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Journal Abstract Search

98 related items for PubMed ID: 10566227

  • 1. [Hemochromatosis. Determination of the C282Y mutation frequency in the population of the Czech Republic and sensitivity of hemochromatosis detection using Guthrie cards].
    Zdárský E, Horák J, Stríteský J, Heirler F.
    Cas Lek Cesk; 1999 Aug 23; 138(16):497-9. PubMed ID: 10566227
    [Abstract] [Full Text] [Related]

  • 2. [Significance and prevalence of the C282Y gene mutation of primary hemochromatosis in the pathogenesis of pophyria cutanea tarda].
    Malina L, Zd'árský E, Dandová S, Michalíková H, Cerná M, Cimburová M.
    Cas Lek Cesk; 2000 Nov 22; 139(23):728-30. PubMed ID: 11191743
    [Abstract] [Full Text] [Related]

  • 3. Unique genetic profile of hereditary hemochromatosis in Russians: high frequency of C282Y mutation in population, but not in patients.
    Potekhina ES, Lavrov AV, Samokhodskaya LM, Efimenko AY, Balatskiy AV, Baev AA, Litvinova MM, Nikitina LA, Shipulin GA, Bochkov NP, Tkachuk VA, Bochkov VN.
    Blood Cells Mol Dis; 2005 Nov 22; 35(2):182-8. PubMed ID: 16055358
    [Abstract] [Full Text] [Related]

  • 4. Searching for hereditary hemochromatosis.
    Laudicina RJ.
    Clin Lab Sci; 2006 Nov 22; 19(3):174-83. PubMed ID: 16910235
    [Abstract] [Full Text] [Related]

  • 5. Hereditary hemochromatosis: detection of C282Y and H63D mutations in HFE gene by means of guthrie cards in population of Czech Republic.
    Cimburova M, Putova I, Provaznikova H, Horak J.
    Genet Epidemiol; 2002 Oct 22; 23(3):260-3. PubMed ID: 12384978
    [Abstract] [Full Text] [Related]

  • 6. [A new method of molecular testing in the differential diagnosis of hereditary hemochromatosis].
    Andrikovics H, Klein I, Kalmár L, Bors A, Jermendy G, Petri I, Kalász L, Váradi A, Tordai A.
    Orv Hetil; 1999 Nov 07; 140(45):2517-22. PubMed ID: 10586619
    [Abstract] [Full Text] [Related]

  • 7. Low penetrant hemochromatosis phenotype in eight families: no evidence of modifiers in the MHC region.
    Sachot S, Moirand R, Jouanolle AM, Mosser J, Fergelot P, Deugnier Y, Brissot P, le Gall JY, David V.
    Blood Cells Mol Dis; 2001 Nov 07; 27(2):518-29. PubMed ID: 11500063
    [Abstract] [Full Text] [Related]

  • 8. DMT1 genetic variability is not responsible for phenotype variability in hereditary hemochromatosis.
    Kelleher T, Ryan E, Barrett S, O'Keane C, Crowe J.
    Blood Cells Mol Dis; 2004 Nov 07; 33(1):35-9. PubMed ID: 15223008
    [Abstract] [Full Text] [Related]

  • 9. C282Y and H63D mutations of the haemochromatosis gene in patients with iron overload.
    Jorquera F, Domínguez A, Díaz-Golpe V, Espinel J, Muñoz F, Herrera A, Fernández-Gundín MJ, Vivas S, Olcoz JL.
    Rev Esp Enferm Dig; 2001 May 07; 93(5):293-302. PubMed ID: 11488107
    [Abstract] [Full Text] [Related]

  • 10. [The prevalence of the Cys282Tyr mutation in the hemochromatosis gene in Cantabria in patients diagnosed with hereditary hemochromatosis].
    Fábrega E, Castro B, Sánchez-Castro L, Benito A, Fernández-Luna JL, Pons-Romero F.
    Med Clin (Barc); 1999 Apr 10; 112(12):451-3. PubMed ID: 10320958
    [Abstract] [Full Text] [Related]

  • 11. [Genetic hemochromatosis].
    Jouanolle AM, David V, Le Gall JY.
    Ann Biol Clin (Paris); 1997 Apr 10; 55(3):189-93. PubMed ID: 9238420
    [Abstract] [Full Text] [Related]

  • 12. A simple genetic test identifies 90% of UK patients with haemochromatosis. The UK Haemochromatosis Consortium.
    The U.
    Gut; 1997 Dec 10; 41(6):841-4. PubMed ID: 9462220
    [Abstract] [Full Text] [Related]

  • 13. Development of a multiplex ARMS test for mutations in the HFE gene associated with hereditary haemochromatosis.
    Baty D, Terron Kwiatkowski A, Mechan D, Harris A, Pippard MJ, Goudie D.
    J Clin Pathol; 1998 Jan 10; 51(1):73-4. PubMed ID: 9577377
    [Abstract] [Full Text] [Related]

  • 14. Determination of gene frequencies for two common haemochromatosis mutations in the Danish population by a novel polymerase chain reaction with sequence-specific primers.
    Steffensen R, Varming K, Jersild C.
    Tissue Antigens; 1998 Sep 10; 52(3):230-5. PubMed ID: 9802602
    [Abstract] [Full Text] [Related]

  • 15. Hemochromatosis and "HLA-H": definite!
    Jazwinska EC, Powell LW.
    Hepatology; 1997 Feb 10; 25(2):495-6. PubMed ID: 9021970
    [Abstract] [Full Text] [Related]

  • 16. Longevity and C282Y mutation for haemochromatosis: survival of C282Y homozygotes does not preclude screening for HFE mutations.
    Willis G, Jennings BA, Wimperis JZ.
    BMJ; 2003 Oct 25; 327(7421):990-1; author reply 991. PubMed ID: 14576264
    [No Abstract] [Full Text] [Related]

  • 17. [Molecular basis in hereditary haemochromatosis].
    Cadet E, Perez AS, Capron D, Rochette J.
    Rev Med Interne; 2005 May 25; 26(5):393-402. PubMed ID: 15893030
    [Abstract] [Full Text] [Related]

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  • 19. Iron overload in light of the identification of a haemochromatosis gene.
    Hollán S.
    Haematologia (Budap); 1997 May 25; 28(3):109-16. PubMed ID: 9283910
    [Abstract] [Full Text] [Related]

  • 20. Significance of linkage disequilibrium between mutation C282Y and a MseI polymorphism in population screening and DNA diagnosis of hemochromatosis.
    de Villiers JN, Kotze MJ.
    Blood Cells Mol Dis; 1999 May 25; 25(3-4):250-2; discussion 253-4. PubMed ID: 10575550
    [Abstract] [Full Text] [Related]

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