81 related articles for article (PubMed ID: 11189980)
1. Prevalence of the Cys282Tyr and His63Asp mutation in Flemish patients with hereditary hemochromatosis.
Van Vlierberghe H; Messiaen L; Hautekeete M; De Paepe A; Elewaut A
Acta Gastroenterol Belg; 2000; 63(3):250-3. PubMed ID: 11189980
[TBL] [Abstract][Full Text] [Related]
2. Hemochromatosis gene HFE Cys282Tyr mutation analysis in a cohort of Northeast German hospitalized patients supports assumption of a North to South allele frequency gradient throughout Germany.
Meier P; Schuff-Werner P; Steiner M
Clin Lab; 2005; 51(9-10):539-43. PubMed ID: 16285477
[TBL] [Abstract][Full Text] [Related]
3. Prevalence of the Cys282Tyr and His63Asp HFE gene mutations in Spanish patients with hereditary hemochromatosis and in controls.
Sánchez M; Bruguera M; Bosch J; Rodés J; Ballesta F; Oliva R
J Hepatol; 1998 Nov; 29(5):725-8. PubMed ID: 9833909
[TBL] [Abstract][Full Text] [Related]
4. Genetic and clinical description of hemochromatosis probands and heterozygotes: evidence that multiple genes linked to the major histocompatibility complex are responsible for hemochromatosis.
Barton JC; Shih WW; Sawada-Hirai R; Acton RT; Harmon L; Rivers C; Rothenberg BE
Blood Cells Mol Dis; 1997; 23(1):135-45; discussion 145a-b. PubMed ID: 9215758
[TBL] [Abstract][Full Text] [Related]
5. An unusual case of hemochromatosis due to a new compound heterozygosity in HFE (p.[Gly43Asp;His63Asp]+[Cys282Tyr]): structural implications with respect to binding with transferrin receptor 1.
Dupradeau FY; Pissard S; Coulhon MP; Cadet E; Foulon K; Fourcade C; Goossens M; Case DA; Rochette J
Hum Mutat; 2008 Jan; 29(1):206. PubMed ID: 18157833
[TBL] [Abstract][Full Text] [Related]
6. [The prevalence of the Cys282Tyr mutation in the hemochromatosis gene in Cantabria in patients diagnosed with hereditary hemochromatosis].
Fábrega E; Castro B; Sánchez-Castro L; Benito A; Fernández-Luna JL; Pons-Romero F
Med Clin (Barc); 1999 Apr; 112(12):451-3. PubMed ID: 10320958
[TBL] [Abstract][Full Text] [Related]
7. Penetrance of Hemochromatosis in HFE Genotypes Resulting in p.Cys282Tyr and p.[Cys282Tyr];[His63Asp] in the eMERGE Network.
Gallego CJ; Burt A; Sundaresan AS; Ye Z; Shaw C; Crosslin DR; Crane PK; Fullerton SM; Hansen K; Carrell D; Kuivaniemi H; Derr K; de Andrade M; McCarty CA; Kitchner TE; Ragon BK; Stallings SC; Papa G; Bochenek J; Smith ME; Aufox SA; Pacheco JA; Patel V; Friesema EM; Erwin AL; Gottesman O; Gerhard GS; Ritchie M; Motulsky AG; Kullo IJ; Larson EB; Tromp G; Brilliant MH; Bottinger E; Denny JC; Roden DM; Williams MS; Jarvik GP
Am J Hum Genet; 2015 Oct; 97(4):512-20. PubMed ID: 26365338
[TBL] [Abstract][Full Text] [Related]
8. [From gene to disease; HFE-mutations in primary haemochromatosis].
Swinkels DW; Jacobs EM
Ned Tijdschr Geneeskd; 2003 Apr; 147(14):652-6. PubMed ID: 12712648
[TBL] [Abstract][Full Text] [Related]
9. [Demonstration of HFE polymorphism in German patients with hereditary hemochromatosis].
