211 related articles for article (PubMed ID: 10216143)
1. Inherited HFE-unrelated hemochromatosis in Italian families.
Camaschella C; Fargion S; Sampietro M; Roetto A; Bosio S; Garozzo G; Arosio C; Piperno A
Hepatology; 1999 May; 29(5):1563-4. PubMed ID: 10216143
[TBL] [Abstract][Full Text] [Related]
2. Linkage to chromosome 1q in Greek families with juvenile hemochromatosis.
Papanikolaou G; Politou M; Roetto A; Bosio S; Sakelaropoulos N; Camaschella C; Loukopoulos D
Blood Cells Mol Dis; 2001; 27(4):744-9. PubMed ID: 11778658
[TBL] [Abstract][Full Text] [Related]
3. [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]
4. Hereditary hemochromatosis in adults without pathogenic mutations in the hemochromatosis gene.
Pietrangelo A; Montosi G; Totaro A; Garuti C; Conte D; Cassanelli S; Fraquelli M; Sardini C; Vasta F; Gasparini P
N Engl J Med; 1999 Sep; 341(10):725-32. PubMed ID: 10471458
[TBL] [Abstract][Full Text] [Related]
5. Mutation analysis of the HLA-H gene in Italian hemochromatosis patients.
Carella M; D'Ambrosio L; Totaro A; Grifa A; Valentino MA; Piperno A; Girelli D; Roetto A; Franco B; Gasparini P; Camaschella C
Am J Hum Genet; 1997 Apr; 60(4):828-32. PubMed ID: 9106528
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Hereditary hemochromatosis: HFE mutation analysis in Greeks reveals genetic heterogeneity.
Papanikolaou G; Politou M; Terpos E; Fourlemadis S; Sakellaropoulos N; Loukopoulos D
Blood Cells Mol Dis; 2000 Apr; 26(2):163-8. PubMed ID: 11001626
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. A candidate gene for hemochromatosis: frequency of the C282Y and H63D mutations.
Jouanolle AM; Fergelot P; Gandon G; Yaouanq J; Le Gall JY; David V
Hum Genet; 1997 Oct; 100(5-6):544-7. PubMed ID: 9341868
[TBL] [Abstract][Full Text] [Related]
10. Juvenile and adult hemochromatosis are distinct genetic disorders.
Camaschella C; Roetto A; Cicilano M; Pasquero P; Bosio S; Gubetta L; Di Vito F; Girelli D; Totaro A; Carella M; Grifa A; Gasparini P
Eur J Hum Genet; 1997; 5(6):371-5. PubMed ID: 9450181
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Hemochromatosis: a genetic defect in iron metabolism.
Jazwinska EC
Bioessays; 1998 Jul; 20(7):562-8. PubMed ID: 9723005
[TBL] [Abstract][Full Text] [Related]
13. [The usefulness of the detection of Cys282Tyr and His63Asp mutations in the diagnosis of hereditary hemochromatosis].
Moreno L; Vallcorba P; Boixeda D; Cabello P; Bermejo F; San Román C
Rev Clin Esp; 1999 Oct; 199(10):632-6. PubMed ID: 10589245
[TBL] [Abstract][Full Text] [Related]
14. The influence of hemochromatosis mutations on iron overload of thalassemia major.
Longo F; Zecchina G; Sbaiz L; Fischer R; Piga A; Camaschella C
Haematologica; 1999 Sep; 84(9):799-803. PubMed ID: 10477452
[TBL] [Abstract][Full Text] [Related]
15. Haemochromatosis in patients with beta-thalassaemia trait.
Piperno A; Mariani R; Arosio C; Vergani A; Bosio S; Fargion S; Sampietro M; Girelli D; Fraquelli M; Conte D; Fiorelli G; Camaschella C
Br J Haematol; 2000 Dec; 111(3):908-14. PubMed ID: 11122155
[TBL] [Abstract][Full Text] [Related]
16. High prevalence of the His63Asp HFE mutation in Italian patients with porphyria cutanea tarda.
Sampietro M; Piperno A; Lupica L; Arosio C; Vergani A; Corbetta N; Malosio I; Mattioli M; Fracanzani AL; Cappellini MD; Fiorelli G; Fargion S
Hepatology; 1998 Jan; 27(1):181-4. PubMed ID: 9425935
[TBL] [Abstract][Full Text] [Related]
17. A pilot C282Y hemochromatosis screening in Italian newborns by TaqMan technology.
Restagno G; Gomez AM; Sbaiz L; De Gobbi M; Roetto A; Bertino E; Fabris C; Fiorucci GC; Fortina P; Camaschella C
Genet Test; 2000; 4(2):177-81. PubMed ID: 10953958
[TBL] [Abstract][Full Text] [Related]
18. Hemochromatosis with HFE gene mutation in a Japanese patient.
Sohda T; Okubo R; Kamimura S; Ohkawara T
Am J Gastroenterol; 2001 Aug; 96(8):2487-8. PubMed ID: 11513196
[TBL] [Abstract][Full Text] [Related]
19. Effects of highly conserved major histocompatibility complex (MHC) extended haplotypes on iron and low CD8+ T lymphocyte phenotypes in HFE C282Y homozygous hemochromatosis patients from three geographically distant areas.
Costa M; Cruz E; Barton JC; Thorstensen K; Morais S; da Silva BM; Pinto JP; Vieira CP; Vieira J; Acton RT; Porto G
PLoS One; 2013; 8(11):e79990. PubMed ID: 24282517
[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]