130 related articles for article (PubMed ID: 38263707)
1. Penetrance, cancer incidence and survival in HFE haemochromatosis-A population-based cohort study.
Schaefer B; Pammer LM; Pfeifer B; Neururer S; Troppmair MR; Panzer M; Wagner S; Pertler E; Gieger C; Kronenberg F; Lamina C; Tilg H; Zoller H
Liver Int; 2024 Mar; 44(3):838-847. PubMed ID: 38263707
[TBL] [Abstract][Full Text] [Related]
2. Genetic modifiers of penetrance to liver endpoints in HFE hemochromatosis: Associations in a large community cohort.
Pilling LC; Atkins JL; Melzer D
Hepatology; 2022 Dec; 76(6):1735-1745. PubMed ID: 35567766
[TBL] [Abstract][Full Text] [Related]
3. Hepatocellular carcinoma and the penetrance of HFE C282Y mutations: a cross sectional study.
Willis G; Bardsley V; Fellows IW; Lonsdale R; Wimperis JZ; Jennings BA
BMC Gastroenterol; 2005 Jun; 5():17. PubMed ID: 15929796
[TBL] [Abstract][Full Text] [Related]
4. Iron-overload-related disease in HFE hereditary hemochromatosis.
Allen KJ; Gurrin LC; Constantine CC; Osborne NJ; Delatycki MB; Nicoll AJ; McLaren CE; Bahlo M; Nisselle AE; Vulpe CD; Anderson GJ; Southey MC; Giles GG; English DR; Hopper JL; Olynyk JK; Powell LW; Gertig DM
N Engl J Med; 2008 Jan; 358(3):221-30. PubMed ID: 18199861
[TBL] [Abstract][Full Text] [Related]
5. Iron overload and HFE gene mutations in Polish patients with liver cirrhosis.
Sikorska K; Romanowski T; Stalke P; Iżycka-Świeszewska E; Bielawski KP
Hepatobiliary Pancreat Dis Int; 2011 Jun; 10(3):270-5. PubMed ID: 21669570
[TBL] [Abstract][Full Text] [Related]
6. Clinical expression of haemochromatosis in Irish C282Y homozygotes identified through family screening.
Gleeson F; Ryan E; Barrett S; Crowe J
Eur J Gastroenterol Hepatol; 2004 Sep; 16(9):859-63. PubMed ID: 15316409
[TBL] [Abstract][Full Text] [Related]
7.
Lucas MR; Atkins JL; Pilling LC; Shearman JD; Melzer D
BMJ Open; 2024 Mar; 14(3):e081926. PubMed ID: 38479735
[TBL] [Abstract][Full Text] [Related]
8. Clinical and genetic heterogeneity in hereditary haemochromatosis: association between lymphocyte counts and expression of iron overload.
Porto G; Cardoso CS; Gordeuk V; Cruz E; Fraga J; Areias J; Oliveira JC; Bravo F; Gangaidzo IT; MacPhail AP; Gomo ZA; Moyo VM; Melo G; Silva C; Justiça B; de Sousa M
Eur J Haematol; 2001 Aug; 67(2):110-8. PubMed ID: 11722599
[TBL] [Abstract][Full Text] [Related]
9. Association of Hemochromatosis HFE p.C282Y Homozygosity With Hepatic Malignancy.
Atkins JL; Pilling LC; Masoli JAH; Kuo CL; Shearman JD; Adams PC; Melzer D
JAMA; 2020 Nov; 324(20):2048-2057. PubMed ID: 33231665
[TBL] [Abstract][Full Text] [Related]
10. Clinical penetrance in hereditary hemochromatosis: estimates of the cumulative incidence of severe liver disease among HFE C282Y homozygotes.
Grosse SD; Gurrin LC; Bertalli NA; Allen KJ
Genet Med; 2018 Apr; 20(4):383-389. PubMed ID: 28771247
[TBL] [Abstract][Full Text] [Related]
11. Correlation between iron status and genetic hemochromatosis (codon C282Y) in a large German population.
Wrede CE; Hutzler S; Bollheimer LC; Buettner R; Hellerbrand C; Schöelmerich J; Palitzsch KD
Isr Med Assoc J; 2004 Jan; 6(1):30-3. PubMed ID: 14740507
[TBL] [Abstract][Full Text] [Related]
12. HFE gene mutation (C282Y) and phenotypic expression among a hospitalised population in a high prevalence area of haemochromatosis.
Distante S; Berg JP; Lande K; Haug E; Bell H
Gut; 2000 Oct; 47(4):575-9. PubMed ID: 10986220
[TBL] [Abstract][Full Text] [Related]
13. Incidence of liver disease in people with HFE mutations.
Willis G; Wimperis JZ; Lonsdale R; Fellows IW; Watson MA; Skipper LM; Jennings BA
Gut; 2000 Mar; 46(3):401-4. PubMed ID: 10673304
[TBL] [Abstract][Full Text] [Related]
14. Penetrance of the C28Y/C282Y genotype of the HFE gene.
Asberg A; Hveem K; Kannelønning K; Irgens WØ
Scand J Gastroenterol; 2007 Sep; 42(9):1073-7. PubMed ID: 17710673
[TBL] [Abstract][Full Text] [Related]
15. Risk of Hepatocellular Carcinoma in Patients with Various HFE Genotypes.
Natarajan Y; Patel P; Chu J; Yu X; Hernaez R; El-Serag H; Kanwal F
Dig Dis Sci; 2023 Jan; 68(1):312-322. PubMed ID: 35790703
[TBL] [Abstract][Full Text] [Related]
16. [Prevalence of hemochromatosis-associated mutations in the hemochromatosis gene in the Danish population].
Larsen LE; Ellervik C; Appleyard M; Nordestgaard BG; Birgens H; Tybjaerg-Hansen A
Ugeskr Laeger; 2002 Sep; 164(39):4545-7. PubMed ID: 12380399
[TBL] [Abstract][Full Text] [Related]
17. Iron-overload and genotypic expression of HFE mutations H63D/C282Y and transferrin receptor Hin6I and BanI polymorphism in german patients with hereditary haemochromatosis.
Gottschalk R; Seidl C; Schilling S; Braner A; Seifried E; Hoelzer D; Kaltwasser JP
Eur J Immunogenet; 2000 Jun; 27(3):129-34. PubMed ID: 10940080
[TBL] [Abstract][Full Text] [Related]
18. Iron loading and morbidity among relatives of HFE C282Y homozygotes identified either by population genetic testing or presenting as patients.
McCune CA; Ravine D; Carter K; Jackson HA; Hutton D; Hedderich J; Krawczak M; Worwood M
Gut; 2006 Apr; 55(4):554-62. PubMed ID: 16174659
[TBL] [Abstract][Full Text] [Related]
19. HFE mutations, iron deficiency and overload in 10,500 blood donors.
Jackson HA; Carter K; Darke C; Guttridge MG; Ravine D; Hutton RD; Napier JA; Worwood M
Br J Haematol; 2001 Aug; 114(2):474-84. PubMed ID: 11529872
[TBL] [Abstract][Full Text] [Related]
20. The 16189 variant of mitochondrial DNA occurs more frequently in C282Y homozygotes with haemochromatosis than those without iron loading.
Livesey KJ; Wimhurst VL; Carter K; Worwood M; Cadet E; Rochette J; Roberts AG; Pointon JJ; Merryweather-Clarke AT; Bassett ML; Jouanolle AM; Mosser A; David V; Poulton J; Robson KJ
J Med Genet; 2004 Jan; 41(1):6-10. PubMed ID: 14729817
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]