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Volumn 68, Issue 12, 2012, Pages 1685-1686

Bevacizumab treatment in hereditary hemorrhagic teleangiectasia

Author keywords

[No Author keywords available]

Indexed keywords

ANTIBODY; BEVACIZUMAB; HEMOGLOBIN; VASCULOTROPIN;

EID: 84871318269     PISSN: 00316970     EISSN: 14321041     Source Type: Journal    
DOI: 10.1007/s00228-012-1308-4     Document Type: Letter
Times cited : (6)

References (10)
  • 1
    • 84864280912 scopus 로고    scopus 로고
    • Bevacizumab-induced serious side-effects: A review of French pharmacovigilance database
    • doi:10.1007/s00228-012-1232-7
    • Taugourdeau-Raymond S, Rouby F, Default A, Jean-Pastor M-J (2012) Bevacizumab-induced serious side-effects: a review of French pharmacovigilance database. Eur J Clin Pharmacol. doi:10.1007/s00228-012-1232-7
    • (2012) Eur J Clin Pharmacol.
    • Taugourdeau-Raymond, S.1    Rouby, F.2    Default, A.3    Jean-Pastor, M.-J.4
  • 2
    • 66349137361 scopus 로고    scopus 로고
    • The effect of bevacizumab (Avastin) treatment on epistaxis in hereditary hemorrhagic telangiectasia
    • Simonds J, Miller F, Mandel J et al (2009) The effect of bevacizumab (Avastin) treatment on epistaxis in hereditary hemorrhagic telangiectasia. Laryngoscope 119:988
    • (2009) Laryngoscope , vol.119 , pp. 988
    • Simonds, J.1    Miller, F.2    Mandel, J.3
  • 3
    • 33747837492 scopus 로고    scopus 로고
    • Dramatic improvement in hereditary hemorrhagic telangiectasia after treatment with the vascular endothelial growth factor (VEGF) antagonist bevacizumab
    • Flieger D, Hainke S, Fischbach W (2006) Dramatic improvement in hereditary hemorrhagic telangiectasia after treatment with the vascular endothelial growth factor (VEGF) antagonist bevacizumab. Ann Hematol 85:631-632
    • (2006) Ann Hematol , vol.85 , pp. 631-632
    • Flieger, D.1    Hainke, S.2    Fischbach, W.3
  • 4
  • 7
    • 57849103993 scopus 로고    scopus 로고
    • Bevacizumab to treat complicated liver vascular malformations in hereditary hemorrhagic telangiectasia: A word of caution
    • author reply 1687-1688
    • Buscarini E, Manfredi G, Zambelli A (2008) Bevacizumab to treat complicated liver vascular malformations in hereditary hemorrhagic telangiectasia: a word of caution. Liver Transpl 14(11):1685-6, author reply 1687-1688
    • (2008) Liver Transpl , vol.14 , Issue.11 , pp. 1685-1686
    • Buscarini, E.1    Manfredi, G.2    Zambelli, A.3
  • 8
    • 39449109211 scopus 로고    scopus 로고
    • Bevacizumab reverses need for liver transplantation in hereditary hemorrhagic telangiectasia
    • Mitchell A, Adams LA, MacQuillan G, Tibballs J, vanden Driesen R (2008) Bevacizumab reverses need for liver transplantation in hereditary hemorrhagic telangiectasia. Liver Transpl 14:210-213
    • (2008) Liver Transpl , vol.14 , pp. 210-213
    • Mitchell, A.1    Adams, L.A.2    MacQuillan, G.3    Tibballs, J.4    Vanden Driesen, R.5
  • 9
    • 65649124507 scopus 로고    scopus 로고
    • Bevacizumab in hereditary hemorrhagic telangiectasia
    • Bose P, Holter JL, Selby GB (2009) Bevacizumab in hereditary hemorrhagic telangiectasia. N Engl J Med 360(20):2143- 2144
    • (2009) N Engl J Med , vol.360 , Issue.20 , pp. 2143-2144
    • Bose, P.1    Holter, J.L.2    Selby, G.B.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.