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

99 related items for PubMed ID: 12651261

  • 61. Homozygous deletion of HFE produces a phenotype similar to the HFE p.C282Y/p.C282Y genotype.
    Le Gac G, Gourlaouen I, Ronsin C, Géromel V, Bourgarit A, Parquet N, Quemener S, Le Maréchal C, Chen JM, Férec C.
    Blood; 2008 Dec 15; 112(13):5238-40. PubMed ID: 18809761
    [Abstract] [Full Text] [Related]

  • 62. The origin and spread of the HFE-C282Y haemochromatosis mutation.
    Distante S, Robson KJ, Graham-Campbell J, Arnaiz-Villena A, Brissot P, Worwood M.
    Hum Genet; 2004 Sep 15; 115(4):269-79. PubMed ID: 15290237
    [Abstract] [Full Text] [Related]

  • 63.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 64. HFE gene mutations in a population of Italian Parkinson's disease patients.
    Biasiotto G, Goldwurm S, Finazzi D, Tunesi S, Zecchinelli A, Sironi F, Pezzoli G, Arosio P.
    Parkinsonism Relat Disord; 2008 Sep 15; 14(5):426-30. PubMed ID: 18325820
    [Abstract] [Full Text] [Related]

  • 65.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 66. Association between HFE mutations and acute myocardial infarction: a study in patients from Northern and Southern Italy.
    Candore G, Balistreri CR, Lio D, Mantovani V, Colonna-Romano G, Chiappelli M, Tampieri C, Licastro F, Branzi A, Averna M, Caruso M, Hoffmann E, Caruso C.
    Blood Cells Mol Dis; 2003 Sep 15; 31(1):57-62. PubMed ID: 12850485
    [Abstract] [Full Text] [Related]

  • 67.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 68. Haemochromatosis gene frequency in a control and diabetic Irish population.
    Kirk L, Bird J, Ramadan S, Samad A, Adebayo G, Lourens W, Williams J.
    Ir J Med Sci; 2009 Mar 15; 178(1):39-42. PubMed ID: 19002551
    [Abstract] [Full Text] [Related]

  • 69.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 70.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 71. Prevalence of HFE mutations in people from North Africa living in southern France.
    Aguilar-Martinez P, Picot MC, Becker F, Boulot P, Montoya F, Mares P, Bachelard B, Henry Y, Delarbre JL, Sarda P, Schved JF.
    Br J Haematol; 2001 Sep 15; 114(4):914-6. PubMed ID: 11564085
    [Abstract] [Full Text] [Related]

  • 72.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 73. Sequence variation and haplotype structure at the human HFE locus.
    Toomajian C, Kreitman M.
    Genetics; 2002 Aug 15; 161(4):1609-23. PubMed ID: 12196404
    [Abstract] [Full Text] [Related]

  • 74. HFE H63D polymorphism is increased in patients with amyotrophic lateral sclerosis of Italian origin.
    Restagno G, Lombardo F, Ghiglione P, Calvo A, Cocco E, Sbaiz L, Mutani R, Chiò A.
    J Neurol Neurosurg Psychiatry; 2007 Mar 15; 78(3):327. PubMed ID: 17308297
    [No Abstract] [Full Text] [Related]

  • 75.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 76. HFE-Related Hemochromatosis in a Chinese Patient: The First Reported Case.
    Zhang W, Wang X, Duan W, Xu A, Zhao X, Huang J, You H, Brissot P, Ou X, Jia J.
    Front Genet; 2020 Mar 15; 11():77. PubMed ID: 32153640
    [Abstract] [Full Text] [Related]

  • 77. Countries of ancestry reported by hemochromatosis probands and control subjects in central Alabama.
    Barton EH, Barton JC, Hollowell WW, Acton RT.
    Ethn Dis; 2004 Mar 15; 14(1):73-81. PubMed ID: 15002926
    [Abstract] [Full Text] [Related]

  • 78. Frequencies of HFE gene mutations associated with haemochromatosis in the population of Libya living in Benghazi.
    Elmrghni S, Dixon RA, Williams DR.
    Int J Clin Exp Med; 2011 Mar 15; 4(3):200-4. PubMed ID: 21977233
    [Abstract] [Full Text] [Related]

  • 79. Prevalence of 845G>A HFE mutation in Slavic populations: an east-west linear gradient in South Slavs.
    Adler G, Clark JS, Łoniewska B, Ciechanowicz A.
    Croat Med J; 2011 Jun 15; 52(3):351-7. PubMed ID: 21674831
    [Abstract] [Full Text] [Related]

  • 80.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 5.