Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Bengt Frode Kase"'
Publikováno v:
Journal of Lipid Research, Vol 41, Iss 7, Pp 1154-1162 (2000)
To extend our knowledge of how the synthesis of free bile acids and bile salts is regulated within the hepatocyte, bile acid-CoA:amino acid N-acyltransferase and bile acid-CoA thioesterase activities were measured in subcellular fractions of human li
Externí odkaz:
https://doaj.org/article/774bc79ef8264b5b9788736ab95ace11
Publikováno v:
Scandinavian Journal of Clinical and Laboratory Investigation. 78:566-574
The risks of developing energy or nutrient deficits are of great concern in infants and children with the rare lymphoedema cholestasis syndrome 1 (LCS1)/Aagenaes syndrome. In adolescents and adults, it is not known whether LCS1 patients need specific
Publikováno v:
Scandinavian Journal of Disability Research. 17:321-334
Today most adults with phenylketonuria (PKU) have followed a protein restricted diet from early infancy. This makes their disorder an invisible impairment which becomes visible only when food is served. When adhering to medical advice in public, adul
Autor:
Åse Fredriksen, Bengt Frode Kase, Anne Berit Guttormsen, Ole Erik Iversen, Klaus Meyer, Jörn Schneede, Helga Refsum, Arve Ulvik, Anne W. Grindflek, Per Magne Ueland
Publikováno v:
Clinical Chemistry. 50:1769-1784
Background: Newborn screening for total homocysteine (tHcy) in blood may identify babies with vitamin B12 (B12) deficiency or homocystinuria, but data on the causes of increased tHcy in screening samples are sparse.Methods: Serum concentrations of tH
Publikováno v:
Lymphatic research and biology. 12(4)
The characterizations of primary lymphedemas in different hereditary diseases are often published as case reports. In this study, 17 out of 20 Norweigian adult patients with lymphedema cholestasis syndrome 1 (LCS1)/Aagenaes syndrome were examined. Th
Autor:
Joseph McPartlin, Christina Westby, Ebba Nexo, Karsten Rasmussen, Per Magne Ueland, Bengt Frode Kase, John M. Scott, Anne Berit Guttormsen, Ingrid Alfheim, Frode Engbaek, Paudy O’Gorman, Robert Clarke, Carole Johnston, Helga Refsum, David Smith, Jan Møller
Publikováno v:
Clinical Chemistry. 46:1150-1156
Background: There is a need for systematic evaluation of methods before their release to the market. We addressed this problem in novel homocysteine assays as part of an European Demonstration Project involving six centers in four countries. Methods:
Autor:
Sedegheh Garagozlian, Kristian Prydz, Bengt Frode Kase, Bente Halvorsen, Svein Olav Kolset, Marianne S. Andresen
Publikováno v:
Biochemical Journal. 343:533-539
High levels of bile acids in the colon may correlate with an increased risk of colon cancer, but the underlying mechanisms are not known. Proteoglycan structures have been shown to change when human colon cells differentiate in vitro. The expression
Publikováno v:
JIMD Reports ISBN: 9783642324413
The main treatment for phenylketonuria (PKU) is a low phenylalanine (Phe) diet, phenylalanine-free protein substitute and low-protein special foods. This study describes dietary composition and nutritional status in late-diagnosed adult patients adhe
Publikováno v:
Pediatric Research. 29:64-69
Infantile Zellweger syndrome belongs to the group of peroxisomal disorders that lack peroxisomes. Both trihydroxycoprostanic acid (THCA), the precursor to cholic acid, and dihydroxycoprostanic acid (DHCA), the precursor to chenodeoxycholic acid, accu
Autor:
Beate, Ørbeck, Kjetil, Sundet, Jens Veilemand, Jørgensen, Bengt Frode, Kase, Sonja, Heyerdahl
Publikováno v:
Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke. 125(22)
We have studied the significance of the thyroxine treatment for neuropsychological functioning in young adults with congenital hypothyroidism.This is a neuropsychological follow-up study of a three-year cohort of early treated congenital hypothyroidi