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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 catheters
Hoda 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 UCMD
Rasha 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 susceptibility
Nagwa 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 Egypt
Zahraa 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 Egypt
Zahraa 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 framework
Claudia 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 disease
Libby 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 disease
Libby 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 mutations
Catherine 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 JAG2
Sandra Coppens, Alison M Barnard, Sanna Puusepp, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 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 catheters
Hoda 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 UCMD
Rasha 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 susceptibility
Nagwa 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 Egypt
Zahraa 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 Egypt
Zahraa 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 framework
Claudia 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 disease
Libby 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 disease
Libby 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 mutations
Catherine 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 JAG2
Sandra Coppens, Alison M Barnard, Sanna Puusepp, et al.
Page
of 2