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Journal Abstract Search

245 related items for PubMed ID: 22924847

  • 1. Clinicopathological study of Japanese patients with genetic iron overload syndromes.
    Hattori A, Miyajima H, Tomosugi N, Tatsumi Y, Hayashi H, Wakusawa S.
    Pathol Int; 2012 Sep; 62(9):612-8. PubMed ID: 22924847
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  • 2. Measurement of serum hepcidin-25 levels as a potential test for diagnosing hemochromatosis and related disorders.
    Kaneko Y, Miyajima H, Piperno A, Tomosugi N, Hayashi H, Morotomi N, Tsuchida K, Ikeda T, Ishikawa A, Ota Y, Wakusawa S, Yoshioka K, Kono S, Pelucchi S, Hattori A, Tatsumi Y, Okada T, Yamagishi M.
    J Gastroenterol; 2010 Nov; 45(11):1163-71. PubMed ID: 20533066
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  • 3. Genetic background of primary iron overload syndromes in Japan.
    Hayashi H, Wakusawa S, Motonishi S, Miyamoto K, Okada H, Inagaki Y, Ikeda T.
    Intern Med; 2006 Nov; 45(20):1107-11. PubMed ID: 17106152
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  • 4. Iron overload in the Asian community.
    Lok CY, Merryweather-Clarke AT, Viprakasit V, Chinthammitr Y, Srichairatanakool S, Limwongse C, Oleesky D, Robins AJ, Hudson J, Wai P, Premawardhena A, de Silva HJ, Dassanayake A, McKeown C, Jackson M, Gama R, Khan N, Newman W, Banait G, Chilton A, Wilson-Morkeh I, Weatherall DJ, Robson KJ.
    Blood; 2009 Jul 02; 114(1):20-5. PubMed ID: 19342478
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  • 14. Mutations in the HFE, TFR2, and SLC40A1 genes in patients with hemochromatosis.
    Del-Castillo-Rueda A, Moreno-Carralero MI, Cuadrado-Grande N, Alvarez-Sala-Walther LA, Enríquez-de-Salamanca R, Méndez M, Morán-Jiménez MJ.
    Gene; 2012 Oct 15; 508(1):15-20. PubMed ID: 22890139
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  • 20. [Pathophysiology and genetics of classic HFE (type 1) hemochromatosis].
    Loréal O, Ropert M, Mosser A, Déhais V, Deugnier Y, David V, Brissot P, Jouanolle AM.
    Presse Med; 2007 Sep 15; 36(9 Pt 2):1271-7. PubMed ID: 17521857
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