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

par El-Gilany, Abdel-Hady, Yahia, Sohier, Wahba, Yahya
Publié dans Ann Saudi Med (2017)

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

par Mitwalli, Maha, Wahba, Yahya, Shaltout, Ali, Gouida, Mona
Publié dans Cent Eur J Immunol (2018)

Cluster of Differentiation 96 in Children with Acute Leukemia: A Single Center Cohort Study

par Mohammad, Hanan, Wahba, Yahya, Gouida, Mona, Shaltout, Ali
Publié dans Indian J Hematol Blood Transfus (2019)

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

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

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

par Yahia, Sohier, El-Hadidy, Mohamed, El-Gilany, Abdel-Hady, Amdel-Hady, Dina, Wahba, Yahya, Al-Haggar, Mohammad
Publié dans Ann Saudi Med (2014)

Psychiatric Disorders and Quality of Life in Egyptian Patients with Chronic Immune Thrombocytopenic Purpura: A Single Center Study

par Yahia, Sohier, Wahba, Yahya, El-Gilany, Abdel-Hady, Abdelmabood, Suzy, El-Hadidy, Mohamed Adel, Darwish, Ahmad, Mansour, Ahmed K.
Publié dans Indian J Hematol Blood Transfus (2018)

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

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