E. Hammouda
Al-Azhar University(EG)
Publications by Year
Research Areas
Muscle Physiology and Disorders, Cardiomyopathy and Myosin Studies, Genetic Neurodegenerative Diseases, Connective tissue disorders research, Nuclear Structure and Function
Most-Cited Works
- → Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy(1999)1,339 cited
- → Truncating mutations in C-terminal titin may cause more severe tibial muscular dystrophy (TMD)(2008)104 cited
- → Periodic Salbutamol in Facioscapulohumeral Muscular Dystrophy: A Randomized Controlled Trial(2009)35 cited
- → A multicenter cross-sectional French study of the impact of COVID-19 on neuromuscular diseases(2021)16 cited
- [Oculopharyngeal muscular dystrophy: study of patients from seven Spanish families with different GCG expansions in PABP2 gene].(2004)
- → Do oxidized low-density lipoproteins link to extra hepatic manifestations in chronic, non-cirrhotic HCV patients?(2024)
- → J - 14 La myopathie liée aux mutations du gène Valosin-Containing-Protein (VCP)(2007)
- → G.P.17.02 New c-terminal titin mutations in Europeans with tibial muscular dystrophy (TMD)(2007)
- → G.P.4.01 Mutational spectrum of the DYSF gene based on a large cohort of dysferlin deficient patients(2007)
- → M.P.4.15 Adipose triglyceride lipase gene (PNPLA2) mutations in patients with myopathy related to neutral lipid storage disease(2007)