Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Amal El-Beshlawy

Showing results (1-10 of 75) with videos related to

Pageof 8
Sort By:
Hematology (Amsterdam, Netherlands)|September 29, 2005
The Egyptian experience with oral iron chelatorsAmal El Beshlawy
Hemoglobin|December 17, 2009
Prevention of hemoglobinopathies in EgyptAmal El-Beshlawy, Ilham Youssry
Blood Cells, Molecules & Diseases|February 23, 2019
Recent trends in treatment of thalassemiaAmal El-Beshlawy, Mona El-Ghamrawy
International Journal of Hematology|October 14, 2011
Challenges of adherence and persistence with iron chelation therapyJohn B Porter, Michael Evangeli, Amal El-Beshlawy
Hemoglobin|December 17, 2009
Fetal globin induction in beta-thalassemiaAmal El-Beshlawy, Mona Hamdy, Mona El Ghamrawy
Haemophilia : the Official Journal of the World Federation of Hemophilia|July 22, 2022
Management of haemophilia A with inhibitors: A regional cross-talkFlora Peyvandi, Kaan Kavakli, Amal El-Beshlawy, et al.
Molecular Genetics and Metabolism Reports|July 17, 2019
Reversal of life-threatening hepatopulmonary syndrome in Gaucher disease by imiglucerase enzyme replacement therapyAmal El Beshlawy, Vagishwari Murugesan, Pramod Kumar Mistry, et al.
Pediatrics|October 3, 2002
Study of 22 Egyptian patients with Diamond-Blackfan anemia, corticosteroids, and cyclosporin therapy resultsAmal El-Beshlawy, Ilham Youssry Ibrahim, Samia Rizk, et al.
Journal of Inherited Metabolic Disease|January 20, 2010
Neuronopathic Gaucher disease: demographic and clinical features of 131 patients enrolled in the International Collaborative Gaucher Group Neurological Outcomes SubregistryAnna Tylki-Szymańska, Ashok Vellodi, Amal El-Beshlawy, et al.
Hemoglobin|March 17, 2007
Study of beta-Thalassemia mutations using the polymerase chain reaction-amplification refractory mutation system and direct DNA sequencing techniques in a group of Egyptian Thalassemia patientsSomaia El-Gawhary, Shahira El-Shafie, Manal Niazi, et al.
Pageof 8

Showing results (1-10 of 75) with videos related to

Sort By:
Pageof 8
Hematology (Amsterdam, Netherlands)|September 29, 2005
The Egyptian experience with oral iron chelatorsAmal El Beshlawy
Hemoglobin|December 17, 2009
Prevention of hemoglobinopathies in EgyptAmal El-Beshlawy, Ilham Youssry
Blood Cells, Molecules & Diseases|February 23, 2019
Recent trends in treatment of thalassemiaAmal El-Beshlawy, Mona El-Ghamrawy
International Journal of Hematology|October 14, 2011
Challenges of adherence and persistence with iron chelation therapyJohn B Porter, Michael Evangeli, Amal El-Beshlawy
Hemoglobin|December 17, 2009
Fetal globin induction in beta-thalassemiaAmal El-Beshlawy, Mona Hamdy, Mona El Ghamrawy
Haemophilia : the Official Journal of the World Federation of Hemophilia|July 22, 2022
Management of haemophilia A with inhibitors: A regional cross-talkFlora Peyvandi, Kaan Kavakli, Amal El-Beshlawy, et al.
Molecular Genetics and Metabolism Reports|July 17, 2019
Reversal of life-threatening hepatopulmonary syndrome in Gaucher disease by imiglucerase enzyme replacement therapyAmal El Beshlawy, Vagishwari Murugesan, Pramod Kumar Mistry, et al.
Pediatrics|October 3, 2002
Study of 22 Egyptian patients with Diamond-Blackfan anemia, corticosteroids, and cyclosporin therapy resultsAmal El-Beshlawy, Ilham Youssry Ibrahim, Samia Rizk, et al.
Journal of Inherited Metabolic Disease|January 20, 2010
Neuronopathic Gaucher disease: demographic and clinical features of 131 patients enrolled in the International Collaborative Gaucher Group Neurological Outcomes SubregistryAnna Tylki-Szymańska, Ashok Vellodi, Amal El-Beshlawy, et al.
Hemoglobin|March 17, 2007
Study of beta-Thalassemia mutations using the polymerase chain reaction-amplification refractory mutation system and direct DNA sequencing techniques in a group of Egyptian Thalassemia patientsSomaia El-Gawhary, Shahira El-Shafie, Manal Niazi, et al.
Pageof 8