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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

496 related items for PubMed ID: 19679982

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  • 2. Congenital sideroblastic anemia of a Saudi child.
    ALBagshi MH, Saloma SH, Albagshi HM.
    Sudan J Paediatr; 2017; 17(1):49-51. PubMed ID: 29213171
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  • 5. Recent advances in the understanding of inherited sideroblastic anaemia.
    Camaschella C.
    Br J Haematol; 2008 Oct; 143(1):27-38. PubMed ID: 18637800
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  • 8. [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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  • 10. Multiple mechanisms for hereditary sideroblastic anemia.
    Furuyama K, Sassa S.
    Cell Mol Biol (Noisy-le-grand); 2002 Feb 23; 48(1):5-10. PubMed ID: 11929048
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  • 11. [Two cases of primary acquired sideroblastic anemia: with special references to the findings in bone marrow culture].
    Koyanagawa Y, Sawada K, Sakurama S, Fukuoka N, Tohma Y, Ieko M, Fujie T, Yamamoto H, Satoh M, Yasukouchi T.
    Rinsho Ketsueki; 1985 Jan 23; 26(1):79-85. PubMed ID: 3999401
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  • 13. [A 2-year-old male patient with congenital sideroblastic anemia and long-term chelation therapy].
    Muntean W, Hauer C, Schmid C.
    Wien Klin Wochenschr; 1989 Apr 28; 101(9):330-4. PubMed ID: 2499990
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  • 15. Late-onset X-linked sideroblastic anemia. Missense mutations in the erythroid delta-aminolevulinate synthase (ALAS2) gene in two pyridoxine-responsive patients initially diagnosed with acquired refractory anemia and ringed sideroblasts.
    Cotter PD, May A, Fitzsimons EJ, Houston T, Woodcock BE, al-Sabah AI, Wong L, Bishop DF.
    J Clin Invest; 1995 Oct 28; 96(4):2090-6. PubMed ID: 7560104
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  • 17. [Neonatal Pearson syndrome. two case studies].
    Collin-Ducasse H, Maillotte AM, Monpoux F, Boutté P, Ferrero-Vacher C, Paquis V.
    Arch Pediatr; 2010 Jan 28; 17(1):38-41. PubMed ID: 19914050
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