Ritter B - Search Results

1

Screening for iron overload using transferrin saturation.

Olsson KS, Eriksson K, Ritter B, Heedman PA. Olsson KS, et al. Among authors: ritter b. Acta Med Scand. 1984;215(2):105-12. doi: 10.1111/j.0954-6820.1984.tb04979.x. Acta Med Scand. 1984. PMID: 6702489

2

The effect of iron fortification of the diet on clinical iron overload in the general population.

Olsson KS, Säfwenberg J, Ritter B. Olsson KS, et al. Among authors: ritter b. Ann N Y Acad Sci. 1988;526:290-300. doi: 10.1111/j.1749-6632.1988.tb55513.x. Ann N Y Acad Sci. 1988. PMID: 3164602

3

Iron deficiency and iron overload in Swedish male adolescents.

Olsson KS, Marsell R, Ritter B, Olander B, Akerblom A, Ostergård H, Larsson O. Olsson KS, et al. Among authors: ritter b. J Intern Med. 1995 Feb;237(2):187-94. doi: 10.1111/j.1365-2796.1995.tb01160.x. J Intern Med. 1995. PMID: 7852922

4

Prevalence of iron overload in central Sweden.

Olsson KS, Ritter B, Rosén U, Heedman PA, Staugård F. Olsson KS, et al. Among authors: ritter b. Acta Med Scand. 1983;213(2):145-50. doi: 10.1111/j.0954-6820.1983.tb03706.x. Acta Med Scand. 1983. PMID: 6837331

5

Liver affection in iron overload studied with serum ferritin and serum aminotransferases.

Olsson KS, Ritter B, Lundin PM. Olsson KS, et al. Among authors: ritter b. Acta Med Scand. 1985;217(1):79-84. doi: 10.1111/j.0954-6820.1985.tb01638.x. Acta Med Scand. 1985. PMID: 3976436

6

HLA-A3-B14 and the origin of the haemochromatosis C282Y mutation: founder effects and recombination events during 12 generations in a Scandinavian family with major iron overload.

Olsson KS, Ritter B, Raha-Chowdhury R. Olsson KS, et al. Among authors: ritter b. Eur J Haematol. 2010 Feb 1;84(2):145-53. doi: 10.1111/j.1600-0609.2009.01376.x. Epub 2009 Nov 12. Eur J Haematol. 2010. PMID: 19912313

7

The HLA-A1-B8 haplotype hitchhiking with the hemochromatosis mutation: does it affect the phenotype?

Olsson KS, Ritter B, Hansson N. Olsson KS, et al. Among authors: ritter b. Eur J Haematol. 2007 Nov;79(5):429-34. doi: 10.1111/j.1600-0609.2007.00953.x. Eur J Haematol. 2007. PMID: 17924859

8

Idiopathic hemochromatosis and chromosomal damage.

Nordenson I, Ritter B, Beckman A, Beckman L. Nordenson I, et al. Among authors: ritter b. Hum Hered. 1992;42(2):143-5. doi: 10.1159/000154055. Hum Hered. 1992. PMID: 1572673

9

HLA haplotype map of river valley populations with hemochromatosis traced through five centuries in Central Sweden.

Olsson KS, Ritter B, Hansson N, Chowdhury RR. Olsson KS, et al. Among authors: ritter b. Eur J Haematol. 2008 Jul;81(1):36-46. doi: 10.1111/j.1600-0609.2008.01078.x. Epub 2008 Mar 19. Eur J Haematol. 2008. PMID: 18363869

10

Transferrin types and expression of hereditary hemochromatosis.

Sikström C, Ritter B, Beckman A, Beckman L. Sikström C, et al. Among authors: ritter b. Hum Genet. 1994 Apr;93(4):483-4. doi: 10.1007/BF00201685. Hum Genet. 1994. PMID: 8168821 No abstract available.

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