Polymorphisms of the sodium voltage-gated channel, alpha subunit 1 (SCN1A -A3184G) gene among children with non-lesional epilepsy: a case-control study

por Ghazala, Esraa, Shahin, Doaa A., Wahba, Yahya
Publicado 2022

Prevalence of congenital heart diseases in children with Down syndrome in Mansoura, Egypt: a retrospective descriptive study

por El-Gilany, Abdel-Hady, Yahia, Sohier, Wahba, Yahya
Publicado 2017

Lymphocyte subgroups and recurrent infections in children with Down syndrome – a prospective case control study

por Mitwalli, Maha, Wahba, Yahya, Shaltout, Ali, Gouida, Mona
Publicado 2018

Prevalence of Helicobacter pylori infection among children with primary nephrotic syndrome: a cross-sectional study

por Mahmoud, Ahmed, Bakr, Ashraf, Elsaid, Afaf, Wahba, Yahya
Publicado 2020

Genetic and biochemical studies of hepatic carcinoma in the Egyptian population

por Elkhoudary, Amany F, Elmougy, Rehab, Elsaid, Afaf, Wahba, Yahya, Abdel-Aziz, Abdel-Aziz F
Publicado 2021

Fanconi Bickel Syndrome: Novel Mutations in GLUT 2 Gene Causing a Distinguished Form of Renal Tubular Acidosis in Two Unrelated Egyptian Families

por Al-Haggar, Mohammad, Sakamoto, Osamu, Shaltout, Ali, El-Hawary, Amany, Wahba, Yahya, Abdel-Hadi, Dina
Publicado 2011

Cell Death Markers in Children with Immune Thrombocytopenic Purpura: A Preliminary Study

por Yahia, Sohier, Eldars, Waleed, Eldegla, Heba, Mansour, Ahmed K., Guaida, Mouna, Abdelkader, Mohamed S. A., Wahba, Yahya
Publicado 2023

Disruptive behavior in Down syndrome children: a cross-sectional comparative study

por Yahia, Sohier, El-Hadidy, Mohamed, El-Gilany, Abdel-Hady, Amdel-Hady, Dina, Wahba, Yahya, Al-Haggar, Mohammad
Publicado 2014

Sporadic Fibrodysplasia Ossificans Progressiva in an Egyptian Infant with c.617G > A Mutation in ACVR1 Gene: A Case Report and Review of Literature

por Al-Haggar, Mohammad, Ahmad, Nermin, Yahia, Sohier, Shams, Amany, Hasaneen, Bothina, Hassan Hassan, Rasha, Wahba, Yahya, Salem, Nanees Abdel-Badie, Abdel-Hady, Dina
Publicado 2013