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.
84 related articles for article (PubMed ID: 17107905)
41. Prevalence of hemochromatosis gene (HFE) mutations in Greece. Papazoglou D; Exiara T; Speletas M; Panagopoulos I; Maltezos E Acta Haematol; 2003; 109(3):137-40. PubMed ID: 12714823 [TBL] [Abstract][Full Text] [Related]
42. HFE genotype, parenchymal iron accumulation, and liver fibrosis in patients with nonalcoholic fatty liver disease. Valenti L; Fracanzani AL; Bugianesi E; Dongiovanni P; Galmozzi E; Vanni E; Canavesi E; Lattuada E; Roviaro G; Marchesini G; Fargion S Gastroenterology; 2010 Mar; 138(3):905-12. PubMed ID: 19931264 [TBL] [Abstract][Full Text] [Related]
43. A search for association between hereditary hemochromatosis HFE gene mutations and type 2 diabetes mellitus in a Polish population. Małecki MT; Klupa T; Waluś M; Czogała W; Greenlaw P; Sieradzki J Med Sci Monit; 2003 Feb; 9(2):BR91-5. PubMed ID: 12601293 [TBL] [Abstract][Full Text] [Related]
44. Diagnostic utility of HFE variants in Spanish patients: association with HLA alleles and role in susceptibility to acute lymphoblastic leukemia. Rodríguez-López R; Donoso M; Fernández-Cavada M; González LM; Margallo A; Corral C; Gallego M; García de Cáceres MT; Herrera T; González C; Vagace JM; Gervasini G Gene; 2013 Feb; 514(1):31-5. PubMed ID: 23178241 [TBL] [Abstract][Full Text] [Related]
45. Prevalence of HFE (hemochromatosis) gene mutations C282Y and H63D in a Romanian population. Voicu PM; Cojocariu C; Petrescu-Danila E; Covic M; Stanciu C; Rusu M Blood Cells Mol Dis; 2009; 42(1):14-5. PubMed ID: 18842428 [No Abstract] [Full Text] [Related]
46. Frequency of the hemochromatosis HFE mutations C282Y, H63D, and S65C in blood donors in the Faroe Islands. Milman N; á Steig T; Koefoed P; Pedersen P; Fenger K; Nielsen FC Ann Hematol; 2005 Mar; 84(3):146-9. PubMed ID: 15042317 [TBL] [Abstract][Full Text] [Related]
47. High prevalence of HFE gene mutations in hemodialysis patients. Mennella G; Valverde S; Forzan S; Fezzi M; Munaretto G; Gessoni G Minerva Urol Nefrol; 2008 Jun; 60(2):81-4. PubMed ID: 18500222 [TBL] [Abstract][Full Text] [Related]
48. Analysis of HFE gene mutations (C282Y, H63D, and S65C) in the Ecuadorian population. Leone PE; Giménez P; Collantes JC; Paz-y-Miño C Ann Hematol; 2005 Feb; 84(2):103-5. PubMed ID: 15517265 [TBL] [Abstract][Full Text] [Related]
49. Mutations of the hemochromatosis gene in Italian candidate blood donors with increased transferrin saturation. Velati C; Marlianici E; Rigamonti D; Barillari G; Chiavilli F; Fugiani P; Garozzo G; Lancieri M; Rinaldi S; Testa D; Sampietro M; Tavazzi D; Delbini P; Fargion S; Fiorelli G Hematol J; 2003; 4(6):436-40. PubMed ID: 14671617 [TBL] [Abstract][Full Text] [Related]
50. Frequency of the C282Y and H63D mutations of the hemochromatosis gene (HFE) in a cohort of 1,000 neonates in Madrid (Spain). Ropero P; Briceño O; Mateo M; Polo M; Mora A; González FA; Villegas A Ann Hematol; 2006 May; 85(5):323-6. PubMed ID: 16520984 [TBL] [Abstract][Full Text] [Related]
51. HFE mutations in heart disease. Dunn T; Blankenship D; Beal N; Allen R; Schechter E; Moore W; Perveen G; Eichner J Heart Vessels; 2008 Sep; 23(5):348-55. PubMed ID: 18810584 [TBL] [Abstract][Full Text] [Related]
53. Prevalence of common HFE and SERPINA1 mutations in patients with hepatocellular carcinoma in a Moroccan population. Ezzikouri S; El Feydi AE; El Kihal L; Afifi R; Benazzouz M; Hassar M; Chafik A; Pineau P; Benjelloun S Arch Med Res; 2008 Feb; 39(2):236-41. PubMed ID: 18164971 [TBL] [Abstract][Full Text] [Related]
54. Mutations in the hemochromatosis gene (HFE) and multiple sclerosis. Ristić S; Lovrecić L; Brajenović-Milić B; Starcević-Cizmarević N; Jazbec SS; Sepcić J; Kapović M; Peterlin B Neurosci Lett; 2005 Aug; 383(3):301-4. PubMed ID: 15955425 [TBL] [Abstract][Full Text] [Related]
55. H63D HFE polymorphisms are associated with increased disease duration and decreased muscle superoxide dismutase-1 expression in amyotrophic lateral sclerosis patients. Su XW; Lee SY; Mitchell RM; Stephens HE; Simmons Z; Connor JR Muscle Nerve; 2013 Aug; 48(2):242-6. PubMed ID: 23813494 [TBL] [Abstract][Full Text] [Related]
56. Prevalence of C282Y and H63D mutations in the haemochromatosis (HFE) gene in Tunisian population. Sassi R; Hmida S; Kaabi H; Hajjej A; Abid A; Abdelkefi S; Yacoub S; Maamar M; Mojaat N; Ben Hamed L; Bellali H; Dridi A; Jridi A; Midouni B; Boukef MK Ann Genet; 2004; 47(4):325-30. PubMed ID: 15581829 [TBL] [Abstract][Full Text] [Related]
58. Acute leukemia in patients past the age of 50. RUBIO F J Am Geriatr Soc; 1960 Aug; 8():644-59. PubMed ID: 14439920 [No Abstract] [Full Text] [Related]
59. Acute leukemia over the age of fifty: a study of its incidence and natural history. GUNZ FW; HOUGH RF Blood; 1956 Oct; 11(10):882-901. PubMed ID: 13363998 [No Abstract] [Full Text] [Related]