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JIMD Reports|September 30, 2016
RARS2 Mutations: Is Pontocerebellar Hypoplasia Type 6 a Mitochondrial Encephalopathy?Tessa van Dijk, Fred van Ruissen, Bregje Jaeger, et al.
European Journal of Cancer (Oxford, England : 1990)|January 1, 1993
The prognostic value of epidermal growth factor receptors, determined by both immunohistochemistry and ligand binding assays, in primary epithelial ovarian cancer: a pilot studyM E van der Burg, S C Henzen-Logmans, J A Foekens, et al.
Journal of Inherited Metabolic Disease|August 28, 2015
Increased mitochondrial ATP production capacity in brain of healthy mice and a mouse model of isolated complex I deficiency after isoflurane anesthesiaGanesh R Manjeri, Richard J Rodenburg, Lionel Blanchet, et al.
Neurogenetics|March 24, 2015
MRPL44 mutations cause a slowly progressive multisystem disease with childhood-onset hypertrophic cardiomyopathyFelix Distelmaier, Tobias B Haack, Claudia B Catarino, et al.
Annals of Clinical and Translational Neurology|October 31, 2014
Phenylbutyrate increases pyruvate dehydrogenase complex activity in cells harboring a variety of defectsRosa Ferriero, Audrey Boutron, Michele Brivet, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|March 1, 1991
BOP/VIP--a new platinum-intensive chemotherapy regimen for poor prognosis germ cell tumoursC R Lewis, S D Fossà, G Mead, et al.
BMC Cardiovascular Disorders|May 28, 2016
Primary skeletal muscle myoblasts from chronic heart failure patients exhibit loss of anti-inflammatory and proliferative activityTahnee Sente, An M Van Berendoncks, An I Jonckheere, et al.
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