Publications by Øystein Aagenæs
64 publications found
Original articles
A nine year follow-up study of patients with lymphoedema cholestasis syndrome 1 (LCS1/Aagenaes syndrome)
Scand J Clin Lab Invest, 78 (7-8), 566-574
DOI 10.1080/00365513.2018.1519723, PubMed 30755100
Hereditary lymphedema, characteristics, and variations in 17 adult patients with lymphedema cholestasis syndrome 1/Aagenaes syndrome
Lymphat Res Biol, 12 (4), 251-7
DOI 10.1089/lrb.2014.0003, PubMed 25317502
CCBE1 mutation in two siblings, one manifesting lymphedema-cholestasis syndrome, and the other, fetal hydrops
PLoS One, 8 (9), e75770
DOI 10.1371/journal.pone.0075770, PubMed 24086631
Advanced hepatocellular carcinoma in adolescence associated with congenital cholestasis: a case description
Case Rep Oncol, 6 (1), 98-103
DOI 10.1159/000348715, PubMed 23626552
Familial occurrence of neonatal diabetes with duplications in chromosome 6q24: treatment with sulfonylurea and 40-yr follow-up
Pediatr Diabetes, 13 (2), 155-62
DOI 10.1111/j.1399-5448.2011.00776.x, PubMed 21518169
Do patients with lymphoedema cholestasis syndrome 1/Aagenaes syndrome need dietary counselling outside cholestatic episodes?
Clin Nutr, 29 (4), 525-30
DOI 10.1016/j.clnu.2010.01.010, PubMed 20170991
Prognosis, with evaluation of general biochemistry, of liver disease in lymphoedema cholestasis syndrome 1 (LCS1/Aagenaes syndrome)
Scand J Gastroenterol, 41 (4), 465-71
DOI 10.1080/00365520500335183, PubMed 16635916
Prognosis, with evaluation of general biochemistry, of liver disease in lymphoedema cholestasis syndrome 1 (LCS1/Aagenaes syndrome)
Scand. J. Gastroenterol., 41 (4), 469-U27
DOI 10.1080/0036552050033518
Evidence for genetic heterogeneity in lymphedema-cholestasis syndrome
J Pediatr, 142 (4), 441-7
DOI 10.1067/mpd.2003.148, PubMed 12712065
Mapping of the locus for cholestasis-lymphedema syndrome (Aagenaes syndrome) to a 6.6-cM interval on chromosome 15q
Am J Hum Genet, 67 (4), 994-9
DOI 10.1086/303080, PubMed 10968776
Homozygous mutation (A228T) in the 5alpha-reductase type 2 gene in a boy with 5alpha-reductase deficiency: genotype-phenotype correlations
Am J Med Genet, 80 (3), 269-72
DOI 10.1002/(SICI)1096-8628(19981116)80:3<269::AID-AJMG18>3.0.CO;2-T, PubMed 9843052
Autosomal glycogenosis of liver and muscle due to phosphorylase kinase deficiency is caused by mutations in the phosphorylase kinase beta subunit (PHKB)
Hum Mol Genet, 6 (7), 1109-15
DOI 10.1093/hmg/6.7.1109, PubMed 9215682
[Familial hypercholesterolemia in children. A management program. Procedures for diagnosis and treatment in our pediatric departments]
Tidsskr Nor Laegeforen, 115 (28), 3514
PubMed 7491607
The effect of 8 years of strict glycaemic control on peripheral nerve function in IDDM patients: the Oslo Study
Diabetologia, 37 (6), 579-84
DOI 10.1007/BF00403376, PubMed 7926342
[Hereditary intrahepatic cholestasis with lymphedema--Aagenaes syndrome]
Tidsskr Nor Laegeforen, 113 (30), 3673-7
PubMed 8278949
Continuous subcutaneous insulin infusion (CSII), multiple injections (MI) and conventional insulin therapy (CT) in self-selecting insulin-dependent diabetic patients. A comparison of metabolic control, acute complications and patient preferences
J Intern Med, 228 (5), 457-64
DOI 10.1111/j.1365-2796.1990.tb00263.x, PubMed 2254715
Microalbuminuria is associated with long term poor glycemic control in adolescent insulin dependent diabetics
Diabetes Res, 12 (2), 71-4
PubMed 2634509
Primordial birdheaded nanism associated with progressive ataxia, early onset insulin resistant diabetes, goiter and primary gonadal insufficiency. A new syndrome
