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

N J BRANDT

Showing results (41-50 of 52) with videos related to

Pageof 6
Sort By:
The Journal of Pediatrics|May 1, 1977
Glutaric aciduria: clinical and laboratory findings in two brothersN Gregersen, N J Brandt, E Christensen, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|February 1, 1982
Nation-wide TSH-screening with low recall rate. Laboratory results of a two-year studyL Hummer, T Munkner, S S Sørensen, et al.
Pediatric Research|October 1, 1982
C6-C10-dicarboxylic aciduria: investigations of a patient with riboflavin responsive multiple acyl-CoA dehydrogenation defectsN Gregersen, H Wintzensen, S K Christensen, et al.
The Southeast Asian Journal of Tropical Medicine and Public Health|June 13, 2001
Design of a pilot study to evaluate tandem mass spectrometry for neonatal screeningH Simonsen, U G Jensen, N J Brandt, et al.
Clinical Chemistry|July 27, 2001
Neonatal screening for galactosemia by quantitative analysis of hexose monophosphates using tandem mass spectrometry: a retrospective studyU G Jensen, N J Brandt, E Christensen, et al.
Acta Paediatrica Scandinavica|January 1, 1982
Metabolic events in infants of diabetic mothers during first 24 hours after birth. III. Changes in plasma amino acidsJ Hertel, G E Andersen, N J Brandt, et al.
Journal of Inherited Metabolic Disease|January 1, 1980
Biochemical studies in a patient with defects in the metabolism of acyl-CoA and sarcosine: another possible case of glutaric aciduria type IIN Gregersen, S Kølvraa, K Rasmussen, et al.
Human Genetics|September 1, 1993
Molecular analysis in patients with mucopolysaccharidosis type II suggests that DXS466 maps within the Hunter geneC Steglich, S Bunge, T Hulsebos, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 11, 1981
Urinary excretion of succinylacetone and delta-aminolevulinic acid in patients with hereditary tyrosinemiaE Christensen, B B Jacobsen, N Gregersen, et al.
Acta Paediatrica Scandinavica|March 1, 1981
Thyroxine-binding globulin deficiency in early childhood. Postnatal changes in serum concentrations of thyroid hormones and thyroid hormone-binding proteinsB B Jacobsen, L C Hansted, N J Brandt, et al.
Pageof 6

Showing results (41-50 of 52) with videos related to

Sort By:
Pageof 6
The Journal of Pediatrics|May 1, 1977
Glutaric aciduria: clinical and laboratory findings in two brothersN Gregersen, N J Brandt, E Christensen, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|February 1, 1982
Nation-wide TSH-screening with low recall rate. Laboratory results of a two-year studyL Hummer, T Munkner, S S Sørensen, et al.
Pediatric Research|October 1, 1982
C6-C10-dicarboxylic aciduria: investigations of a patient with riboflavin responsive multiple acyl-CoA dehydrogenation defectsN Gregersen, H Wintzensen, S K Christensen, et al.
The Southeast Asian Journal of Tropical Medicine and Public Health|June 13, 2001
Design of a pilot study to evaluate tandem mass spectrometry for neonatal screeningH Simonsen, U G Jensen, N J Brandt, et al.
Clinical Chemistry|July 27, 2001
Neonatal screening for galactosemia by quantitative analysis of hexose monophosphates using tandem mass spectrometry: a retrospective studyU G Jensen, N J Brandt, E Christensen, et al.
Acta Paediatrica Scandinavica|January 1, 1982
Metabolic events in infants of diabetic mothers during first 24 hours after birth. III. Changes in plasma amino acidsJ Hertel, G E Andersen, N J Brandt, et al.
Journal of Inherited Metabolic Disease|January 1, 1980
Biochemical studies in a patient with defects in the metabolism of acyl-CoA and sarcosine: another possible case of glutaric aciduria type IIN Gregersen, S Kølvraa, K Rasmussen, et al.
Human Genetics|September 1, 1993
Molecular analysis in patients with mucopolysaccharidosis type II suggests that DXS466 maps within the Hunter geneC Steglich, S Bunge, T Hulsebos, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 11, 1981
Urinary excretion of succinylacetone and delta-aminolevulinic acid in patients with hereditary tyrosinemiaE Christensen, B B Jacobsen, N Gregersen, et al.
Acta Paediatrica Scandinavica|March 1, 1981
Thyroxine-binding globulin deficiency in early childhood. Postnatal changes in serum concentrations of thyroid hormones and thyroid hormone-binding proteinsB B Jacobsen, L C Hansted, N J Brandt, et al.
Pageof 6