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Annals of Neurology|October 24, 1997
New familial mitochondrial encephalopathy with macrocephaly, cardiomyopathy, and complex I deficiencyC Dionisi-Vici, W Ruitenbeek, G Fariello, et al.
Annals of Clinical Biochemistry|November 1, 1992
Enzyme activities of the mitochondrial energy generating system in skeletal muscle tissue of preterm and fullterm neonatesW Sperl, R C Sengers, J M Trijbels, et al.
Biochemical and Biophysical Research Communications|March 2, 1999
Mapping of the human Voltage-Dependent Anion Channel isoforms 1 and 2 reconsideredA Messina, M Oliva, C Rosato, et al.
Neuropediatrics|July 13, 1999
Pontocerebellar hypoplasia associated with respiratory-chain defectsT J de Koning, L S de Vries, F Groenendaal, et al.
European Journal of Pediatrics|September 15, 1999
Cerebral palsy and pyruvate dehydrogenase deficiency: identification of two new mutations in the E1alpha geneW Lissens, P Vreken, P G Barth, et al.
European Journal of Pediatrics|April 1, 1990
Deficiency of the alpha and beta subunits of pyruvate dehydrogenase in a patient with lactic acidosis and unexpected sudden deathW Sperl, W Ruitenbeek, C M Kerkhof, et al.
Computers in Biology and Medicine|January 1, 1985
Computerized calculation of in vitro generation of ATP and creatine phosphate induced by respiration in human muscle mitochondriaJ C Fischer, W Ruitenbeek, A M Stadhouders, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 29, 1985
Differential investigation of the capacity of succinate oxidation in human skeletal muscleJ C Fischer, W Ruitenbeek, J A Berden, et al.
Neuropediatrics|February 1, 1991
MELAS syndrome. Report of two patients, and comparison with data of 24 patients derived from the literatureJ L van Hellenberg Hubar, F J Gabreëls, W Ruitenbeek, et al.
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