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Nature Reviews. Neurology|November 20, 2018
POLG-related disorders and their neurological manifestationsShamima Rahman, William C CopelandJournal of Inherited Metabolic Disease|January 26, 2019
Disorders of riboflavin metabolismShanti Balasubramaniam, John Christodoulou, Shamima RahmanJournal of Inherited Metabolic Disease|June 14, 2024
Mitochondrial membrane synthesis, remodelling and cellular traffickingMartina Messina, Frédéric M Vaz, Shamima RahmanJournal of Inherited Metabolic Disease|March 28, 2019
Cerebral folate deficiency: Analytical tests and differential diagnosisSimon Pope, Rafael Artuch, Simon Heales, et al.Journal of Inherited Metabolic Disease|January 3, 2024
Gene therapy for mitochondrial disordersNandaki Keshavan, Michal Minczuk, Carlo Viscomi, et al.Annals of Neurology|September 25, 2024
Interferon Stimulated Gene Expression Is a Biomarker for Primary Mitochondrial DiseaseNandaki Keshavan, Lana Mhaldien, Kimberly Gilmour, et al.BMC Pediatrics|March 6, 2014
Gentamicin, genetic variation and deafness in preterm childrenMaria Bitner-Glindzicz, Shamima Rahman, Kathy Chant, et al.Scandinavian Journal of Clinical and Laboratory Investigation|January 3, 2012
Plasma thiol status is altered in children with mitochondrial diseasesHeli Salmi, James V Leonard, Shamima Rahman, et al.Journal of Inherited Metabolic Disease|December 19, 2020
An international classification of inherited metabolic disorders (ICIMD)Carlos R Ferreira, Shamima Rahman, Markus Keller, et al.European Journal of Pediatrics|March 21, 2003
Mitochondrial HMG-CoA synthase deficiency: identification of two further patients carrying two novel mutationsNicole I Wolf, Shamima Rahman, Peter T Clayton, et al.Pageof 16