The definition of neuronopathic Gaucher disease R Schiffmann, J Sevigny, A Rolfs, EH Davies, O Goker‐Alpan, ... Journal of inherited metabolic disease 43 (5), 1056-1059, 2020 | 58 | 2020 |
Genotyping of intron 22-related rearrangements of F8 by inverse-shifting PCR in Egyptian hemophilia A patients H Abou-Elew, H Ahmed, H Raslan, M Abdelwahab, R Hammoud, ... Annals of hematology 90, 579-584, 2011 | 40 | 2011 |
Lysosomal storage disorders in Egyptian children MA Elmonem, IG Mahmoud, DA Mehaney, SA Sharaf, SA Hassan, ... The Indian Journal of Pediatrics 83, 805-813, 2016 | 35 | 2016 |
Intracranial hemorrhage in acute and chronic childhood immune thrombocytopenic purpura over a ten-year period: an Egyptian multicenter study M Elalfy, N Elbarbary, N Khaddah, M Abdelwahab, F El Rashidy, ... Acta haematologica 123 (1), 59-63, 2009 | 35 | 2009 |
Long-term follow-up and sudden unexpected death in Gaucher disease type 3 in Egypt M Abdelwahab, D Blankenship, R Schiffmann Neurology: Genetics 2 (2), e55, 2016 | 27 | 2016 |
Clinical phenotype, fibrinogen supplementation, and health-related quality of life in patients with afibrinogenemia A Casini, S von Mackensen, C Santoro, C Djambas Khayat, M Belhani, ... Blood, The Journal of the American Society of Hematology 137 (22), 3127-3136, 2021 | 23 | 2021 |
Throwing a spotlight on under-recognized manifestations of Gaucher disease: Pulmonary involvement, lymphadenopathy and Gaucheroma U Ramaswami, E Mengel, A Berrah, M AlSayed, A Broomfield, A Donald, ... Molecular genetics and metabolism 133 (4), 335-344, 2021 | 18 | 2021 |
Prevalence of hepatitis C virus infection and human immunodeficiency virus in a cohort of Egyptian hemophiliac children MS Abdelwahab, MS El-Raziky, NA Kaddah, HH Abou-Elew Annals of Saudi medicine 32 (2), 200-202, 2012 | 18 | 2012 |
Profiling the mutational landscape of coagulation factor V deficiency EM Paraboschi, M Menegatti, V Rimoldi, M Borhany, M Abdelwahab, ... haematologica 105 (4), e180, 2020 | 14 | 2020 |
Previously unrecognized behavioral phenotype in Gaucher disease type 3 M Abdelwahab, M Potegal, EG Shapiro, I Nestrasil Neurology: Genetics 3 (3), e158, 2017 | 12 | 2017 |
Mesenteric and mediastinal lymphadenopathy in Egyptian children with Gaucher disease types 1 and 3 treated with enzyme replacement therapy M Abdelwahab, HM SeifEldien Journal of pediatric hematology/oncology 37 (5), e316-e322, 2015 | 12 | 2015 |
Scoring system to facilitate diagnosis of Gaucher disease A Mehta, O Rivero‐Arias, M Abdelwahab, S Campbell, A McMillan, ... Internal Medicine Journal 50 (12), 1538-1546, 2020 | 9 | 2020 |
Rare coagulation disorders: a study of 70 cases in the Egyptian population M Abdelwahab, N Khaddah Haemophilia 5 (18), e386-e388, 2012 | 9 | 2012 |
Investigation of a dysmorphic facial phenotype in patients with Gaucher disease types 2 and 3 E Daykin, N Fleischer, M Abdelwahab, N Hassib, R Schiffmann, E Ryan, ... Molecular Genetics and Metabolism 134 (3), 274-280, 2021 | 3 | 2021 |
Management of type 3 Gaucher disease M Abdelwahab Current Medical Literature 10 (4), 93, 2012 | 2 | 2012 |
High incidence of intracranial haemorrhage in Egyptian children with congenital afibrinogenaemia M Abdelwahab, P de Moerloose, A Casini Haemophilia 29 (2), 572-577, 2023 | 1 | 2023 |
Mortality and morbidity in mild vs severe hemophilia A and B; 15 years' experience; retrospective multi-center outcome M Abdelwahab, M Elalfy Haemophilia 24, 63-64, 2018 | 1 | 2018 |
Cardiac assessment in Egyptian type 3 Gaucher disease and report of calcifications in homozygous L444P mutation M Abdelwahab, A Fattouh, H Hamza, D Abdelaziz Molecular Genetics and Metabolism 1 (120), S17, 2017 | 1 | 2017 |
Splenectomy in eight Egyptian patients with type III Gaucher disease: An 8year prospective study M Abdelwahab Molecular Genetics and Metabolism 2 (114), S11, 2015 | 1 | 2015 |
Abnormal behavioral features in Egyptian children with type III Gaucher disease M Abdelwahab, E Shapiro, I Nestrasil Molecular Genetics and Metabolism 2 (114), S11, 2015 | 1 | 2015 |