290 related articles for article (PubMed ID: 11001800)
1. Nonexpressing homozygotes for C282Y hemochromatosis: minority or majority of cases?
Adams PC
Mol Genet Metab; 2000; 71(1-2):81-6. PubMed ID: 11001800
[TBL] [Abstract][Full Text] [Related]
2. Hepatic iron overload: direct HFE (HLA-H) mutation analysis vs quantitative iron assays for the diagnosis of hereditary hemochromatosis.
Press RD; Flora K; Gross C; Rabkin JM; Corless CL
Am J Clin Pathol; 1998 May; 109(5):577-84. PubMed ID: 9576576
[TBL] [Abstract][Full Text] [Related]
3. [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]
4. 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]
5. A primer for predicting risk of disease in HFE-linked hemochromatosis.
Adams PC; Walker AP; Acton RT
Genet Test; 2001; 5(4):311-6. PubMed ID: 11960576
[TBL] [Abstract][Full Text] [Related]
6. Update on hereditary hemochromatosis and the HFE gene.
Brandhagen DJ; Fairbanks VF; Batts KP; Thibodeau SN
Mayo Clin Proc; 1999 Sep; 74(9):917-21. PubMed ID: 10488796
[TBL] [Abstract][Full Text] [Related]
7. Genotypic/phenotypic correlations in genetic hemochromatosis: evolution of diagnostic criteria.
Adams PC; Chakrabarti S
Gastroenterology; 1998 Feb; 114(2):319-23. PubMed ID: 9453492
[TBL] [Abstract][Full Text] [Related]
8. Clinical manifestations of hemochromatosis in HFE C282Y homozygotes identified by screening.
McLaren GD; McLaren CE; Adams PC; Barton JC; Reboussin DM; Gordeuk VR; Acton RT; Harris EL; Speechley MR; Sholinsky P; Dawkins FW; Snively BM; Vogt TM; Eckfeldt JH;
Can J Gastroenterol; 2008 Nov; 22(11):923-30. PubMed ID: 19018338
[TBL] [Abstract][Full Text] [Related]
9. Penetrance of the C28Y/C282Y genotype of the HFE gene.
Asberg A; Hveem K; Kannelønning K; Irgens WØ
Scand J Gastroenterol; 2007 Sep; 42(9):1073-7. PubMed ID: 17710673
[TBL] [Abstract][Full Text] [Related]
10. Underdiagnosis of hereditary haemochromatosis: lack of presentation or penetration?
Ryan E; Byrnes V; Coughlan B; Flanagan AM; Barrett S; O'Keane JC; Crowe J
Gut; 2002 Jul; 51(1):108-12. PubMed ID: 12077102
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Hereditary haemochromatosis: diagnosis and management in the gene era.
Olynyk JK
Liver; 1999 Apr; 19(2):73-80. PubMed ID: 10220735
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. The S65C mutation in Spain. Implications for iron overload screening.
Remacha AF; Barceló MJ; Sardà MP; Blesa I; Altés A; Baiget M
Haematologica; 2000 Dec; 85(12):1324-5. PubMed ID: 11114141
[TBL] [Abstract][Full Text] [Related]
16. Screening for hereditary hemochromatosis in siblings and children of affected patients. A cost-effectiveness analysis.
El-Serag HB; Inadomi JM; Kowdley KV
Ann Intern Med; 2000 Feb; 132(4):261-9. PubMed ID: 10681280
[TBL] [Abstract][Full Text] [Related]
17. [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]
18. Abnormal regulation of HFE mRNA expression does not contribute to primary iron overload.
Vercesi E; Cerani P; Rolandi V; Rovati A; Bergamaschi G
Haematologica; 2000 Aug; 85(8):787-91. PubMed ID: 10942923
[TBL] [Abstract][Full Text] [Related]
19. Pitfalls in the genetic diagnosis of hereditary hemochromatosis.
Jeffrey GP; Adams PC
Genet Test; 2000; 4(2):143-6. PubMed ID: 10953953
[TBL] [Abstract][Full Text] [Related]
20. [Iron in the era of molecular biology].
Deugnier Y; Moirand R; Brissot P; David V
Pathol Biol (Paris); 1999 Nov; 47(9):938-44. PubMed ID: 10609274
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]