Sign in to NCBI
  • RSS feed iconRSS
  • Save search
  • Advanced
  • Help

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination
We are sorry, but NCBI web applications do not support your browser and may not function properly. More information

    Results: 1 to 20 of 57

    1.

    Hereditary hemochromatosis.

    Crownover BK, Covey CJ.

    Am Fam Physician. 2013 Feb 1;87(3):183-90. Review.

    PMID:
    23418762
    [PubMed - indexed for MEDLINE]

    Related citations

    2.

    Hereditary hemochromatosis: implications for South Dakota physicians.

    Stampe C, Weiland K.

    S D Med. 2013 Jan;66(1):15, 17-8.

    PMID:
    23342715
    [PubMed - indexed for MEDLINE]

    Related citations

    3.

    Diagnostic utility of HFE variants in Spanish patients: association with HLA alleles and role in susceptibility to acute lymphoblastic leukemia.

    Rodríguez-López R, Donoso M, Fernández-Cavada M, González LM, Margallo A, Corral C, Gallego M, García de Cáceres MT, Herrera T, González C, Vagace JM, Gervasini G.

    Gene. 2013 Feb 1;514(1):31-5. doi: 10.1016/j.gene.2012.10.090. Epub 2012 Nov 21.

    PMID:
    23178241
    [PubMed - indexed for MEDLINE]

    Related citations

    4.

    Iranian hereditary hemochromatosis patients: baseline characteristics, laboratory data and gene mutations.

    Zamani F, Bagheri Z, Bayat M, Fereshtehnejad SM, Basi A, Najmabadi H, Ajdarkosh H.

    Med Sci Monit. 2012 Oct;18(10):CR622-9.

    PMID:
    23018356
    [PubMed - indexed for MEDLINE]
    Free PMC Article

    Related citations

    5.

    H63D mutation in HFE gene is common in Indians and is associated with the European haplotype.

    Dhillon BK, Prakash S, Chandak GR, Chawla YK, Das R.

    J Genet. 2012 Aug;91(2):229-32. No abstract available.

    PMID:
    22942096
    [PubMed - indexed for MEDLINE]
    Free Article

    Related citations

    6.

    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. doi: 10.1016/j.gene.2012.07.069. Epub 2012 Aug 4.

    PMID:
    22890139
    [PubMed - indexed for MEDLINE]

    Related citations

    7.

    Phlebotomy patterns in haemochromatosis patients and their contribution to the blood supply.

    Walkden D, Badami K, McGonigal G.

    N Z Med J. 2012 Jul 29;125(1358):29-34.

    PMID:
    22864154
    [PubMed - indexed for MEDLINE]

    Related citations

    8.

    Sample-to-SNP kit: a reliable, easy and fast tool for the detection of HFE p.H63D and p.C282Y variations associated to hereditary hemochromatosis.

    Nielsen PB, Petersen MS, Ystaas V, Andersen RV, Hansen KM, Blaabjerg V, Refstrup M.

    Gene. 2012 Oct 1;507(1):79-84. doi: 10.1016/j.gene.2012.06.020. Epub 2012 Jun 23.

    PMID:
    22735619
    [PubMed - indexed for MEDLINE]

    Related citations

    9.

    HFE gene C282Y, H63D and S65C mutations frequency in the Transylvania region, Romania.

    Trifa AP, Popp RA, Militaru MS, Farcaş MF, Crişan TO, Gana I, Cucuianu A, Pop IV.

    J Gastrointestin Liver Dis. 2012 Jun;21(2):177-80.

    PMID:
    22720307
    [PubMed - indexed for MEDLINE]
    Free Article

    Related citations

    10.

    Porphyria cutanea tarda in the Basque Country: significance of HFE gene mutations and of external factors.

    Castiella A, Zapata E, Otazua P, Zubiaurre L.

    Liver Int. 2012 Nov;32(10):1597. doi: 10.1111/j.1478-3231.2012.02834.x. Epub 2012 Jun 11. No abstract available.

    PMID:
    22680055
    [PubMed - indexed for MEDLINE]

    Related citations

    11.

    Hemochromatosis: discovery of the HFE gene.

    Bacon BR.

    Mo Med. 2012 Mar-Apr;109(2):133-6.

    PMID:
    22675794
    [PubMed - indexed for MEDLINE]

    Related citations

    12.

    Diagnosis of hereditary hemochromatosis in the era of genetic testing.

    Trieß C, von Figura G, Stuhrmann M, Butzeck B, Krayenbuehl PA, Strnad P, Kulaksiz H.

