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Ariella Weinberg Shokrun
Ariella Weinberg Shokrun
Medicine
Endocrinology
Internal medicine
Mutation
Neonatal diabetes
4
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The Novel R211Q POP1 Homozygous Mutation Causes Severe Short Stature But Uniquely Only Subtle Skeletal Dysplasia
2018
Maha Abdulhadi-Atwan
Tehila Klopshtock
Muna Sharaf
Ariella Weinberg Shokrun
Ephrat Levy-Lahad
David Zangen
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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?
2018
Adi Auerbach
Amitay Cohen
Eran Lavi
Najwa Abdulhaq
Ariella Weinberg Shokrun
Ephrat Levy-Lahad
Rina Hemi
Zangen David
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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
2016
Adi Auerbach
Noa Ofek Shlomai
Ariella Weinberg Shokrun
Ephrat Levy-Lahad
David Zangen
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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
2015
Abdulsalam Abu Libdeh
Ariella Weinberg Shokrun
Ephrat Levy-Lahad
Osnat Admoni
Yardena Tenenbaum-Rakover
David Zangen
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