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E A Kvittingen

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Scandinavian Journal of Clinical and Laboratory Investigation. Supplementum|January 1, 1990
Diagnosis of metabolic disease by measurement of intracellular enzyme activityE A Kvittingen
Journal of Inherited Metabolic Disease|January 1, 1991
Tyrosinaemia type I--an updateE A Kvittingen
Scandinavian Journal of Clinical and Laboratory Investigation. Supplementum|January 1, 1986
Hereditary tyrosinemia type I--an overviewE A Kvittingen
Journal of Inherited Metabolic Disease|January 1, 1995
Tyrosinaemia--treatment and outcomeE A Kvittingen
Scandinavian Journal of Clinical and Laboratory Investigation. Supplementum|January 1, 1986
The pre- and post-natal diagnosis of tyrosinemia type I and the detection of the carrier state by assay of fumarylacetoacetaseE A Kvittingen, E Brodtkorb
American Journal of Human Genetics|December 1, 1994
Identification of a frequent pseudodeficiency mutation in the fumarylacetoacetase gene, with implications for diagnosis of tyrosinemia type IH Rootwelt, E Brodtkorb, E A Kvittingen
Acta Paediatrica Japonica : Overseas Edition|August 1, 1988
Outcome of therapy of hereditary tyrosinemiaS Halvorsen, E A Kvittingen, A Flatmark
Pediatric Research|July 1, 1983
Deficient fumarylacetoacetate fumarylhydrolase activity in lymphocytes and fibroblasts from patients with hereditary tyrosinemiaE A Kvittingen, S Halvorsen, E Jellum
Biomedical & Environmental Mass Spectrometry|October 1, 1988
Mass spectrometry in diagnosis of metabolic disordersE Jellum, E A Kvittingen, O Stokke
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 1, 1981
Assay of fumarylacetoacetate fumarylhydrolase in human liver-deficient activity in a case of hereditary tyrosinemiaE A Kvittingen, E Jellum, O Stokke
Pageof 5

Showing results (1-10 of 50) with videos related to

Sort By:
Pageof 5
Scandinavian Journal of Clinical and Laboratory Investigation. Supplementum|January 1, 1990
Diagnosis of metabolic disease by measurement of intracellular enzyme activityE A Kvittingen
Journal of Inherited Metabolic Disease|January 1, 1991
Tyrosinaemia type I--an updateE A Kvittingen
Scandinavian Journal of Clinical and Laboratory Investigation. Supplementum|January 1, 1986
Hereditary tyrosinemia type I--an overviewE A Kvittingen
Journal of Inherited Metabolic Disease|January 1, 1995
Tyrosinaemia--treatment and outcomeE A Kvittingen
Scandinavian Journal of Clinical and Laboratory Investigation. Supplementum|January 1, 1986
The pre- and post-natal diagnosis of tyrosinemia type I and the detection of the carrier state by assay of fumarylacetoacetaseE A Kvittingen, E Brodtkorb
American Journal of Human Genetics|December 1, 1994
Identification of a frequent pseudodeficiency mutation in the fumarylacetoacetase gene, with implications for diagnosis of tyrosinemia type IH Rootwelt, E Brodtkorb, E A Kvittingen
Acta Paediatrica Japonica : Overseas Edition|August 1, 1988
Outcome of therapy of hereditary tyrosinemiaS Halvorsen, E A Kvittingen, A Flatmark
Pediatric Research|July 1, 1983
Deficient fumarylacetoacetate fumarylhydrolase activity in lymphocytes and fibroblasts from patients with hereditary tyrosinemiaE A Kvittingen, S Halvorsen, E Jellum
Biomedical & Environmental Mass Spectrometry|October 1, 1988
Mass spectrometry in diagnosis of metabolic disordersE Jellum, E A Kvittingen, O Stokke
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 1, 1981
Assay of fumarylacetoacetate fumarylhydrolase in human liver-deficient activity in a case of hereditary tyrosinemiaE A Kvittingen, E Jellum, O Stokke
Pageof 5