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Journal Abstract Search

203 related items for PubMed ID: 15865879

  • 1. Recent advances in the molecular biology of congenital polycythemias and polycythemia vera.
    Gregg XT, Prchal JT.
    Curr Hematol Rep; 2005 May; 4(3):238-42. PubMed ID: 15865879
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  • 3. Evaluation of "increased" hemoglobin in the JAK2 mutations era: a diagnostic algorithm based on genetic tests.
    Tefferi A, Pardanani A.
    Mayo Clin Proc; 2007 May; 82(5):599-604. PubMed ID: 17493421
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  • 4. Polycythemia and oxygen sensing.
    Maran J, Prchal J.
    Pathol Biol (Paris); 2004 Jun; 52(5):280-4. PubMed ID: 15217714
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  • 5. Genetically heterogeneous origins of idiopathic erythrocytosis.
    Percy MJ.
    Hematology; 2007 Apr; 12(2):131-9. PubMed ID: 17454194
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  • 6. Disruption of oxygen homeostasis underlies congenital Chuvash polycythemia.
    Ang SO, Chen H, Hirota K, Gordeuk VR, Jelinek J, Guan Y, Liu E, Sergueeva AI, Miasnikova GY, Mole D, Maxwell PH, Stockton DW, Semenza GL, Prchal JT.
    Nat Genet; 2002 Dec; 32(4):614-21. PubMed ID: 12415268
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  • 7. Congenital polycythemias/erythrocytoses.
    Gordeuk VR, Stockton DW, Prchal JT.
    Haematologica; 2005 Jan; 90(1):109-16. PubMed ID: 15642677
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  • 11. Polycythemia vera and other primary polycythemias.
    Prchal JT.
    Curr Opin Hematol; 2005 Mar; 12(2):112-6. PubMed ID: 15725900
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  • 12. Molecular basis for polycythemia.
    Prchal JF, Prchal JT.
    Curr Opin Hematol; 1999 Mar; 6(2):100-9. PubMed ID: 10088640
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  • 13. Pathogenetic mechanisms of polycythemia vera and congenital polycythemic disorders.
    Prchal JT.
    Semin Hematol; 2001 Jan; 38(1 Suppl 2):10-20. PubMed ID: 11242597
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  • 14. Congenital disorder of oxygen sensing: association of the homozygous Chuvash polycythemia VHL mutation with thrombosis and vascular abnormalities but not tumors.
    Gordeuk VR, Sergueeva AI, Miasnikova GY, Okhotin D, Voloshin Y, Choyke PL, Butman JA, Jedlickova K, Prchal JT, Polyakova LA.
    Blood; 2004 May 15; 103(10):3924-32. PubMed ID: 14726398
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  • 15. [Not just another kinase. New knowledge about myeloproliferative disease].
    Bjerrum OW.
    Ugeskr Laeger; 2006 Sep 25; 168(39):3293. PubMed ID: 17032590
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  • 16. Mutations in the VHL gene in sporadic apparently congenital polycythemia.
    Pastore YD, Jelinek J, Ang S, Guan Y, Liu E, Jedlickova K, Krishnamurti L, Prchal JT.
    Blood; 2003 Feb 15; 101(4):1591-5. PubMed ID: 12393546
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  • 18. Markers of myeloproliferative diseases in childhood polycythemia vera and essential thrombocythemia.
    Teofili L, Giona F, Martini M, Cenci T, Guidi F, Torti L, Palumbo G, Amendola A, Foà R, Larocca LM.
    J Clin Oncol; 2007 Mar 20; 25(9):1048-53. PubMed ID: 17369568
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  • 19. JAKing up hematopoietic proliferation.
    Shannon K, Van Etten RA.
    Cancer Cell; 2005 Apr 20; 7(4):291-3. PubMed ID: 15837617
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  • 20. Polycythemia vera: scientific advances and current practice.
    Tefferi A, Spivak JL.
    Semin Hematol; 2005 Oct 20; 42(4):206-20. PubMed ID: 16210034
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