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Magy  Abdelwahab
Magy Abdelwahab
Cairo University Paediatric Hospital, Kasr ElAiny Hospital
Dirección de correo verificada de kasralainy.edu.eg
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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
582020
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
402011
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
352016
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
352009
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
272016
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
232021
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
182021
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
182012
Profiling the mutational landscape of coagulation factor V deficiency
EM Paraboschi, M Menegatti, V Rimoldi, M Borhany, M Abdelwahab, ...
haematologica 105 (4), e180, 2020
142020
Previously unrecognized behavioral phenotype in Gaucher disease type 3
M Abdelwahab, M Potegal, EG Shapiro, I Nestrasil
Neurology: Genetics 3 (3), e158, 2017
122017
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
122015
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
92020
Rare coagulation disorders: a study of 70 cases in the Egyptian population
M Abdelwahab, N Khaddah
Haemophilia 5 (18), e386-e388, 2012
92012
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
32021
Management of type 3 Gaucher disease
M Abdelwahab
Current Medical Literature 10 (4), 93, 2012
22012
High incidence of intracranial haemorrhage in Egyptian children with congenital afibrinogenaemia
M Abdelwahab, P de Moerloose, A Casini
Haemophilia 29 (2), 572-577, 2023
12023
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
12018
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
12017
Splenectomy in eight Egyptian patients with type III Gaucher disease: An 8year prospective study
M Abdelwahab
Molecular Genetics and Metabolism 2 (114), S11, 2015
12015
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
12015
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Artículos 1–20