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

F J van Sprang

Showing results (21-30 of 30) with videos related to

Pageof 3
Sort By:
You have reached the last page of results.This site can display upto 30 results.
European Journal of Pediatrics|July 1, 1981
A case of formiminoglutamic aciduria. Clinical and biochemical studiesM Duran, D Ketting, P K de Bree, et al.
Advances in Experimental Medicine and Biology|January 1, 1984
New defects of pyrimidine metabolismS K Wadman, F A Beemer, P K de Bree, et al.
Lancet (London, England)|July 1, 1989
Sudden infant death and long-chain 3-hydroxyacyl-CoA dehydrogenaseR J Wanders, M Duran, L Ijlst, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of a new inborn error of mitochondrial fatty acid beta-oxidationR J Wanders, L IJlst, A H van Gennip, et al.
Journal of Inherited Metabolic Disease|January 1, 1988
Beta-mannosidosis in two brothers with hearing lossL Dorland, M Duran, F E Hoefnagels, et al.
Helvetica Paediatrica Acta|December 1, 1976
Lethal neonatal argininosuccinate lyase deficiency in four children from one sibshipC van der Heiden, L J Gerards, J P van Biervliet, et al.
European Journal of Pediatrics|October 1, 1988
3-Methylglutaconic aciduria: a phenotype in which activity of 3-methylglutaconyl-coenzyme A hydratase is normalK M Gibson, W L Nyhan, L Sweetman, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 31, 1990
Rapid diagnosis of 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency via enzyme activity measurements in leukocytes or platelets using a simple spectrophotometric methodR J Wanders, P H Zoeters, R B Schutgens, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 30, 1983
Urinary excretion of deuterated metabolites in patients with tyrosinemia type I after oral loading with deuterated L-tyrosineS K Wadman, M Duran, D Ketting, et al.
European Journal of Pediatrics|November 1, 1988
Adenylosuccinase deficiency: an inborn error of purine nucleotide synthesisJ Jaeken, S K Wadman, M Duran, et al.
Pageof 3

Showing results (21-30 of 30) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
European Journal of Pediatrics|July 1, 1981
A case of formiminoglutamic aciduria. Clinical and biochemical studiesM Duran, D Ketting, P K de Bree, et al.
Advances in Experimental Medicine and Biology|January 1, 1984
New defects of pyrimidine metabolismS K Wadman, F A Beemer, P K de Bree, et al.
Lancet (London, England)|July 1, 1989
Sudden infant death and long-chain 3-hydroxyacyl-CoA dehydrogenaseR J Wanders, M Duran, L Ijlst, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of a new inborn error of mitochondrial fatty acid beta-oxidationR J Wanders, L IJlst, A H van Gennip, et al.
Journal of Inherited Metabolic Disease|January 1, 1988
Beta-mannosidosis in two brothers with hearing lossL Dorland, M Duran, F E Hoefnagels, et al.
Helvetica Paediatrica Acta|December 1, 1976
Lethal neonatal argininosuccinate lyase deficiency in four children from one sibshipC van der Heiden, L J Gerards, J P van Biervliet, et al.
European Journal of Pediatrics|October 1, 1988
3-Methylglutaconic aciduria: a phenotype in which activity of 3-methylglutaconyl-coenzyme A hydratase is normalK M Gibson, W L Nyhan, L Sweetman, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 31, 1990
Rapid diagnosis of 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency via enzyme activity measurements in leukocytes or platelets using a simple spectrophotometric methodR J Wanders, P H Zoeters, R B Schutgens, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 30, 1983
Urinary excretion of deuterated metabolites in patients with tyrosinemia type I after oral loading with deuterated L-tyrosineS K Wadman, M Duran, D Ketting, et al.
European Journal of Pediatrics|November 1, 1988
Adenylosuccinase deficiency: an inborn error of purine nucleotide synthesisJ Jaeken, S K Wadman, M Duran, et al.
Pageof 3