Congenital Hypothyroidism: Influence of Disease Severity and L-Thyroxine Treatment on Intellectual, Motor, and School-Associated Outcomes in Young Adults von Oerbeck, Beate, Sundet, Kjetil, Kase, Bengt F, Heyerdahl, Sonja

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Screening for Serum Total Homocysteine in Newborn Children von Refsum, Helga, Grindflek, Anne W, Ueland, Per M, Fredriksen, Ase, Meyer, Klaus, Ulvik, Arve, Guttormsen, Anne B, Iversen, Ole E, Schneede, Jorn, Kase, Bengt F

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Congenital hypothyroidism: no adverse effects of high dose thyroxine treatment on adult memory, attention, and behaviour von Oerbeck, B, Sundet, K, Kase, B F, Heyerdahl, S

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Evaluation of Novel Assays in Clinical Chemistry: Quantification of Plasma Total Homocysteine von Nexo, Ebba, Engbaek, Frode, Ueland, Per Magne, Westby, Christina, O'Gorman, Paudy, Johnston, Carole, Kase, Bengt Frode, Guttormsen, Anne B, Alfheim, Ingrid, McPartlin, Joseph, Smith, David, Moller, Jan, Rasmussen, Karsten, Clarke, Robert, Scott, John M, Refsum, Helga

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Severe hypothyroidism due to atrophic thyroiditis from second year of life influenced developmental outcome von JOERGENSEN, J. V, OERBECK, B, JEBSEN, P, HEYERDAHL, S, KASE, B. F

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Urinary Peptides in Rett Syndrome von Solaas, K. M., Skjeldal, O., Gardner, M. L. G., Kase, B. F., Reichelt, K. L.

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Linear growth in early treated children with congenital hypothyroidism von Heyerdahl, S, Ilicki, A, Karlberg, J, Kase, BF, Larsson, A

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Subcellular organization of bile acid amidation in human liver: a key issue in regulating the biosynthesis of bile salts von Solaas, K, Ulvestad, A, Söreide, O, Kase, B F

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The study of delivery condition including age of mothers, parity, gravida, amount of blood loss and neonatal condition at 13 primary health centre (PHC) of Lagos state in Nigeria von Suzui, E, Tsukada, Y, Kase, F

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Peroxisomal Bile Acid-CoA: Amino-Acid N-Acyltransferase in Rat Liver von Kase, B F, Björkhem, I

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Presence of choloyl- and chenodeoxycholoyl-coenzyme A thioesterase activity in human liver von Solaas, K., Sletta, R. J., Søreide, O., Kase, B. F.

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LET dependence of cell death and chromatin-break induction in normal human cells irradiated by neon-ion beams von SUZUKI, Y. KASE, T. KANAI, F. YATAGAI and M. WATANABE, M.

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Studies on the degradation of [U-3H]-phytanic acid and [U-3H]-pristanic acid in cultured fibroblasts from children with peroxisomal disorders von Kase, B. F., Björkhem, I.

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Infantile Refsum's disease: A generalized peroxisomal disorder: Case report with postmortem examination von Torvik, A., Torp, S., Kase, B.F., Ek, J., Skjeldal, O., Stokke, O.

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Peroxisomal chain-shortening of thromboxane B2 : evidence for impaired degradation of thromboxane B2 in Zellweger syndrome von DICZFALUSY, U, VESTERQVIST, O, FRODE KASE, B, LUND, E, ALEXSON, S. E. H

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Formation of cholic acid from 3 alpha, 7 alpha, 12 alpha-trihydroxy-5 beta-cholestanoic acid by rat liver peroxisomes von Kase, F, Björkhem, I, Pedersen, J I

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Mutations in the iduronate-2-sulfatase gene in five Norwegians with Hunter syndrome von OLSEN, T. C, EIKEN, H. G, KNAPPSKOG, P. M, KASE, B. F, MANSSON, J.-E, BOMAN, H, APOLD, J

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Characterization of an Acyl-CoA Thioesterase That Functions as a Major Regulator of Peroxisomal Lipid Metabolism von Hunt, Mary C, Solaas, Karianne, Kase, B Frode, Alexson, Stefan E H

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Simple diagnosis of the Zellweger syndrome by gas-liquid chromatography of dimethylacetals von Björkhem, I, Sisfontes, L, Boström, B, Kase, B F, Blomstrand, R

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Intellectual development in children with congenital hypothyroidism in relation to recommended thyroxine treatment von Heyerdahl, Sonja, Kase, Bengt Frode, Lie, Sverre Olaf

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