    Dig Dis Sci. 2012 Nov;57(11):2988-94. doi: 10.1007/s10620-012-2243-z. Epub 2012 Jun 7.

    PMID:
    22674401
    [PubMed - indexed for MEDLINE]

    Related citations

    13.

    The functional significance of E277K and V295A HFE mutations.

    Silva B, Martins R, Proença D, Fleming R, Faustino P.

    Br J Haematol. 2012 Aug;158(3):399-408. doi: 10.1111/j.1365-2141.2012.09164.x. Epub 2012 May 25.

    PMID:
    22624560
    [PubMed - indexed for MEDLINE]

    Related citations

    14.

    Alternative polyadenylation and nonsense-mediated decay coordinately regulate the human HFE mRNA levels.

    Martins R, Proença D, Silva B, Barbosa C, Silva AL, Faustino P, Romão L.

    PLoS One. 2012;7(4):e35461. doi: 10.1371/journal.pone.0035461. Epub 2012 Apr 18.

    PMID:
    22530027
    [PubMed - indexed for MEDLINE]
    Free PMC Article

    Related citations

    15.

    An association study of HFE gene mutation with idiopathic male infertility in the Chinese Han population.

    Yu XY, Wang BB, Xin ZC, Liu T, Ma K, Jiang J, Fang X, Yu LH, Peng YF, Ma X.

    Asian J Androl. 2012 Jul;14(4):599-603. doi: 10.1038/aja.2012.1. Epub 2012 Apr 16.

    PMID:
    22504868
    [PubMed - indexed for MEDLINE]

    Related citations

    16.

    The H63D mutation of the hemochromatosis gene is associated with sustained virological response in chronic hepatitis C patients treated with interferon-based therapy: a meta-analysis.

    Li SH, Zhao H, Ren YY, Liu YZ, Song G, Ding P, Ding YP, Wang GQ.

    Tohoku J Exp Med. 2012;226(4):293-9.

    PMID:
    22499121
    [PubMed - indexed for MEDLINE]
    Free Article

    Related citations

    17.

    Effect of HFE gene polymorphism on sustained virological response in patients with chronic hepatitis C and elevated serum ferritin.

    Coelho-Borges S, Cheinquer H, Wolff FH, Cheinquer N, Krug L, Ashton-Prolla P.

    Arq Gastroenterol. 2012 Jan-Mar;49(1):9-13.

    PMID:
    22481680
    [PubMed - indexed for MEDLINE]
    Free Article

    Related citations

    18.

    Study of the HFE gene common polymorphisms in French patients with sporadic amyotrophic lateral sclerosis.

    Praline J, Blasco H, Vourc'h P, Rat V, Gendrot C, Camu W, Andres CR; French ALS Study Group.

    J Neurol Sci. 2012 Jun 15;317(1-2):58-61. doi: 10.1016/j.jns.2012.02.029. Epub 2012 Mar 14.

    PMID:
    22425014
    [PubMed - indexed for MEDLINE]

    Related citations

    19.

    Metals and the liver.

    Maxwell KL, Kowdley KV.

    Curr Opin Gastroenterol. 2012 May;28(3):217-22. doi: 10.1097/MOG.0b013e3283521d82. Review.

    PMID:
    22395570
    [PubMed - indexed for MEDLINE]

    Related citations

    20.

    Validation of an unlabeled probe melting analysis assay combined with high-throughput extractions for genotyping of the most common variants in HFE-associated hereditary hemochromatosis, C282Y, H63D, and S65C.

    Sumner K, Hubley L, Pont-Kingdon G, Mitchell S, Wayman T, Wilson A, Meadows C, Elenitoba-Johnson K, Pattison D, Dobrowolski S, Best H, Lyon E.

    Genet Test Mol Biomarkers. 2012 Jul;16(7):656-60. doi: 10.1089/gtmb.2011.0204. Epub 2012 Feb 24.

    PMID:
    22364140
    [PubMed - indexed for MEDLINE]

    Related citations

      Display Settings:

      Format
      Items per page
      Sort by

      Send to:

      Choose Destination

      Supplemental Content

      Filters: Manage Filters

      7 free full-text articles in PubMed Central

      See all (7)...

      Find related data

      Search details

      See more...

      Recent activity

      Clear Turn Off Turn On

      Your browsing activity is empty.

      Activity recording is turned off.

      Turn recording back on

      See more...
      You are here: NCBI > Literature > PubMed
      Write to the Help Desk