128 related articles for article (PubMed ID: 29731342)
1. Radiological features of crystal-induced arthropathy associated with hereditary hemochromatosis with homozygous C282Y mutation.
García García M
Reumatol Clin (Engl Ed); 2020; 16(2 Pt 1):122-124. PubMed ID: 29731342
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
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. HFE p.C282Y homozygosity predisposes to rapid serum ferritin rise after menopause: A genotype-stratified cohort study of hemochromatosis in Australian women.
Warne CD; Zaloumis SG; Bertalli NA; Delatycki MB; Nicoll AJ; McLaren CE; Hopper JL; Giles GG; Anderson GJ; Olynyk JK; Powell LW; Allen KJ; Gurrin LC;
J Gastroenterol Hepatol; 2017 Apr; 32(4):797-802. PubMed ID: 27784128
[TBL] [Abstract][Full Text] [Related]
6. Rare HFE variants are the most frequent cause of hemochromatosis in non-c282y homozygous patients with hemochromatosis.
Hamdi-Rozé H; Beaumont-Epinette MP; Ben Ali Z; Le Lan C; Loustaud-Ratti V; Causse X; Loreal O; Deugnier Y; Brissot P; Jouanolle AM; Bardou-Jacquet E
Am J Hematol; 2016 Dec; 91(12):1202-1205. PubMed ID: 27518069
[TBL] [Abstract][Full Text] [Related]
7. Expression of HLA-linked hemochromatosis in subjects homozygous or heterozygous for the C282Y mutation.
Crawford DH; Jazwinska EC; Cullen LM; Powell LW
Gastroenterology; 1998 May; 114(5):1003-8. PubMed ID: 9558290
[TBL] [Abstract][Full Text] [Related]
8. Hemochromatosis in Ireland and HFE.
Ryan E; O'keane C; Crowe J
Blood Cells Mol Dis; 1998 Dec; 24(4):428-32. PubMed ID: 9851896
[TBL] [Abstract][Full Text] [Related]
9. Correlation between genotype and phenotype in hereditary hemochromatosis: analysis of 61 cases.
Sham RL; Ou CY; Cappuccio J; Braggins C; Dunnigan K; Phatak PD
Blood Cells Mol Dis; 1997 Aug; 23(2):314-20. PubMed ID: 9410475
[TBL] [Abstract][Full Text] [Related]
10. Transient elevation of serum ferritin in a Sri Lankan with homozygosity for H63D mutation in the HFE gene: a case report.
Wickramasinghe W; Karunathilaka C; Jayasinghe S; Gooneratne L
J Med Case Rep; 2020 Jul; 14(1):93. PubMed ID: 32641120
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Hemochromatosis Mutations, Brain Iron Imaging, and Dementia in the UK Biobank Cohort.
Atkins JL; Pilling LC; Heales CJ; Savage S; Kuo CL; Kuchel GA; Steffens DC; Melzer D
J Alzheimers Dis; 2021; 79(3):1203-1211. PubMed ID: 33427739
[TBL] [Abstract][Full Text] [Related]
13. Increased capacity of lymphocytes from hereditary hemochromatosis patients homozygous for the C282Y HFE mutation to respond to the genotoxic effect of diepoxybutane.
Porto B; Vieira R; Porto G
Mutat Res; 2009 Feb; 673(1):37-42. PubMed ID: 19146986
[TBL] [Abstract][Full Text] [Related]
14. GNPAT variant (D519G) is not associated with an elevated serum ferritin or iron removed by phlebotomy in patients referred for C282Y-linked hemochromatosis.
Levstik A; Stuart A; Adams PC
Ann Hepatol; 2016 Nov-Dec 2016; 15(6):907-910. PubMed ID: 27740525
[TBL] [Abstract][Full Text] [Related]
15. Haemochromatosis arthropathy - a conundrum of the Celtic curse.
Kiely PD
J R Coll Physicians Edinb; 2018 Sep; 48(3):233-238. PubMed ID: 30191911
[TBL] [Abstract][Full Text] [Related]
16. Hereditary hemochromatosis in north-eastern Romania.
Voicu PM; Cojocariu C; Petrescu-Dănilă E; Stanciu C; Covic M; Rusu M; Trifan A
Rev Med Chir Soc Med Nat Iasi; 2010; 114(4):982-7. PubMed ID: 21495455
[TBL] [Abstract][Full Text] [Related]
17. [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]
18. A genotypic study of 217 unrelated probands diagnosed as "genetic hemochromatosis" on "classical" phenotypic criteria.
Brissot P; Moirand R; Jouanolle AM; Guyader D; Le Gall JY; Deugnier Y; David V
J Hepatol; 1999 Apr; 30(4):588-93. PubMed ID: 10207799
[TBL] [Abstract][Full Text] [Related]
19. [Hereditary hemochromatosis: molecular diagnosis and effect of treatment].
Szczeklik W; Dropiński J; Dziedzina S; Szułdrzyński K; Biesiada G; Mach T; Sanak M
Pol Arch Med Wewn; 2004 May; 111(5):593-6. PubMed ID: 15508811
[TBL] [Abstract][Full Text] [Related]
20. Hereditary Hemochromatosis Associations with Frailty, Sarcopenia and Chronic Pain: Evidence from 200,975 Older UK Biobank Participants.
Tamosauskaite J; Atkins JL; Pilling LC; Kuo CL; Kuchel GA; Ferrucci L; Melzer D
J Gerontol A Biol Sci Med Sci; 2019 Feb; 74(3):337-342. PubMed ID: 30657865
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]