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J A Smeitink

Showing results (1-10 of 79) with videos related to

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Tijdschrift Voor Kindergeneeskunde|April 1, 1989
[Sarcoidosis]J M van Proosdij, J A Smeitink
Clinical Genetics|July 8, 2017
Mining for mitochondrial mechanisms: Linking known syndromes to mitochondrial functionD M Panneman, J A Smeitink, R J Rodenburg
Lancet (London, England)|October 6, 1999
Mitochondrial toxicity induced by nucleoside-analogue reverse-transcriptase inhibitors is a key factor in the pathogenesis of antiretroviral-therapy-related lipodystrophyK Brinkman, J A Smeitink, J A Romijn, et al.
Current Opinion in Neurology|November 28, 2001
Mitochondrial oxidative phosphorylation system assembly in man: recent achievementsM J Coenen, L P van den Heuvel, J A Smeitink
Mitochondrion|August 27, 2005
Biochemical examination of fibroblasts in the diagnosis and research of oxidative phosphorylation (OXPHOS) defectsL P van den Heuvel, J A Smeitink, R J T Rodenburg
Lancet (London, England)|May 22, 1993
Phenylpyruvate, fetal damage, and maternal phenylketonuria syndromeL Dorland, B T Poll-The, M Duran, et al.
European Journal of Pediatrics|March 1, 1993
A retrospective study of patients with the hereditary syndrome of congenital cataract, mitochondrial myopathy of heart and skeletal muscle and lactic acidosisG J van Ekeren, A M Stadhouders, J A Smeitink, et al.
American Journal of Medical Genetics|October 2, 2001
Respiratory chain complex I deficiencyR H Triepels, L P Van Den Heuvel, J M Trijbels, et al.
Annals of Neurology|April 13, 2000
Simvastatin and plasma very-long-chain fatty acids in X-linked adrenoleukodystrophyA Verrips, M A Willemsen, E Rubio-Gozalbo, et al.
European Journal of Pediatrics|February 24, 2001
Nuclear genes and oxidative phosphorylation disorders: a reviewJ A Smeitink, R C Sengers, F J Trijbels, et al.
Pageof 8

Showing results (1-10 of 79) with videos related to

Sort By:
Pageof 8
Tijdschrift Voor Kindergeneeskunde|April 1, 1989
[Sarcoidosis]J M van Proosdij, J A Smeitink
Clinical Genetics|July 8, 2017
Mining for mitochondrial mechanisms: Linking known syndromes to mitochondrial functionD M Panneman, J A Smeitink, R J Rodenburg
Lancet (London, England)|October 6, 1999
Mitochondrial toxicity induced by nucleoside-analogue reverse-transcriptase inhibitors is a key factor in the pathogenesis of antiretroviral-therapy-related lipodystrophyK Brinkman, J A Smeitink, J A Romijn, et al.
Current Opinion in Neurology|November 28, 2001
Mitochondrial oxidative phosphorylation system assembly in man: recent achievementsM J Coenen, L P van den Heuvel, J A Smeitink
Mitochondrion|August 27, 2005
Biochemical examination of fibroblasts in the diagnosis and research of oxidative phosphorylation (OXPHOS) defectsL P van den Heuvel, J A Smeitink, R J T Rodenburg
Lancet (London, England)|May 22, 1993
Phenylpyruvate, fetal damage, and maternal phenylketonuria syndromeL Dorland, B T Poll-The, M Duran, et al.
European Journal of Pediatrics|March 1, 1993
A retrospective study of patients with the hereditary syndrome of congenital cataract, mitochondrial myopathy of heart and skeletal muscle and lactic acidosisG J van Ekeren, A M Stadhouders, J A Smeitink, et al.
American Journal of Medical Genetics|October 2, 2001
Respiratory chain complex I deficiencyR H Triepels, L P Van Den Heuvel, J M Trijbels, et al.
Annals of Neurology|April 13, 2000
Simvastatin and plasma very-long-chain fatty acids in X-linked adrenoleukodystrophyA Verrips, M A Willemsen, E Rubio-Gozalbo, et al.
European Journal of Pediatrics|February 24, 2001
Nuclear genes and oxidative phosphorylation disorders: a reviewJ A Smeitink, R C Sengers, F J Trijbels, et al.
Pageof 8