Thorstensen K - Search Results

1

High prevalence of hereditary thrombotic thrombocytopenic purpura in central Norway: from clinical observation to evidence.

von Krogh AS, Quist-Paulsen P, Waage A, Langseth ØO, Thorstensen K, Brudevold R, Tjønnfjord GE, Largiadèr CR, Lämmle B, Kremer Hovinga JA. von Krogh AS, et al. Among authors: thorstensen k. J Thromb Haemost. 2016 Jan;14(1):73-82. doi: 10.1111/jth.13186. Epub 2016 Jan 8. J Thromb Haemost. 2016. PMID: 26566785 Free article.

2

Thrombotic thrombocytopenic purpura in 2 siblings: defective platelet function and plasma factor deficiency occurring simultaneously.

Waage A, Siegel J, Thorstensen K, Lamvik J. Waage A, et al. Among authors: thorstensen k. Scand J Haematol. 1986 Jan;36(1):55-7. doi: 10.1111/j.1600-0609.1986.tb02649.x. Scand J Haematol. 1986. PMID: 3952464

3

High headache prevalence among women with hemochromatosis: the Nord-Trøndelag health study.

Hagen K, Stovner LJ, Asberg A, Thorstensen K, Bjerve KS, Hveem K. Hagen K, et al. Among authors: thorstensen k. Ann Neurol. 2002 Jun;51(6):786-9. doi: 10.1002/ana.10209. Ann Neurol. 2002. PMID: 12112089

4

Screening for C282Y homozygosity in a Norwegian population (HUNT2): The sensitivity and specificity of transferrin saturation.

Thorstensen K, Kvitland MA, Irgens WØ, Hveem K, Asberg A. Thorstensen K, et al. Scand J Clin Lab Invest. 2010 Apr;70(2):92-7. doi: 10.3109/00365510903527838. Scand J Clin Lab Invest. 2010. PMID: 20073670

5

[A 40-year-old woman with anemia].

Kildahl-Andersen O, Thorstensen K, Sagen E, Dahl IM, Tjønnfjord G. Kildahl-Andersen O, et al. Among authors: thorstensen k. Tidsskr Nor Laegeforen. 2006 Nov 16;126(22):2958-9. Tidsskr Nor Laegeforen. 2006. PMID: 17144048 Norwegian.

6

Screening for hemochromatosis: high prevalence and low morbidity in an unselected population of 65,238 persons.

Asberg A, Hveem K, Thorstensen K, Ellekjter E, Kannelønning K, Fjøsne U, Halvorsen TB, Smethurst HB, Sagen E, Bjerve KS. Asberg A, et al. Among authors: thorstensen k. Scand J Gastroenterol. 2001 Oct;36(10):1108-15. doi: 10.1080/003655201750422747. Scand J Gastroenterol. 2001. PMID: 11589387

7

Prevalence of haemochromatosis gene mutations in Parkinson's disease.

Aamodt AH, Stovner LJ, Thorstensen K, Lydersen S, White LR, Aasly JO. Aamodt AH, et al. Among authors: thorstensen k. J Neurol Neurosurg Psychiatry. 2007 Mar;78(3):315-7. doi: 10.1136/jnnp.2006.101352. Epub 2006 Oct 20. J Neurol Neurosurg Psychiatry. 2007. PMID: 17056630 Free PMC article.

8

Iron loading in HFE p.C282Y homozygotes found by population screening: relationships to HLA-type and T-lymphocyte subsets.

Thorstensen K, Kvitland MA, Irgens WØ, Åsberg A, Borch-Iohnsen B, Moen T, Hveem K. Thorstensen K, et al. Scand J Clin Lab Invest. 2017 Nov;77(7):477-485. doi: 10.1080/00365513.2017.1342136. Epub 2017 Jul 5. Scand J Clin Lab Invest. 2017. PMID: 28678636

9

Hereditary hemochromatosis: the clinical significance of the S65C mutation.

Asberg A, Thorstensen K, Hveem K, Bjerve KS. Asberg A, et al. Among authors: thorstensen k. Genet Test. 2002 Spring;6(1):59-62. doi: 10.1089/109065702760093933. Genet Test. 2002. PMID: 12180078

10

Lower hemoglobin with lower ferritin - results from the HUNT 2 Study.

Åsberg A, Borch-Iohnsen B, Mikkelsen G, Thorstensen K, Åsberg AE. Åsberg A, et al. Among authors: thorstensen k. Scand J Clin Lab Invest. 2015 Apr;75(2):152-5. doi: 10.3109/00365513.2014.993335. Epub 2015 Jan 16. Scand J Clin Lab Invest. 2015. PMID: 25594798

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