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R Scholte

Showing results (51-60 of 83) with videos related to

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Journal of the Neurological Sciences|January 1, 1987
Cytochrome c oxidase deficiency in subacute necrotizing encephalomyelopathyW F Arts, H R Scholte, M C Loonen, et al.
Journal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|May 1, 1990
Primary carnitine deficiencyH R Scholte, R Rodrigues Pereira, P C de Jonge, et al.
Journal of Neurology|January 1, 1993
Mitochondrial encephalomyopathy, lactic acidosis and stroke in adults: two casesH P Kremer, A Keyser, A R Wintzen, et al.
The Journal of Pediatrics|May 1, 1988
de Toni-Fanconi-Debré syndrome with Leigh syndrome revealing severe muscle cytochrome c oxidase deficiencyH Ogier, A Lombes, H R Scholte, et al.
Journal of the Neurological Sciences|April 1, 1988
Defect in succinate oxidation by isolated muscle mitochondria in a patient with symmetrical lesions in the basal gangliaJ J Martin, F L Van de Vyver, H R Scholte, et al.
American Journal of Human Genetics|April 1, 1996
Genetic and biochemical impairment of mitochondrial complex I activity in a family with Leber hereditary optic neuropathy and hereditary spastic dystoniaD D De Vries, L N Went, G W Bruyn, et al.
Annals of Human Genetics|May 31, 2007
Fatal malonyl CoA decarboxylase deficiency due to maternal uniparental isodisomy of the telomeric end of chromosome 16S Malvagia, L Papi, A Morrone, et al.
Pathology, Research and Practice|November 1, 1988
Mitochondrial myopathies with necrotizing encephalopathy of the Leigh typeJ Peiffer, B Kustermann-Kuhn, W Mortier, et al.
Annals of Neurology|April 18, 1998
Very long chain acyl-coenzyme A dehydrogenase deficiency with adult onsetA H Smelt, B J Poorthuis, W Onkenhout, et al.
Hepatology (Baltimore, Md.)|July 1, 1997
Effect of lamivudine on morphology and function of mitochondria in patients with chronic hepatitis BP Honkoop, R A de Man, H R Scholte, et al.
Pageof 9

Showing results (51-60 of 83) with videos related to

Sort By:
Pageof 9
Journal of the Neurological Sciences|January 1, 1987
Cytochrome c oxidase deficiency in subacute necrotizing encephalomyelopathyW F Arts, H R Scholte, M C Loonen, et al.
Journal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|May 1, 1990
Primary carnitine deficiencyH R Scholte, R Rodrigues Pereira, P C de Jonge, et al.
Journal of Neurology|January 1, 1993
Mitochondrial encephalomyopathy, lactic acidosis and stroke in adults: two casesH P Kremer, A Keyser, A R Wintzen, et al.
The Journal of Pediatrics|May 1, 1988
de Toni-Fanconi-Debré syndrome with Leigh syndrome revealing severe muscle cytochrome c oxidase deficiencyH Ogier, A Lombes, H R Scholte, et al.
Journal of the Neurological Sciences|April 1, 1988
Defect in succinate oxidation by isolated muscle mitochondria in a patient with symmetrical lesions in the basal gangliaJ J Martin, F L Van de Vyver, H R Scholte, et al.
American Journal of Human Genetics|April 1, 1996
Genetic and biochemical impairment of mitochondrial complex I activity in a family with Leber hereditary optic neuropathy and hereditary spastic dystoniaD D De Vries, L N Went, G W Bruyn, et al.
Annals of Human Genetics|May 31, 2007
Fatal malonyl CoA decarboxylase deficiency due to maternal uniparental isodisomy of the telomeric end of chromosome 16S Malvagia, L Papi, A Morrone, et al.
Pathology, Research and Practice|November 1, 1988
Mitochondrial myopathies with necrotizing encephalopathy of the Leigh typeJ Peiffer, B Kustermann-Kuhn, W Mortier, et al.
Annals of Neurology|April 18, 1998
Very long chain acyl-coenzyme A dehydrogenase deficiency with adult onsetA H Smelt, B J Poorthuis, W Onkenhout, et al.
Hepatology (Baltimore, Md.)|July 1, 1997
Effect of lamivudine on morphology and function of mitochondria in patients with chronic hepatitis BP Honkoop, R A de Man, H R Scholte, et al.
Pageof 9