Whole exome sequencing identifies a new mutation in the SLC19A2 gene leading to thiamine‐responsive megaloblastic anemia in an Egyptian family

by Khalda Amr, Patrycja Pawlikowska, Said Aoufouchi, Filippo Rosselli, Ghada El‐Kamah
Published 2019-07-01

A novel mutation in the leptin gene (W121X) in an Egyptian family

by Inas Mazen, Khalda Amr, Sally Tantawy, I. Sadaf Farooqi, Mona El Gammal
Published 2014-01-01

Genetic susceptibility for insulin resistance among Egyptian women

by Moushira Errfan Zaki, Khalda Amr, Asmaa E. Elkhouly, Naglaa Abu-Mandil Hassan
Published 2016-06-01

Clinical and Mutational Spectrum of Xeroderma Pigmentosum in Egypt: Identification of Six Novel Mutations and Implications for Ancestral Origins

by Eman Rabie, Khalda Amr, Suher Zada, Heba El-Sayed, Mohamad El Darouti, Ghada El-Kamah
Published 2021-02-01

Association of vitamin D receptor gene polymorphism (VDR) with vitamin D deficiency, metabolic and inflammatory markers in Egyptian obese women

by Moushira Zaki, Sanaa Kamal, Walaa A. Basha, Eman Youness, Wafaa Ezzat, Hala El-Bassyouni, Khalda Amr
Published 2017-09-01

Higher Expression of Toll-like Receptors 3, 7, 8, and 9 in Pityriasis Rosea

by Mostafa Abou El-Ela, Mohamed El-Komy, Rania Abdel Hay, Rehab Hegazy, Amin Sharobim, Laila Rashed, Khalda Amr
Published 2017-03-01