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Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 20, 2005
Laboratory diagnosis of defects of creatine biosynthesis and transport
Nanda M Verhoeven, Gajja S Salomons, Cornelis Jakobs
Clinical Chemistry
|
June 21, 2003
Disease-related metabolites in culture medium of fibroblasts from patients with D-2-hydroxyglutaric aciduria, L-2-hydroxyglutaric aciduria, and combined D/L-2-hydroxyglutaric aciduria
Eduard A Struys, Nanda M Verhoeven, Birthe Roos, et al.
FEBS Letters
|
January 27, 2004
Investigations by mass isotopomer analysis of the formation of D-2-hydroxyglutarate by cultured lymphoblasts from two patients with D-2-hydroxyglutaric aciduria
Eduard A Struys, Nanda M Verhoeven, Henri Brunengraber, et al.
The Journal of Biological Chemistry
|
April 25, 2012
Identification of a human trans-3-hydroxy-L-proline dehydratase, the first characterized member of a novel family of proline racemase-like enzymes
Wouter F Visser, Nanda M Verhoeven-Duif, Tom J de Koning
Clinical Chemistry
|
May 29, 2004
Measurement of urinary D- and L-2-hydroxyglutarate enantiomers by stable-isotope-dilution liquid chromatography-tandem mass spectrometry after derivatization with diacetyl-L-tartaric anhydride
Eduard A Struys, Erwin E W Jansen, Nanda M Verhoeven, et al.
The Journal of Biological Chemistry
|
February 15, 2025
Anaplerosis by medium-chain fatty acids through complex interplay with glucose and glutamine metabolism
Hannah M German, Jolita Ciapaite, Nanda M Verhoeven-Duif, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences
|
November 29, 2005
A novel, quantitative assay for homocarnosine in cerebrospinal fluid using stable-isotope dilution liquid chromatography-tandem mass spectrometry
Erwin E W Jansen, K Michael Gibson, Yosuke Shigematsu, et al.
Journal of Inherited Metabolic Disease
|
February 11, 2014
The potential of exosomes in diagnosis and treatment of inborn errors of metabolism
Bas W M van Balkom, Jaap van Doorn, Nanda M Verhoeven-Duif, et al.
Journal of Inherited Metabolic Disease
|
May 24, 2019
Pathophysiology of propionic and methylmalonic acidemias. Part 2: Treatment strategies
Hanneke A Haijes, Peter M van Hasselt, Judith J M Jans, et al.
Molecular Genetics and Metabolism
|
July 6, 2004
Evaluation of pentitol metabolism in mammalian tissues provides new insight into disorders of human sugar metabolism
Jojanneke H J Huck, Birthe Roos, Cornelis Jakobs, et al.
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Search research articles
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Showing results (1-10 of 107) with videos related to
Sort By:
Page
of 11
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 20, 2005
Laboratory diagnosis of defects of creatine biosynthesis and transport
Nanda M Verhoeven, Gajja S Salomons, Cornelis Jakobs
Clinical Chemistry
|
June 21, 2003
Disease-related metabolites in culture medium of fibroblasts from patients with D-2-hydroxyglutaric aciduria, L-2-hydroxyglutaric aciduria, and combined D/L-2-hydroxyglutaric aciduria
Eduard A Struys, Nanda M Verhoeven, Birthe Roos, et al.
FEBS Letters
|
January 27, 2004
Investigations by mass isotopomer analysis of the formation of D-2-hydroxyglutarate by cultured lymphoblasts from two patients with D-2-hydroxyglutaric aciduria
Eduard A Struys, Nanda M Verhoeven, Henri Brunengraber, et al.
The Journal of Biological Chemistry
|
April 25, 2012
Identification of a human trans-3-hydroxy-L-proline dehydratase, the first characterized member of a novel family of proline racemase-like enzymes
Wouter F Visser, Nanda M Verhoeven-Duif, Tom J de Koning
Clinical Chemistry
|
May 29, 2004
Measurement of urinary D- and L-2-hydroxyglutarate enantiomers by stable-isotope-dilution liquid chromatography-tandem mass spectrometry after derivatization with diacetyl-L-tartaric anhydride
Eduard A Struys, Erwin E W Jansen, Nanda M Verhoeven, et al.
The Journal of Biological Chemistry
|
February 15, 2025
Anaplerosis by medium-chain fatty acids through complex interplay with glucose and glutamine metabolism
Hannah M German, Jolita Ciapaite, Nanda M Verhoeven-Duif, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences
|
November 29, 2005
A novel, quantitative assay for homocarnosine in cerebrospinal fluid using stable-isotope dilution liquid chromatography-tandem mass spectrometry
Erwin E W Jansen, K Michael Gibson, Yosuke Shigematsu, et al.
Journal of Inherited Metabolic Disease
|
February 11, 2014
The potential of exosomes in diagnosis and treatment of inborn errors of metabolism
Bas W M van Balkom, Jaap van Doorn, Nanda M Verhoeven-Duif, et al.
Journal of Inherited Metabolic Disease
|
May 24, 2019
Pathophysiology of propionic and methylmalonic acidemias. Part 2: Treatment strategies
Hanneke A Haijes, Peter M van Hasselt, Judith J M Jans, et al.
Molecular Genetics and Metabolism
|
July 6, 2004
Evaluation of pentitol metabolism in mammalian tissues provides new insight into disorders of human sugar metabolism
Jojanneke H J Huck, Birthe Roos, Cornelis Jakobs, et al.
Page
of 11