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

D Ketting

Showing results (51-60 of 55) with videos related to

Pageof 6
Sort By:
You have reached the last page of results.This site can display upto 55 results.
Developmental Medicine and Child Neurology|June 1, 1977
Report of a patient with severe, chronic lactic acidaemia and pyruvate carboxylase deficiencyJ P Van Biervliet, L Bruinvis, C van der Heiden, 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.
The Journal of Pediatrics|September 1, 1985
Octanoic acidemia and octanoylcarnitine excretion with dicarboxylic aciduria due to defective oxidation of medium-chain fatty acidsM Duran, G Mitchell, J B de Klerk, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 20, 1976
D-Glyceric acidemia in a patient with chronic metabolic acidosisS K Wadman, M Duran, D Ketting, 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.
Pageof 6

Showing results (51-60 of 55) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 55 results.
Developmental Medicine and Child Neurology|June 1, 1977
Report of a patient with severe, chronic lactic acidaemia and pyruvate carboxylase deficiencyJ P Van Biervliet, L Bruinvis, C van der Heiden, 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.
The Journal of Pediatrics|September 1, 1985
Octanoic acidemia and octanoylcarnitine excretion with dicarboxylic aciduria due to defective oxidation of medium-chain fatty acidsM Duran, G Mitchell, J B de Klerk, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 20, 1976
D-Glyceric acidemia in a patient with chronic metabolic acidosisS K Wadman, M Duran, D Ketting, 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.
Pageof 6