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125 related items for PubMed ID: 38980801

  • 1. HFE and Non-HFE Hereditary Hemochromatosis Based on Screening of 854 Individuals: 12 Years of an Iranian Experience.
    Zarifian Yeganeh R, Akbari Kelishomi M, Ahmadpour Jenaghard A, Salmani B, Vahidi Z, Makvand M, Azad M, Kooshki M, Bouraqi Y, Azarkeivan A, Najmabadi H, Neishabury M.
    Genet Test Mol Biomarkers; 2024 Jul; 28(7):289-296. PubMed ID: 38980801
    [Abstract] [Full Text] [Related]

  • 2. Hereditary hemochromatosis: mutations in genes involved in iron homeostasis in Brazilian patients.
    Santos PC, Cançado RD, Pereira AC, Schettert IT, Soares RA, Pagliusi RA, Hirata RD, Hirata MH, Teixeira AC, Figueiredo MS, Chiattone CS, Krieger JE, Guerra-Shinohara EM.
    Blood Cells Mol Dis; 2011 Apr 15; 46(4):302-7. PubMed ID: 21411349
    [Abstract] [Full Text] [Related]

  • 3. Transferrin receptor-2 gene and non-C282Y homozygous patients with hemochromatosis.
    Aguilar-Martinez P, Esculié-Coste C, Bismuth M, Giansily-Blaizot M, Larrey D, Schved JF.
    Blood Cells Mol Dis; 2001 Apr 15; 27(1):290-3. PubMed ID: 11358390
    [Abstract] [Full Text] [Related]

  • 4. Analysis of HFE and non-HFE gene mutations in Brazilian patients with hemochromatosis.
    Bittencourt PL, Marin ML, Couto CA, Cançado EL, Carrilho FJ, Goldberg AC.
    Clinics (Sao Paulo); 2009 Apr 15; 64(9):837-41. PubMed ID: 19759876
    [Abstract] [Full Text] [Related]

  • 5. HFE C282Y homozygotes aged 25-29 years at HEIRS Study initial screening.
    Barton JC, Acton RT, Leiendecker-Foster C, Lovato L, Adams PC, McLaren GD, Eckfeldt JH, McLaren CE, Reboussin DM, Gordeuk VR, Speechley MR, Reiss JA, Press RD, Dawkins FW, Hemochromatosis and Iron Overload Screening (HEIRS) Study Research Investigators.
    Genet Test; 2007 Apr 15; 11(3):269-75. PubMed ID: 17949288
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. Mutations in the HFE, TFR2, and SLC40A1 genes in patients with hemochromatosis.
    Del-Castillo-Rueda A, Moreno-Carralero MI, Cuadrado-Grande N, Alvarez-Sala-Walther LA, Enríquez-de-Salamanca R, Méndez M, Morán-Jiménez MJ.
    Gene; 2012 Oct 15; 508(1):15-20. PubMed ID: 22890139
    [Abstract] [Full Text] [Related]

  • 8. Iron-overload and genotypic expression of HFE mutations H63D/C282Y and transferrin receptor Hin6I and BanI polymorphism in german patients with hereditary haemochromatosis.
    Gottschalk R, Seidl C, Schilling S, Braner A, Seifried E, Hoelzer D, Kaltwasser JP.
    Eur J Immunogenet; 2000 Jun 15; 27(3):129-34. PubMed ID: 10940080
    [Abstract] [Full Text] [Related]

  • 9. Identification of novel mutations in hemochromatosis genes by targeted next generation sequencing in Italian patients with unexplained iron overload.
    Badar S, Busti F, Ferrarini A, Xumerle L, Bozzini P, Capelli P, Pozzi-Mucelli R, Campostrini N, De Matteis G, Marin Vargas S, Giorgetti A, Delledonne M, Olivieri O, Girelli D.
    Am J Hematol; 2016 Jun 15; 91(4):420-5. PubMed ID: 26799139
    [Abstract] [Full Text] [Related]

