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Journal Abstract Search

128 related items for PubMed ID: 18325820

  • 1. HFE gene mutations in a population of Italian Parkinson's disease patients.
    Biasiotto G, Goldwurm S, Finazzi D, Tunesi S, Zecchinelli A, Sironi F, Pezzoli G, Arosio P.
    Parkinsonism Relat Disord; 2008; 14(5):426-30. PubMed ID: 18325820
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  • 2. Prevalence of H63D, S65C, and C282Y hereditary hemochromatosis gene variants in Madeira Island (Portugal).
    Spínola C, Brehm A, Spínola H.
    Ann Hematol; 2011 Jan; 90(1):29-32. PubMed ID: 20714725
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  • 3. Prevalence of H63D, S65C and C282Y hereditary hemochromatosis gene mutations in Slovenian population by an improved high-throughput genotyping assay.
    Cukjati M, Vaupotic T, Rupreht R, Curin-Serbec V.
    BMC Med Genet; 2007 Nov 23; 8():69. PubMed ID: 18036208
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  • 4. Screening for mutations of the HFE gene in Parkinson's disease patients with hyperechogenicity of the substantia nigra.
    Akbas N, Hochstrasser H, Deplazes J, Tomiuk J, Bauer P, Walter U, Behnke S, Riess O, Berg D.
    Neurosci Lett; 2006 Oct 16; 407(1):16-9. PubMed ID: 16935420
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  • 5. Frequency of the HFE gene mutations in five Italian populations.
    Candore G, Mantovani V, Balistreri CR, Lio D, Colonna-Romano G, Cerreta V, Carru C, Deiana L, Pes G, Menardi G, Perotti L, Miotti V, Bevilacqua E, Amoroso A, Caruso C.
    Blood Cells Mol Dis; 2002 Oct 16; 29(3):267-73. PubMed ID: 12547216
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  • 7. Association of HFE common mutations with Parkinson's disease, Alzheimer's disease and mild cognitive impairment in a Portuguese cohort.
    Guerreiro RJ, Bras JM, Santana I, Januario C, Santiago B, Morgadinho AS, Ribeiro MH, Hardy J, Singleton A, Oliveira C.
    BMC Neurol; 2006 Jul 06; 6():24. PubMed ID: 16824219
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  • 8. Frequency of the C282Y and H63D mutations of the hemochromatosis gene (HFE) in 2501 ethnic Danes.
    Milman N, Pedersen P, Ovesen L, Melsen GV, Fenger K.
    Ann Hematol; 2004 Oct 06; 83(10):654-7. PubMed ID: 15141324
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  • 9. Analysis of HFE gene mutations (C282Y, H63D, and S65C) in the Ecuadorian population.
    Leone PE, Giménez P, Collantes JC, Paz-y-Miño C.
    Ann Hematol; 2005 Feb 06; 84(2):103-5. PubMed ID: 15517265
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  • 13. Analysis of HFE and TFR2 mutations in selected blood donors with biochemical parameters of iron overload.
    De Gobbi M, Daraio F, Oberkanins C, Moritz A, Kury F, Fiorelli G, Camaschella C.
    Haematologica; 2003 Apr 06; 88(4):396-401. PubMed ID: 12681966
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  • 16. Two novel missense mutations of the HFE gene (I105T and G93R) and identification of the S65C mutation in Alabama hemochromatosis probands.
    Barton JC, Sawada-Hirai R, Rothenberg BE, Acton RT.
    Blood Cells Mol Dis; 1999 Apr 06; 25(3-4):147-55. PubMed ID: 10575540
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  • 20. [The importance of DNA analysis of C282Y, H63D and S65C mutations in the HFE gene].
    Drastíková M, Beránek M, Hegerová J, Putzová D.
    Cas Lek Cesk; 2012 Apr 06; 151(9):428-31. PubMed ID: 23102134
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