Effect of near normoglycaemia for two years on progression of early diabetic retinopathy, nephropathy, and neuropathy: the Oslo study von Dahl-Jørgensen, K, Brinchmann-Hansen, O, Hanssen, K F, Ganes, T, Kierulf, P, Smeland, E, Sandvik, L, Aagenaes, O

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Autosomal Glycogenosis of Liver and Muscle Due to Phosphorylase Kinase Deficiency is Caused by Mutations in the Phosphorylase Kinase β Subunit (PHKB) von Burwinkel, Barbara, Maichele, Andrea J., Aagenaes, Øystein, Bakker, Henk D., Lerner, Aaron, Shin, Yoon S., Strachan, Judith A., Kilimann, Manfred W.

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Hereditary Cholestasis with Lymphoedema (Aagenaes Syndrome, Cholestasis-Lymphoedema Syndrome): New Cases and Follow-up from Infancy to Adult Age von Aagenaes, O

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Rapid tightening of blood glucose control leads to transient deterioration of retinopathy in insulin dependent diabetes mellitus: the Oslo study von Dahl-Jørgensen, K, Brinchmann-Hansen, O, Hanssen, K F, Sandvik, L, Aagenaes, O

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Tobacco use prevention in Norway--a terrible example? von Aagenaes, O

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Mapping of the Locus for Cholestasis-Lymphedema Syndrome (Aagenaes Syndrome) to a 6.6-cM Interval on Chromosome 15q von Bull, Laura N., Roche, Erin, Song, Eyun J., Pedersen, Jan, Knisely, A.S., van der Hagen, C.B., Eiklid, Kristin, Aagenaes, Øystein, Freimer, Nelson B.

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No difference in the parental origin of susceptibility HLA class II haplotypes among Norwegian patients with insulin-dependent diabetes mellitus von Undlien, D E, Akselsen, H E, Joner, G, Dahl-Jorgensen, K, Aagenaes, O, Sovik, O, Thorsby, E, Rønningen, K S

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Diabetic complications in a prepubertal adolescent von Sørensen, E, Aagenaes, O

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Evidence for genetic heterogeneity in lymphedema-cholestasis syndrome von Frühwirth, Martin, Janecke, Andreas R., Müller, Thomas, Carlton, Victoria E.H., Kronenberg, Florian, Offner, Felix, Knisely, A.S., Geleff, Silvana, Song, Eyun J., Simma, Burkhard, Königsrainer, Alfred, Margreiter, Raimund, van der Hagen, C.B., Eiklid, Kristin, Aagenaes, Øystein, Bull, Laura, Ellemunter, Helmut

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The Baerum issue von Aagenaes, Ø

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The effect of 8 years of strict glycaemic control on peripheral nerve function in IDDM patients: the Oslo Study von Amthor, K F, Dahl-Jørgensen, K, Berg, T J, Heier, M S, Sandvik, L, Aagenaes, O, Hanssen, K F

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Hereditary cholestasis with lymphoedema (Aagenaes syndrome, cholestasis-lymphoedema syndrome) von AAGENAES, Ø

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Hereditary recurrent intrahepatic cholestasis from birth von Aagenaes, O., van der Hagen, C. B., Refsum, S.

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Lymphoedema in Hereditary Recurrent Cholestasis from Birth von Aagenaes, Øystein, Sigstad, Helge, Bjørn-Hansen, Ragnar

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Wilsons disease in childhood. Surviving severe haemolytic crisis with coma von Aagenaes, O, Berg, K

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Pathology and pathogenesis of liver disease in alpha-1-antitrypsin deficient individuals von Aagenaes, O., TFagerhol, M., Elgjo, K., Munthe, E., Hovig, T.

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Growth Hormone Treatment in Achondroplasia: 2 Year Results of a Dose-Response Study von Hagenäs, Lars, Aagenaes, Øystein, Eklöf, Ole, Hertel, Thomas, Kaitila, Ilkka, Mohnike, Klaus, Perhentuupa, Jaako, Ritzén, Martin, Sipilä, Ilkka, Müller, Jørn

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Cholestatic jaundice in infancy. The importance of familial and genetic factors in aetiology and prognosis von Henriksen, N T, Drabløs, P A, Aagenaes, O

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The human Y chrosome and the etiology of true hermaphroditism with the report of a case with XX-XY sex chromosome mosaicism von Brogger, A, Aagenaes, O

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Homozygous mutation (A228T) in the 5alpha-reductase type 2 gene in a boy with 5alpha-reductase deficiency: genotype-phenotype correlations von Nordenskjöld, A, Magnus, O, Aagenaes, O, Knudtzon, J

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