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Clinical Medicine (London, England)|January 18, 2019
The utility of phenomics in diagnosis of inherited metabolic disordersJoyeeta Rahman, Shamima RahmanLancet (London, England)|June 16, 2018
Mitochondrial medicine in the omics eraJoyeeta Rahman, Shamima RahmanFrontiers in Genetics|February 19, 2019
Systems Biology Approaches Toward Understanding Primary Mitochondrial DiseasesElaina M Maldonado, Fatma Taha, Joyeeta Rahman, et al.Journal of Inherited Metabolic Disease|July 4, 2020
Moving towards clinical trials for mitochondrial diseasesRobert D S Pitceathly, Nandaki Keshavan, Joyeeta Rahman, et al.Nature Reviews. Endocrinology|October 8, 2016
Mitochondrial disease and endocrine dysfunctionJasmine Chow, Joyeeta Rahman, John C Achermann, 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 RahmanPageof 16