78 related articles for article (PubMed ID: 10448186)
1. HFE gene mutation and transferrin saturation in very low birthweight infants.
Maier RF; Witt H; Bührer C; Mönch E; Köttgen E
Arch Dis Child Fetal Neonatal Ed; 1999 Sep; 81(2):F144-5. PubMed ID: 10448186
[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. HFE S65C variant is not associated with increased transferrin saturation in voluntary blood donors.
Arya N; Chakrabrati S; Hegele RA; Adams PC
Blood Cells Mol Dis; 1999; 25(5-6):354-7. PubMed ID: 10660483
[TBL] [Abstract][Full Text] [Related]
4. Immunohistochemistry of the Hfe protein in patients with hereditary hemochromatosis, iron deficiency anemia, and normal controls.
Byrnes V; Ryan E; O'Keane C; Crowe J
Blood Cells Mol Dis; 2000 Feb; 26(1):2-8. PubMed ID: 10772870
[TBL] [Abstract][Full Text] [Related]
5. Iron status and HFE genotype in erythrocyte pyruvate kinase deficiency: study of Italian cases.
Zanella A; Bianchi P; Iurlo A; Boschetti C; Taioli E; Vercellati C; Zappa M; Fermo E; Tavazzi D; Sampietro M
Blood Cells Mol Dis; 2001; 27(3):653-61. PubMed ID: 11482880
[TBL] [Abstract][Full Text] [Related]
6. A population-based study of the clinical expression of the hemochromatosis gene.
Olynyk JK; Cullen DJ; Aquilia S; Rossi E; Summerville L; Powell LW
N Engl J Med; 1999 Sep; 341(10):718-24. PubMed ID: 10471457
[TBL] [Abstract][Full Text] [Related]
7. Relation between HFE mutations and mild iron-overload expression.
Mura C; Le Gac G; Raguénes O; Mercier AY; Le Guen A; Férec C
Mol Genet Metab; 2000 Apr; 69(4):295-301. PubMed ID: 10870847
[TBL] [Abstract][Full Text] [Related]
8. [Relationship between HFE gene and hereditary hemochromatosis].
Meng H; Hou Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Apr; 19(2):159-62. PubMed ID: 11941597
[TBL] [Abstract][Full Text] [Related]
9. HFE gene variants modify the association between maternal lead burden and infant birthweight: a prospective birth cohort study in Mexico City, Mexico.
Cantonwine D; Hu H; Téllez-Rojo MM; Sánchez BN; Lamadrid-Figueroa H; Ettinger AS; Mercado-García A; Hernández-Avila M; Wright RO
Environ Health; 2010 Jul; 9():43. PubMed ID: 20659343
[TBL] [Abstract][Full Text] [Related]
10. HFE genotype and parameters of iron metabolism in German first-time blood donors - evidence for an increased transferrin saturation in C282Y heterozygotes.
Raddatz D; Legler T; Lynen R; Addicks N; Ramadori G
Z Gastroenterol; 2003 Nov; 41(11):1069-76. PubMed ID: 14648375
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. HFE based re-evaluation of heterozygous hemochromatosis.
Moirand R; Guyader D; Mendler MH; Jouanolle AM; Le Gall JY; David V; Brissot P; Deugnier Y
Am J Med Genet; 2002 Sep; 111(4):356-61. PubMed ID: 12210292
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. [Genetic hemochromatosis and the HFE gene].
Moirand R
Bull Acad Natl Med; 2000; 184(2):325-35; discussion 335-6. PubMed ID: 10989541
[TBL] [Abstract][Full Text] [Related]
16. HFE gene mutation (C282Y) and phenotypic expression among a hospitalised population in a high prevalence area of haemochromatosis.
Distante S; Berg JP; Lande K; Haug E; Bell H
Gut; 2000 Oct; 47(4):575-9. PubMed ID: 10986220
[TBL] [Abstract][Full Text] [Related]
17. Iron uptake from plasma transferrin by the duodenum is impaired in the Hfe knockout mouse.
Trinder D; Olynyk JK; Sly WS; Morgan EH
Proc Natl Acad Sci U S A; 2002 Apr; 99(8):5622-6. PubMed ID: 11943867
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Mutation analysis of the transferrin receptor-2 gene in patients with iron overload.
Lee PL; Halloran C; West C; Beutler E
Blood Cells Mol Dis; 2001; 27(1):285-9. PubMed ID: 11358389
[TBL] [Abstract][Full Text] [Related]
20. Frequencies of C282Y and H63D mutations and transferrin saturation indices in the Korean population.
Choi SJ; Min WK; Chun S; Park H; Kim JW; Park CJ; Chi HS
Clin Chem Lab Med; 2002 Jul; 40(7):689-92. PubMed ID: 12241015
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
