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J Rodenburg

Showing results (71-80 of 214) with videos related to

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Developmental Disabilities Research Reviews|September 7, 2010
Complex I disorders: causes, mechanisms, and development of treatment strategies at the cellular levelFederica Valsecchi, Werner J H Koopman, Ganesh R Manjeri, et al.
European Journal of Surgical Oncology : the Journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology|November 24, 2005
Discrepancy between second and first opinion in surgical oncological patientsW A M Mellink, S C Henzen-Logmans, A H H Bongaerts, et al.
Analytical Biochemistry|October 25, 2001
Development of an androgen reporter gene assay (AR-LUX) utilizing a human cell line with an endogenously regulated androgen receptorB M Blankvoort, E M de Groene, A P van Meeteren-Kreikamp, et al.
International Journal of Cancer|September 9, 1992
Receptors for hormones and growth factors and (onco)-gene amplification in human ovarian cancerE M Berns, J G Klijn, S C Henzen-Logmans, et al.
American Journal of Ophthalmology Case Reports|May 17, 2024
Leber's hereditary optic neuropathy like disease in <i>MT-ATP6</i> variant m.8969G>ACansu de Muijnck, Mary J van Schooneveld, Astrid S Plomp, et al.
Cardiovascular Research|July 13, 2016
Mitochondrial complex I dysfunction and altered NAD(P)H kinetics in rat myocardium in cardiac right ventricular hypertrophy and failureRob C I Wüst, Heder J de Vries, Liesbeth T Wintjes, et al.
Brain & Development|March 11, 2008
MR spectroscopy of the brain in Leigh syndromeP E Sijens, G P A Smit, L A Rödiger, et al.
Journal of Inherited Metabolic Disease|June 9, 2009
Coenzyme Q(10) is decreased in fibroblasts of patients with methylmalonic aciduria but not in mevalonic aciduriaD Haas, P Niklowitz, F Hörster, et al.
Journal of Inherited Metabolic Disease|January 13, 2022
Mitochondrial RNA processing defect caused by a SUPV3L1 mutation in two siblings with a novel neurodegenerative syndromeSelma L van Esveld, Richard J Rodenburg, Fathiya Al-Murshedi, et al.
Molecular Syndromology|November 1, 2012
A Diagnostic Algorithm for Mitochondrial Disorders in Estonian ChildrenK Joost, R J Rodenburg, A Piirsoo, et al.
Pageof 22

Showing results (71-80 of 214) with videos related to

Sort By:
Pageof 22
Developmental Disabilities Research Reviews|September 7, 2010
Complex I disorders: causes, mechanisms, and development of treatment strategies at the cellular levelFederica Valsecchi, Werner J H Koopman, Ganesh R Manjeri, et al.
European Journal of Surgical Oncology : the Journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology|November 24, 2005
Discrepancy between second and first opinion in surgical oncological patientsW A M Mellink, S C Henzen-Logmans, A H H Bongaerts, et al.
Analytical Biochemistry|October 25, 2001
Development of an androgen reporter gene assay (AR-LUX) utilizing a human cell line with an endogenously regulated androgen receptorB M Blankvoort, E M de Groene, A P van Meeteren-Kreikamp, et al.
International Journal of Cancer|September 9, 1992
Receptors for hormones and growth factors and (onco)-gene amplification in human ovarian cancerE M Berns, J G Klijn, S C Henzen-Logmans, et al.
American Journal of Ophthalmology Case Reports|May 17, 2024
Leber's hereditary optic neuropathy like disease in <i>MT-ATP6</i> variant m.8969G>ACansu de Muijnck, Mary J van Schooneveld, Astrid S Plomp, et al.
Cardiovascular Research|July 13, 2016
Mitochondrial complex I dysfunction and altered NAD(P)H kinetics in rat myocardium in cardiac right ventricular hypertrophy and failureRob C I Wüst, Heder J de Vries, Liesbeth T Wintjes, et al.
Brain & Development|March 11, 2008
MR spectroscopy of the brain in Leigh syndromeP E Sijens, G P A Smit, L A Rödiger, et al.
Journal of Inherited Metabolic Disease|June 9, 2009
Coenzyme Q(10) is decreased in fibroblasts of patients with methylmalonic aciduria but not in mevalonic aciduriaD Haas, P Niklowitz, F Hörster, et al.
Journal of Inherited Metabolic Disease|January 13, 2022
Mitochondrial RNA processing defect caused by a SUPV3L1 mutation in two siblings with a novel neurodegenerative syndromeSelma L van Esveld, Richard J Rodenburg, Fathiya Al-Murshedi, et al.
Molecular Syndromology|November 1, 2012
A Diagnostic Algorithm for Mitochondrial Disorders in Estonian ChildrenK Joost, R J Rodenburg, A Piirsoo, et al.
Pageof 22