Acta Paediatr Scand, 78 (3), 488-93
DOI 10.1111/j.1651-2227.1989.tb11119.x, PubMed 2662702
[Microalbuminuria. An important marker for diabetic nephropathy and macrovascular disease]
Tidsskr Nor Laegeforen, 108 (26), 2168-70
PubMed 3206421
Reduction of urinary albumin excretion after 4 years of continuous subcutaneous insulin infusion in insulin-dependent diabetes mellitus. The Oslo Study
Acta Endocrinol (Copenh), 117 (1), 19-25
DOI 10.1530/acta.0.1170019, PubMed 3289293
Screening for cystic fibrosis among newborns in Norway by measurement of serum/plasma trypsin-like immunoreactivity. Results of a 2 1/2-year pilot project
Scand J Gastroenterol Suppl, 143, 13-8
DOI 10.3109/00365528809090208, PubMed 3164498
Elevated albumin excretion rate is common among poorly controlled adolescent insulin dependent diabetics
Diabetes Res, 6 (1), 43-6
PubMed 3690956
Sorbitol as a sweetener in the diet of insulin-dependent diabetes
Acta Med Scand, 221 (2), 165-70
DOI 10.1111/j.0954-6820.1987.tb01262.x, PubMed 3296669
Increase in insulin antibodies during continuous subcutaneous insulin infusion and multiple-injection therapy in contrast to conventional treatment
Diabetes, 36 (1), 1-5
DOI 10.2337/diab.36.1.1, PubMed 3539672
Effect of near normoglycaemia for two years on progression of early diabetic retinopathy, nephropathy, and neuropathy: the Oslo study
Br Med J (Clin Res Ed), 293 (6556), 1195-9
DOI 10.1136/bmj.293.6556.1195, PubMed 3096429
[Treatment of children and adolescents with diabetes. Special problems]
Tidsskr Nor Laegeforen, 106 (29), 2415-7
PubMed 3787604
Diabetic control is improved by guar gum and wheat bran supplementation
Diabet Med, 3 (3), 230-3
DOI 10.1111/j.1464-5491.1986.tb00750.x, PubMed 3030619
Wilsons disease in childhood. Surviving severe haemolytic crisis with coma
Acta Pharmacol Toxicol (Copenh), 59 Suppl 7, 202-5
DOI 10.1111/j.1600-0773.1986.tb02744.x, PubMed 3776564
Rapid tightening of blood glucose control leads to transient deterioration of retinopathy in insulin dependent diabetes mellitus: the Oslo study
Br Med J (Clin Res Ed), 290 (6471), 811-5
DOI 10.1136/bmj.290.6471.811, PubMed 3919804
[Determination of urinary glucose. Simple determination of urinary glucose with a new semi-quantitative reagent stick; the Diabur Test 5000]
Tidsskr Nor Laegeforen, 104 (26), 1803-6
PubMed 6495272
[New methods for subcutaneous insulin administration. A year's experience with the insulin pump and multiple insulin injection therapy]
Tidsskr Nor Laegeforen, 104 (13), 856-61
PubMed 6379982
[Reye's syndrome in Norway 1977-1981]
Tidsskr Nor Laegeforen, 104 (1), 12-3
PubMed 6695363
The effect of cooking upon the blood glucose response to ingested carrots and potatoes
Diabetes Care, 7 (3), 221-3
DOI 10.2337/diacare.7.3.221, PubMed 6734389
Increase in blood glucose in insulin-dependent diabetics after intake of various fruits
Acta Med Scand, 212 (5), 281-3
DOI 10.1111/j.0954-6820.1982.tb03214.x, PubMed 6758494
Cholestatic jaundice in infancy. The importance of familial and genetic factors in aetiology and prognosis
Arch Dis Child, 56 (8), 622-7
DOI 10.1136/adc.56.8.622, PubMed 7271301
Effect of different kinds of fibre on postprandial blood glucose in insulin-dependent diabetics
Acta Med Scand, 208 (5), 389-91
DOI 10.1111/j.0954-6820.1980.tb01218.x, PubMed 6257055
Sucrose and sorbitol as sweeteners in the diet of insulin-dependent diabetics
Acta Med Scand, 207 (5), 371-3
DOI 10.1111/j.0954-6820.1980.tb09740.x, PubMed 6992517
Plasma glucose and insulin responses to orally administered carbohydrate-rich foodstuffs
Nutr Metab, 24 (3), 168-75
DOI 10.1159/000176338, PubMed 7003441
