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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

207 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]
    of 11.