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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

141 related items for PubMed ID: 11778658

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  • 3. 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
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  • 4. HLA haplotype map of river valley populations with hemochromatosis traced through five centuries in Central Sweden.
    Olsson KS, Ritter B, Hansson N, Chowdhury RR.
    Eur J Haematol; 2008 Jul; 81(1):36-46. PubMed ID: 18363869
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  • 6. 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 Jul; 5(6):371-5. PubMed ID: 9450181
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  • 7. 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
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  • 10. Linkage disequilibrium and extended haplotypes in the HLA-A to D6S105 region: implications for mapping the hemochromatosis gene (HFE).
    Gandon G, Jouanolle AM, Chauvel B, Mauvieux V, le Treut A, Feingold J, Le Gall JY, David V, Yaouanq J.
    Hum Genet; 1996 Jan; 97(1):103-13. PubMed ID: 8557248
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  • 12. Exclusion of ZIRTL as candidate gene of juvenile hemochromatosis and refinement of the critical interval on 1q21.
    Roetto A, Alberti F, Daraio F, Cali A, Cazzola M, Totaro A, Gasparini P, Camaschella C.
    Blood Cells Mol Dis; 2000 Jun; 26(3):205-10. PubMed ID: 10950940
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  • 13. Human leukocyte antigen haplotypes and HFE mutations in Spanish hereditary hemochromatosis and sporadic porphyria cutanea tarda.
    Gonzalez-Hevilla M, de Salamanca RE, Morales P, Martínez-Laso J, Fontanellas A, Castro MJ, Rojo R, Moscoso J, Zamora J, Serrano-Vela JI, Arnaiz-Villena A.
    J Gastroenterol Hepatol; 2005 Mar; 20(3):456-62. PubMed ID: 15740492
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  • 14. Isolation and characterisation of cosmids to intervals within a 4.5Mb region at 6p21.3.
    Jazwinska EC, Cullen LM, Zournazi A, Burt MJ, Van Der Griend B, Goldwurm S, Little PF.
    DNA Seq; 1997 Mar; 8(3):147-50. PubMed ID: 10668959
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  • 15. Hereditary hemochromatosis in Spain.
    Sánchez M, Bruguera M, Quintero E, Barrio Y, Mazzara R, Rodés J, Oliva R.
    Genet Test; 2000 Mar; 4(2):171-6. PubMed ID: 10953957
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  • 16. 46,XX, inv(6)(p21.1p23) in a pedigree with hereditary haemochromatosis.
    Venditti CP, Seese NK, Gerhard GS, Ten Elshof AE, Chorney KA, Mowrey PN, Lacey PG, Knoll JH, Chorney MJ.
    J Med Genet; 1997 Jan; 34(1):24-7. PubMed ID: 9032645
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  • 17. Genetic hemochromatosis, a Celtic disease: is it now time for population screening?
    Byrnes V, Ryan E, Barrett S, Kenny P, Mayne P, Crowe J.
    Genet Test; 2001 Jan; 5(2):127-30. PubMed ID: 11551098
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  • 18. Genetic hemochromatosis: why is discovery of the HLA-H gene of interest to rheumatologists?
    Puéchal X.
    Rev Rhum Engl Ed; 1997 Oct; 64(10):527-9. PubMed ID: 9385688
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  • 19. 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
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  • 20. Characterization of a recombinant that locates the hereditary hemochromatosis gene telomeric to HLA-F.
    Calandro LM, Baer DM, Sensabaugh GF.
    Hum Genet; 1995 Sep; 96(3):339-42. PubMed ID: 7649553
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