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- Clinical and genetic features of Calpainopathies in Saudi Arabia - a descriptive cross-sectional study. Journal Articles
- Dysferlin aggregation in limbâgirdle muscular dystrophy type 2B/myoshi myopathy necessitates mutational screen for diagnosis Journal Articles
- Neurotrophins, cytokines, oxidative parameters and funcionality in Progressive Muscular Dystrophies Journal Articles
- Redox State and Mitochondrial Respiratory Chain Function in Skeletal Muscle of LGMD2A Patients Journal Articles
- Variants in CAPN3 Causing Autosomal Dominant Limb-Girdle Muscular Dystrophy Combined With Calpain-3 Deficiency. Journal Articles