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Journal Abstract Search

295 related items for PubMed ID: 36309641

  • 1. Neonatal hemochromatosis with εγδβ-thalassemia: a case report and analysis of serum iron regulators.
    Tsuge M, Kodera A, Sumitomo H, Araki T, Yoshida R, Yasui K, Sato H, Washio Y, Washio K, Shigehara K, Yashiro M, Yagi T, Tsukahara H.
    BMC Pediatr; 2022 Oct 29; 22(1):622. PubMed ID: 36309641
    [Abstract] [Full Text] [Related]

  • 2. Liver iron concentrations and urinary hepcidin in beta-thalassemia.
    Origa R, Galanello R, Ganz T, Giagu N, Maccioni L, Faa G, Nemeth E.
    Haematologica; 2007 May 29; 92(5):583-8. PubMed ID: 17488680
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  • 3. An RNAi therapeutic targeting Tmprss6 decreases iron overload in Hfe(-/-) mice and ameliorates anemia and iron overload in murine β-thalassemia intermedia.
    Schmidt PJ, Toudjarska I, Sendamarai AK, Racie T, Milstein S, Bettencourt BR, Hettinger J, Bumcrot D, Fleming MD.
    Blood; 2013 Feb 14; 121(7):1200-8. PubMed ID: 23223430
    [Abstract] [Full Text] [Related]

  • 4. New thiazolidinones reduce iron overload in mouse models of hereditary hemochromatosis and β-thalassemia.
    Liu J, Liu W, Liu Y, Miao Y, Guo Y, Song H, Wang F, Zhou H, Ganz T, Yan B, Liu S.
    Haematologica; 2019 Sep 14; 104(9):1768-1781. PubMed ID: 30792208
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  • 6. Iron and hepcidin: a story of recycling and balance.
    Camaschella C.
    Hematology Am Soc Hematol Educ Program; 2013 Sep 14; 2013():1-8. PubMed ID: 24319154
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  • 8. Transfusion suppresses erythropoiesis and increases hepcidin in adult patients with β-thalassemia major: a longitudinal study.
    Pasricha SR, Frazer DM, Bowden DK, Anderson GJ.
    Blood; 2013 Jul 04; 122(1):124-33. PubMed ID: 23656728
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  • 9. Iron overload across the spectrum of non-transfusion-dependent thalassaemias: role of erythropoiesis, splenectomy and transfusions.
    Porter JB, Cappellini MD, Kattamis A, Viprakasit V, Musallam KM, Zhu Z, Taher AT.
    Br J Haematol; 2017 Jan 04; 176(2):288-299. PubMed ID: 27917462
    [Abstract] [Full Text] [Related]

  • 10. Oral ferroportin inhibitor vamifeport for improving iron homeostasis and erythropoiesis in β-thalassemia: current evidence and future clinical development.
    Porter J, Taher A, Viprakasit V, Kattamis A, Coates TD, Garbowski M, Dürrenberger F, Manolova V, Richard F, Cappellini MD.
    Expert Rev Hematol; 2021 Jul 04; 14(7):633-644. PubMed ID: 34324404
    [Abstract] [Full Text] [Related]

  • 11. Alpha- and Beta-thalassemia: Rapid Evidence Review.
    Baird DC, Batten SH, Sparks SK.
    Am Fam Physician; 2022 Mar 01; 105(3):272-280. PubMed ID: 35289581
    [Abstract] [Full Text] [Related]

  • 12. The association between growth differentiation factor-15, erythroferrone, and iron status in thalassemic patients.
    Youssry I, Samy RM, AbdelMohsen M, Salama NM.
    Pediatr Res; 2024 Mar 01; 95(4):1095-1100. PubMed ID: 37464096
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  • 14. Iron Status in Newly Diagnosed β-Thalassemia Major: High Rate of Iron Status due to Erythropoiesis Drive.
    Susanah S, Rakhmilla LE, Ghozali M, Trisaputra JO, Moestopo O, Sribudiani Y, Idjradinata PS, Maskoen AM.
    Biomed Res Int; 2021 Mar 01; 2021():5560319. PubMed ID: 33954177
    [Abstract] [Full Text] [Related]

  • 15. 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 01; 45(11):1163-71. PubMed ID: 20533066
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  • 16. Minihepcidins improve ineffective erythropoiesis and splenomegaly in a new mouse model of adult β-thalassemia major.
    Casu C, Chessa R, Liu A, Gupta R, Drakesmith H, Fleming R, Ginzburg YZ, MacDonald B, Rivella S.
    Haematologica; 2020 Jul 01; 105(7):1835-1844. PubMed ID: 31582543
    [Abstract] [Full Text] [Related]

  • 17. Iron status in patients with pyruvate kinase deficiency: neonatal hyperferritinaemia associated with a novel frameshift deletion in the PKLR gene (p.Arg518fs), and low hepcidin to ferritin ratios.
    Mojzikova R, Koralkova P, Holub D, Zidova Z, Pospisilova D, Cermak J, Striezencova Laluhova Z, Indrak K, Sukova M, Partschova M, Kucerova J, Horvathova M, Divoky V.
    Br J Haematol; 2014 May 01; 165(4):556-63. PubMed ID: 24533562
    [Abstract] [Full Text] [Related]

  • 18. New therapeutic targets in transfusion-dependent and -independent thalassemia.
    Cappellini MD, Motta I.
    Hematology Am Soc Hematol Educ Program; 2017 Dec 08; 2017(1):278-283. PubMed ID: 29222267
    [Abstract] [Full Text] [Related]

  • 19. Serum Hepcidin as a Diagnostic Marker of Severe Iron Overload in Beta-thalassemia Major.
    Kaddah AM, Abdel-Salam A, Farhan MS, Ragab R.
    Indian J Pediatr; 2017 Oct 08; 84(10):745-750. PubMed ID: 28600663
    [Abstract] [Full Text] [Related]

  • 20. Clinical relevance of anemia and transfusion iron overload in myelodysplastic syndromes.
    Cazzola M, Della Porta MG, Malcovati L.
    Hematology Am Soc Hematol Educ Program; 2008 Oct 08; ():166-75. PubMed ID: 19074076
    [Abstract] [Full Text] [Related]

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