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

O Borud

Showing results (1-10 of 20) with videos related to

Pageof 2
Sort By:
Scandinavian Journal of Clinical and Laboratory Investigation|September 1, 1977
Metabolic studies on normal and pyruvate dehydrogenase deficient cultured human fibroblastsO Borud, J H Stroomme
Journal of Inherited Metabolic Disease|January 1, 1982
Normal 2-aminobutyrate oxidation and increased valine oxidation in fibroblasts deficient in pyruvate dehydrogenaseO Borud, J E Pettersen
Journal of Inherited Metabolic Disease|January 1, 1978
Secondary metabolic changes in fibroblasts from six patients with hereditary lactic acidosisO Borud, J H Strømme
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 17, 1976
Dopamine-beta-hydroxylase activity in serum following acute myocardial infarction: an evaluation of this parameter for routine use as an index of sympathetic activityT Gutteberg, O Borud, J H Stromme
Journal of Inherited Metabolic Disease|January 1, 1980
Combined iminoglycinuria and cystine- and dibasic aminoaciduria in patients with propionic acidaemia and 3-methylcrotonylglycinuriaP Purkiss, R A Chalmers, O Borud
Acta Paediatrica (Oslo, Norway : 1992)|September 1, 1994
Lactate and pyruvate concentrations in capillary blood from newbornsJ Nielsen, L M Ytrebø, O Borud
ORL; Journal for Oto-Rhino-Laryngology and Its Related Specialties|January 1, 1977
Hereditary deafness in the cat. Free amino acid and sugar content in the perilymphH H Elverland, I W Mair, O Borud
Pediatric Research|January 1, 1976
Fatal lactic acidosis in a newborn attributable to a congenital defect of pyruvate dehydrogenaseJ H Strömme, O Borud, P J Moe
Journal of Mental Deficiency Research|June 1, 1989
Cystathioninuria in Down's syndromeA Hestnes, O Borud, H Lunde, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 1, 1977
Gas chromatographic and mass spectrometric studies on urinary organic acids in a patient with congenital lactic acidosis due to pyruvate decarboxylase deficiencyR A Chalmers, A M Lawson, O Borud
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Scandinavian Journal of Clinical and Laboratory Investigation|September 1, 1977
Metabolic studies on normal and pyruvate dehydrogenase deficient cultured human fibroblastsO Borud, J H Stroomme
Journal of Inherited Metabolic Disease|January 1, 1982
Normal 2-aminobutyrate oxidation and increased valine oxidation in fibroblasts deficient in pyruvate dehydrogenaseO Borud, J E Pettersen
Journal of Inherited Metabolic Disease|January 1, 1978
Secondary metabolic changes in fibroblasts from six patients with hereditary lactic acidosisO Borud, J H Strømme
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 17, 1976
Dopamine-beta-hydroxylase activity in serum following acute myocardial infarction: an evaluation of this parameter for routine use as an index of sympathetic activityT Gutteberg, O Borud, J H Stromme
Journal of Inherited Metabolic Disease|January 1, 1980
Combined iminoglycinuria and cystine- and dibasic aminoaciduria in patients with propionic acidaemia and 3-methylcrotonylglycinuriaP Purkiss, R A Chalmers, O Borud
Acta Paediatrica (Oslo, Norway : 1992)|September 1, 1994
Lactate and pyruvate concentrations in capillary blood from newbornsJ Nielsen, L M Ytrebø, O Borud
ORL; Journal for Oto-Rhino-Laryngology and Its Related Specialties|January 1, 1977
Hereditary deafness in the cat. Free amino acid and sugar content in the perilymphH H Elverland, I W Mair, O Borud
Pediatric Research|January 1, 1976
Fatal lactic acidosis in a newborn attributable to a congenital defect of pyruvate dehydrogenaseJ H Strömme, O Borud, P J Moe
Journal of Mental Deficiency Research|June 1, 1989
Cystathioninuria in Down's syndromeA Hestnes, O Borud, H Lunde, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 1, 1977
Gas chromatographic and mass spectrometric studies on urinary organic acids in a patient with congenital lactic acidosis due to pyruvate decarboxylase deficiencyR A Chalmers, A M Lawson, O Borud
Pageof 2