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Neuroscience and Biobehavioral Reviews|May 17, 2021
Effect of neuropsychiatric medications on mitochondrial function: For better or for worseTim L Emmerzaal, Gerben Nijkamp, Marin Veldic, et al.
American Journal of Human Genetics|May 7, 2005
Deficiency of the ADP-forming succinyl-CoA synthase activity is associated with encephalomyopathy and mitochondrial DNA depletionOrly Elpeleg, Chaya Miller, Eli Hershkovitz, et al.
Drug Discovery Today|July 18, 2015
Can folic acid have a role in mitochondrial disorders?Aida Ormazabal, Mercedes Casado, Marta Molero-Luis, et al.
Journal of Inherited Metabolic Disease|April 16, 2016
The pleiotropic effects of decanoic acid treatment on mitochondrial function in fibroblasts from patients with complex I deficient Leigh syndromeMarta Kanabus, Elisa Fassone, Sean David Hughes, et al.
Molecular Therapy. Advances|July 12, 2026
Next generation AAV-F capsid gene therapy rescues disease pathology in a model of pyruvate dehydrogenase complex deficiencyAnna Keegan, Özge Çetin, Ellie M Chilcott, et al.
Journal of Inherited Metabolic Disease|November 17, 2011
Further delineation of pontocerebellar hypoplasia type 6 due to mutations in the gene encoding mitochondrial arginyl-tRNA synthetase, RARS2Emma Glamuzina, Ruth Brown, Kieran Hogarth, et al.
Rapid Communications in Mass Spectrometry : RCM|April 18, 2013
Coenzyme Q10 quantification in muscle, fibroblasts and cerebrospinal fluid by liquid chromatography/tandem mass spectrometry using a novel deuterated internal standardKate E C Duberley, Iain P Hargreaves, Korn-Anong Chaiwatanasirikul, et al.
Journal of Inherited Metabolic Disease|September 3, 2017
The presence of anaemia negatively influences survival in patients with POLG diseaseOmar Hikmat, Charalampos Tzoulis, Claus Klingenberg, et al.
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