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Scientific Reports|April 27, 2017
A statistical algorithm showing coenzyme Q10 and citrate synthase as biomarkers for mitochondrial respiratory chain enzyme activitiesD Yubero, A Adin, R Montero, et al.Revista De Neurologia|June 18, 2004
[Familiar chronic progressive external ophthalmoplegia of mitochondrial origin]M Pineda, A Playán-Ariso, M J Alcaine-Villarroya, et al.Revista De Neurologia|December 29, 2000
[Mitochondrial encephalomyelitis, lactic acidosis and cerebrovascular accidents (MELAS) in pediatric age with the A3243G mutation in the tRNALeu(UUR) gene of mitochondrial DNA]L Coelho-Miranda, A Playan, R Artuch, et al.Orphanet Journal of Rare Diseases|February 1, 2018
Hypermanganesemia due to mutations in SLC39A14: further insights into Mn deposition in the central nervous systemL Marti-Sanchez, J D Ortigoza-Escobar, A Darling, et al.Clinical Genetics|March 19, 2010
Molecular characterization of five patients with homocystinuria due to severe methylenetetrahydrofolate reductase deficiencyR Urreizti, A A Moya-García, A Pino-Ángeles, et al.Pageof 8