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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

244 related articles for article (PubMed ID: 17483072)

  • 61. Should we screen for hereditary hemochromatosis in healthy Lebanese: a pilot study.
    Mahfouz RA; Sarieddine DS; Charafeddine KM; Abdul Khalik RN; Cortas NK; Daher RT
    Mol Biol Rep; 2012 Jan; 39(1):753-9. PubMed ID: 21553046
    [TBL] [Abstract][Full Text] [Related]  

  • 62. The effect of the hemochromatosis (HFE) genotype on lead load and iron metabolism among lead smelter workers.
    Fan G; Du G; Li H; Lin F; Sun Z; Yang W; Feng C; Zhu G; Li Y; Chen Y; Jiao H; Zhou F
    PLoS One; 2014; 9(7):e101537. PubMed ID: 24988074
    [TBL] [Abstract][Full Text] [Related]  

  • 63. C282Y hemochromatosis gene mutation and iron parameters in dialysis patients.
    Fernández Rodríguez AM; Gascón LH; García La Orden I; Santos JP; Samper RG; Letosa RM; Palop Cubillo L; Rodríguez Pérez JC; Rodríguez-Gallego JC
    Clin Nephrol; 2011 Apr; 75(4):328-35. PubMed ID: 21426887
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Phenotypic expression of the C282Y/Q283P compound heterozygosity in HFE and molecular modeling of the Q283P mutation effect.
    Le Gac G; Dupradeau FY; Mura C; Jacolot S; Scotet V; Esnault G; Mercier AY; Rochette J; Férec C
    Blood Cells Mol Dis; 2003; 30(3):231-7. PubMed ID: 12737937
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Can defects in transferrin receptor 2 and hereditary hemochromatosis genes account for iron overload in HbH disease?
    Chan V; Wong MS; Ooi C; Chen FE; Chim CS; Liang RH; Todd D; Chan TK
    Blood Cells Mol Dis; 2003; 30(1):107-11. PubMed ID: 12667993
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Heterozygous recipient and donor HFE mutations associated with a hereditary haemochromatosis phenotype after liver transplantation.
    Wigg AJ; Harley H; Casey G
    Gut; 2003 Mar; 52(3):433-5. PubMed ID: 12584229
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Penetrance of hemochromatosis.
    Waalen J; Felitti V; Gelbart T; Ho NJ; Beutler E
    Blood Cells Mol Dis; 2002; 29(3):418-32. PubMed ID: 12678056
    [TBL] [Abstract][Full Text] [Related]  

  • 68. The C282Y mutation causing hereditary hemochromatosis does not produce a null allele.
    Levy JE; Montross LK; Cohen DE; Fleming MD; Andrews NC
    Blood; 1999 Jul; 94(1):9-11. PubMed ID: 10381492
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Vibrio vulnificus septicemia in a patient with the hemochromatosis HFE C282Y mutation.
    Gerhard GS; Levin KA; Price Goldstein J; Wojnar MM; Chorney MJ; Belchis DA
    Arch Pathol Lab Med; 2001 Aug; 125(8):1107-9. PubMed ID: 11473471
    [TBL] [Abstract][Full Text] [Related]  

  • 70. When and how should we screen for hereditary hemochromatosis?
    Chalès G; Guggenbuhl P
    Joint Bone Spine; 2003 Aug; 70(4):263-70. PubMed ID: 12951308
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Epidemic pathogenic selection: an explanation for hereditary hemochromatosis?
    Moalem S; Percy ME; Kruck TP; Gelbart RR
    Med Hypotheses; 2002 Sep; 59(3):325-9. PubMed ID: 12208162
    [TBL] [Abstract][Full Text] [Related]  

  • 72. HFE genotypes in patients with chronic pancreatitis and pancreatic adenocarcinoma.
    Hucl T; Kylanpää-Bäck ML; Witt H; Künzli B; Lempinen M; Schneider A; Kemppainen E; Löhr M; Friess H; Ockenga J; Rosendahl J; Schulz HU; Gress T; Singer MV; Pfützer RH
    Genet Med; 2007 Jul; 9(7):479-83. PubMed ID: 17666895
    [TBL] [Abstract][Full Text] [Related]  

  • 73. What's new in hemochromatosis.
    Gochee PA; Powell LW
    Curr Opin Hematol; 2001 Mar; 8(2):98-104. PubMed ID: 11224684
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Phenotypic expression of the C282Y/Q283P compound heterozygosity in HFE and molecular modeling of the Q283P mutation effect.
    Oberkanins C
    Blood Cells Mol Dis; 2003; 31(2):173; author reply 174. PubMed ID: 12972020
    [No Abstract]   [Full Text] [Related]  

  • 75. Frequency of the S65C mutation in the hemochromatosis gene in Brazil.
    Oliveira VC; Caxito FA; Gomes KB; Castro AM; Pardini VC; Ferreira AC
    Genet Mol Res; 2009 Jul; 8(3):794-8. PubMed ID: 19681031
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Screening for hemochromatosis in Turkey.
    Bozkaya H; Bektas M; Metin O; Erkan O; Ibrahimoglu D; Dalva K; Akbiyik F; Gurel S; Bozdayi AM; Akay C; Yurdaydin C; Aslan O; Uzunalimoglu O
    Dig Dis Sci; 2004 Mar; 49(3):444-9. PubMed ID: 15139495
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Incidence of cardiac arrhythmias in asymptomatic hereditary hemochromatosis subjects with C282Y homozygosity.
    Shizukuda Y; Tripodi DJ; Zalos G; Bolan CD; Yau YY; Leitman SF; Waclawiw MA; Rosing DR
    Am J Cardiol; 2012 Mar; 109(6):856-60. PubMed ID: 22196777
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Heme carrier protein 1 (HCP1) genetic variants in the Hemochromatosis and Iron Overload Screening (HEIRS) Study participants.
    Wang X; Leiendecker-Foster C; Acton RT; Barton JC; McLaren CE; McLaren GD; Gordeuk VR; Eckfeldt JH
    Blood Cells Mol Dis; 2009; 42(2):150-4. PubMed ID: 19176287
    [TBL] [Abstract][Full Text] [Related]  

  • 79. Involvement of ApoE E4 and H63D in sporadic Alzheimer's disease in a folate-supplemented Ontario population.
    Percy M; Moalem S; Garcia A; Somerville MJ; Hicks M; Andrews D; Azad A; Schwarz P; Beheshti Zavareh R; Birkan R; Choo C; Chow V; Dhaliwal S; Duda V; Kupferschmidt AL; Lam K; Lightman D; Machalek K; Mar W; Nguyen F; Rytwinski PJ; Svara E; Tran M; Wheeler K; Yeung L; Zanibbi K; Zener R; Ziraldo M; Freedman M
    J Alzheimers Dis; 2008 May; 14(1):69-84. PubMed ID: 18525129
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Hemochromatosis, alcoholism and unhealthy dietary fat: a case report.
    Shobi V; Adeseye A; Billy B; Medhat K
    J Med Case Rep; 2021 Feb; 15(1):84. PubMed ID: 33596964
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.