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List of works by Yahya Wahba

A novel fibrillin-1 mutation in an egyptian marfan family: A proband showing nephrotic syndrome due to focal segmental glomerulosclerosis.

scientific article published in January 2017

CD40 and CD72 expression and prognostic values among children with systemic lupus erythematosus: a case-control study

scientific article published on 22 July 2020

CYP2C9 (*2&*3) and CYP2C19 (*2&*3) polymorphisms among children with nonlesional epilepsy: a single-center study

scientific article published on 18 July 2020

Camurati-Engelmann disease: New clinical insights in an Egyptian case report

scientific article published on 21 September 2017

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

scientific article published on 05 June 2019

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

scientific article published on November 2014

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

scientific article published on 28 July 2011

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

scientific article published on 30 October 2018

Mutation analysis of the GLUT2 gene in three unrelated Egyptian families with Fanconi–Bickel syndrome: revisited gene atlas for renumbering ⬇️

scientific article published on February 18, 2012

Novel homozygous SLC29A3 mutations among two unrelated Egyptian families with spectral features of H-syndrome.

scientific article published on 4 June 2014

Oxidative stress and vitamin D receptor BsmI gene polymorphism in Egyptian children with systemic lupus erythematosus: a single center study

scientific article published on 01 May 2019

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

scientific article

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

scientific article published on 11 October 2018

Rapunzel syndrome (gastric trichobezoar), a rare presentation with generalised oedema: case report and review of the literature.

scientific article

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

scientific article published on 23 January 2013

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