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 *

119 related articles for article (PubMed ID: 11078576)

  • 1. Erratum: are hereditary hemochromatosis mutations involved in alzheimer disease?
    Moalem S; Percy ME; Andrews DF; Kruck TP; Wong S; Dalton AJ; Mehta P; Fedor B; Warren AC
    Am J Med Genet; 2000 Nov; 95(2):189. PubMed ID: 11078576
    [No Abstract]   [Full Text] [Related]  

  • 2. Are hereditary hemochromatosis mutations involved in Alzheimer disease?
    Moalem S; Percy ME; Andrews DF; Kruck TP; Wong S; Dalton AJ; Mehta P; Fedor B; Warren AC
    Am J Med Genet; 2000 Jul; 93(1):58-66. PubMed ID: 10861683
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Association of porphyria cutanea tarda with hereditary hemochromatosis.
    Mehrany K; Drage LA; Brandhagen DJ; Pittelkow MR
    J Am Acad Dermatol; 2004 Aug; 51(2):205-11. PubMed ID: 15280838
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prevalence of the Cys282Tyr and His63Asp HFE gene mutations in Spanish patients with hereditary hemochromatosis and in controls.
    Sánchez M; Bruguera M; Bosch J; Rodés J; Ballesta F; Oliva R
    J Hepatol; 1998 Nov; 29(5):725-8. PubMed ID: 9833909
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Non-HFE-related hereditary iron overload].
    Aguilar-Martinez P
    Presse Med; 2007 Sep; 36(9 Pt 2):1279-91. PubMed ID: 17540536
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Autosomal dominant hereditary hemochromatosis associated with a novel ferroportin mutation and unique clinical features.
    Sham RL; Phatak PD; West C; Lee P; Andrews C; Beutler E
    Blood Cells Mol Dis; 2005; 34(2):157-61. PubMed ID: 15727899
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 27(1):290-3. PubMed ID: 11358390
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Correlation between genotype and phenotype in hereditary hemochromatosis: analysis of 61 cases.
    Sham RL; Ou CY; Cappuccio J; Braggins C; Dunnigan K; Phatak PD
    Blood Cells Mol Dis; 1997 Aug; 23(2):314-20. PubMed ID: 9410475
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hereditary hemochromatosis: missed diagnosis or misdiagnosis?
    Cherfane CE; Hollenbeck RD; Go J; Brown KE
    Am J Med; 2013 Nov; 126(11):1010-5. PubMed ID: 24054178
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mutations of the HFE gene and the risk of hepatocellular carcinoma.
    Racchi O; Mangerini R; Rapezzi D; Gaetani GF; Nobile MT; Picciotto A; Ferraris AM
    Blood Cells Mol Dis; 1999; 25(5-6):350-3. PubMed ID: 10660482
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hereditary hemochromatosis: an opportunity for gene therapy.
    Ezquer F; Núñez MT; Rojas A; Asenjo J; Israel Y
    Biol Res; 2006; 39(1):113-24. PubMed ID: 16629172
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Autosomal dominant hereditary hemochromatosis associated with two novel Ferroportin 1 mutations in Spain.
    Bach V; Remacha A; Altés A; Barceló MJ; Molina MA; Baiget M
    Blood Cells Mol Dis; 2006; 36(1):41-5. PubMed ID: 16257244
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Screening for hereditary hemochromatosis: a clinical practice guideline from the American College of Physicians.
    Qaseem A; Aronson M; Fitterman N; Snow V; Weiss KB; Owens DK;
    Ann Intern Med; 2005 Oct; 143(7):517-21. PubMed ID: 16204164
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Diagnosis of hereditary hemochromatosis with molecular analysis of DNA in patients with anti-HCV positive liver cirrhosis. Clinical case].
    Carella AM; Bianco G; Carella M; Gasparini P
    Minerva Med; 1998 Sep; 89(9):323-7. PubMed ID: 9856121
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Human leukocyte antigen haplotypes and HFE mutations in Spanish hereditary hemochromatosis and sporadic porphyria cutanea tarda.
    Gonzalez-Hevilla M; de Salamanca RE; Morales P; Martínez-Laso J; Fontanellas A; Castro MJ; Rojo R; Moscoso J; Zamora J; Serrano-Vela JI; Arnaiz-Villena A
    J Gastroenterol Hepatol; 2005 Mar; 20(3):456-62. PubMed ID: 15740492
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hereditary hemochromatosis.
    Pietrangelo A
    Biochim Biophys Acta; 2006 Jul; 1763(7):700-10. PubMed ID: 16891003
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Clinical research and preliminarily exploration of genetic basis on a hereditary hemochromatosis pedigree].
    Jiang J; Huang JM; Qian W; Yang L; Ye J; Hou XH
    Zhonghua Gan Zang Bing Za Zhi; 2010 Nov; 18(11):842-4. PubMed ID: 21138633
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetics of iron storage and hemochromatosis.
    Beutler E; Felitti V; Gelbart T; Ho N
    Drug Metab Dispos; 2001 Apr; 29(4 Pt 2):495-9. PubMed ID: 11259339
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hemochromatosis in Ireland and HFE.
    Ryan E; O'keane C; Crowe J
    Blood Cells Mol Dis; 1998 Dec; 24(4):428-32. PubMed ID: 9851896
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Recognition and management of hereditary hemochromatosis.
    Brandhagen DJ; Fairbanks VF; Baldus W
    Am Fam Physician; 2002 Mar; 65(5):853-60. PubMed ID: 11898957
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.