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Journal of Medical Genetics|September 14, 2012
Complex I deficiency: clinical features, biochemistry and molecular geneticsElisa Fassone, Shamima RahmanBMJ Case Reports|October 9, 2013
Treatable Leigh-like encephalopathy presenting in adolescenceElisa Fassone, Yehani Wedatilake, Catherine J DeVile, et al.Journal of Medical Genetics|September 21, 2011
Mutations in the mitochondrial complex I assembly factor NDUFAF1 cause fatal infantile hypertrophic cardiomyopathyElisa Fassone, Jan-Willem Taanman, Iain P Hargreaves, et al.Journal of Inherited Metabolic Disease|April 16, 2016
The pleiotropic effects of decanoic acid treatment on mitochondrial function in fibroblasts from patients with complex I deficient Leigh syndromeMarta Kanabus, Elisa Fassone, Sean David Hughes, et al.Journal of Inherited Metabolic Disease|May 16, 2013
Gastrointestinal and hepatic manifestations of mitochondrial disordersShamima RahmanDevelopmental Medicine and Child Neurology|January 31, 2012
Mitochondrial disease and epilepsyShamima RahmanBrain Communications|January 16, 2025
Complex I deficiency remains the most frequent cause of Leigh syndrome spectrumShamima RahmanEpilepsy & Behavior : E&B|July 12, 2015
Pathophysiology of mitochondrial disease causing epilepsy and status epilepticusShamima RahmanEpilepsy & Behavior : E&B|November 4, 2019
Advances in the treatment of mitochondrial epilepsiesShamima RahmanPageof 17