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Volumn 98, Issue 3, 2007, Pages 702-704

Haemostatic proteins gene polymorphisms in patients with unusual vein thrombosis and Ph-myeloproliferative disorders [10]

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD CLOTTING FACTOR 11; BLOOD CLOTTING FACTOR 5 LEIDEN; FIBRINOGEN; FIBRINOGEN RECEPTOR; JANUS KINASE 2;

EID: 34548700610     PISSN: 03406245     EISSN: None     Source Type: Journal    
DOI: 10.1160/TH07-02-0142     Document Type: Letter
Times cited : (5)

References (15)
  • 1
    • 20144363192 scopus 로고    scopus 로고
    • Acquired mutation of the tyrosine kinase JAK2 in human myelo-proliferative disorders
    • Baxter EJ, Scoff LM, Campbell PJ, et al. Acquired mutation of the tyrosine kinase JAK2 in human myelo-proliferative disorders. Lancet 2005; 365: 1054-1061.
    • (2005) Lancet , vol.365 , pp. 1054-1061
    • Baxter, E.J.1    Scoff, L.M.2    Campbell, P.J.3
  • 2
    • 17644424955 scopus 로고    scopus 로고
    • A gain-of-function mutation of JAK2 in myeloproliferative disorders
    • Kralovics R, Passamonti F, Buster AS, et al. A gain-of-function mutation of JAK2 in myeloproliferative disorders. N Engl J Med 2005; 352: 1779-1790.
    • (2005) N Engl J Med , vol.352 , pp. 1779-1790
    • Kralovics, R.1    Passamonti, F.2    Buster, A.S.3
  • 3
    • 27744606173 scopus 로고    scopus 로고
    • JAK2 mutation in essential thrombocythemia: Clinical association and long-term pronostic relevance
    • Wolanskyj AP, Lasho TL, Schwager SM, et al. JAK2 mutation in essential thrombocythemia: clinical association and long-term pronostic relevance. Br J Haematol 2005; 131: 208-213.
    • (2005) Br J Haematol , vol.131 , pp. 208-213
    • Wolanskyj, A.P.1    Lasho, T.L.2    Schwager, S.M.3
  • 4
    • 34548672958 scopus 로고    scopus 로고
    • SDF1-3′ A gene polymorphism: Risk factor for thrombotic events in Philadelphia - negative chronic myeloproliferative disorders
    • Vanelli C, Biondi ML, Turri O, et al. SDF1-3′ A gene polymorphism: risk factor for thrombotic events in Philadelphia - negative chronic myeloproliferative disorders. Haematologica 2005; 90 (Suppl 3): 66.
    • (2005) Haematologica , vol.90 , Issue.SUPPL. 3 , pp. 66
    • Vanelli, C.1    Biondi, M.L.2    Turri, O.3
  • 5
    • 34548671075 scopus 로고    scopus 로고
    • Endothelial nitric oxide syntetase gene polymorphisms (G894T and T786C) in essential thromboythemia
    • Gardellini A, Biondi ML, Turri O, et al. Endothelial nitric oxide syntetase gene polymorphisms (G894T and T786C) in essential thromboythemia. Haematologica 2005; 90 (Suppl 3): 66.
    • (2005) Haematologica , vol.90 , Issue.SUPPL. 3 , pp. 66
    • Gardellini, A.1    Biondi, M.L.2    Turri, O.3
  • 6
    • 2042477375 scopus 로고    scopus 로고
    • Hemostatic gene polymorphisms and the prevalence of thrombotic complications in polycythemia vera and essential thrombocythemia
    • Afshar-Karghan V, Lopez JA, Gray LA, et al. Hemostatic gene polymorphisms and the prevalence of thrombotic complications in polycythemia vera and essential thrombocythemia. Blood Coagul Fibrinolysis 2004; 15: L21-24.
    • (2004) Blood Coagul Fibrinolysis , vol.15
    • Afshar-Karghan, V.1    Lopez, J.A.2    Gray, L.A.3
  • 7
    • 0033999779 scopus 로고    scopus 로고
    • Cause of portal or hepatic venous thrombosis in adults: The role of multiple concurrent factors
    • Dernninger MH, Chait Y, Casadevall N, et al. Cause of portal or hepatic venous thrombosis in adults: the role of multiple concurrent factors. Hepatology 2000; 31: 587-591.
    • (2000) Hepatology , vol.31 , pp. 587-591
    • Dernninger, M.H.1    Chait, Y.2    Casadevall, N.3
  • 8
    • 0036818776 scopus 로고    scopus 로고
