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Magy Abdelwahab

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Journal of Pediatric Hematology/Oncology|December 19, 2014
Mesenteric and Mediastinal Lymphadenopathy in Egyptian Children With Gaucher Disease Types 1 and 3 Treated With Enzyme Replacement TherapyMagy Abdelwahab, Hadeel M SeifEldien
Neurology. Genetics|April 29, 2016
Long-term follow-up and sudden unexpected death in Gaucher disease type 3 in EgyptMagy Abdelwahab, Derek Blankenship, Raphael Schiffmann
Haemophilia : the Official Journal of the World Federation of Hemophilia|December 31, 2022
High incidence of intracranial haemorrhage in Egyptian children with congenital afibrinogenaemiaMagy Abdelwahab, Philippe de Moerloose, A Casini
Neurology. Genetics|June 22, 2017
Previously unrecognized behavioral phenotype in Gaucher disease type 3Magy Abdelwahab, Michael Potegal, Elsa G Shapiro, et al.
Journal of Clinical Medicine|February 13, 2025
Home Enzyme Replacement Therapy in Gaucher Disease: A ReviewBeata Kieć-Wilk, Paul Guijt, Michaela Dan, et al.
Molecular Genetics and Metabolism|October 19, 2021
Investigation of a dysmorphic facial phenotype in patients with Gaucher disease types 2 and 3Emily Daykin, Nicole Fleischer, Magy Abdelwahab, et al.
Annals of Hematology|November 13, 2010
Genotyping of intron 22-related rearrangements of F8 by inverse-shifting PCR in Egyptian hemophilia A patientsHeba Abou-Elew, Hanan Ahmed, Hanan Raslan, et al.
Acta Haematologica|December 4, 2009
Intracranial hemorrhage in acute and chronic childhood immune thrombocytopenic purpura over a ten-year period: an Egyptian multicenter studyMohsen Elalfy, Nancy Elbarbary, Normine Khaddah, et al.
Orphanet Journal of Rare Diseases|February 20, 2026
Exploring delayed diagnosis in Gaucher disease: insights from a community survey and potential solutionsDiana Paulina Peña Aragón, Tanya Collin-Histed, Magy Abdelwahab, et al.
Internal Medicine Journal|November 11, 2020
Scoring system to facilitate diagnosis of Gaucher diseaseAtul Mehta, Oliver Rivero-Arias, Magy Abdelwahab, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Journal of Pediatric Hematology/Oncology|December 19, 2014
Mesenteric and Mediastinal Lymphadenopathy in Egyptian Children With Gaucher Disease Types 1 and 3 Treated With Enzyme Replacement TherapyMagy Abdelwahab, Hadeel M SeifEldien
Neurology. Genetics|April 29, 2016
Long-term follow-up and sudden unexpected death in Gaucher disease type 3 in EgyptMagy Abdelwahab, Derek Blankenship, Raphael Schiffmann
Haemophilia : the Official Journal of the World Federation of Hemophilia|December 31, 2022
High incidence of intracranial haemorrhage in Egyptian children with congenital afibrinogenaemiaMagy Abdelwahab, Philippe de Moerloose, A Casini
Neurology. Genetics|June 22, 2017
Previously unrecognized behavioral phenotype in Gaucher disease type 3Magy Abdelwahab, Michael Potegal, Elsa G Shapiro, et al.
Journal of Clinical Medicine|February 13, 2025
Home Enzyme Replacement Therapy in Gaucher Disease: A ReviewBeata Kieć-Wilk, Paul Guijt, Michaela Dan, et al.
Molecular Genetics and Metabolism|October 19, 2021
Investigation of a dysmorphic facial phenotype in patients with Gaucher disease types 2 and 3Emily Daykin, Nicole Fleischer, Magy Abdelwahab, et al.
Annals of Hematology|November 13, 2010
Genotyping of intron 22-related rearrangements of F8 by inverse-shifting PCR in Egyptian hemophilia A patientsHeba Abou-Elew, Hanan Ahmed, Hanan Raslan, et al.
Acta Haematologica|December 4, 2009
Intracranial hemorrhage in acute and chronic childhood immune thrombocytopenic purpura over a ten-year period: an Egyptian multicenter studyMohsen Elalfy, Nancy Elbarbary, Normine Khaddah, et al.
Orphanet Journal of Rare Diseases|February 20, 2026
Exploring delayed diagnosis in Gaucher disease: insights from a community survey and potential solutionsDiana Paulina Peña Aragón, Tanya Collin-Histed, Magy Abdelwahab, et al.
Internal Medicine Journal|November 11, 2020
Scoring system to facilitate diagnosis of Gaucher diseaseAtul Mehta, Oliver Rivero-Arias, Magy Abdelwahab, et al.
Pageof 2