These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
144 related articles for article (PubMed ID: 20145272)
1. The Southern French registry of genetic hemochromatosis: a tool for determining clinical prevalence of the disorder and genotype penetrance. Aguilar-Martinez P; Bismuth M; Blanc F; Blanc P; Cunat S; Dereure O; Dujols P; Giansily-Blaizot M; Jorgensen C; Konate A; Larrey D; Le Quellec A; Mura T; Raingeard I; Ramos J; Renard E; Rousseau F; Schved JF; Picot MC Haematologica; 2010 Apr; 95(4):551-6. PubMed ID: 20145272 [TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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. Hereditary hemochromatosis in a Brazilian university hospital in São Paulo State (1990-2000). Martinelli AL; Filho R; Cruz S; Franco R; Tavella M; Secaf M; Ramalho L; Zucoloto S; Rodrigues S; Zago M Genet Mol Res; 2005 Mar; 4(1):31-8. PubMed ID: 15841433 [TBL] [Abstract][Full Text] [Related]
6. Transferrin receptor-2 gene and non-C282Y homozygous patients with hemochromatosis. Aguilar-Martinez P; Esculié-Coste C; Bismuth M; Giansily-Blaizot M; Larrey D; Schved JF Blood Cells Mol Dis; 2001; 27(1):290-3. PubMed ID: 11358390 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. [Molecular genetic diagnostics and screening of hereditary hemochromatosis]. Zlocha J; Kovács L; Pozgayová S; Kupcová V; Durínová S Vnitr Lek; 2006 Jun; 52(6):602-8. PubMed ID: 16871764 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. Prevalence of hemochromatosis-related symptoms among individuals with mutations in the HFE gene. Waalen J; Felitti V; Gelbart T; Ho NJ; Beutler E Mayo Clin Proc; 2002 Jun; 77(6):522-30. PubMed ID: 12059121 [TBL] [Abstract][Full Text] [Related]
13. Expression of the HFE hemochromatosis gene in a community-based population of elderly women. Rossi E; Kuek C; Beilby JP; Jeffrey GP; Devine A; Prince RL J Gastroenterol Hepatol; 2004 Oct; 19(10):1150-4. PubMed ID: 15377292 [TBL] [Abstract][Full Text] [Related]
14. The biochemical and clinical penetrance of individuals diagnosed with genetic haemochromatosis by predictive genetic testing. Watkins S; Thorburn D; Joshi N; Neilson M; Joyce T; Spooner R; Cooke A; Mills PR; Morris AJ; Stanley AJ Eur J Gastroenterol Hepatol; 2008 May; 20(5):379-83. PubMed ID: 18403938 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Clinical Penetrance of Hereditary Hemochromatosis-Related End-Organ Damage of C282Y Homozygosity, A Newfoundland Experience. Lim DR; Vidyasankar G; Phua C; Borgaonkar M Clin Transl Gastroenterol; 2020 Nov; 11(11):e00258. PubMed ID: 33259166 [TBL] [Abstract][Full Text] [Related]
17. Reduced phenotypic expression in genetic hemochromatosis with time: Role of exposure to non-genetic modifiers. Deugnier Y; Morcet J; Lainé F; Hamdi-Roze H; Bollard AS; Guyader D; Moirand R; Bardou-Jacquet E J Hepatol; 2019 Jan; 70(1):118-125. PubMed ID: 30244162 [TBL] [Abstract][Full Text] [Related]
18. Hemochromatosis and iron-overload screening in a racially diverse population. Adams PC; Reboussin DM; Barton JC; McLaren CE; Eckfeldt JH; McLaren GD; Dawkins FW; Acton RT; Harris EL; Gordeuk VR; Leiendecker-Foster C; Speechley M; Snively BM; Holup JL; Thomson E; Sholinsky P; N Engl J Med; 2005 Apr; 352(17):1769-78. PubMed ID: 15858186 [TBL] [Abstract][Full Text] [Related]
19. Contribution of different HFE genotypes to iron overload disease: a pooled analysis. Burke W; Imperatore G; McDonnell SM; Baron RC; Khoury MJ Genet Med; 2000; 2(5):271-7. PubMed ID: 11399207 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]