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Journal Abstract Search

128 related items for PubMed ID: 10772871

  • 1. Clinical and molecular aspects of juvenile hemochromatosis in Saguenay-Lac-Saint-Jean (Quebec, canada).
    Rivard SR, Mura C, Simard H, Simard R, Grimard D, Le Gac G, Raguenes O, Férec C, De Braekeleer M.
    Blood Cells Mol Dis; 2000 Feb; 26(1):10-4. PubMed ID: 10772871
    [Abstract] [Full Text] [Related]

  • 2. H63D homozygotes with hyperferritinaemia: Is this genotype, the primary cause of iron overload?
    de Diego C, Opazo S, Murga MJ, Martínez-Castro P.
    Eur J Haematol; 2007 Jan; 78(1):66-71. PubMed ID: 17042772
    [Abstract] [Full Text] [Related]

  • 3. Genetic screening for HFE hemochromatosis in 6,020 Danish men: penetrance of C282Y, H63D, and S65C variants.
    Pedersen P, Milman N.
    Ann Hematol; 2009 Aug; 88(8):775-84. PubMed ID: 19159930
    [Abstract] [Full Text] [Related]

  • 4. Survival after liver transplantation in patients with hepatic iron overload: the national hemochromatosis transplant registry.
    Kowdley KV, Brandhagen DJ, Gish RG, Bass NM, Weinstein J, Schilsky ML, Fontana RJ, McCashland T, Cotler SJ, Bacon BR, Keeffe EB, Gordon F, Polissar N, National Hemochromatosis Transplant Registry.
    Gastroenterology; 2005 Aug; 129(2):494-503. PubMed ID: 16083706
    [Abstract] [Full Text] [Related]

  • 5. Homozygous p.M172K mutation of the TFR2 gene in an Italian family with type 3 hereditary hemochromatosis and early onset iron overload.
    Majore S, Milano F, Binni F, Stuppia L, Cerrone A, Tafuri A, De Bernardo C, Palka G, Grammatico P.
    Haematologica; 2006 Aug; 91(8 Suppl):ECR33. PubMed ID: 16923517
    [Abstract] [Full Text] [Related]

  • 6. [Hemochromatosis--from an underdiagnosed curiosity to a common disease].
    Hagve TA, Asberg A, Ulvik R, Borch-Iohnsen B, Thorstensen K.
    Tidsskr Nor Laegeforen; 2009 Apr 30; 129(9):863-6. PubMed ID: 19415085
    [Abstract] [Full Text] [Related]

  • 7. Screening for hemochromatosis in asymptomatic subjects with or without a family history.
    Powell LW, Dixon JL, Ramm GA, Purdie DM, Lincoln DJ, Anderson GJ, Subramaniam VN, Hewett DG, Searle JW, Fletcher LM, Crawford DH, Rodgers H, Allen KJ, Cavanaugh JA, Bassett ML.
    Arch Intern Med; 2006 Feb 13; 166(3):294-301. PubMed ID: 16476869
    [Abstract] [Full Text] [Related]

  • 8. Is there a threshold of hepatic iron concentration that leads to cirrhosis in C282Y hemochromatosis?
    Adams PC.
    Am J Gastroenterol; 2001 Feb 13; 96(2):567-9. PubMed ID: 11232708
    [Abstract] [Full Text] [Related]

  • 9. Mutation analysis in the HFE gene in patients with hereditary haemochromatosis in Saguenay-Lac-Saint-Jean (Quebec, Canada).
    Rivard SR, Mura C, Simard H, Simard R, Grimard D, Le Gac G, Raguenes O, Férec C, De Braekeleer M.
    Br J Haematol; 2000 Mar 13; 108(4):854-8. PubMed ID: 10792295
    [Abstract] [Full Text] [Related]

  • 10. A novel ferroportin mutation in a Canadian family with autosomal dominant hemochromatosis.
    Morris TJ, Litvinova MM, Ralston D, Mattman A, Holmes D, Lockitch G.
    Blood Cells Mol Dis; 2005 Mar 13; 35(3):309-14. PubMed ID: 16111902
    [Abstract] [Full Text] [Related]

  • 11. Hemochromatosis (HFE) and transferrin receptor-1 (TFRC1) genes in sporadic porphyria cutanea tarda (sPCT).
    Lamoril J, Andant C, Gouya L, Malonova E, Grandchamp B, Martásek P, Deybac JC, Puy H.
    Cell Mol Biol (Noisy-le-grand); 2002 Feb 13; 48(1):33-41. PubMed ID: 11929045
    [Abstract] [Full Text] [Related]

  • 12. [Idiopathic hemochromatosis].
    Marin MG.
    Minerva Med; 1985 Mar 31; 76(13):627-34. PubMed ID: 2986052
    [Abstract] [Full Text] [Related]

  • 13. Juvenile hemochromatosis in the southeastern United States: a report of seven cases in two kinships.
    Barton JC, Rao SV, Pereira NM, Gelbart T, Beutler E, Rivers CA, Acton RT.
    Blood Cells Mol Dis; 2002 Mar 31; 29(1):104-15. PubMed ID: 12482411
    [Abstract] [Full Text] [Related]

  • 14. The relationship between iron overload, clinical symptoms, and age in 410 patients with genetic hemochromatosis.
    Adams PC, Deugnier Y, Moirand R, Brissot P.
    Hepatology; 1997 Jan 31; 25(1):162-6. PubMed ID: 8985284
    [Abstract] [Full Text] [Related]

  • 15. Population genetics of hereditary hemochromatosis in Saguenay Lac-Saint-Jean (Quebec, Canada).
    de Braekeleer M, Vigneault A, Simard H.
    Ann Genet; 1992 Jan 31; 35(4):202-7. PubMed ID: 1296515
    [Abstract] [Full Text] [Related]

  • 16. Successful pregnancy following gonadotropin therapy in a young female with juvenile idiopathic hemochromatosis and secondary hypogonadotropic hypogonadism.
    Farina G, Pedrotti C, Cerani P, Rovati A, Strada E, Bergamaschi G, Montanari L.
    Haematologica; 1995 Jan 31; 80(4):335-7. PubMed ID: 7590503
    [Abstract] [Full Text] [Related]

  • 17. [Endocrine consequences of hemochromatosis].
    Young J.
    Presse Med; 2007 Sep 31; 36(9 Pt 2):1319-25. PubMed ID: 17524608
    [Abstract] [Full Text] [Related]

  • 18. The dysmetabolic iron overload syndrome is clinically and genetically distinct from HFE-related genetic hemochromatosis.
    Rovati A, Bergamaschi G, Casula S, Cerani P, Grasso M, Cazzola M.
    Haematologica; 1999 Feb 31; 84(2):182-3. PubMed ID: 10091420
    [No Abstract] [Full Text] [Related]

  • 19. [Genetic hemochromatosis].
    Jouanolle AM, Gandon G, Le Gall JY, David V.
    Ann Biol Clin (Paris); 1998 Jul 31; 56 Spec No():31-5. PubMed ID: 9827212
    [No Abstract] [Full Text] [Related]

  • 20. Secondary hypothyroidism in hereditary hemochromatosis: recovery after iron depletion.
    Hudec M, Grigerova M, Walsh CH.
    Thyroid; 2008 Feb 31; 18(2):255-7. PubMed ID: 18205549
    [Abstract] [Full Text] [Related]

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