Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

J M Trijbels

Showing results (31-40 of 177) with videos related to

Pageof 18
Sort By:
Journal of Inherited Metabolic Disease|January 1, 1990
Heterogeneous tissue expression of enzyme defects in mitochondrial myopathiesW Sperl, W Ruitenbeek, J M Trijbels, et al.
Acta Paediatrica Scandinavica|January 1, 1974
The IMP dehydrogenase catalysed reaction in erythrocytes of normal individuals and patients with hypoxanthine guanine phosphoribosyltransferase deficiencyE J Lommen, R A de Abreu, J M Trijbels, et al.
Metabolism: Clinical and Experimental|May 1, 1989
Reproducibility of urinary 3-methylhistidine excretion in human subjects consuming freely selected dietsH P Peters, M A van Erp-Baart, J M Trijbels, et al.
Journal of Chromatography. B, Biomedical Applications|October 6, 1995
Determination of extracellular and intracellular thiopurines and methylthiopurines by high-performance liquid chromatographyC W Keuzenkamp-Jansen, R A De Abreu, J P Bökkerink, et al.
Leukemia Research|July 1, 1995
High-dose 6-mercaptopurine infusions and tumor lysis syndromeC W Keuzenkamp-Jansen, J P Bökkerink, R A De Abreu, et al.
Virchows Archiv. A, Pathological Anatomy and Histopathology|January 1, 1983
Fatal lipid storage myopathy with deficiency of cytochrome-c-oxidase and carnitine. A contribution to the combined cytochemical-finestructural identification of cytochrome-c-oxidase in longterm frozen muscleJ Müller-Höcker, D Pongratz, T Deufel, et al.
The Journal of Pediatrics|June 1, 1975
Congenital cataract and mitochondrial myopathy of skeletal and heart muscle associated with lactic acidosis after exerciseR C Sengers, J M Trijbels, J L Willems, 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.
Acta Paediatrica Scandinavica|May 1, 1970
The influence of adenine on the clinical features and purine metabolism in the Lesch-Nyhan syndromeS P van der Zee, E J Lommen, J M Trijbels, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Alternative methionine degradation via the transamination pathway: an option for therapy for homocystinuria due to cystathionine synthase deficiencyH J Blom, G H Boers, A Tangerman, et al.
Pageof 18

Showing results (31-40 of 177) with videos related to

Sort By:
Pageof 18
Journal of Inherited Metabolic Disease|January 1, 1990
Heterogeneous tissue expression of enzyme defects in mitochondrial myopathiesW Sperl, W Ruitenbeek, J M Trijbels, et al.
Acta Paediatrica Scandinavica|January 1, 1974
The IMP dehydrogenase catalysed reaction in erythrocytes of normal individuals and patients with hypoxanthine guanine phosphoribosyltransferase deficiencyE J Lommen, R A de Abreu, J M Trijbels, et al.
Metabolism: Clinical and Experimental|May 1, 1989
Reproducibility of urinary 3-methylhistidine excretion in human subjects consuming freely selected dietsH P Peters, M A van Erp-Baart, J M Trijbels, et al.
Journal of Chromatography. B, Biomedical Applications|October 6, 1995
Determination of extracellular and intracellular thiopurines and methylthiopurines by high-performance liquid chromatographyC W Keuzenkamp-Jansen, R A De Abreu, J P Bökkerink, et al.
Leukemia Research|July 1, 1995
High-dose 6-mercaptopurine infusions and tumor lysis syndromeC W Keuzenkamp-Jansen, J P Bökkerink, R A De Abreu, et al.
Virchows Archiv. A, Pathological Anatomy and Histopathology|January 1, 1983
Fatal lipid storage myopathy with deficiency of cytochrome-c-oxidase and carnitine. A contribution to the combined cytochemical-finestructural identification of cytochrome-c-oxidase in longterm frozen muscleJ Müller-Höcker, D Pongratz, T Deufel, et al.
The Journal of Pediatrics|June 1, 1975
Congenital cataract and mitochondrial myopathy of skeletal and heart muscle associated with lactic acidosis after exerciseR C Sengers, J M Trijbels, J L Willems, 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.
Acta Paediatrica Scandinavica|May 1, 1970
The influence of adenine on the clinical features and purine metabolism in the Lesch-Nyhan syndromeS P van der Zee, E J Lommen, J M Trijbels, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Alternative methionine degradation via the transamination pathway: an option for therapy for homocystinuria due to cystathionine synthase deficiencyH J Blom, G H Boers, A Tangerman, et al.
Pageof 18