140 related articles for article (PubMed ID: 2361583)
1. [Possibility of the development of non-transfusion hemosiderosis in beta-thalassemia, caused by association with HLA-linked hemochromatosis].
Settarova DA; Donskov SI; Manishkina RP; Krasavtseva TK; Klinika EG
Gematol Transfuziol; 1990 Mar; 35(3):16-8. PubMed ID: 2361583
[TBL] [Abstract][Full Text] [Related]
2. A study of 609 HLA haplotypes marking for the hemochromatosis gene: (1) mapping of the gene near the HLA-A locus and characters required to define a heterozygous population and (2) hypothesis concerning the underlying cause of hemochromatosis-HLA association.
Simon M; Le Mignon L; Fauchet R; Yaouanq J; David V; Edan G; Bourel M
Am J Hum Genet; 1987 Aug; 41(2):89-105. PubMed ID: 3475981
[TBL] [Abstract][Full Text] [Related]
3. Serum ferritin in haemodialysis patients: is there a relationship to 'haemochromatosis alleles' HLA A3, B7, B14?
Maher ER; Curtis JR
Nephron; 1986; 43(1):43-4. PubMed ID: 3486371
[TBL] [Abstract][Full Text] [Related]
4. Coincidental nontransfusional iron overload and thalassemia minor: association with HLA-linked hemochromatosis.
Edwards CQ; Skolnick MH; Kushner JP
Blood; 1981 Oct; 58(4):844-8. PubMed ID: 7272512
[TBL] [Abstract][Full Text] [Related]
5. Serum ferritin in haemodialysis patients: role of blood transfusions and 'haemochromatosis alleles' HLA A3, B7 and B14.
Gómez E; Ortega F; Peces R; Gago E; Marín R; Alvarez Grande J
Nephron; 1984; 36(2):106-10. PubMed ID: 6607419
[TBL] [Abstract][Full Text] [Related]
6. Iron overload in subjects with beta-thalassaemia trait: role of idiopathic haemochromatosis gene.
Fargion S; Piperno A; Panaiotopoulos N; Taddei MT; Fiorelli G
Br J Haematol; 1985 Nov; 61(3):487-90. PubMed ID: 3877523
[TBL] [Abstract][Full Text] [Related]
7. Idiopathic haemochromatosis and HLA antigens in Italy: is A3 Bw35 HLA haplotype a marker for idiopathic haemochromatosis gene in north east regions?
Piperno A; Fargion S; Panaiotopoulos N; Del Ninno E; Taddei MT; Fiorelli G
J Clin Pathol; 1986 Feb; 39(2):125-8. PubMed ID: 3485115
[TBL] [Abstract][Full Text] [Related]
8. Mapping the locus for hereditary hemochromatosis: localization between HLA-B and HLA-A.
Edwards CQ; Griffen LM; Dadone MM; Skolnick MH; Kushner JP
Am J Hum Genet; 1986 Jun; 38(6):805-11. PubMed ID: 3460331
[TBL] [Abstract][Full Text] [Related]
9. Is all genetic (hereditary) hemochromatosis HLA-associated.
Powell LW; Bassett ML; Axelsen E; Ferluga J; Halliday JW
Ann N Y Acad Sci; 1988; 526():23-33. PubMed ID: 3260461
[TBL] [Abstract][Full Text] [Related]
10. [Heredity and genetics of hemochromatosis].
Yaouanq J
Rev Med Interne; 1989; 10(6):541-7. PubMed ID: 2488506
[No Abstract] [Full Text] [Related]
11. Major histocompatibility complex class I associations in iron overload: evidence for a new link between the HFE H63D mutation, HLA-A29, and non-classical forms of hemochromatosis.
Porto G; Alves H; Rodrigues P; Cabeda JM; Portal C; Ruivo A; Justiça B; Wolff R; De Sousa M
Immunogenetics; 1998 Apr; 47(5):404-10. PubMed ID: 9510559
[TBL] [Abstract][Full Text] [Related]
12. An HLA-All association with the hemochromatosis allele?
Le Mignon L; Simon M; Fauchet R; Edan G; Le Reun M; Brissot P; Genetet B; Bourel M
Clin Genet; 1983 Sep; 24(3):171-6. PubMed ID: 6578890
[TBL] [Abstract][Full Text] [Related]
13. Human leukocyte antigen haplotypes and HFE mutations in Spanish hereditary hemochromatosis and sporadic porphyria cutanea tarda.
Gonzalez-Hevilla M; de Salamanca RE; Morales P; Martínez-Laso J; Fontanellas A; Castro MJ; Rojo R; Moscoso J; Zamora J; Serrano-Vela JI; Arnaiz-Villena A
J Gastroenterol Hepatol; 2005 Mar; 20(3):456-62. PubMed ID: 15740492
[TBL] [Abstract][Full Text] [Related]
14. [Correlation of HLA antigens and idiopathic hemochromatosis in Hungary].
Czink E; Gyódi E; Német K; Hollán Z
Orv Hetil; 1991 Feb; 132(8):409-10, 413-5. PubMed ID: 2003028
[TBL] [Abstract][Full Text] [Related]
15. Iron overload disorders: natural history, pathogenesis, diagnosis, and therapy.
McLaren GD; Muir WA; Kellermeyer RW
Crit Rev Clin Lab Sci; 1983; 19(3):205-66. PubMed ID: 6373141
[TBL] [Abstract][Full Text] [Related]
16. Was the C282Y mutation an Irish Gaelic mutation that the Vikings helped disseminate? HLA haplotype observations of hemochromatosis from the west coast of Sweden.
Olsson KS; Konar J; Dufva IH; Ricksten A; Raha-Chowdhury R
Eur J Haematol; 2011 Jan; 86(1):75-82. PubMed ID: 20946107
[TBL] [Abstract][Full Text] [Related]
17. 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
Eur J Haematol; 2010 Feb; 84(2):145-53. PubMed ID: 19912313
[TBL] [Abstract][Full Text] [Related]
18. Association between a 10 kb Pvu II restriction fragment of genomic DNA with the hemochromatosis gene.
Lucotte G; Coulondre C
Exp Clin Immunogenet; 1986; 3(4):219-23. PubMed ID: 2908538
[TBL] [Abstract][Full Text] [Related]
19. HLA-linked hemochromatosis alleles in sporadic porphyria cutanea tarda.
Edwards CQ; Griffen LM; Goldgar DE; Skolnick MH; Kushner JP
Gastroenterology; 1989 Oct; 97(4):972-81. PubMed ID: 2789160
[TBL] [Abstract][Full Text] [Related]
20. Nontransfusional iron overload in thalassemia. Association with hereditary hemochromatosis.
Rees DC; Singh BM; Luo LY; Wickramasinghe S; Thein SL
Ann N Y Acad Sci; 1998 Jun; 850():490-4. PubMed ID: 9668593
[No Abstract] [Full Text] [Related]
[Next] [New Search]