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Epilepsy & Behavior : E&B|November 4, 2019
Advances in the treatment of mitochondrial epilepsiesShamima RahmanJournal of Inherited Metabolic Disease|May 13, 2015
Emerging aspects of treatment in mitochondrial disordersShamima RahmanJournal of Inherited Metabolic Disease|October 5, 2020
Seeking impact: Global perspectives on outcome measure selection for translational and clinical research for primary mitochondrial disordersAmy Goldstein, Shamima RahmanMolecular Genetics and Metabolism|July 30, 2024
Natural history of deoxyguanosine kinase deficiencyNandaki Keshavan, Shamima RahmanJournal of Medical Genetics|September 14, 2012
Complex I deficiency: clinical features, biochemistry and molecular geneticsElisa Fassone, Shamima RahmanEssays in Biochemistry|July 8, 2018
Natural history of mitochondrial disorders: a systematic reviewNandaki Keshavan, Shamima RahmanEndocrine Reviews|February 1, 2025
Endocrine Dysfunction in Primary Mitochondrial DiseasesRachel Varughese, Shamima RahmanPediatric Nephrology (Berlin, Germany)|December 13, 2012
Mitochondrial disease--an important cause of end-stage renal failureShamima Rahman, Andrew M HallArchives of Disease in Childhood|June 26, 2017
Recognition, investigation and management of mitochondrial diseaseJames E Davison, Shamima RahmanPageof 16