All Stories

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

    Article • Lupus, July 2020, SAGE Publications

    Assistant Professor Yahya Wahba

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

    Article • Acta Neurologica Belgica, July 2020, Springer Science + Business Media

    Assistant Professor Yahya Wahba

  3. Neurocutaneous melanosis is not always a benign disease

    Article • Indian Journal of Dermatology Venereology and Leprology, January 2020, Medknow

    Assistant Professor Yahya Wahba

  4. Comparison of Soybean-based Oil and MCT-olive-fish-soy Oil Intravenous Lipid Emulsions on Soluble Adhesion Markers in Preterm Neonates with Sepsis: A Randomized Controlled Trial

    Article • Indian Pediatrics, August 2019, Springer Science + Business Media

    Assistant Professor Yahya Wahba

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

    Article • Indian Journal of Hematology and Blood Transfusion, June 2019, Springer Science + Business Media

    Assistant Professor Yahya Wahba

  6. Vitamin D receptor gene (VDR) and oxidative stress (OS) play important roles in pathogenesis of SLE.

    Article • Lupus, May 2019, SAGE Publications

    Assistant Professor Yahya Wahba

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

    Article • Indian Journal of Hematology and Blood Transfusion, October 2018, Springer Science + Business Media

    Assistant Professor Yahya Wahba

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

    Article • Central European Journal of Immunology, January 2018, Termedia Sp. z.o.o.

    Assistant Professor Yahya Wahba

  9. Pre versus post application of a 0.12% chlorhexidine based oral hygiene protocol in an Egyptian pediatric intensive care unit: Practice and effects

    Article • The Egyptian Journal of Critical Care Medicine, December 2017, Wolters Kluwer Health

    Assistant Professor Yahya Wahba

  10. Rapunzel syndrome: An Egyptian Case Report

    Article • Paediatrics and International Child Health, October 2017, Taylor & Francis

    Assistant Professor Yahya Wahba, Sohier Yahia

  11. Camurati–Engelmann disease: New clinical insights in an Egyptian case report

    Article • Journal of Orthopaedic Science, September 2017, Elsevier

    Assistant Professor Yahya Wahba

  12. Prevalence of congenital heart diseases in down syndrome in Mansoura ,Egypt

    Article • Annals of Saudi Medicine, September 2017, King Faisal Specialist Hospital and Research Centre

    Prof Abdel-Hady A El-Gilany, Assistant Professor Yahya Wahba, Sohier Yahia

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

    Article • Saudi Journal of Kidney Diseases and Transplantation, January 2017, Medknow

    Assistant Professor Yahya Wahba

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

    Article • Annals of Saudi Medicine, November 2014, King Faisal Specialist Hospital and Research Centre

    Assistant Professor Yahya Wahba

  15. Diabetes in MUCH

    Article • Pediatric Diabetes, June 2014, Wiley

    Professor Mohammad Mohammad Al-Haggar, Assistant Professor Yahya Wahba

  16. Sporadic Fibrodysplasia Ossificans Progressiva in an Egyptian Infant with c.617G > A Mutation inACVR1Gene: A Case Report and Review of Literature

    Article • Case Reports in Genetics, January 2013, Hindawi Publishing Corporation

    Assistant Professor Yahya Wahba

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

    Article • Clinical and Experimental Nephrology, February 2012, Springer Science + Business Media

    Assistant Professor Yahya Wahba

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

    Article • Case Reports in Nephrology, January 2011, Hindawi Publishing Corporation

    Assistant Professor Yahya Wahba