 Human Mutation Causes Neonatal Diabetes followed by Severe Infantile Obesity Associated with Paradoxical Upregulated Ghrelin Levels - Do Beta-cells Secrete Ghrelin? | ESPE2018
Adi Auerbach; Amitay Cohen; Eran Lavi; Najwa Abdulhaq; Ariella Weinberg Shokrun; Ephrat Levy-Lahad; Rina Hemi; Zangen David
http://abstracts.eurospe.org/hrp/0089/hrp0089p3-p125.htm
Published: 2018-08-28

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Neonatal Diabetes due to NKX2.2 Mutation - Genotype, Clinical Phenotype and Therapeutic Challenges in a Very Low Birth Weight Diabetic Neonate | ESPE2016
Adi Auerbach; Noa Ofek Shlomai; Ariella Weinberg Shokrun; Ephrat Levy-Lahad; David Zangen
http://abstracts.eurospe.org/hrp/0086/hrp0086rfc9.1.htm
Published: 2016-08-19

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Founder Effect and the Clinical and Molecular Characteristics in a Cohort of Classical and Non-Classical Congenital Lipoid Adrenal Hyperplasia Due To StAR Mutations | ESPE2015
Abdulsalam Abu-Libdeh; Ariella Weinberg Shokrun; Ephrat Levy-Lahad; Osnat Admoni; Yardena Tenenbaum-Rakover; David Zangen
http://abstracts.eurospe.org/hrp/0084/hrp0084p1-9.htm
Published: 2015-08-26

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