N. Waked

Association of Plasminogen Activator Inhibitor 1 (PAI-1) 4G/5G Polymorphism and Susceptibility to SLE in Egyptian Children and Adolescents: A Multicenter Study

H. Shehata, M. Attia, Nagwa E. Akeel, 2020, Journal of inflammation research.

Association of interleukin-17A gene polymorphisms and susceptibility to systemic lupus erythematosus in Egyptian children and adolescents: a multi-centre study

A. Elhewala, A. Sobeih, A. Sherif, 2020, Lupus.

Vitamin D receptor gene FokI polymorphism in Egyptian children and adolescents with SLE: A case-control study

A. Khalil, M. Fathy, Y. Ali, 2017, Lupus.

Vitamin D deficiency and vitamin D receptor FokI polymorphism as risk factors for COVID-19

Muaddi Alharbi, H. Shehata, Thoraya A Hosny, 2022, Pediatric Research.

Ficolin‐1 gene (FCN1) −144 C/A polymorphism is associated with adverse outcome of severe pneumonia in the under‐five Egyptian children: A multicenter study

M. Abdel-Aziz, A. Elhewala, N. Abdelaal, 2020, Pediatric pulmonology.

Clinical, neuroimaging, and genetic characteristics of megalencephalic leukoencephalopathy with subcortical cysts in Egyptian patients.

I. Mahmoud, L. Selim, Marwa Salah Mahmoud, 2014, Pediatric neurology.

Vitamin D deficiency and vitamin D receptor FokI polymorphism as risk factors for COVID-19

Muaddi Alharbi, H. Shehata, Thoraya A Hosny, 2022, Pediatric Research.