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.
121 related articles for article (PubMed ID: 19796184)
21. Juvenile hemochromatosis due to G320V/Q116X compound heterozygosity of hemojuvelin in an Irish patient. Daraio F; Ryan E; Gleeson F; Roetto A; Crowe J; Camaschella C Blood Cells Mol Dis; 2005; 35(2):174-6. PubMed ID: 15967692 [TBL] [Abstract][Full Text] [Related]
22. Effect of correcting transferrin saturation for body mass index in HFE C282Y homozygotes. Waalen J; Beutler E J Hepatol; 2006 Feb; 44(2):433-4; author reply 434-5. PubMed ID: 16364490 [No Abstract] [Full Text] [Related]
23. Hereditary haemochromatosis caused by homozygous HJV mutation evolved through paternal disomy. Neřoldová M; Fraňková S; Stránecký V; Honsová E; Lukšan O; Beneš M; Michalová K; Kmoch S; Jirsa M Clin Genet; 2015; 87(1):96-8. PubMed ID: 24635876 [No Abstract] [Full Text] [Related]
24. [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]
25. Haemochromatosis gene C282Y homozygotes in an elderly male population. Willis G; Wimperis JZ; Smith KC; Fellows IW; Jennings BA Lancet; 1999 Jul; 354(9174):221-2. PubMed ID: 10421310 [TBL] [Abstract][Full Text] [Related]
27. Frequency and spectrum of hemochromatosis mutations in Tunisia. Zorai A; Harteveld CL; Rachdi R; Dellagi K; Abbes S; Delbini P; Giordano PC Hematol J; 2003; 4(6):433-5. PubMed ID: 14671616 [TBL] [Abstract][Full Text] [Related]
28. Prevalence of the G320V mutation of the HJV gene, associated with juvenile hemochromatosis, in Greece. Pissia M; Polonifi K; Politou M; Lilakos K; Sakellaropoulos N; Papanikolaou G Haematologica; 2004 Jun; 89(6):742-3. PubMed ID: 15194541 [TBL] [Abstract][Full Text] [Related]
29. Distribution of HFE gene mutations in Slovenian patients with hereditary hemochromatosis. Stepec S; Makuc J; Markovic S; Medica I; Peterlin B Ann Hematol; 2008 Aug; 87(8):667-9. PubMed ID: 18317757 [No Abstract] [Full Text] [Related]
30. [Hemochromatosis, a public health problem]. Aguilar Martinez P Soins; 2007 Jun; (716):34-5. PubMed ID: 17718029 [No Abstract] [Full Text] [Related]
31. Letter by Sullivan regarding article, "HFE C282Y homozygosity is associated with lower total and low-density lipoprotein cholesterol: the hemochromatosis and iron overload screening study". Sullivan JL Circ Cardiovasc Genet; 2009 Jun; 2(3):e1. PubMed ID: 20031587 [No Abstract] [Full Text] [Related]
32. 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]
33. Hemochromatosis gene mutation--could it be a disease marker for myelodysplasia? Várkonyi J; Andrikovics H; Tordai A Leuk Res; 2009 Jan; 33(1):201-2. PubMed ID: 18462792 [No Abstract] [Full Text] [Related]
34. Hypogonadism and reduced bone mineral density in heterozygous H63D mutation in the HFE gene: an unusual presentation of hereditary hemochromatosis. Francucci CM; Gatti C; Camilletti A; Fiscaletti P; Caudarella R; Boscaro M J Androl; 2007; 28(1):21-6. PubMed ID: 16988327 [No Abstract] [Full Text] [Related]
35. Frequency of the hemochromatosis gene mutations in the population of Serbia and Montenegro. Sarić M; Zamurović Lj; Keckarević-Marković M; Keckarević D; Stevanović M; Savić-Pavićević D; Jović J; Romac S Clin Genet; 2006 Aug; 70(2):170-2. PubMed ID: 16879202 [No Abstract] [Full Text] [Related]