Erhardt A; Niederau C; Osman Y; Hassan M; Häussinger D
Dtsch Med Wochenschr; 1999 Dec; 124(48):1448-52. PubMed ID: 10615325
[TBL] [Abstract][Full Text] [Related]
10. Predominance of the HLA-H Cys282Tyr mutation in Austrian patients with genetic haemochromatosis.
Datz C; Lalloz MR; Vogel W; Graziadei I; Hackl F; Vautier G; Layton DM; Maier-Dobersberger T; Ferenci P; Penner E; Sandhofer F; Bomford A; Paulweber B
J Hepatol; 1997 Nov; 27(5):773-9. PubMed ID: 9382962
[TBL] [Abstract][Full Text] [Related]
11. Mutation analysis of the HLA-H gene in Italian hemochromatosis patients.
Carella M; D'Ambrosio L; Totaro A; Grifa A; Valentino MA; Piperno A; Girelli D; Roetto A; Franco B; Gasparini P; Camaschella C
Am J Hum Genet; 1997 Apr; 60(4):828-32. PubMed ID: 9106528
[TBL] [Abstract][Full Text] [Related]
12. Homozygosity for the predominant Cys282Tyr mutation and absence of disease expression in hereditary haemochromatosis.
Rhodes DA; Raha-Chowdhury R; Cox TM; Trowsdale J
J Med Genet; 1997 Sep; 34(9):761-4. PubMed ID: 9321765
[TBL] [Abstract][Full Text] [Related]
13. Molecular analysis of HLA-H gene mutations in New Zealand patients with haemochromatosis.
Burt MJ; Upton JD; Morison IM; Chapman BA; Faed JM; George PM
N Z Med J; 1997 Nov; 110(1056):429-32. PubMed ID: 9418837
[TBL] [Abstract][Full Text] [Related]
14. Haemochromatosis: automated detection of the two point mutations in the HFE gene: Cys282Tyr and His63Asp.
Klingler KR; Zech D; Wielckens K
Clin Chem Lab Med; 2000 Dec; 38(12):1225-30. PubMed ID: 11205685
[TBL] [Abstract][Full Text] [Related]
15. A PCR-SSP method for detecting the His63Asp mutation in the HFE gene associated with hereditary haemochromatosis.
Smillie D
Mol Pathol; 1998 Aug; 51(4):232-3. PubMed ID: 9893753
[TBL] [Abstract][Full Text] [Related]
16. Mutation analysis of the HFE gene associated with hereditary hemochromatosis in African Americans.
Monaghan KG; Rybicki BA; Shurafa M; Feldman GL
Am J Hematol; 1998 Jul; 58(3):213-7. PubMed ID: 9662273
[TBL] [Abstract][Full Text] [Related]
17. Adult onset hereditary hemochromatosis is associated with a novel recurrent Hemojuvelin (HJV) gene mutation in north Indians.
Dhillon BK; Chopra G; Jamwal M; Chandak GR; Duseja A; Malhotra P; Chawla YK; Garewal G; Das R
Blood Cells Mol Dis; 2018 Nov; 73():14-21. PubMed ID: 30195625
[TBL] [Abstract][Full Text] [Related]
18. No evidence of increased risk of colorectal cancer in individuals heterozygous for the Cys282Tyr haemochromatosis mutation.
Macdonald GA; Tarish J; Whitehall VJ; McCann SJ; Mellick GD; Buttenshaw RL; Johnson AG; Young J; Leggett BA
J Gastroenterol Hepatol; 1999 Dec; 14(12):1188-91. PubMed ID: 10634155
[TBL] [Abstract][Full Text] [Related]
19. Rapid diagnosis of asymptomatic hereditary haemochromatosis by detection of the Cys282Tyr mutation in the HLA-H gene.
Aslam S; Standen GR
Postgrad Med J; 1997 Sep; 73(863):573-4. PubMed ID: 9373599
[TBL] [Abstract][Full Text] [Related]
20. High prevalence of the Cys282Tyr HFE mutation facilitates an improved diagnostic service for hereditary haemochromatosis in South Africa.
de Villiers JN; Hillerman R; de Jong G; Langenhoven E; Rossouw H; Marx MP; Kotze MJ
S Afr Med J; 1999 Mar; 89(3):279-82. PubMed ID: 10226674
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
