Hoda Abdel‐Hamid

Zagazig University — Egypt

Biochemistry, Genetics and Molecular Biology · Life Sciences

23h-index3.9kcitations66works1.02yr avg
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Research Topics

Muscle Physiology and Disorders(26), Neurogenetic and Muscular Disorders Research(10), Cardiomyopathy and Myosin Studies(5), Genetic Neurodegenerative Diseases(5), Congenital heart defects research(5)

Publications65 total

Role of CT dacryocystography in the management of lacrimal drainage system obstruction
The Egyptian Journal of Otolaryngology·2025· 1 citedOpen Access
Access to novel therapies for Duchenne muscular dystrophy—Insights from expert treating physicians
Annals of the Child Neurology Society·2024· 4 citedOpen Access
Impact of Use Of Local Phenytoin On postoperative outcomes of pediatric tonsillectomy
Zagazig University Medical Journal·2024
Field Application of some Pyrethroid Insecticides against Cutworm, Agrotis ipsilon and Their Effect on Toxicity and Histological Changes
Journal of Plant Protection and Pathology /Journal of Plant Protection and Pathology·2024Open Access
Nerve conduction velocity studies in infantile Krabbe disease demonstrate long term continued progression of peripheral demyelinating neuropathy after hematopoietic stem cell transplantation (HSCT)
Molecular Genetics and Metabolism·2024
Effect of hypofractionated radiotherapy on lung functions in breast cancer patients
Egyptian Journal of Chest Diseases and Tuberculosis·2023· 2 citedOpen Access
Dual-energy X-ray absorptiometry measures of lean body mass as a biomarker for progression in boys with Duchenne muscular dystrophy
Scientific Reports·2022· 10 citedOpen Access
Quantitative magnetic resonance imaging measures as biomarkers of disease progression in boys with Duchenne muscular dystrophy: a phase 2 trial of domagrozumab
Journal of Neurology·2022· 23 citedOpen Access
Pilot study of nuclear scintigraphy to assess cough clearance in DMD
Pediatric Pulmonology·2022Open Access
Pilot Study of Nuclear Scintigraphy To Assess Cough Clearance in DMD
2022Open Access
A homozygous <i>CAP2</i> pathogenic variant in a neonate presenting with rapidly progressive cardiomyopathy and nemaline rods
American Journal of Medical Genetics Part A·2021· 15 cited
Meta-analyses of deflazacort versus prednisone/prednisolone in patients with nonsense mutation Duchenne muscular dystrophy
Journal of Comparative Effectiveness Research·2021· 15 citedOpen Access
Rasch Analysis of the Pediatric Quality of Life Inventory 4.0 Generic Core Scales Administered to Patients With Duchenne Muscular Dystrophy
Value in Health·2021· 11 citedOpen Access
A Combined Prospective and Retrospective Comparison of Long-Term Functional Outcomes Suggests Delayed Loss of Ambulation and Pulmonary Decline with Long-Term Eteplirsen Treatment
Journal of Neuromuscular Diseases·2021· 48 citedOpen Access
Open-Label Evaluation of Eteplirsen in Patients with Duchenne Muscular Dystrophy Amenable to Exon 51 Skipping: PROMOVI Trial
Journal of Neuromuscular Diseases·2021· 107 citedOpen Access
Corrigendum to “Randomized phase 2 trial and open-label extension of domagrozumab in Duchenne muscular dystrophy” [Neuromuscular Disorders, Vol. 30 (6) 2020, 492-502]
Neuromuscular Disorders·2021· 12 citedOpen Access
Medical management of muscle weakness in Duchenne muscular dystrophy
PLoS ONE·2020· 8 citedOpen Access
Clinical Reasoning: A 14-year-old boy with acute weakness, paresthesias, and headache
Neurology·2020· 4 citedOpen Access
Randomized phase 2 trial and open-label extension of domagrozumab in Duchenne muscular dystrophy
Neuromuscular Disorders·2020· 63 citedOpen Access
Combination therapy with nusinersen and AVXS-101 in SMA type 1
Neurology·2019· 47 cited
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Frequent Co-authors

Craig M. McDonald(21), Anne M. Connolly(17), Jean K. Mah(16), Paula R. Clemens(12), Erik Henricson(11), Monique M. Ryan(11), Tina Duong(10), Yoram Nevo(10), Peter Karachunski(10), Eugenio Mercuri(10), Russell J. Butterfield(10), Avital Cnaan(9), M. Tulinius(9), Nancy L. Kuntz(9), Richard T. Abresch(8), Carolina Tesi Rocha(8), Alberto Dubrovsky(8), Michela Guglieri(8), Lauren P. Morgenroth(7), Robert T. Leshner(7)