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Volumn 18, Issue 7, 2012, Pages 819-827

Prevalence and clinical outcomes of the 46/1 haplotype, Janus kinase 2 mutations, and ten-eleven translocation 2 mutations in budd-chiari syndrome and their impact on thrombotic complications post Liver Transplantation

Author keywords

[No Author keywords available]

Indexed keywords

JANUS KINASE 2;

EID: 84863972671     PISSN: 15276465     EISSN: 15276473     Source Type: Journal    
DOI: 10.1002/lt.23443     Document Type: Article
Times cited : (30)

References (41)
  • 1
    • 0025103267 scopus 로고
    • Classification of hepatic venous outflow obstruction: Ambiguous terminology of the Budd-Chiari syndrome
    • Ludwig J, Hashimoto E, McGill DB, van Heerden JA,. Classification of hepatic venous outflow obstruction: ambiguous terminology of the Budd-Chiari syndrome. Mayo Clin Proc 1990; 65: 51-55.
    • (1990) Mayo Clin Proc , vol.65 , pp. 51-55
    • Ludwig, J.1    Hashimoto, E.2    McGill, D.B.3    Van Heerden, J.A.4
  • 3
    • 0025105575 scopus 로고
    • In vitro colony culture and chromosomal studies in hepatic and portal vein thrombosis-possible evidence of an occult myeloproliferative state
    • Pagliuca A, Mufti GJ, Janossa-Tahernia M, Eridani S, Westwood NB, Thumpston J, et al. In vitro colony culture and chromosomal studies in hepatic and portal vein thrombosis-possible evidence of an occult myeloproliferative state. Q J Med 1990; 76: 981-989.
    • (1990) Q J Med , vol.76 , pp. 981-989
    • Pagliuca, A.1    Mufti, G.J.2    Janossa-Tahernia, M.3    Eridani, S.4    Westwood, N.B.5    Thumpston, J.6
  • 4
    • 0021972984 scopus 로고
    • Primary myeloproliferative disorder and hepatic vein thrombosis. A prospective study of erythroid colony formation in vitro in 20 patients with Budd-Chiari syndrome
    • Valla D, Casadevall N, Lacombe C, Varet B, Goldwasser E, Franco D, et al. Primary myeloproliferative disorder and hepatic vein thrombosis. A prospective study of erythroid colony formation in vitro in 20 patients with Budd-Chiari syndrome. Ann Intern Med 1985; 103: 329-334.
    • (1985) Ann Intern Med , vol.103 , pp. 329-334
    • Valla, D.1    Casadevall, N.2    Lacombe, C.3    Varet, B.4    Goldwasser, E.5    Franco, D.6
  • 5
    • 0023945861 scopus 로고
    • Etiology of portal vein thrombosis in adults. A prospective evaluation of primary myeloproliferative disorders
    • Valla D, Casadevall N, Huisse MG, Tulliez M, Grange JD, Muller O, et al. Etiology of portal vein thrombosis in adults. A prospective evaluation of primary myeloproliferative disorders. Gastroenterology 1988; 94: 1063-1069.
    • (1988) Gastroenterology , vol.94 , pp. 1063-1069
    • Valla, D.1    Casadevall, N.2    Huisse, M.G.3    Tulliez, M.4    Grange, J.D.5    Muller, O.6
  • 6
    • 0030731923 scopus 로고    scopus 로고
    • Spontaneous erythroid colony formation as the clue to an underlying myeloproliferative disorder in patients with Budd-Chiari syndrome or portal vein thrombosis
    • De Stefano V, Teofili L, Leone G, Michiels JJ,. Spontaneous erythroid colony formation as the clue to an underlying myeloproliferative disorder in patients with Budd-Chiari syndrome or portal vein thrombosis. Semin Thromb Hemost 1997; 23: 411-418.
    • (1997) Semin Thromb Hemost , vol.23 , pp. 411-418
    • De Stefano, V.1    Teofili, L.2    Leone, G.3    Michiels, J.J.4
  • 7
    • 17844383458 scopus 로고    scopus 로고
    • A unique clonal JAK2 mutation leading to constitutive signalling causes polycythemia vera
    • James C, Ugo V, Le Couedic JP, et al. A unique clonal JAK2 mutation leading to constitutive signalling causes polycythemia vera. Nature 2005; 434: 1144-1148.
