173 related articles for article (PubMed ID: 9833909)
1. 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]
2. 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]
3. 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]
4. HFE gene mutations in coronary atherothrombotic disease.
Calado RT; Franco RF; Pazin-Filho A; Simões MV; Marin-Neto JA; Zago MA
Braz J Med Biol Res; 2000 Mar; 33(3):301-6. PubMed ID: 10719381
[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. 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]
7. [The usefulness of the detection of Cys282Tyr and His63Asp mutations in the diagnosis of hereditary hemochromatosis].
Moreno L; Vallcorba P; Boixeda D; Cabello P; Bermejo F; San Román C
Rev Clin Esp; 1999 Oct; 199(10):632-6. PubMed ID: 10589245
[TBL] [Abstract][Full Text] [Related]
8. HFE codon 63/282 (H63D/C282Y) dimorphism in German patients with genetic hemochromatosis.
Gottschalk R; Seidl C; Löffler T; Seifried E; Hoelzer D; Kaltwasser JP
Tissue Antigens; 1998 Mar; 51(3):270-5. PubMed ID: 9550327
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. Increased frequency of the haemochromatosis Cys282Tyr mutation in sporadic porphyria cutanea tarda.
Roberts AG; Whatley SD; Morgan RR; Worwood M; Elder GH
Lancet; 1997 Feb; 349(9048):321-3. PubMed ID: 9024376
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. A candidate gene for hemochromatosis: frequency of the C282Y and H63D mutations.
Jouanolle AM; Fergelot P; Gandon G; Yaouanq J; Le Gall JY; David V
Hum Genet; 1997 Oct; 100(5-6):544-7. PubMed ID: 9341868
[TBL] [Abstract][Full Text] [Related]
15. High prevalence of the His63Asp HFE mutation in Italian patients with porphyria cutanea tarda.
Sampietro M; Piperno A; Lupica L; Arosio C; Vergani A; Corbetta N; Malosio I; Mattioli M; Fracanzani AL; Cappellini MD; Fiorelli G; Fargion S
Hepatology; 1998 Jan; 27(1):181-4. PubMed ID: 9425935
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Rapid screening of the Cys282Tyr and His63Asp mutations in the HFE gene.
Jardi R; Rodriguez-Frias F; Buti M; Costa X; Cotrina M; Olive G; Pascual C; Esteban R; Guardia J
J Hepatol; 2000 Feb; 32(2):362-3. PubMed ID: 10707881
[No Abstract] [Full Text] [Related]
18. [Frequency of HFE gene mutations and genotype-phenotype correlations in patients with hereditary hemochromatosis in Switzerland].
Himmelmann A; Bortoluzzi L; Jansen S; Fehr J
Schweiz Med Wochenschr; 2000 Aug; 130(31-32):1112-9. PubMed ID: 11008304
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Mutation analysis of the HFE gene in German hemochromatosis patients and controls using automated SSCP-based capillary electrophoresis and a new PCR-ELISA technique.
Hellerbrand C; Bosserhoff AK; Seegers S; Lingner G; Wrede C; Lock G; Schölmerich J; Büttner R
Scand J Gastroenterol; 2001 Nov; 36(11):1211-6. PubMed ID: 11686223
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
