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Rasha El Sherif

Showing results (1-10 of 11) with videos related to

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Hemodialysis International. International Symposium on Home Hemodialysis|November 25, 2011
Carriage of Staphylococcus aureus in the nose of patients on regular dialysis treatment using hemodialysis cathetersHoda Abdel Hamid Maamoun, Amin Roshdy Soliman, Rasha El Sherif
Neurology. Genetics|March 28, 2024
Splicing Switching of Alternative Last Exons Due to a Deletion Including Canonical Polyadenylation Site in <i>COL6A2</i> Gene Causes Recessive UCMDRasha El Sherif, Yoshihiko Saito, Tomonari Awaya, et al.
Arab Journal of Gastroenterology : the Official Publication of the Pan-Arab Association of Gastroenterology|March 26, 2019
Virulent Escherichia coli strains among Egyptian patients with acute diarrhoea versus urinary tract infection, and their antibiotic susceptibilityNagwa Tharwat, Rasha El-Sherif, Sherif Elnagdy, et al.
Value in Health Regional Issues|October 20, 2023
Early Cost-Utility Analysis of Ataluren and Eteplirsen in the Treatment of Duchenne Muscular Dystrophy in EgyptZahraa Shehata, Andrew Metry, Hoda Rabea, et al.
Value in Health Regional Issues|September 26, 2022
Estimating Societal Cost of Illness and Patients' Quality of Life of Duchenne Muscular Dystrophy in EgyptZahraa Hassan Shehata, Hoda Rabea, Rasha El Sherif, et al.
Neuromuscular Disorders : NMD|April 17, 2026
Bridging past and future: the evolution of genetic diagnosis in FSHD and the role of emerging technologies in a globalized frameworkClaudia Strafella, Hannes Erdmann, Jorge Alfredo Bevilacqua, et al.
Orphanet Journal of Rare Diseases|September 7, 2018
Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare diseaseLibby Wood, Guillaume Bassez, Corinne Bleyenheuft, et al.
Orphanet Journal of Rare Diseases|August 17, 2019
Correction to: Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare diseaseLibby Wood, Guillaume Bassez, Corinne Bleyenheuft, et al.
Human Mutation|January 22, 2015
The TREAT-NMD DMD Global Database: analysis of more than 7,000 Duchenne muscular dystrophy mutationsCatherine L Bladen, David Salgado, Soledad Monges, et al.
American Journal of Human Genetics|April 16, 2021
A form of muscular dystrophy associated with pathogenic variants in JAG2Sandra Coppens, Alison M Barnard, Sanna Puusepp, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Hemodialysis International. International Symposium on Home Hemodialysis|November 25, 2011
Carriage of Staphylococcus aureus in the nose of patients on regular dialysis treatment using hemodialysis cathetersHoda Abdel Hamid Maamoun, Amin Roshdy Soliman, Rasha El Sherif
Neurology. Genetics|March 28, 2024
Splicing Switching of Alternative Last Exons Due to a Deletion Including Canonical Polyadenylation Site in <i>COL6A2</i> Gene Causes Recessive UCMDRasha El Sherif, Yoshihiko Saito, Tomonari Awaya, et al.
Arab Journal of Gastroenterology : the Official Publication of the Pan-Arab Association of Gastroenterology|March 26, 2019
Virulent Escherichia coli strains among Egyptian patients with acute diarrhoea versus urinary tract infection, and their antibiotic susceptibilityNagwa Tharwat, Rasha El-Sherif, Sherif Elnagdy, et al.
Value in Health Regional Issues|October 20, 2023
Early Cost-Utility Analysis of Ataluren and Eteplirsen in the Treatment of Duchenne Muscular Dystrophy in EgyptZahraa Shehata, Andrew Metry, Hoda Rabea, et al.
Value in Health Regional Issues|September 26, 2022
Estimating Societal Cost of Illness and Patients' Quality of Life of Duchenne Muscular Dystrophy in EgyptZahraa Hassan Shehata, Hoda Rabea, Rasha El Sherif, et al.
Neuromuscular Disorders : NMD|April 17, 2026
Bridging past and future: the evolution of genetic diagnosis in FSHD and the role of emerging technologies in a globalized frameworkClaudia Strafella, Hannes Erdmann, Jorge Alfredo Bevilacqua, et al.
Orphanet Journal of Rare Diseases|September 7, 2018
Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare diseaseLibby Wood, Guillaume Bassez, Corinne Bleyenheuft, et al.
Orphanet Journal of Rare Diseases|August 17, 2019
Correction to: Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare diseaseLibby Wood, Guillaume Bassez, Corinne Bleyenheuft, et al.
Human Mutation|January 22, 2015
The TREAT-NMD DMD Global Database: analysis of more than 7,000 Duchenne muscular dystrophy mutationsCatherine L Bladen, David Salgado, Soledad Monges, et al.
American Journal of Human Genetics|April 16, 2021
A form of muscular dystrophy associated with pathogenic variants in JAG2Sandra Coppens, Alison M Barnard, Sanna Puusepp, et al.
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