    • (2005) Nature , vol.434 , pp. 1144-1148
    • James, C.1    Ugo, V.2    Le Couedic, J.P.3
  • 8
    • 17844383458 scopus 로고    scopus 로고
    • A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera
    • James C, Ugo V, Le Couédic JP, Staerk J, Delhommeau F, Lacout C, et al. A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera. Nature 2005; 434: 1144-1148.
    • (2005) Nature , vol.434 , pp. 1144-1148
    • James, C.1    Ugo, V.2    Le Couédic, J.P.3    Staerk, J.4    Delhommeau, F.5    Lacout, C.6
  • 11
    • 66149155797 scopus 로고    scopus 로고
    • Vascular disorders of the liver
    • for American Association for the Study of Liver Diseases
    • DeLeve LD, Valla DC, Garcia-Tsao G,; for American Association for the Study of Liver Diseases. Vascular disorders of the liver. Hepatology 2009; 49: 1729-1764.
    • (2009) Hepatology , vol.49 , pp. 1729-1764
    • Deleve, L.D.1    Valla, D.C.2    Garcia-Tsao, G.3
  • 12
    • 21344467318 scopus 로고    scopus 로고
    • Widespread occurrence of the JAK2 V617F mutation in chronic myeloproliferative disorders
    • Jones AV, Kreil S, Zoi K, Waghorn K, Curtis C, Zhang L, et al. Widespread occurrence of the JAK2 V617F mutation in chronic myeloproliferative disorders. Blood 2005; 106: 2162-2168.
    • (2005) Blood , vol.106 , pp. 2162-2168
    • Jones, A.V.1    Kreil, S.2    Zoi, K.3    Waghorn, K.4    Curtis, C.5    Zhang, L.6
  • 13
    • 33750550297 scopus 로고    scopus 로고
    • Concurrent MPL515 and JAK2V617F mutations in myelofibrosis: Chronology of clonal emergence and changes in mutant allele burden over time
    • Lasho TL, Pardanani A, McClure RF, Mesa RA, Levine RL, Gilliland DG, Tefferi A,. Concurrent MPL515 and JAK2V617F mutations in myelofibrosis: chronology of clonal emergence and changes in mutant allele burden over time. Br J Haematol 2006; 135: 683-687.
    • (2006) Br J Haematol , vol.135 , pp. 683-687
    • Lasho, T.L.1    Pardanani, A.2    McClure, R.F.3    Mesa, R.A.4    Levine, R.L.5    Gilliland, D.G.6    Tefferi, A.7
  • 14
    • 54049123194 scopus 로고    scopus 로고
    • Genetic complexity of myeloproliferative neoplasms
    • Kralovics R,. Genetic complexity of myeloproliferative neoplasms. Leukemia 2008; 22: 1841-1848.
    • (2008) Leukemia , vol.22 , pp. 1841-1848
    • Kralovics, R.1
  • 15
    • 33745623666 scopus 로고    scopus 로고
    • Genetic and clinical implications of the Val617Phe JAK2 mutation in 72 families with myeloproliferative disorders
    • Bellanné-Chantelot C, Chaumarel I, Labopin M, Bellanger F, Barbu V, De Toma C, et al. Genetic and clinical implications of the Val617Phe JAK2 mutation in 72 families with myeloproliferative disorders. Blood 2006; 108: 346-352.
    • (2006) Blood , vol.108 , pp. 346-352
    • Bellanné-Chantelot, C.1    Chaumarel, I.2    Labopin, M.3    Bellanger, F.4    Barbu, V.5    De Toma, C.6
  • 16
    • 54049129782 scopus 로고    scopus 로고
    • Increased risks of polycythemia vera, essential thrombocythemia, and myelofibrosis among 24,577 first-degree relatives of 11,039 patients with myeloproliferative neoplasms in Sweden
    • Landgren O, Goldin LR, Kristinsson SY, Helgadottir EA, Samuelsson J, Björkholm M,. Increased risks of polycythemia vera, essential thrombocythemia, and myelofibrosis among 24,577 first-degree relatives of 11,039 patients with myeloproliferative neoplasms in Sweden. Blood 2008; 112: 2199-2204.
