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Journal Abstract Search

317 related items for PubMed ID: 17493421

  • 1.
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  • 2. The complete evaluation of erythrocytosis: congenital and acquired.
    Patnaik MM, Tefferi A.
    Leukemia; 2009 May; 23(5):834-44. PubMed ID: 19295544
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  • 3. Molecular study of congenital erythrocytosis in 70 unrelated patients revealed a potential causal mutation in less than half of the cases (Where is/are the missing gene(s)?).
    Bento C, Almeida H, Maia TM, Relvas L, Oliveira AC, Rossi C, Girodon F, Fernandez-Lago C, Aguado-Diaz A, Fraga C, Costa RM, Araújo AL, Silva J, Vitória H, Miguel N, Silveira MP, Martin-Nuñez G, Ribeiro ML.
    Eur J Haematol; 2013 Oct; 91(4):361-8. PubMed ID: 23859443
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  • 5. The role of serum erythropoietin level and JAK2 V617F allele burden in the diagnosis of polycythaemia vera.
    Ancochea A, Alvarez-Larrán A, Morales-Indiano C, García-Pallarols F, Martínez-Avilés L, Angona A, Senín A, Bellosillo B, Besses C.
    Br J Haematol; 2014 Nov; 167(3):411-7. PubMed ID: 25040297
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  • 6. Current diagnostic criteria for the chronic myeloproliferative disorders (MPD) essential thrombocythemia (ET), polycythemia vera (PV) and chronic idiopathic myelofibrosis (CIMF).
    Michiels JJ, Bernema Z, Van Bockstaele D, De Raeve H, Schroyens W.
    Pathol Biol (Paris); 2007 Mar; 55(2):92-104. PubMed ID: 16919893
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  • 9. Usefulness of JAK2V617F mutation in distinguishing idiopathic erythrocytosis from polycythemia vera.
    Rossi D, Cortini F, Deambrogi C, Barbieri C, Cerri M, Franceschetti S, Conconi A, Capello D, Gaidano G.
    Leuk Res; 2007 Jan; 31(1):97-101. PubMed ID: 16620973
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  • 14. Bone marrow morphologic features in polycythemia vera with JAK2 exon 12 mutations.
    Lakey MA, Pardanani A, Hoyer JD, Nguyen PL, Lasho TL, Tefferi A, Hanson CA.
    Am J Clin Pathol; 2010 Jun; 133(6):942-8. PubMed ID: 20472853
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  • 15. [High hemoglobin, not always polycythaemia vera. Weak evidence for the effect of venesection in other erythrocytoses].
    Hultcrantz M, Admasie J, Beshara S, Landin B, Palmblad J.
    Lakartidningen; 2010 Jun; 109(51-52):2354-7. PubMed ID: 23367550
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  • 18. The frequency of JAK2 exon 12 mutations in idiopathic erythrocytosis patients with low serum erythropoietin levels.
    Percy MJ, Scott LM, Erber WN, Harrison CN, Reilly JT, Jones FG, Green AR, McMullin MF.
    Haematologica; 2007 Dec; 92(12):1607-14. PubMed ID: 18055983
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  • 19. Elevated serum erythropoietin levels in patients with Budd-Chiari syndrome secondary to polycythemia vera: clinical implications for the role of JAK2 mutation analysis.
    Thurmes PJ, Steensma DP.
    Eur J Haematol; 2006 Jul; 77(1):57-60. PubMed ID: 16827884
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  • 20. [Polycythemia vera].
    Gemünden C, Gerber B.
    Praxis (Bern 1994); 2012 May 09; 101(10):631-9, 641; quiz 640. PubMed ID: 22565553
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