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Journal Abstract Search

92 related items for PubMed ID: 21320560

  • 1. SLC40A1-R178G mutation and ferroportin disease.
    Speletas M, Onoufriadis E, Kioumi A, Germenis AE.
    J Hepatol; 2011 Sep; 55(3):730-731. PubMed ID: 21320560
    [No Abstract] [Full Text] [Related]

  • 2. SLC40A1-R178G or R178Q and ferroportin disease? A call for vigilance in mutation reporting.
    Wallace DF.
    J Hepatol; 2013 Aug; 59(2):396-7. PubMed ID: 23523714
    [No Abstract] [Full Text] [Related]

  • 3. Reply to: "SLC40A1-R178G or R178Q and ferroportin disease? A call for vigilance in mutation reporting".
    Speletas M, Kioumi A, Germenis AE.
    J Hepatol; 2013 Aug; 59(2):397. PubMed ID: 23523713
    [No Abstract] [Full Text] [Related]

  • 4. 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; 140(7):2056-63, 2063.e1. PubMed ID: 21396368
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  • 6. 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; 53(5):941-9. PubMed ID: 20691492
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  • 9. A novel mutation in the SLC40A1 gene associated with reduced iron export in vitro.
    Moreno-Carralero MI, Muñoz-Muñoz JA, Cuadrado-Grande N, López-Rodríguez R, José Hernández-Alfaro M, del-Castillo-Rueda A, Enríquez-de-Salamanca R, Méndez M, Morán-Jiménez MJ.
    Am J Hematol; 2014 Jul; 89(7):689-94. PubMed ID: 24644245
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  • 12. The ferroportin disease.
    Pietrangelo A.
    Blood Cells Mol Dis; 2004 Jul; 32(1):131-8. PubMed ID: 14757427
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  • 14. Iron overload due to mutations in ferroportin.
    De Domenico I, Ward DM, Musci G, Kaplan J.
    Haematologica; 2006 Jan; 91(1):92-5. PubMed ID: 16434376
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  • 15. [Practical use of genetic markers other than C282Y in iron overload disorders].
    Brissot P.
    Gastroenterol Clin Biol; 2002 Nov; 26(11):991-3. PubMed ID: 12483130
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  • 18. The impact of the mutations of the HFE gene and of the SLC11A3 gene on iron overload in Greek thalassemia intermedia and beta(s)/beta(thal) anemia patients.
    Politou M, Kalotychou V, Pissia M, Rombos Y, Sakellaropoulos N, Papanikolaou G.
    Haematologica; 2004 Apr; 89(4):490-2. PubMed ID: 15075083
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  • 19. Ferroportin 1 (SCL40A1) variant associated with iron overload in African-Americans.
    Beutler E, Barton JC, Felitti VJ, Gelbart T, West C, Lee PL, Waalen J, Vulpe C.
    Blood Cells Mol Dis; 2003 Apr; 31(3):305-9. PubMed ID: 14636643
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  • 20. Gene symbol: SLC40A1. Disease: Primary iron overload.
    Zaahl MG, Merryweather-Clarke AT, Kotze MJ, van der Merwe S, Warnich L, Robson KJ.
    Hum Genet; 2005 May; 116(6):541. PubMed ID: 15991323
    [No Abstract] [Full Text] [Related]

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