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Rasha El Sherif
Observed names:
R M El Sherif,
R. EL Sherif,
R. El Sherif,
R.M. El Sherif,
Rasha El SHERIF,
Rasha el Sherif
show all 6
Institution:
New Giza University
Observed institutions:
Ain Shams University,
Cairo University,
Kyoto University,
National Center of Neurology and Psychiatry,
New Giza University,
National Institute of Neuroscience
show all 6
ORCID:
0000-0002-5285-2462
Observed ORCID:
0000-0002-5285-2462
OpenAlex ID:
A5088336452
The TREAT-NMD DMD Global Database: Analysis of More than 7,000 Duchenne Muscular Dystrophy Mutations
2015
·
Catherine L. Bladen
, David Salgado
, et al.
·
Human Mutation
·
765
PDF
Clinical Outcomes in Duchenne Muscular Dystrophy: A Study of 5345 Patients from the TREAT-NMD DMD Global Database
2017
·
Zaïda Koeks
, Catherine L. Bladen
, et al.
·
Journal of Neuromuscular Diseases
·
195
PDF
A form of muscular dystrophy associated with pathogenic variants in JAG2
2021
·
Sandra Coppens
, Alison M. Barnard
, et al.
·
The American Journal of Human Genetics
·
41
PDF
Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease
2018
·
Libby Wood
, Guillaume Bassez
, et al.
·
Orphanet Journal of Rare Diseases
·
32
PDF
Estimating Societal Cost of Illness and Patients’ Quality of Life of Duchenne Muscular Dystrophy in Egypt
2022
·
Zahraa Hassan Shehata
, Hoda Rabea
, et al.
·
Value in Health Regional Issues
·
14
PDF
A form of muscular dystrophy associated with pathogenic variants in JAG2
2021
·
Sandra Coppens
, Alison M. Barnard
, et al.
·
The American Journal of Human Genetics
·
11
PDF
Patterns of dystrophin gene deletion in Egyptian Duchenne/Becker muscular dystrophy patients.
2007
·
R M El Sherif
, N Aly Fahmy
, et al.
·
Europe PMC (PubMed Central)
·
10
Three novel recessive DYSF mutations identified in three patients with muscular dystrophy, limb-girdle, type 2B
2018
·
Mariko Okubo
, Aritoshi Iida
, et al.
·
Journal of the Neurological Sciences
·
7
Early Cost-Utility Analysis of Ataluren and Eteplirsen in the Treatment of Duchenne Muscular Dystrophy in Egypt
2023
·
Zahraa Shehata
, Andrew Metry
, et al.
·
Value in Health Regional Issues
·
5
PDF
Carriage of S taphylococcus aureus in the nose of patients on regular dialysis treatment using hemodialysis catheters
2011
·
Hoda Abdel Hamid MAAMOUN
, Amin Roshdy SOLIMAN
, et al.
·
Hemodialysis International
·
5
A novel homozygous nonsense variant in COL12A1 causes myopathic Ehlers‐Danlos syndrome: A case report and literature review
2024
·
Rasha El Sherif
, Yoshihiko Saito
, et al.
·
Neuropathology and Applied Neurobiology
·
4
“Boule du biceps” in dysferlinopathy
2019
·
Rasha El Sherif
, Rasha S. Hussein
, et al.
·
Neurology
·
3
Bridging past and future: the evolution of genetic diagnosis in FSHD and the role of emerging technologies in a globalized framework
2026
·
Claudia Strafella
, Hannes Erdmann
, et al.
·
Neuromuscular Disorders
·
1
Splicing Switching of Alternative Last Exons Due to a Deletion Including Canonical Polyadenylation Site in COL6A2 Gene Causes Recessive UCMD
2024
·
Rasha El Sherif
, Yoshihiko Saito
, et al.
·
Neurology Genetics
·
1
VP291 The clinical, imaging and genetic characteristics in a large cohort of LGMDR1 patients from an Egyptian referral center
2023
·
R. El Sherif
, I. Nishino
·
Neuromuscular Disorders
·
1
A 53‐year‐old man with a 16‐year history of asymmetrical proximal muscle weakness, facial muscle weakness, and scapular winging
2023
·
Jantima Tanboon
, Rasha El Sherif
, et al.
·
Brain Pathology
·
1
PDF
Correction to: Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease
2019
·
Libby Wood
, Guillaume Bassez
, et al.
·
Orphanet Journal of Rare Diseases
·
1
Clinical, muscle pathology and genetic features of GNE myopathy patients in Egypt: Case report
2016
·
R. EL Sherif
, I. Nishino
, et al.
·
Neuromuscular Disorders
·
1
4.16eP Heterozygous DOK7-related congenital myasthenic syndrome responsive to salbutamol: a case series from Iraq
2026
·
Akram Alnajati
, Rasha El Sherif
, et al.
·
Neuromuscular Disorders
403PImpact of healthcare disparities, specialized care, and socioeconomic factors on Duchenne muscular dystrophy patient’s outcome: insights from Egyptian referral center
2025
·
R. El Sherif
, L. Lowes
·
Neuromuscular Disorders
494PThe Egyptian neuromuscular registry: a comprehensive platform for research, and clinical trial readiness for limb girdle muscular dystrophy
2025
·
D. Hamed
, R. El Sherif
·
Neuromuscular Disorders
500PFirst neuromuscular center experience in Iraq clinical, radiological, histopathological, and genetic findings from 10 families with LGMDR2
2025
·
A. Ali
, S. Omairi
, et al.
·
Neuromuscular Disorders
504VPLimb-girdle muscular dystrophy R1 in Egyptian and regional patients: clinical spectrum, genetics, and registry insights
2025
·
R. Mowafy
, N. Minami
, et al.
·
Neuromuscular Disorders
687VP Splicing switching of alternative last exons due to a deletion including canonical polyadenylation site in COL6A2 gene causes recessive UCMD
2024
·
Y. Saito
, R. El Sherif
, et al.
·
Neuromuscular Disorders
Registries and Care of Nmd
2021
·
R. El Sherif
, M. Gamal
, et al.
·
Neuromuscular Disorders
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Works count:
30
Citation count:
1,098
H-index:
7
I10-index:
7
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