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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.Developmental Medicine and Child Neurology|September 25, 2012
Inborn errors of metabolism causing epilepsyShamima Rahman, Emma J Footitt, Sophia Varadkar, 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.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 12, 2013
Brown-Vialetto-van Laere syndrome: a riboflavin responsive neuronopathy of infancy with singular featuresCarlotta Spagnoli, Matthew C Pitt, Shamima Rahman, et al.Molecular Genetics and Metabolism|February 1, 2026
Clinical and biochemical footprints of primary mitochondrial disorders: proposed nosologyMartina Messina, Rebecca Ganetzky, Carlos R Ferreira, et al.Annals of Neurology|October 28, 2015
Leigh syndrome: One disorder, more than 75 monogenic causesNicole J Lake, Alison G Compton, Shamima Rahman, et al.Plos One|July 4, 2018
Near infrared spectroscopy with a vascular occlusion test as a biomarker in children with mitochondrial and other neuro-genetic disordersSainath Raman, Latifa Chentouf, Catherine DeVile, et al.Pageof 17