    • (2008) Blood , vol.112 , pp. 2199-2204
    • Landgren, O.1    Goldin, L.R.2    Kristinsson, S.Y.3    Helgadottir, E.A.4    Samuelsson, J.5    Björkholm, M.6
  • 18
    • 63449099560 scopus 로고    scopus 로고
    • JAK2 haplotype is a major risk factor for the development of myeloproliferative neoplasms
    • Jones AV, Chase A, Silver RT, Oscier D, Zoi K, Wang YL, et al. JAK2 haplotype is a major risk factor for the development of myeloproliferative neoplasms. Nat Genet 2009; 41: 446-449.
    • (2009) Nat Genet , vol.41 , pp. 446-449
    • Jones, A.V.1    Chase, A.2    Silver, R.T.3    Oscier, D.4    Zoi, K.5    Wang, Y.L.6
  • 20
    • 63449127583 scopus 로고    scopus 로고
    • A germline JAK2 SNP is associated with predisposition to the development of JAK2(V617F)-positive myeloproliferative neoplasms
    • Kilpivaara O, Mukherjee S, Schram AM, Wadleigh M, Mullally A, Ebert BL, et al. A germline JAK2 SNP is associated with predisposition to the development of JAK2(V617F)-positive myeloproliferative neoplasms. Nat Genet 2009; 41: 455-459.
    • (2009) Nat Genet , vol.41 , pp. 455-459
    • Kilpivaara, O.1    Mukherjee, S.2    Schram, A.M.3    Wadleigh, M.4    Mullally, A.5    Ebert, B.L.6
  • 21
    • 67650924270 scopus 로고    scopus 로고
    • Detection of mutant TET2 in myeloid malignancies other than myeloproliferative neoplasms: CMML, MDS, MDS/MPN and AML
    • Tefferi A, Lim KH, Abdel-Wahab O, Lasho TL, Patel J, Patnaik MM, et al. Detection of mutant TET2 in myeloid malignancies other than myeloproliferative neoplasms: CMML, MDS, MDS/MPN and AML. Leukemia 2009; 23: 1343-1345.
    • (2009) Leukemia , vol.23 , pp. 1343-1345
    • Tefferi, A.1    Lim, K.H.2    Abdel-Wahab, O.3    Lasho, T.L.4    Patel, J.5    Patnaik, M.M.6
  • 22
    • 67349124376 scopus 로고    scopus 로고
    • TET2 mutations and their clinical correlates in polycythemia vera, essential thrombocythemia and myelofibrosis
    • Tefferi A, Pardanani A, Lim KH, Abdel-Wahab O, Lasho TL, Patel J, et al. TET2 mutations and their clinical correlates in polycythemia vera, essential thrombocythemia and myelofibrosis. Leukemia 2009; 23: 905-911.
    • (2009) Leukemia , vol.23 , pp. 905-911
    • Tefferi, A.1    Pardanani, A.2    Lim, K.H.3    Abdel-Wahab, O.4    Lasho, T.L.5    Patel, J.6
  • 25
    • 33751002644 scopus 로고    scopus 로고
    • Aiming at minimal invasiveness as a therapeutic strategy for Budd-Chiari syndrome
    • Plessier A, Sibert A, Consigny Y, Hakime A, Zappa M, Denninger MH, et al. Aiming at minimal invasiveness as a therapeutic strategy for Budd-Chiari syndrome. Hepatology 2006; 44: 1308-1316.
    • (2006) Hepatology , vol.44 , pp. 1308-1316
    • Plessier, A.1    Sibert, A.2    Consigny, Y.3    Hakime, A.4    Zappa, M.5    Denninger, M.H.6
  • 26
    • 0016480047 scopus 로고
    • The Budd-Chiari syndrome: Correlation between hepatic scintigraphy and the clinical, radiological, and pathological findings in nineteen cases of hepatic venous outflow obstruction
    • Tavill AS, Wood EJ, Kreel L, Jones EA, Gregory M, Sherlock S,. The Budd-Chiari syndrome: correlation between hepatic scintigraphy and the clinical, radiological, and pathological findings in nineteen cases of hepatic venous outflow obstruction. Gastroenterology 1975; 68: 509-518.