    • Thrombocythosis and recurrent hepatic outflow obstruction (Budd-Chiari syndrome) after successful thrombolysis: Case report and literature review
    • Randi NL, Sartori MT, Luzzatto G, et al. Thrombocythosis and recurrent hepatic outflow obstruction (Budd-Chiari syndrome) after successful thrombolysis: case report and literature review. Clin Appl Thromb/Hemost 2002; 8: 369-374.
    • (2002) Clin Appl Thromb/Hemost , vol.8 , pp. 369-374
    • Randi, N.L.1    Sartori, M.T.2    Luzzatto, G.3
  • 9
    • 33746772110 scopus 로고    scopus 로고
    • The relationship between beta fibrinogen gene-455G/A polymorphisms and Budd-Chiari syndrome
    • Wang SY, Wei YF, Li JD. The relationship between beta fibrinogen gene-455G/A polymorphisms and Budd-Chiari syndrome. Zhonghua Nei Ke Za Zhi 2004;43:753-755.
    • (2004) Zhonghua Nei Ke Za Zhi , vol.43 , pp. 753-755
    • Wang, S.Y.1    Wei, Y.F.2    Li, J.D.3
  • 10
    • 2442465593 scopus 로고    scopus 로고
    • Association after linkage analysis indicates that homozygosity for 46 C/T polymorphism in F12 gene is a genetic risk factor for venous thrombosis
    • Tirado I, Soria MJ, Mateo J, et al. Association after linkage analysis indicates that homozygosity for 46 C/T polymorphism in F12 gene is a genetic risk factor for venous thrombosis. Thromb Haemost 2004; 91: 899-904.
    • (2004) Thromb Haemost , vol.91 , pp. 899-904
    • Tirado, I.1    Soria, M.J.2    Mateo, J.3
  • 11
    • 0032901326 scopus 로고    scopus 로고
    • Diagnostic criteria and prognosis in polycythemia vera and essential thrombocythemia
    • Murphy S. Diagnostic criteria and prognosis in polycythemia vera and essential thrombocythemia. Semin Hematol 1999; 36: 9-13.
    • (1999) Semin Hematol , vol.36 , pp. 9-13
    • Murphy, S.1
  • 12
    • 33751161677 scopus 로고    scopus 로고
    • Clonality status and Jak 2 V617F mutation in children with essential thrombocythemia
    • Randi ML, Putti MC, Scapin M, et al. Clonality status and Jak 2 V617F mutation in children with essential thrombocythemia. Blood 2006; 108: 3600-3602.
    • (2006) Blood , vol.108 , pp. 3600-3602
    • Randi, M.L.1    Putti, M.C.2    Scapin, M.3
  • 13
    • 28244442441 scopus 로고    scopus 로고
    • Definition of subtypes of essential thrombocythemia and relation to polycythemia vera based on Jak2 V617F mutation status: A prospective study
    • Campbell PJ, Scott LM, Buck G, et al. Definition of subtypes of essential thrombocythemia and relation to polycythemia vera based on Jak2 V617F mutation status: a prospective study. Lancet 2005; 366: 1945-1953.
    • (2005) Lancet , vol.366 , pp. 1945-1953
    • Campbell, P.J.1    Scott, L.M.2    Buck, G.3
  • 14
    • 25844461158 scopus 로고    scopus 로고
    • The Jak2V617F mutation, PRV-1 over-expression and EEC formation define a similar cohort of MPD patients
    • Goerttler PS, Steimle C, Marz E, et al. The Jak2V617F mutation, PRV-1 over-expression and EEC formation define a similar cohort of MPD patients. Blood 2005; 106: 2862-2864.
    • (2005) Blood , vol.106 , pp. 2862-2864
    • Goerttler, P.S.1    Steimle, C.2    Marz, E.3
  • 15
    • 0033555392 scopus 로고    scopus 로고
    • A large proportion of patients with a diagnosis of essential thrombocythemia do not have a clonal disorder and may be at lower risk of thrombotic complications
    • Harrison CN, Gale RE, Machin SJ, et al. A large proportion of patients with a diagnosis of essential thrombocythemia do not have a clonal disorder and may be at lower risk of thrombotic complications. Blood 1999; 993: 417-424.
    • (1999) Blood , vol.993 , pp. 417-424
    • Harrison, C.N.1    Gale, R.E.2    Machin, S.J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.