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Richard J T Rodenburg

Showing results (1-10 of 61) with videos related to

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Journal of Inherited Metabolic Disease|May 5, 2010
Biochemical diagnosis of mitochondrial disordersRichard J T Rodenburg
Journal of Inherited Metabolic Disease|August 30, 2011
Mitochondrial ATP synthase: architecture, function and pathologyAn I Jonckheere, Jan A M Smeitink, Richard J T Rodenburg
International Journal of Chronic Obstructive Pulmonary Disease|December 1, 2007
Mitochondrial function in diaphragm of emphysematous hamsters after treatment with nandroloneHanneke J H Wijnhoven, Leo Ennen, Richard J T Rodenburg, et al.
Mitochondrion|May 23, 2006
Females with PDHA1 gene mutations: a diagnostic challengeMarjolein Willemsen, Richard J T Rodenburg, Alexandra Teszas, et al.
Brain & Development|July 21, 2019
ARX-associated infantile epileptic-dyskinetic encephalopathy with responsiveness to valproate for controlling seizures and reduced activity of muscle mitochondrial complex IVAnna Ka-Yee Kwong, Vanessa Loi-Yan Chu, Richard J T Rodenburg, et al.
International Immunopharmacology|December 8, 2005
Beta-adrenergic receptor agonists induce the release of granulocyte chemotactic protein-2, oncostatin M, and vascular endothelial growth factor from macrophagesKitty C M Verhoeckx, Robert P Doornbos, Renger F Witkamp, et al.
The Analyst|January 1, 2004
Detection of hormonal anabolic compounds in calf urine and unverified growth-promoting preparations: application of the AR-LUX bioassay for screening and determination of androgenic activityBarry M G Blankvoort, Jac M M J G Aarts, Robert Schilt, et al.
American Journal of Human Genetics|December 23, 2006
Leigh syndrome with nephropathy and CoQ10 deficiency due to decaprenyl diphosphate synthase subunit 2 (PDSS2) mutationsLuis Carlos López, Markus Schuelke, Catarina M Quinzii, et al.
Proteomics|March 30, 2004
A combination of proteomics, principal component analysis and transcriptomics is a powerful tool for the identification of biomarkers for macrophage maturation in the U937 cell lineKitty C M Verhoeckx, Sabina Bijlsma, Els M de Groene, et al.
BBA Clinical|June 23, 2016
Three families with 'de novo' m.3243A > G mutationPaul de Laat, Mirian C H Janssen, Charlotte L Alston, et al.
Pageof 7

Showing results (1-10 of 61) with videos related to

Sort By:
Pageof 7
Journal of Inherited Metabolic Disease|May 5, 2010
Biochemical diagnosis of mitochondrial disordersRichard J T Rodenburg
Journal of Inherited Metabolic Disease|August 30, 2011
Mitochondrial ATP synthase: architecture, function and pathologyAn I Jonckheere, Jan A M Smeitink, Richard J T Rodenburg
International Journal of Chronic Obstructive Pulmonary Disease|December 1, 2007
Mitochondrial function in diaphragm of emphysematous hamsters after treatment with nandroloneHanneke J H Wijnhoven, Leo Ennen, Richard J T Rodenburg, et al.
Mitochondrion|May 23, 2006
Females with PDHA1 gene mutations: a diagnostic challengeMarjolein Willemsen, Richard J T Rodenburg, Alexandra Teszas, et al.
Brain & Development|July 21, 2019
ARX-associated infantile epileptic-dyskinetic encephalopathy with responsiveness to valproate for controlling seizures and reduced activity of muscle mitochondrial complex IVAnna Ka-Yee Kwong, Vanessa Loi-Yan Chu, Richard J T Rodenburg, et al.
International Immunopharmacology|December 8, 2005
Beta-adrenergic receptor agonists induce the release of granulocyte chemotactic protein-2, oncostatin M, and vascular endothelial growth factor from macrophagesKitty C M Verhoeckx, Robert P Doornbos, Renger F Witkamp, et al.
The Analyst|January 1, 2004
Detection of hormonal anabolic compounds in calf urine and unverified growth-promoting preparations: application of the AR-LUX bioassay for screening and determination of androgenic activityBarry M G Blankvoort, Jac M M J G Aarts, Robert Schilt, et al.
American Journal of Human Genetics|December 23, 2006
Leigh syndrome with nephropathy and CoQ10 deficiency due to decaprenyl diphosphate synthase subunit 2 (PDSS2) mutationsLuis Carlos López, Markus Schuelke, Catarina M Quinzii, et al.
Proteomics|March 30, 2004
A combination of proteomics, principal component analysis and transcriptomics is a powerful tool for the identification of biomarkers for macrophage maturation in the U937 cell lineKitty C M Verhoeckx, Sabina Bijlsma, Els M de Groene, et al.
BBA Clinical|June 23, 2016
Three families with 'de novo' m.3243A > G mutationPaul de Laat, Mirian C H Janssen, Charlotte L Alston, et al.
Pageof 7