    • (1975) Gastroenterology , vol.68 , pp. 509-518
    • Tavill, A.S.1    Wood, E.J.2    Kreel, L.3    Jones, E.A.4    Gregory, M.5    Sherlock, S.6
  • 28
    • 0028999114 scopus 로고
    • Which is the best surgery for Budd-Chiari syndrome: Venous decompression or liver transplantation? A single-center experience with 50 patients
    • Ringe B, Lang H, Oldhafer KJ, Gebel M, Flemming P, Georgii A, et al. Which is the best surgery for Budd-Chiari syndrome: venous decompression or liver transplantation? A single-center experience with 50 patients. Hepatology 1995; 21: 1337-1344.
    • (1995) Hepatology , vol.21 , pp. 1337-1344
    • Ringe, B.1    Lang, H.2    Oldhafer, K.J.3    Gebel, M.4    Flemming, P.5    Georgii, A.6
  • 29
    • 33646782921 scopus 로고    scopus 로고
    • Favourable medium term outcome following hepatic vein recanalisation and/or transjugular intrahepatic portosystemic shunt for Budd Chiari syndrome
    • Eapen CE, Velissaris D, Heydtmann M, Gunson B, Olliff S, Elias E,. Favourable medium term outcome following hepatic vein recanalisation and/or transjugular intrahepatic portosystemic shunt for Budd Chiari syndrome. Gut 2006; 55: 878-884.
    • (2006) Gut , vol.55 , pp. 878-884
    • Eapen, C.E.1    Velissaris, D.2    Heydtmann, M.3    Gunson, B.4    Olliff, S.5    Elias, E.6
  • 30
    • 84859383697 scopus 로고    scopus 로고
    • Results of liver transplantation in the treatment of Budd-Chiari syndrome
    • Mackiewicz A, Kotulski M, Zieniewicz K, Krawczyk M., Results of liver transplantation in the treatment of Budd-Chiari syndrome. Ann Transplant 2012; 17: 5-10.
    • (2012) Ann Transplant , vol.17 , pp. 5-10
    • MacKiewicz, A.1    Kotulski, M.2    Zieniewicz, K.3    Krawczyk, M.4
  • 32
    • 32444442580 scopus 로고    scopus 로고
    • Liver transplantation for Budd-Chiari syndrome: A European study on 248 patients from 51 centres
    • Mentha G, Giostra E, Majno PE, Bechstein WO, Neuhaus P, O'Grady J, et al. Liver transplantation for Budd-Chiari syndrome: a European study on 248 patients from 51 centres. J Hepatol 2006; 44: 520-528.
    • (2006) J Hepatol , vol.44 , pp. 520-528
    • Mentha, G.1    Giostra, E.2    Majno, P.E.3    Bechstein, W.O.4    Neuhaus, P.5    O'Grady, J.6
  • 33
    • 66749118350 scopus 로고    scopus 로고
    • Identification of MPL W515L/K mutations in patients with primary myelofibrosis and essential thrombocythaemia by allele-specific polymerase chain reaction
    • Daly S, Conneally E, Langabeer SE,. Identification of MPL W515L/K mutations in patients with primary myelofibrosis and essential thrombocythaemia by allele-specific polymerase chain reaction. Acta Haematol 2009; 121: 221-222.
    • (2009) Acta Haematol , vol.121 , pp. 221-222
    • Daly, S.1    Conneally, E.2    Langabeer, S.E.3
  • 34
    • 36148993604 scopus 로고    scopus 로고
    • Prevalence and prognostic significance of allelic imbalance by single-nucleotide polymorphism analysis in low-risk myelodysplastic syndromes
    • Mohamedali A, Gäken J, Twine NA, Ingram W, Westwood N, Lea NC, et al. Prevalence and prognostic significance of allelic imbalance by single-nucleotide polymorphism analysis in low-risk myelodysplastic syndromes. Blood 2007; 110: 3365-3373.