The effect of exercise on diabetic control and hemoglobin A1 (HbA1) in children
Acta Paediatr Scand Suppl, 283, 53-6
DOI 10.1111/j.1651-2227.1980.tb15313.x, PubMed 6938115
Hereditary cholestasis combined with peripheral pulmonary stenosis and other anomalies
Acta Paediatr Scand, 66 (1), 7-15
DOI 10.1111/j.1651-2227.1977.tb07801.x, PubMed 831382
Standardization of types of insulin and of its concentrations and syringes [proceedings]
Acta Paediatr Belg, 30 (2), 126-7
PubMed 888696
[Letter: Toxic effects of amino acids]
Tidsskr Nor Laegeforen, 96 (12), 725
PubMed 820016
Pathology and pathogenesis of liver disease in alpha-1-antitrypsin deficient individuals
Postgrad Med J, 50 (584), 365-75
DOI 10.1136/pgmj.50.584.365, PubMed 4549449
[Total parenteral feeding in pediatrics]
Tidsskr Nor Laegeforen, 94 (10), 663-4
PubMed 4207895
Neonatal cholestasis in alpha-1-antitrypsin deficient children. Clinical, genetic, histological and immunohistochemical findings
Acta Paediatr Scand, 61 (6), 632-42
DOI 10.1111/j.1651-2227.1972.tb15960.x, PubMed 4117022
[Practical accomplishment of dietary treatment in children]
Tidsskr Nor Laegeforen, 92 (26), 1695-6
PubMed 4672949
[Dietary treatment of diabetic children]
Tidsskr Nor Laegeforen, 92 (26), 1666-70
PubMed 5078266
Fatal congenital lactic acidosis in two siblings. I. Clinical and pathological findings
Acta Paediatr Scand, 60 (2), 129-37
DOI 10.1111/j.1651-2227.1971.tb06632.x, PubMed 5548117
Lymphoedema in hereditary recurrent cholestasis from birth
Arch Dis Child, 45 (243), 690-5
DOI 10.1136/adc.45.243.690, PubMed 5477684
Primary lymphoedema combined with hereditary recurrent intrahepatic cholestasis
Acta Med Scand, 188 (3), 213-9
DOI 10.1111/j.0954-6820.1970.tb08028.x, PubMed 5526945
Hereditary recurrent intrahepatic cholestasis from birth
Arch Dis Child, 43 (232), 646-57
DOI 10.1136/adc.43.232.646, PubMed 5702224
[Antibiotic therapy in childhood]
Tidsskr Nor Laegeforen, 88 (10), 967-72
PubMed 5686812
Infant mortality problems in Norway
Vital Health Stat 3 Anal Stud (8), 1-40
PubMed 5299271
[Treatment of erythroblastosis fetalis]
Tidsskr Nor Laegeforen, 87 (18), Suppl:1581-5
PubMed 5626949
The smaller of twins and hypoglycemia
Acta Paediatr Scand, Suppl 177:114+
DOI 10.1111/j.1651-2227.1967.tb05254.x, PubMed 5587681
The human Y chrosome and the etiology of true hermaphroditism with the report of a case with XX-XY sex chromosome mosaicism
Hereditas, 53 (1), 231-46
PubMed 5889237
Hereditary spastic paraplegia. A family with ten injured
Acta Psychiatr Scand, 34 (4), 489-94
DOI 10.1111/j.1600-0447.1959.tb07537.x, PubMed 13791321
Review articles
Hereditary cholestasis with lymphoedema (Aagenaes syndrome, cholestasis-lymphoedema syndrome). New cases and follow-up from infancy to adult age
Scand J Gastroenterol, 33 (4), 335-45
DOI 10.1080/00365529850170955, PubMed 9605254
Other articles
[The Baerum issue]
Tidsskr Nor Laegeforen, 121 (8), 983-4
PubMed 11332398
[Tobacco use prevention in Norway--a terrible example?]
Tidsskr Nor Laegeforen, 119 (7), 999
PubMed 10210964
No difference in the parental origin of susceptibility HLA class II haplotypes among Norwegian patients with insulin-dependent diabetes mellitus
Am J Hum Genet, 57 (6), 1511-4
PubMed 8533785
[Early surgical treatment of biliary atresia]
Tidsskr Nor Laegeforen, 114 (20), 2426-7
PubMed 7646625
Diabetic complications in a prepubertal adolescent
Arch Dis Child, 63 (11), 1397-8
DOI 10.1136/adc.63.11.1397, PubMed 3060025
Hereditary recurrent cholestasis with lymphoedema--two new families
Acta Paediatr Scand, 63 (3), 465-71
DOI 10.1111/j.1651-2227.1974.tb04832.x, PubMed 4857709