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Anemia

Free Subscription 26.12.2011 1 Am J Hematol 1 Am J Kidney Dis 5 Blood 2 Haematologica 11 Hemoglobin 4 J Pediatr Hematol Oncol 2 Nephrol Dial Transplant

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Single Articles

Am J Hematol

1. KAMEL S , Lu Z, Sikaris K
   Comment on: Neutropenia and anemia with reduced serum vitamin B(12).
   Am J Hematol. 2011 Oct 20. doi: 10.1002/ajh.22226.
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   Am J Kidney Dis

2. MACDOUGALL IC
   New Anemia Therapies: Translating Novel Strategies From Bench to Bedside.
   Am J Kidney Dis. 2011.
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   Blood

3. DA SILVA MC , Zuccherato LW, Lucena FC, Soares-Souza GB, et al
   Extensive admixture in Brazilian sickle cell patients: implications for the mapping of genetic modifiers.
   Blood. 2011;118:4493-5.
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4. KUENTZ M , Robin M, Dhedin N, Hicheri Y, et al
   Is there still a place for myeloablative regimen to transplant young adults with sickle cell disease?
   Blood. 2011;118:4491-2.
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5. GALLAGHER PG
   HbA(2): at the borderline of the KLF.
   Blood. 2011;118:4301-2.
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6. PERSEU L , Satta S, Moi P, Demartis FR, et al
   KLF1 gene mutations cause borderline HbA(2).
   Blood. 2011;118:4454-8.
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7. GINZBURG Y , Rivella S
   beta-thalassemia: a model for elucidating the dynamic regulation of ineffective erythropoiesis and iron metabolism.
   Blood. 2011;118:4321-30.
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   Haematologica

8. WALNE A , Dokal A, Plagnol V, Beswick R, et al
   Exome sequencing identifies MPL as a causative gene in familial aplastic anemia.
   Haematologica. 2011.
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9. KONOPACKI J , Procher R, Robin M, Bieri S, et al
   Long-term follow-up after allogeneic stem cell transplantation in patients with severe aplastic anemia after cyclophosphamide plus antithymocyte globulin conditioning.
   Haematologica. 2011.
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   Hemoglobin

10. POGGI M , Sorrentino F, Pascucci C, Monti S, et al
    Malignancies in beta-thalassemia patients: first description of two cases of thyroid cancer and review of the literature.
    Hemoglobin. 2011;35:439-46.
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11. LIAO C , Pan M, Han J, Yang X, et al
    Early prenatal diagnosis of thalassemia: the first report of experience in mainland China.
    Hemoglobin. 2011;35:434-8.
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12. GUEST EM , Neville KA, Hoyer JD, Safo MK, et al
    Hb Lake Tapawingo [alpha46(CE4)Phe-->Ser; HBA2:c.140T>C]: a new unstable alpha chain hemoglobin variant associated with low systemic arterial saturation.
    Hemoglobin. 2011;35:411-6.
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13. DANIEL Y , Hill K, Inusa B, Thein SL, et al
    Sickle cell/beta0-thalassemia associated with the 1393 bp deletion can be associated with a severe phenotype.
    Hemoglobin. 2011;35:406-10.
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14. MOKHTAR GM , Tantawy AA, Adly AA, Ismail EA, et al
    Clinicopathological and radiological study of Egyptian beta-thalassemia intermedia and beta-thalassemia major patients: relation to complications and response to therapy.
    Hemoglobin. 2011;35:382-405.
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15. FERNANDES AC , Shimmoto MM, Furuzawa GK, Vicari P, et al
    Molecular analysis of beta-thalassemia patients: first identification of mutations HBB:c.93-2A>G and HBB:c.114G>A in Brazil.
    Hemoglobin. 2011;35:358-66.
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16. ABUZENADAH AM , Hussein IM, Damanhouri GA, A-Sayes FM, et al
    Molecular basis of beta-thalassemia in the western province of Saudi Arabia: identification of rare beta-thalassemia mutations.
    Hemoglobin. 2011;35:346-57.
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17. WANEESORN J , Panyasai S, Kongthai K, Singboottra P, et al
    Comparison between capillary electrophoresis and high performance liquid chromatography for detection and quantification of Hb constant spring [Hb CS; alpha142, Term-->Gln (TAA>CAA IN alpha2)].
    Hemoglobin. 2011;35:338-45.
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18. RAHIMINEJAD MS , Zeinali S, Afrasiabi A, Valeshabad AK, et al
    beta-Thalassemia mutations found during 1 year of prenatal diagnoses in Fars Province, Iran.
    Hemoglobin. 2011;35:331-7.
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19. MOOSAVI SF , Amirian A, Zarbakhsh B, Kordafshari A, et al
    The carrier frequency of alpha-globin gene triplication in an Iranian population with normal or borderline hematological parameters.
    Hemoglobin. 2011;35:323-30.
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20. JOLY P , Lacan P, Garcia C, Meley R, et al
    A novel deletion/insertion caused by a replication error in the beta-globin gene locus control region.
    Hemoglobin. 2011;35:316-22.
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    J Pediatr Hematol Oncol

21. DWINNELL SJ , Coad S, Butler B, Albersheim S, et al
    In Utero diagnosis and management of a fetus with homozygous alpha-Thalassemia in the second trimester: a case report and literature review.
    J Pediatr Hematol Oncol. 2011;33:e358-60.
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22. BUCHBINDER DK , Zadeh T, Nugent D
    A patient with familial bone marrow failure and an inversion of chromosome 8.
    J Pediatr Hematol Oncol. 2011;33:626-7.
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23. CHONAT S , Saah E, Gera R, Scott-Emuakpor A, et al
    Co-occurrence of Chiari malformations and sickle cell disease-a diagnostic dilemma: a report of 4 cases and review of literature.
    J Pediatr Hematol Oncol. 2011;33:624-5.
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24. SABIO H , Dixon N, Patel N, Obiaga C, et al
    Thalassemia-like phenotype in a novel complex hemoglobinopathy With alpha, beta, delta globin chain abnormalities.
    J Pediatr Hematol Oncol. 2011;33:589-91.
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    Nephrol Dial Transplant

25. GRANGER VALLEE A , Canaud B
    Statins and resistance to erythropoiesis-stimulating agents: are the two associated?
    Nephrol Dial Transplant. 2011;26:2715-6.
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26. PANICHI V , Rosati A, Bigazzi R, Paoletti S, et al
    Anaemia and resistance to erythropoiesis-stimulating agents as prognostic factors in haemodialysis patients: results from the RISCAVID study.
    Nephrol Dial Transplant. 2011;26:2641-8.
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