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Inas Mazen

Showing results (31-40 of 49) with videos related to

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American Journal of Medical Genetics. Part A|August 19, 2015
Clinical and molecular characterization of seven Egyptian families with autosomal recessive robinow syndrome: Identification of four novel ROR2 gene mutationsMona Aglan, Khalda Amr, Samira Ismail, et al.
American Journal of Medical Genetics. Part A|December 22, 2018
GAPO syndrome in seven new patients: Identification of five novel ANTXR1 mutations including the first large intragenic deletionMohamed S Abdel-Hamid, Samira Ismail, Maha S Zaki, et al.
Endocrine Connections|October 19, 2025
Continuity of care in Klinefelter syndrome: age-adapted modules for standardized clinical data collection (I-KS)Corinna Grasemann, Claus H Gravholt, Lexi Breen, et al.
European Journal of Endocrinology|March 5, 2014
Analysis of the gene coding for steroidogenic factor 1 (SF1, NR5A1) in a cohort of 50 Egyptian patients with 46,XY disorders of sex developmentSally Tantawy, Inas Mazen, Hala Soliman, et al.
The Journal of Clinical Endocrinology and Metabolism|July 18, 2015
Severe Early-Onset Obesity Due to Bioinactive Leptin Caused by a p.N103K Mutation in the Leptin GeneMartin Wabitsch, Jan-Bernd Funcke, Julia von Schnurbein, et al.
American Journal of Medical Genetics. Part A|April 23, 2018
Identification of a novel homozygous ALX4 mutation in two unrelated patients with frontonasal dysplasia type-2Mona El-Ruby, Alaa El-Din Fayez, Sara H El-Dessouky, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|July 22, 2021
Expanding DSD Phenotypes Associated with Variants in the DEAH-Box RNA Helicase DHX37Housna Zidoune, Laetitia Martinerie, Daisylyn S Tan, et al.
Science Advances|January 4, 2023
In vitro cellular reprogramming to model gonad development and its disordersNitzan Gonen, Caroline Eozenou, Richard Mitter, et al.
The Journal of Clinical Endocrinology and Metabolism|November 3, 2025
Gonadal Function And Its Evolution In 46, XX Testicular/Ovotesticular DSDMargherita Sepich, Silvano Bertelloni, Nina Tyutyusheva, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|August 5, 2021
Testosterone Therapy and Its Monitoring in Adolescent Boys with Hypogonadism: Results of an International Survey from the I-DSD RegistryMarianna R Stancampiano, Angela K Lucas-Herald, Jillian Bryce, et al.
Pageof 5

Showing results (31-40 of 49) with videos related to

Sort By:
Pageof 5
American Journal of Medical Genetics. Part A|August 19, 2015
Clinical and molecular characterization of seven Egyptian families with autosomal recessive robinow syndrome: Identification of four novel ROR2 gene mutationsMona Aglan, Khalda Amr, Samira Ismail, et al.
American Journal of Medical Genetics. Part A|December 22, 2018
GAPO syndrome in seven new patients: Identification of five novel ANTXR1 mutations including the first large intragenic deletionMohamed S Abdel-Hamid, Samira Ismail, Maha S Zaki, et al.
Endocrine Connections|October 19, 2025
Continuity of care in Klinefelter syndrome: age-adapted modules for standardized clinical data collection (I-KS)Corinna Grasemann, Claus H Gravholt, Lexi Breen, et al.
European Journal of Endocrinology|March 5, 2014
Analysis of the gene coding for steroidogenic factor 1 (SF1, NR5A1) in a cohort of 50 Egyptian patients with 46,XY disorders of sex developmentSally Tantawy, Inas Mazen, Hala Soliman, et al.
The Journal of Clinical Endocrinology and Metabolism|July 18, 2015
Severe Early-Onset Obesity Due to Bioinactive Leptin Caused by a p.N103K Mutation in the Leptin GeneMartin Wabitsch, Jan-Bernd Funcke, Julia von Schnurbein, et al.
American Journal of Medical Genetics. Part A|April 23, 2018
Identification of a novel homozygous ALX4 mutation in two unrelated patients with frontonasal dysplasia type-2Mona El-Ruby, Alaa El-Din Fayez, Sara H El-Dessouky, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|July 22, 2021
Expanding DSD Phenotypes Associated with Variants in the DEAH-Box RNA Helicase DHX37Housna Zidoune, Laetitia Martinerie, Daisylyn S Tan, et al.
Science Advances|January 4, 2023
In vitro cellular reprogramming to model gonad development and its disordersNitzan Gonen, Caroline Eozenou, Richard Mitter, et al.
The Journal of Clinical Endocrinology and Metabolism|November 3, 2025
Gonadal Function And Its Evolution In 46, XX Testicular/Ovotesticular DSDMargherita Sepich, Silvano Bertelloni, Nina Tyutyusheva, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|August 5, 2021
Testosterone Therapy and Its Monitoring in Adolescent Boys with Hypogonadism: Results of an International Survey from the I-DSD RegistryMarianna R Stancampiano, Angela K Lucas-Herald, Jillian Bryce, et al.
Pageof 5