    • (2007) Blood , vol.110 , pp. 3365-3373
    • Mohamedali, A.1    Gäken, J.2    Twine, N.A.3    Ingram, W.4    Westwood, N.5    Lea, N.C.6
  • 35
    • 78149454504 scopus 로고    scopus 로고
    • Next-generation sequencing of the TET2 gene in 355 MDS and CMML patients reveals low-abundance mutant clones with early origins, but indicates no definite prognostic value
    • Smith AE, Mohamedali AM, Kulasekararaj A, Lim Z, Gäken J, Lea NC, et al. Next-generation sequencing of the TET2 gene in 355 MDS and CMML patients reveals low-abundance mutant clones with early origins, but indicates no definite prognostic value. Blood 2010; 116: 3923-3932.
    • (2010) Blood , vol.116 , pp. 3923-3932
    • Smith, A.E.1    Mohamedali, A.M.2    Kulasekararaj, A.3    Lim, Z.4    Gäken, J.5    Lea, N.C.6
  • 37
    • 0037184339 scopus 로고    scopus 로고
    • Hematologic aspects of liver transplantation for Budd-Chiari syndrome with special reference to myeloproliferative disorders
    • Melear JM, Goldstein RM, Levy MF, Molmenti EP, Cooper B, Netto GJ, et al. Hematologic aspects of liver transplantation for Budd-Chiari syndrome with special reference to myeloproliferative disorders. Transplantation 2002; 74: 1090-1095.
    • (2002) Transplantation , vol.74 , pp. 1090-1095
    • Melear, J.M.1    Goldstein, R.M.2    Levy, M.F.3    Molmenti, E.P.4    Cooper, B.5    Netto, G.J.6
  • 38
    • 79961022740 scopus 로고    scopus 로고
    • Long-term follow-up of liver transplantation for Budd-Chiari syndrome with antithrombotic therapy based on the etiology
    • Chinnakotla S, Klintmalm GB, Kim P, Tomiyama K, Klintmalm E, Davis GL, et al. Long-term follow-up of liver transplantation for Budd-Chiari syndrome with antithrombotic therapy based on the etiology. Transplantation 2011; 92: 341-345.
    • (2011) Transplantation , vol.92 , pp. 341-345
    • Chinnakotla, S.1    Klintmalm, G.B.2    Kim, P.3    Tomiyama, K.4    Klintmalm, E.5    Davis, G.L.6
  • 39
    • 79954585767 scopus 로고    scopus 로고
    • The JAK2 46/1 haplotype in Budd-Chiari syndrome and portal vein thrombosis
    • For European Network For Vascular Disorders Of the Liver
    • Smalberg JH, Koehler E, Darwish Murad S, Plessier A, Seijo S, Trebicka J, et al.; for European Network for Vascular Disorders of the Liver. The JAK2 46/1 haplotype in Budd-Chiari syndrome and portal vein thrombosis. Blood 2011; 117: 3968-3973.
    • (2011) Blood , vol.117 , pp. 3968-3973
    • Smalberg, J.H.1    Koehler, E.2    Darwish Murad, S.3    Plessier, A.4    Seijo, S.5    Trebicka, J.6
  • 40
    • 42249108660 scopus 로고    scopus 로고
    • Thrombosis and anticoagulation in liver disease
    • Valla DC,. Thrombosis and anticoagulation in liver disease. Hepatology 2008; 47: 1384-1393.
    • (2008) Hepatology , vol.47 , pp. 1384-1393
    • Valla, D.C.1
  • 41
    • 68249099452 scopus 로고    scopus 로고
    • Etiology, management, and outcome of the Budd-Chiari syndrome
    • For European Network For Vascular Disorders Ofthe Liver
    • Darwish Murad S, Plessier A, Hernandez-Guerra M, Fabris F, Eapen CE, Bahr MJ, et al.; for European Network for Vascular Disorders of the Liver. Etiology, management, and outcome of the Budd-Chiari syndrome. Ann Intern Med 2009; 151: 167-175.
    • (2009) Ann Intern Med , vol.151 , pp. 167-175
    • Darwish Murad, S.1    Plessier, A.2    Hernandez-Guerra, M.3    Fabris, F.4    Eapen, C.E.5    Bahr, M.J.6


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