S. Ekladious

CD209-336A/G promotor polymorphism and its clinical associations in sickle cell disease Egyptian Pediatric patients.

R. Afifi, S. Yousry, R. E. Hussein, 2017, Hematology/oncology and stem cell therapy.

Genetic profiling of CAH Egyptian children: rapid guide to clinical interpretation of common mutations

M. Hafez, N. Musa, A. Ibrahim, 2020, Journal of Endocrinological Investigation.

ASSOCIATION OF HEME OXYGENASE-1 HMOX-1 GENE POLYMORPHISM WITH SICKLE CELL DISEASE IN EGYPTIAN PATIENTS

N. Zayed, R. Hassan, A. Kamal, 2006 .

CYP21A2 genetic profile in 14 Egyptian children with suspected congenital adrenal hyperplasia: a diagnostic challenge

M. Hafez, N. Musa, A. Ibrahim, 2018, Annals of the New York Academy of Sciences.

Validation of a Proposed Warfarin Dosing Algorithm Based on the Genetic Make-Up of Egyptian Patients

S. Sharaf, M. S. Issac, Hazem S. Abou-Youssef, 2013, Molecular Diagnosis & Therapy.

Comparative study between single versus dual trigger for poor responders in GnRH‐antagonist ICSI cycles: A randomized controlled study

A. Maged, A. Shohayeb, E. Hussein, 2020, International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics.

Highly Sensitive Serum miRNA Panel for the Diagnosis of Hepatocellular Carcinoma in Egyptian Patients with HCV-Related HCC.

M. Khairy, A. Elsharkawy, A. Yosry, 2022, Laboratoriums Medizin.

Impact of shift work on sleep problems, hormonal changes, and features of metabolic syndrome in a sample of Egyptian industrial workers: a cross-sectional study

A. Samir, Marwa El-Sharkawy, S. Ekladious, 2018 .