  • 10. Hereditary hemochromatosis in a Brazilian university hospital in São Paulo State (1990-2000).
    Martinelli AL, Filho R, Cruz S, Franco R, Tavella M, Secaf M, Ramalho L, Zucoloto S, Rodrigues S, Zago M.
    Genet Mol Res; 2005 Mar 31; 4(1):31-8. PubMed ID: 15841433
    [Abstract] [Full Text] [Related]

  • 11. Correlation of genotype and phenotype in 32 patients with hereditary hemochromatosis in China.
    Wu L, Zhang W, Li Y, Zhou D, Zhang B, Xu A, Wu Z, Wu L, Li S, Wang X, Zhao X, Wang Q, Li M, Wang Y, You H, Huang J, Ou X, Jia J.
    Orphanet J Rare Dis; 2021 Sep 28; 16(1):398. PubMed ID: 34583728
    [Abstract] [Full Text] [Related]

  • 12. Genetic modifiers of penetrance to liver endpoints in HFE hemochromatosis: Associations in a large community cohort.
    Pilling LC, Atkins JL, Melzer D.
    Hepatology; 2022 Dec 28; 76(6):1735-1745. PubMed ID: 35567766
    [Abstract] [Full Text] [Related]

  • 13. [Molecular genetic diagnostics and screening of hereditary hemochromatosis].
    Zlocha J, Kovács L, Pozgayová S, Kupcová V, Durínová S.
    Vnitr Lek; 2006 Jun 28; 52(6):602-8. PubMed ID: 16871764
    [Abstract] [Full Text] [Related]

  • 14. Transferrin receptor 2 (TfR2) and HFE mutational analysis in non-C282Y iron overload: identification of a novel TfR2 mutation.
    Mattman A, Huntsman D, Lockitch G, Langlois S, Buskard N, Ralston D, Butterfield Y, Rodrigues P, Jones S, Porto G, Marra M, De Sousa M, Vatcher G.
    Blood; 2002 Aug 01; 100(3):1075-7. PubMed ID: 12130528
    [Abstract] [Full Text] [Related]

  • 15. Low frequency of HFE gene mutations in Croatian patients suspected of having hereditary hemochromatosis.
    Milić S, Ristić S, Starčević-Čizmarević N, Brajenović-Milić B, Crnić-Martinović M, Kapović M, Peterlin B, Štimac D.
    Med Sci Monit; 2011 Oct 01; 17(10):CR552-6. PubMed ID: 21959608
    [Abstract] [Full Text] [Related]

  • 16. The global prevalence of HFE and non-HFE hemochromatosis estimated from analysis of next-generation sequencing data.
    Wallace DF, Subramaniam VN.
    Genet Med; 2016 Jun 01; 18(6):618-26. PubMed ID: 26633544
    [Abstract] [Full Text] [Related]

  • 17. 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 01; 88(4):396-401. PubMed ID: 12681966
    [Abstract] [Full Text] [Related]

  • 18. Mutation analysis of the HFE gene in German hemochromatosis patients and controls using automated SSCP-based capillary electrophoresis and a new PCR-ELISA technique.
    Hellerbrand C, Bosserhoff AK, Seegers S, Lingner G, Wrede C, Lock G, Schölmerich J, Büttner R.
    Scand J Gastroenterol; 2001 Nov 01; 36(11):1211-6. PubMed ID: 11686223
    [Abstract] [Full Text] [Related]

  • 19. HFE mutations and hemochromatosis in Danish patients admitted for HFE genotyping.
    Koefoed P, Dalhoff K, Dissing J, Kramer I, Milman N, Pedersen P, Simonsen K, Tygstrup N, Nielsen FC.
    Scand J Clin Lab Invest; 2002 Nov 01; 62(7):527-35. PubMed ID: 12512743
    [Abstract] [Full Text] [Related]

  • 20. Elevated MCP-1 serum levels are associated with the H63D mutation and not the C282Y mutation in hereditary hemochromatosis.
    Lawless MW, White M, Mankan AK, O'Dwyer MJ, Norris S.
    Tissue Antigens; 2007 Oct 01; 70(4):294-300. PubMed ID: 17767550
    [Abstract] [Full Text] [Related]

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