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Journal Abstract Search

221 related items for PubMed ID: 10483144

  • 1.
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  • 2. [An infant case of sideroblastic anemia that responded to oral pyridoxine].
    Kudo K, Ito M, Horibe K, Iwase K, Kojima S.
    Rinsho Ketsueki; 1999 Aug; 40(8):667-72. PubMed ID: 10496043
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  • 4. [Vitamin B6-sensitive hereditary sideroblastic anemia].
    Heller T, Höchstetter V, Basler M, Borck V.
    Dtsch Med Wochenschr; 2004 Jan 23; 129(4):141-4. PubMed ID: 14724775
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  • 7. [Familial pyridoxine-responsive sideroblastic anaemia. One case (author's transl)].
    Garbarz M, Bernard JF, Boivin P.
    Nouv Presse Med; 1980 Nov 22; 9(44):3345-7. PubMed ID: 7443486
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  • 8. Multiple mechanisms for hereditary sideroblastic anemia.
    Furuyama K, Sassa S.
    Cell Mol Biol (Noisy-le-grand); 2002 Feb 22; 48(1):5-10. PubMed ID: 11929048
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  • 9. Erythroid 5-aminolevulinate synthase and X-linked sideroblastic anemia.
    Ferreira GC.
    J Fla Med Assoc; 1993 Jul 22; 80(7):481-3. PubMed ID: 8089650
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  • 11. [Successful treatment of X-linked sideroblastic anemia with ALAS2 R452H mutation using vitamin B6].
    Kawakami T, Nakazawa H, Kawakami F, Matsuzawa S, Sudo Y, Sakai H, Nishina S, Senoo N, Senoo Y, Komatsu M, Umemura T, Yamaguchi T, Kosho T, Fujiwara T, Harigae H, Ishida F.
    Rinsho Ketsueki; 2018 Jul 22; 59(4):401-406. PubMed ID: 29743399
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  • 12. [Sideroblastic anemia preceded by essential thrombocythemia with 20q- chromosome abnormality].
    Yamada K, Nakamaki T, Yokoyama A, Hino K, Tomoyasu S, Sakurai M, Tsuruoka N.
    Rinsho Ketsueki; 1993 Sep 22; 34(9):1027-32. PubMed ID: 8230746
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  • 14. [Congenital sideroblastic anemia-a new family with identification of K156E mutation of ALAS2 gene and literature review].
    Cui R, Xu Z, Qin T, Zhang Y, Xiao Z.
    Zhonghua Xue Ye Xue Za Zhi; 2014 Feb 22; 35(2):142-6. PubMed ID: 24606657
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  • 16. Hereditary sideroblastic anemia and glucose-6-phosphate dehydrogenase deficiency in a Negro family.
    Prasad AS, Tranchida L, Konno ET, Berman L, Albert S, Sing CF, Brewer GJ.
    J Clin Invest; 1968 Jun 22; 47(6):1415-24. PubMed ID: 4871209
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  • 17. Congenital sideroblastic anemia without clinical iron overload. A case report.
    Pignon JM, Breton-Gorius J, Bachir D, Rochant H.
    Nouv Rev Fr Hematol (1978); 1990 Jun 22; 32(4):281-4. PubMed ID: 2290714
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  • 19. [A family of hereditary refractory sideroblastic anemia with markedly reduced delta-aminolevulinic acid synthetase activity in bone marrow erythroblasts].
    Hirabayashi N, Utsumi M, Nakashima I, Yasuma A, Aoki N.
    Rinsho Ketsueki; 1976 Jan 22; 17(1):45-50. PubMed ID: 987283
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  • 20. Disparate phenotypic expression of ALAS2 R452H (nt 1407 G --> A) in two brothers, one with severe sideroblastic anemia and iron overload, hepatic cirrhosis, and hepatocellular carcinoma.
    Barton JC, Lee PL.
    Blood Cells Mol Dis; 2006 Jan 22; 36(3):342-6. PubMed ID: 16540354
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