Scientific Programme, ePosters & Abstracts
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Neonatal Severe Hyperparathyroidism - Using Genetics to Determine Treatment | ESPE2019 Ziv Carmit Avnon; Rachel Beeri; Ephrat Levy-Lahad; Adi Aurbach; Floris Levy-Khademi http://abstracts.eurospe.org/hrp/0092/hrp0092P3-296 Published: 2019-08-22
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The Novel Founder Homozygous V225M Mutation in the 17HSDB3 Gene Causes Aberrant Splicing and Severe XY-DSD | ESPE2019 Floris Levy-Khademi; Sharon Zeligson; Tehila Klopstock; Boris Chertin; Carmit Avnon-Ziv; Paul Renbaum; Eran Lavi; Muna Sharaf; S http://abstracts.eurospe.org/hrp/0092/hrp0092P1-128 Published: 2019-08-22
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The Founder Homozygous NR5A1 Gene Mutation p.R103Q Causes Asplenia and Severe XY-DSD and XX-DSD in a Palestinian Cohort | ESPE2019 Maha Abdulhadi-Atwan; Guy Hidesh; Abdulsalam Abulibdeh; Harry Hirsch; Tehila Klopstock; Ephrat Levy-Lahad; David Zangen http://abstracts.eurospe.org/hrp/0092/hrp0092RFC3.3 Published: 2019-08-22
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A Novel Genetic Aetiology for Familial Neonatal Central Diabetes Insipidus | ESPE2019 Eran lavi; Muna Sharaf; Abdulsalam Abu-Libdeh; Pinchas Renbaum; Ephrat Levy-Lahad; David Zangen http://abstracts.eurospe.org/hrp/0092/hrp0092FC11.3 Published: 2019-08-22
Neonatal Severe Hyperparathyroidism - Using Genetics to Determine Treatment | ESPE2019 Ziv Carmit Avnon; Rachel Beeri; Ephrat Levy-Lahad; Adi Aurbach; Floris Levy-Khademi http://abstracts.eurospe.org/hrp/0092/hrp0092p3-296.html Published: 2019-08-22
The Novel Founder Homozygous V225M Mutation in the 17HSDB3 Gene Causes Aberrant Splicing and Severe XY-DSD | ESPE2019 Floris Levy-Khademi; Sharon Zeligson; Tehila Klopstock; Boris Chertin; Carmit Avnon-Ziv; Paul Renbaum; Eran Lavi; Muna Sharaf; S http://abstracts.eurospe.org/hrp/0092/hrp0092p1-128.html Published: 2019-08-22
The Founder Homozygous NR5A1 Gene Mutation p.R103Q Causes Asplenia and Severe XY-DSD and XX-DSD in a Palestinian Cohort | ESPE2019 Maha Abdulhadi-Atwan; Guy Hidesh; Abdulsalam Abulibdeh; Harry Hirsch; Tehila Klopstock; Ephrat Levy-Lahad; David Zangen http://abstracts.eurospe.org/hrp/0092/hrp0092rfc3.3.html Published: 2019-08-22
A Novel Genetic Aetiology for Familial Neonatal Central Diabetes Insipidus | ESPE2019 Eran lavi; Muna Sharaf; Abdulsalam Abu-Libdeh; Pinchas Renbaum; Ephrat Levy-Lahad; David Zangen http://abstracts.eurospe.org/hrp/0092/hrp0092fc11.3.html Published: 2019-08-22
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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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The Novel R211Q POP1 Homozygous Mutation Causes Severe Short Stature But Uniquely Only Subtle Skeletal Dysplasia | ESPE2018 Maha Abdulhadi-Atwan; Tehila Klopshtock; Muna Sharaf; Ariella Weinberg-Shokrun; Ephrat Levy-Lahad; David Zangen http://abstracts.eurospe.org/hrp/0089/hrp0089rfc2.6.htm Published: 2018-08-28
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