| Prevalence of congenital heart diseases in children with Down syndrome in Mansoura, Egypt: a retrospective descriptive study AH El-Gilany, S Yahia, Y Wahba Annals of Saudi medicine 37 (5), 386-392, 2017 | 37 | 2017 |
| Rapunzel syndrome (gastric trichobezoar), a rare presentation with generalised oedema: case report and review of the literature I Nour, M Abd Alatef, A Megahed, S Yahia, Y Wahba, AE Shabaan Paediatrics and International Child Health 39 (1), 76-78, 2019 | 25 | 2019 |
| Burden of family caregivers of Down syndrome children: a cross-sectional study N Alam El-Deen, AA Alwakeel, AH El-Gilany, Y Wahba Family Practice 38 (2), 159-164, 2021 | 17 | 2021 |
| Disruptive behavior in Down syndrome children: a cross-sectional comparative study S Yahia, M El-Hadidy, AH El-Gilany, D Amdel-Hady, Y Wahba, ... Annals of Saudi medicine 34 (6), 517-521, 2014 | 16 | 2014 |
| Fanconi Bickel Syndrome: Novel Mutations in GLUT 2 Gene Causing a Distinguished Form of Renal Tubular Acidosis in Two Unrelated Egyptian Families M Al-Haggar, O Sakamoto, A Shaltout, A El-Hawary, Y Wahba, ... Case Reports in Nephrology 2011 (1), 754369, 2011 | 15 | 2011 |
| Lymphocyte subgroups and recurrent infections in children with Down syndrome–a prospective case control study M Mitwalli, Y Wahba, A Shaltout, M Gouida Central European Journal of Immunology 43 (3), 248-254, 2018 | 14 | 2018 |
| Novel homozygous SLC29A3 mutations among two unrelated Egyptian families with spectral features of H‐syndrome M Al‐Haggar, N Salem, Y Wahba, N Ahmad, L Jonard, D Abdel‐Hady, ... Pediatric Diabetes 16 (4), 305-316, 2015 | 13 | 2015 |
| Mutation analysis of the GLUT2 gene in three unrelated Egyptian families with Fanconi–Bickel syndrome: revisited gene atlas for renumbering M Al-Haggar, O Sakamoto, A Shaltout, A Al-Hawari, Y Wahba, ... Clinical and experimental nephrology 16, 604-610, 2012 | 12 | 2012 |
| The potential impact of CYP2D6 (* 2/* 4/* 10) gene variants among Egyptian epileptic children: a preliminary study AM Elsaid, RF Zahran, SM Elmetwaly, Y Wahba, H Megahed, RM Elshazli Gene 832, 146585, 2022 | 11 | 2022 |
| Oxidative stress and vitamin D receptor BsmI gene polymorphism in Egyptian children with systemic lupus erythematosus: a single center study H Fouad, S Yahia, A Elsaid, A Hammad, Y Wahba, AH El-Gilany, ... Lupus 28 (6), 771-777, 2019 | 11 | 2019 |
| CYP2C9 (*2&*3) and CYP2C19 (*2&*3) polymorphisms among children with nonlesional epilepsy: a single-center study S Eltalal, M El Ayouty, A El-Said, Y Wahba Acta Neurologica Belgica 121, 1623-1631, 2021 | 10 | 2021 |
| Polymorphisms of interleukin 4 and interleukin 4 receptor genes and bronchial asthma risk among Egyptian children A Elsaid, RMS Shoaib, SS Badr, Y Wahba, SEN Ayyad Clinical Biochemistry 93, 66-72, 2021 | 10 | 2021 |
| Sporadic Fibrodysplasia Ossificans Progressiva in an Egyptian Infant with c.617G > A Mutation in ACVR1 Gene: A Case Report and Review of Literature M Al-Haggar, N Ahmad, S Yahia, A Shams, B Hasaneen, ... Case Reports in Genetics 2013 (1), 834605, 2013 | 10 | 2013 |
| Mutation in the SLC29A3 Gene in an Egyptian patient with H syndrome: a case report and review of literature HT El-Bassyouni, MM Thomas, AMS Tosson Journal of Pediatric Genetics 9 (02), 109-113, 2020 | 9 | 2020 |
| CD40 and CD72 expression and prognostic values among children with systemic lupus erythematosus: a case–control study A Asmiyou, AM Bakr, DA Shahin, Y Wahba Lupus 29 (10), 1270-1276, 2020 | 8 | 2020 |
| Pre versus post application of a 0.12% chlorhexidine based oral hygiene protocol in an Egyptian pediatric intensive care unit: Practice and effects MM Gomaa, Y Wahba, MA El-Bayoumi Egyptian Journal of Critical Care Medicine 5 (3), 87-91, 2017 | 7 | 2017 |
| Cluster of differentiation 96 in children with acute leukemia: A single center cohort study H Mohammad, Y Wahba, M Gouida, A Shaltout Indian Journal of Hematology and Blood Transfusion 36 (1), 178-182, 2020 | 6 | 2020 |
| Psychiatric disorders and quality of life in Egyptian patients with chronic immune thrombocytopenic purpura: a single center study S Yahia, Y Wahba, AH El-Gilany, S Abdelmabood, MA El-Hadidy, ... Indian Journal of Hematology and Blood Transfusion 35, 347-351, 2019 | 6 | 2019 |
| Polymorphisms of the sodium voltage-gated channel, alpha subunit 1 (SCN1A -A3184G) gene among children with non-lesional epilepsy: a case-control study E Ghazala, DA Shahin, Y Wahba Italian Journal of Pediatrics 48 (1), 157, 2022 | 5 | 2022 |
| Neurocutaneous melanosis is not always a benign disease S Abd El Mabood, Y Wahba, S Yahia, MM Sarhan, AK Mansour, ... Indian Journal of Dermatology, Venereology and Leprology 86, 335, 2020 | 5 | 2020 |
