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Journal 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 RahmanLancet (London, England)|June 16, 2018
Mitochondrial medicine in the omics eraJoyeeta Rahman, Shamima RahmanEssays in Biochemistry|July 8, 2018
Natural history of mitochondrial disorders: a systematic reviewNandaki Keshavan, Shamima RahmanClinical Medicine (London, England)|January 18, 2019
The utility of phenomics in diagnosis of inherited metabolic disordersJoyeeta Rahman, Shamima RahmanEndocrine Reviews|February 1, 2025
Endocrine Dysfunction in Primary Mitochondrial DiseasesRachel Varughese, Shamima RahmanJournal of Medical Genetics|March 8, 2011
Kearns-Sayre syndrome caused by defective R1/p53R2 assemblyRobert D S Pitceathly, Elisa Fassone, Jan-Willem Taanman, et al.Pediatric Nephrology (Berlin, Germany)|December 13, 2012
Mitochondrial disease--an important cause of end-stage renal failureShamima Rahman, Andrew M HallPageof 17