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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 Cancer (Oxford, England : 1990)|January 1, 1995
Meta-iodobenzylguanidine (MIBG) inhibits malate and succinate driven mitochondrial ATP synthesis in the human neuroblastoma cell line SK-N-BE(2c)J Cornelissen, R J Wanders, C Van den Bogert, et al.
Pediatrics|November 5, 2003
Short-chain Acyl-CoA dehydrogenase deficiency: studies in a large family adding to the complexity of the disorderLevinus A Bok, Peter Vreken, Frits A Wijburg, et al.
Molecular Genetics and Metabolism|April 28, 2004
Identification of fatty aldehyde dehydrogenase in the breakdown of phytol to phytanic acidDaan M van den Brink, Joram N I van Miert, Georges Dacremont, et al.
Journal of Inherited Metabolic Disease|October 25, 2013
Valproyl-CoA inhibits the activity of ATP- and GTP-dependent succinate:CoA ligasesPaula B M Luís, Jos Ruiter, Lodewijk IJlst, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 13, 2016
A movement disorder with dystonia and ataxia caused by a mutation in the HIBCH geneGudrun Schottmann, Akosua Sarpong, Carmen Lorenz, et al.
Breast Cancer Research : BCR|May 4, 2018
The combined effect of mammographic texture and density on breast cancer risk: a cohort studyJohanna O P Wanders, Carla H van Gils, Nico Karssemeijer, et al.
Survey of Ophthalmology|September 21, 2010
Adult Refsum disease: a form of tapetoretinal dystrophy accessible to therapyKlaus Rüether, Eleanor Baldwin, Minne Casteels, et al.
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