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Journal Abstract Search

142 related items for PubMed ID: 12406098

  • 1. Genetic hyperferritinaemia and reticuloendothelial iron overload associated with a three base pair deletion in the coding region of the ferroportin gene (SLC11A3).
    Cazzola M, Cremonesi L, Papaioannou M, Soriani N, Kioumi A, Charalambidou A, Paroni R, Romtsou K, Levi S, Ferrari M, Arosio P, Christakis J.
    Br J Haematol; 2002 Nov; 119(2):539-46. PubMed ID: 12406098
    [Abstract] [Full Text] [Related]

  • 2. Autosomal dominant reticuloendothelial iron overload associated with a 3-base pair deletion in the ferroportin 1 gene (SLC11A3).
    Devalia V, Carter K, Walker AP, Perkins SJ, Worwood M, May A, Dooley JS.
    Blood; 2002 Jul 15; 100(2):695-7. PubMed ID: 12091367
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  • 3. A Japanese family with ferroportin disease caused by a novel mutation of SLC40A1 gene: hyperferritinemia associated with a relatively low transferrin saturation of iron.
    Koyama C, Wakusawa S, Hayashi H, Ueno T, Suzuki R, Yano M, Saito H, Okazaki T.
    Intern Med; 2005 Sep 15; 44(9):990-3. PubMed ID: 16258219
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  • 4. Hyperferritinaemia in the absence of iron overload.
    Arnold JD, Mumford AD, Lindsay JO, Hegde U, Hagan M, Hawkins JR.
    Gut; 1997 Sep 15; 41(3):408-10. PubMed ID: 9378401
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  • 5. Role of ferritin and ferroportin genes in unexplained hyperferritinaemia.
    Cazzola M.
    Best Pract Res Clin Haematol; 2005 Jun 15; 18(2):251-63. PubMed ID: 15737888
    [Abstract] [Full Text] [Related]

  • 6. Two Dutch families with hereditary hyperferritinaemia-cataract syndrome and heterozygosity for an HFE-related haemochromatosis gene mutation.
    Simsek S, Nanayakkara PW, Keek JM, Faber LM, Bruin KF, Pals G.
    Neth J Med; 2003 Sep 15; 61(9):291-5. PubMed ID: 14692443
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  • 7. A linkage between hereditary hyperferritinaemia not related to iron overload and autosomal dominant congenital cataract.
    Girelli D, Olivieri O, De Franceschi L, Corrocher R, Bergamaschi G, Cazzola M.
    Br J Haematol; 1995 Aug 15; 90(4):931-4. PubMed ID: 7669675
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  • 8. Mild iron overload in patients carrying the HFE S65C gene mutation: a retrospective study in patients with suspected iron overload and healthy controls.
    Holmström P, Marmur J, Eggertsen G, Gåfvels M, Stål P.
    Gut; 2002 Nov 15; 51(5):723-30. PubMed ID: 12377814
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  • 9. Identification of mutations in SLC40A1 that affect ferroportin function and phenotype of human ferroportin iron overload.
    Mayr R, Griffiths WJ, Hermann M, McFarlane I, Halsall DJ, Finkenstedt A, Douds A, Davies SE, Janecke AR, Vogel W, Cox TM, Zoller H.
    Gastroenterology; 2011 Jun 15; 140(7):2056-63, 2063.e1. PubMed ID: 21396368
    [Abstract] [Full Text] [Related]

  • 10. 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 15; 78(1):66-71. PubMed ID: 17042772
    [Abstract] [Full Text] [Related]

  • 11. Genetic and clinical heterogeneity of ferroportin disease.
    Cremonesi L, Forni GL, Soriani N, Lamagna M, Fermo I, Daraio F, Galli A, Pietra D, Malcovati L, Ferrari M, Camaschella C, Cazzola M.
    Br J Haematol; 2005 Dec 15; 131(5):663-70. PubMed ID: 16351644
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  • 13. Iron overload in Africans and African-Americans and a common mutation in the SCL40A1 (ferroportin 1) gene.
    Gordeuk VR, Caleffi A, Corradini E, Ferrara F, Jones RA, Castro O, Onyekwere O, Kittles R, Pignatti E, Montosi G, Garuti C, Gangaidzo IT, Gomo ZA, Moyo VM, Rouault TA, MacPhail P, Pietrangelo A.
    Blood Cells Mol Dis; 2003 Dec 15; 31(3):299-304. PubMed ID: 14636642
    [Abstract] [Full Text] [Related]

  • 14. Autosomal dominant iron overload due to a novel mutation of ferroportin1 associated with parenchymal iron loading and cirrhosis.
    Wallace DF, Clark RM, Harley HA, Subramaniam VN.
    J Hepatol; 2004 Apr 15; 40(4):710-3. PubMed ID: 15030991
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  • 15. Causes of iron overload in blood donors - a clinical study.
    Laursen AH, Bjerrum OW, Friis-Hansen L, Hansen TO, Marott JL, Magnussen K.
    Vox Sang; 2018 Feb 15; 113(2):110-119. PubMed ID: 29230833
    [Abstract] [Full Text] [Related]

  • 16. Hereditary hyperferritinaemia-cataract syndrome: a challenging diagnosis for the hepatogastroenterologist.
    Ferrante M, Geubel AP, Fevery J, Marogy G, Horsmans Y, Nevens F.
    Eur J Gastroenterol Hepatol; 2005 Nov 15; 17(11):1247-53. PubMed ID: 16215440
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  • 19. Ferroportin disease: a systematic meta-analysis of clinical and molecular findings.
    Mayr R, Janecke AR, Schranz M, Griffiths WJ, Vogel W, Pietrangelo A, Zoller H.
    J Hepatol; 2010 Nov 15; 53(5):941-9. PubMed ID: 20691492
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