297 related articles for article (PubMed ID: 24401005)
1. Age-dependent ferritin elevations and HFE C282Y mutation as risk factors for symptomatic knee osteoarthritis in males: a longitudinal cohort study.
Kennish L; Attur M; Oh C; Krasnokutsky S; Samuels J; Greenberg JD; Huang X; Abramson SB
BMC Musculoskelet Disord; 2014 Jan; 15():8. PubMed ID: 24401005
[TBL] [Abstract][Full Text] [Related]
2. Ferritin concentrations in synovial fluid are higher in osteoarthritis patients with HFE gene mutations (C282Y or H63D).
Carroll GJ; Sharma G; Upadhyay A; Jazayeri JA
Scand J Rheumatol; 2010; 39(5):413-20. PubMed ID: 20560808
[TBL] [Abstract][Full Text] [Related]
3. Association of heterozygous hemochromatosis C282Y gene mutation with hand osteoarthritis.
Ross JM; Kowalchuk RM; Shaulinsky J; Ross L; Ryan D; Phatak PD
J Rheumatol; 2003 Jan; 30(1):121-5. PubMed ID: 12508400
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Differences in hepatic phenotype between hemochromatosis patients with HFE C282Y homozygosity and other HFE genotypes.
Cheng R; Barton JC; Morrison ED; Phatak PD; Krawitt EL; Gordon SC; Kowdley KV
J Clin Gastroenterol; 2009 Jul; 43(6):569-73. PubMed ID: 19359997
[TBL] [Abstract][Full Text] [Related]
6. Patatin-like phospholipase domain containing-3 gene I148M polymorphism, steatosis, and liver damage in hereditary hemochromatosis.
Valenti L; Maggioni P; Piperno A; Rametta R; Pelucchi S; Mariani R; Dongiovanni P; Fracanzani AL; Fargion S
World J Gastroenterol; 2012 Jun; 18(22):2813-20. PubMed ID: 22719190
[TBL] [Abstract][Full Text] [Related]
7. Mild iron overload in patients carrying the HFE S65C gene mutation: a retrospective study in patients with suspected iron overload and healthy controls.
Holmström P; Marmur J; Eggertsen G; Gåfvels M; Stål P
Gut; 2002 Nov; 51(5):723-30. PubMed ID: 12377814
[TBL] [Abstract][Full Text] [Related]
8. Primary osteoarthritis in the ankle joint is associated with finger metacarpophalangeal osteoarthritis and the H63D mutation in the HFE gene: evidence for a hemochromatosis-like polyarticular osteoarthritis phenotype.
Carroll GJ
J Clin Rheumatol; 2006 Jun; 12(3):109-13. PubMed ID: 16755236
[TBL] [Abstract][Full Text] [Related]
9. Hemochromatosis gene mutations, body iron stores, dietary iron, and risk of colorectal adenoma in women.
Chan AT; Ma J; Tranah GJ; Giovannucci EL; Rifai N; Hunter DJ; Fuchs CS
J Natl Cancer Inst; 2005 Jun; 97(12):917-26. PubMed ID: 15956653
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. HFE C282Y heterozygosity in hepatocellular carcinoma: evidence for an increased prevalence.
Hellerbrand C; Pöppl A; Hartmann A; Schölmerich J; Lock G
Clin Gastroenterol Hepatol; 2003 Jul; 1(4):279-84. PubMed ID: 15017669
[TBL] [Abstract][Full Text] [Related]
12. Increased risk of death from iron overload among 422 treated probands with HFE hemochromatosis and serum levels of ferritin greater than 1000 μg/L at diagnosis.
Barton JC; Barton JC; Acton RT; So J; Chan S; Adams PC
Clin Gastroenterol Hepatol; 2012 Apr; 10(4):412-6. PubMed ID: 22265917
[TBL] [Abstract][Full Text] [Related]
13. Reference centiles for serum ferritin and percentage of transferrin saturation, with application to mutations of the HFE gene.
Koziol JA; Ho NJ; Felitti VJ; Beutler E
Clin Chem; 2001 Oct; 47(10):1804-10. PubMed ID: 11568090
[TBL] [Abstract][Full Text] [Related]
14. HFE mutations and chronic hepatitis C: H63D and C282Y heterozygosity are independent risk factors for liver fibrosis and cirrhosis.
Erhardt A; Maschner-Olberg A; Mellenthin C; Kappert G; Adams O; Donner A; Willers R; Niederau C; Häussinger D
J Hepatol; 2003 Mar; 38(3):335-42. PubMed ID: 12586300
[TBL] [Abstract][Full Text] [Related]
15. HFE C282Y/H63D compound heterozygotes are at low risk of hemochromatosis-related morbidity.
Gurrin LC; Bertalli NA; Dalton GW; Osborne NJ; Constantine CC; McLaren CE; English DR; Gertig DM; Delatycki MB; Nicoll AJ; Southey MC; Hopper JL; Giles GG; Anderson GJ; Olynyk JK; Powell LW; Allen KJ;
Hepatology; 2009 Jul; 50(1):94-101. PubMed ID: 19554541
[TBL] [Abstract][Full Text] [Related]
16. HFE mutations, hepatic iron, and fibrosis: ethnic-specific association of NASH with C282Y but not with fibrotic severity.
Chitturi S; Weltman M; Farrell GC; McDonald D; Kench J; Liddle C; Samarasinghe D; Lin R; Abeygunasekera S; George J
Hepatology; 2002 Jul; 36(1):142-9. PubMed ID: 12085358
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. The common HFE variants C282Y and H63D are not associated with primary OA of the hip or knee.
Loughlin J; Carr A; Chapman K
J Rheumatol; 2005 Feb; 32(2):391-2; author reply 392. PubMed ID: 15693075
[No Abstract] [Full Text] [Related]
19. Prevalence of coronary heart disease associated with HFE mutations in adults attending a health appraisal center.
Waalen J; Felitti V; Gelbart T; Ho NJ; Beutler E
Am J Med; 2002 Oct; 113(6):472-9. PubMed ID: 12427496
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
