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R Scholte

Showing results (61-70 of 83) with videos related to

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Journal of Immunological Methods|August 21, 2007
A simplified and reliable assay for complex I in human blood lymphocytesL E A de Wit, L Spruijt, G C Schoonderwoerd, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Confocal scanning laser microscopy of mitochondria: a possible tool in the diagnosis of mitochondrial disordersM H Ruiters, E A van Spronsen, O H Skjeldal, et al.
Neuromuscular Disorders : NMD|July 23, 1998
Infantile fibre type disproportion, myofibrillar lysis and cardiomyopathy: a disorder in three unrelated Dutch familiesP G Barth, R J Wanders, W Ruitenbeek, et al.
Journal of Human Genetics|February 1, 2003
A novel splice site mutation in neonatal carnitine palmitoyl transferase II deficiencyRoel J P Smeets, Jan A M Smeitink, Ben A Semmekrot, et al.
Neurology|March 1, 1986
Riboflavin-responsive lipid-storage myopathy and glutaric aciduria type II of early adult onsetM de Visser, H R Scholte, R B Schutgens, et al.
Human Genetics|September 10, 1999
Identification of two novel mutations in OCTN2 of three patients with systemic carnitine deficiencyF M Vaz, H R Scholte, J Ruiter, et al.
Neuromuscular Disorders : NMD|September 8, 2004
Increased risk for cardiorespiratory failure associated with the A3302G mutation in the mitochondrial DNA encoded tRNALeu(UUR) geneB J C van den Bosch, I F M de Coo, A T M Hendrickx, et al.
Neuromuscular Disorders : NMD|July 17, 1999
Myopathy in very-long-chain acyl-CoA dehydrogenase deficiency: clinical and biochemical differences with the fatal cardiac phenotypeH R Scholte, R N Van Coster, P C de Jonge, et al.
Biochimica Et Biophysica Acta|July 25, 1990
Oxidative phosphorylation in human muscle in patients with ocular myopathy and after general anaesthesiaH R Scholte, E Agsteribbe, H F Busch, et al.
Nucleic Acids Research|October 12, 2000
Mutation analysis of the entire mitochondrial genome using denaturing high performance liquid chromatographyB J van Den Bosch, R F de Coo, H R Scholte, et al.
Pageof 9

Showing results (61-70 of 83) with videos related to

Sort By:
Pageof 9
Journal of Immunological Methods|August 21, 2007
A simplified and reliable assay for complex I in human blood lymphocytesL E A de Wit, L Spruijt, G C Schoonderwoerd, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Confocal scanning laser microscopy of mitochondria: a possible tool in the diagnosis of mitochondrial disordersM H Ruiters, E A van Spronsen, O H Skjeldal, et al.
Neuromuscular Disorders : NMD|July 23, 1998
Infantile fibre type disproportion, myofibrillar lysis and cardiomyopathy: a disorder in three unrelated Dutch familiesP G Barth, R J Wanders, W Ruitenbeek, et al.
Journal of Human Genetics|February 1, 2003
A novel splice site mutation in neonatal carnitine palmitoyl transferase II deficiencyRoel J P Smeets, Jan A M Smeitink, Ben A Semmekrot, et al.
Neurology|March 1, 1986
Riboflavin-responsive lipid-storage myopathy and glutaric aciduria type II of early adult onsetM de Visser, H R Scholte, R B Schutgens, et al.
Human Genetics|September 10, 1999
Identification of two novel mutations in OCTN2 of three patients with systemic carnitine deficiencyF M Vaz, H R Scholte, J Ruiter, et al.
Neuromuscular Disorders : NMD|September 8, 2004
Increased risk for cardiorespiratory failure associated with the A3302G mutation in the mitochondrial DNA encoded tRNALeu(UUR) geneB J C van den Bosch, I F M de Coo, A T M Hendrickx, et al.
Neuromuscular Disorders : NMD|July 17, 1999
Myopathy in very-long-chain acyl-CoA dehydrogenase deficiency: clinical and biochemical differences with the fatal cardiac phenotypeH R Scholte, R N Van Coster, P C de Jonge, et al.
Biochimica Et Biophysica Acta|July 25, 1990
Oxidative phosphorylation in human muscle in patients with ocular myopathy and after general anaesthesiaH R Scholte, E Agsteribbe, H F Busch, et al.
Nucleic Acids Research|October 12, 2000
Mutation analysis of the entire mitochondrial genome using denaturing high performance liquid chromatographyB J van Den Bosch, R F de Coo, H R Scholte, et al.
Pageof 9