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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

42 related items for PubMed ID: 16466945

  • 1. Unique genetic profile of hereditary haemochromatosis in Russians: High frequency of C282Y mutation in population, but not in patients.
    McCune CA, Worwood M.
    Blood Cells Mol Dis; 2006; 36(2):329; author reply 330. PubMed ID: 16466945
    [No Abstract] [Full Text] [Related]

  • 2. 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; 35(2):182-8. PubMed ID: 16055358
    [Abstract] [Full Text] [Related]

  • 3. Was the C282Y mutation an Irish Gaelic mutation that the Vikings help disseminate?
    Whittington CA.
    Med Hypotheses; 2006; 67(6):1270-3. PubMed ID: 16920278
    [Abstract] [Full Text] [Related]

  • 4. [Value of genetic diagnosis of C282Y mutation in patients with hereditary hemochromatosis].
    Ocran K, Schmidt HH.
    Z Gastroenterol; 2000 Feb; 38(2):205-7. PubMed ID: 10721178
    [No Abstract] [Full Text] [Related]

  • 5. Genetic screening for HFE hemochromatosis in 6,020 Danish men: penetrance of C282Y, H63D, and S65C variants.
    Pedersen P, Milman N.
    Ann Hematol; 2009 Aug; 88(8):775-84. PubMed ID: 19159930
    [Abstract] [Full Text] [Related]

  • 6. Hereditary hemochromatosis screening: effect of mutation penetrance and prevalence on cost-effectiveness of testing algorithms.
    Gagné G, Reinharz D, Laflamme N, Adams PC, Rousseau F.
    Clin Genet; 2007 Jan; 71(1):46-58. PubMed ID: 17204047
    [Abstract] [Full Text] [Related]

  • 7. Letter regarding article by Ellervik et al, "hereditary hemochromatosis and risk of ischemic heart disease: a prospective study and a case-control study".
    Goland S, Malnick SD.
    Circulation; 2006 Jan 03; 113(1):e10; author reply e10. PubMed ID: 16391159
    [No Abstract] [Full Text] [Related]

  • 8. Longevity and C282Y mutation for haemochromatosis: data do not support conclusion.
    Li AC, Powell J.
    BMJ; 2003 Oct 25; 327(7421):990; author reply 991. PubMed ID: 14576265
    [No Abstract] [Full Text] [Related]

  • 9. Detection of the C282Y and H63D polymorphisms associated with hereditary hemochromatosis using the ABI 7500 fast real time PCR platform.
    Tafe LJ, Belloni DR, Tsongalis GJ.
    Diagn Mol Pathol; 2007 Jun 25; 16(2):112-5. PubMed ID: 17525682
    [Abstract] [Full Text] [Related]

  • 10. Analysis of C282Y and H63D mutations of the hemochromatosis gene (HFE) in blood donors from Córdoba, Argentina.
    Soria NW, Cossy Isasi S, Chaig MR, Gerez de Burgos NM.
    Ann Hematol; 2009 Jan 25; 88(1):77-9. PubMed ID: 18633618
    [No Abstract] [Full Text] [Related]

  • 11. Searching for hereditary hemochromatosis.
    Laudicina RJ.
    Clin Lab Sci; 2006 Jan 25; 19(3):174-83. PubMed ID: 16910235
    [Abstract] [Full Text] [Related]

  • 12. Hemochromatosis-associated gene mutations in patients with myelodysplastic syndromes with refractory anemia with ringed sideroblasts.
    Nearman ZP, Szpurka H, Serio B, Warshawksy I, Theil K, Lichtin A, Sekeres MA, Maciejewski JP.
    Am J Hematol; 2007 Dec 25; 82(12):1076-9. PubMed ID: 17654685
    [Abstract] [Full Text] [Related]

  • 13. Hereditary hemochromatosis genotypes and risk of ischemic stroke.
    Ellervik C, Tybjaerg-Hansen A, Appleyard M, Sillesen H, Boysen G, Nordestgaard BG.
    Neurology; 2007 Mar 27; 68(13):1025-31. PubMed ID: 17389307
    [Abstract] [Full Text] [Related]

  • 14. Hemochromatosis gene mutations, liver function tests and iron status in alcohol-dependent patients admitted for detoxification.
    Robinson G, Narasimhan S, Weatherall M, Beasley R.
    J Gastroenterol Hepatol; 2007 Jun 27; 22(6):852-4. PubMed ID: 17565641
    [Abstract] [Full Text] [Related]

  • 15. Homozygous p.M172K mutation of the TFR2 gene in an Italian family with type 3 hereditary hemochromatosis and early onset iron overload.
    Majore S, Milano F, Binni F, Stuppia L, Cerrone A, Tafuri A, De Bernardo C, Palka G, Grammatico P.
    Haematologica; 2006 Aug 27; 91(8 Suppl):ECR33. PubMed ID: 16923517
    [Abstract] [Full Text] [Related]

  • 16. Hereditary hemochromatosis: screening and management.
    Waalen J, Beutler E.
    Curr Hematol Rep; 2006 Mar 27; 5(1):34-40. PubMed ID: 16537044
    [Abstract] [Full Text] [Related]

  • 17. Population-based study of the relationship between mutations in the hemochromatosis (HFE) gene and arthritis.
    Sherrington CA, Knuiman MW, Divitini ML, Bartholomew HC, Cullen DJ, Olynyk JK.
    J Gastroenterol Hepatol; 2006 Mar 27; 21(3):595-8. PubMed ID: 16638105
    [Abstract] [Full Text] [Related]

  • 18. [C677T mutation in methylentetrahydrofolatereductase gene in patients with venous thromboses from the central region of Russia correlates with a high risk of pulmonary artery thromboembolism].
    Avdonin PV, Kirienko AI, Kozhevnikova LM, Shostak NA, Babadaeva NM, Leont'ev SG, Petukhov EB, Kubatiev AA, Savel'ev VS.
    Ter Arkh; 2006 Mar 27; 78(6):70-6. PubMed ID: 16881367
    [Abstract] [Full Text] [Related]

  • 19. The clinical penetrance of hereditary hemochromatosis.
    Beutler E, Felitti VJ.
    Hepatology; 2003 Mar 27; 37(3):711. PubMed ID: 12601368
    [No Abstract] [Full Text] [Related]

  • 20. [Hereditary hemochromatosis].
    Arnold C, Köck J, von Weizsäcker F, Blum HE.
    Dtsch Med Wochenschr; 1998 Mar 27; 123(13):397-8. PubMed ID: 9556696
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 3.