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Volumn 180, Issue 8, 2009, Pages 833-835

Hereditary hemorrhagic telangiectasia

Author keywords

[No Author keywords available]

Indexed keywords

ANTIFIBRINOLYTIC AGENT; ETHINYLESTRADIOL; IRON; NORETHISTERONE;

EID: 65349140104     PISSN: 08203946     EISSN: 14882329     Source Type: Journal    
DOI: 10.1503/cmaj.081739     Document Type: Article
Times cited : (27)

References (18)
  • 1
    • 0042130535 scopus 로고    scopus 로고
    • The prevalence and manifestations of hereditary hemorrhagic telangiectasia in the Afro-Caribbean population of the Netherlands Antilles: A family screening
    • Westermann CJ, Rosina AF, De Vries, V, et al. The prevalence and manifestations of hereditary hemorrhagic telangiectasia in the Afro-Caribbean population of the Netherlands Antilles: a family screening. Am J Med Genet A 2003;116A:324-8.
    • (2003) Am J Med Genet A , vol.116 A , pp. 324-328
    • Westermann, C.J.1    Rosina, A.F.2    De Vries, V.3
  • 2
    • 0026683949 scopus 로고
    • Hereditary haemorrhagic telangiectasia: A clinical analysis
    • Porteous ME, Burn J, Proctor SJ. Hereditary haemorrhagic telangiectasia: a clinical analysis. J Med Genet 1992;29:527-30.
    • (1992) J Med Genet , vol.29 , pp. 527-530
    • Porteous, M.E.1    Burn, J.2    Proctor, S.J.3
  • 3
    • 33749239827 scopus 로고    scopus 로고
    • Hereditary haemorrhagic telangiectasia: Mutation detection, test sensitivity and novel mutations
    • Prigoda NL, Savas S, Abdalla SA, et al. Hereditary haemorrhagic telangiectasia: mutation detection, test sensitivity and novel mutations. J Med Genet 2006; 43:722-8.
    • (2006) J Med Genet , vol.43 , pp. 722-728
    • Prigoda, N.L.1    Savas, S.2    Abdalla, S.A.3
  • 4
    • 55849086919 scopus 로고    scopus 로고
    • Genotype-phenotype relationship for localization and age distribution of telangiectases in hereditary hemorrhagic telangiectasia
    • Letteboer TG, Mager HJ, Snijder RJ, et al. Genotype-phenotype relationship for localization and age distribution of telangiectases in hereditary hemorrhagic telangiectasia. Am J Med Genet A2008;146A:2733-9.
    • (2008) Am J Med Genet A , vol.146 A , pp. 2733-2739
    • Letteboer, T.G.1    Mager, H.J.2    Snijder, R.J.3
  • 5
    • 65349150596 scopus 로고    scopus 로고
    • Hereditary hemorrhagic telangiectasia: Epistaxis and hemoptysis
    • Nada S, Bhatt SP. Hereditary hemorrhagic telangiectasia: epistaxis and hemoptysis. CMAJ 2009;180:838.
    • (2009) CMAJ , vol.180 , pp. 838
    • Nada, S.1    Bhatt, S.P.2
  • 6
    • 65349131269 scopus 로고    scopus 로고
    • Hereditary hemorrhagic telangiectasia: Fatigue and dyspnea
    • Irani F, Kasmani R. Hereditary hemorrhagic telangiectasia: fatigue and dyspnea. CMAJ2009;180:839.
    • (2009) CMAJ , vol.180 , pp. 839
    • Irani, F.1    Kasmani, R.2
  • 7
    • 65349157718 scopus 로고    scopus 로고
    • Hereditary hemorrhagic telangiectasia: Transient ischemic attacks
    • Manawadu D, Vethanayagam D, Ahmed SN. Hereditary hemorrhagic telangiectasia: transient ischemic attacks. CMAJ2009;180:836-7.
    • (2009) CMAJ , vol.180 , pp. 836-837
    • Manawadu, D.1    Vethanayagam, D.2    Ahmed, S.N.3
  • 8
    • 0034007163 scopus 로고    scopus 로고
    • Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome)
    • Shovlin CL, Guttmacher AE, Buscarini E, et al. Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome). Am J Med Genet 2000;91:66-7.
    • (2000) Am J Med Genet , vol.91 , pp. 66-67
    • Shovlin, C.L.1    Guttmacher, A.E.2    Buscarini, E.3
  • 9
    • 0025230351 scopus 로고
    • Treatment of bleeding gastrointestinal vascular malformations with oestrogen-progesterone
    • van Cutsem E, Rutgeerts P, Vantrappen G. Treatment of bleeding gastrointestinal vascular malformations with oestrogen-progesterone. Lancet 1990;335:953-5.
    • (1990) Lancet , vol.335 , pp. 953-955
    • van Cutsem, E.1    Rutgeerts, P.2    Vantrappen, G.3
  • 10
    • 0032799731 scopus 로고    scopus 로고
    • Hereditary haemorrhagic telangiectasia and pulmonary arteriovenous malformations: Issues in clinical management and review of pathogenic mechanisms
    • Shovlin CL, Letarte M. Hereditary haemorrhagic telangiectasia and pulmonary arteriovenous malformations: issues in clinical management and review of pathogenic mechanisms. Thorax 1999;54:714-29.
    • (1999) Thorax , vol.54 , pp. 714-729
    • Shovlin, C.L.1    Letarte, M.2
  • 11
    • 0031846341 scopus 로고    scopus 로고
    • Pulmonary arteriovenous malformations. A state of the art review
    • Gossage JR, Kanj G. Pulmonary arteriovenous malformations. A state of the art review. Am J Respir Crit Care Med 1998;158:643-61.
    • (1998) Am J Respir Crit Care Med , vol.158 , pp. 643-661
    • Gossage, J.R.1    Kanj, G.2
  • 12
    • 47349107056 scopus 로고    scopus 로고
    • Estimates of maternal risks of pregnancy for women with hereditary haemorrhagic telangiectasia (Osler- Weber-Rendu syndrome): Suggested approach for obstetric services
    • Shovlin CL, Sodhi V, McCarthy A, et al. Estimates of maternal risks of pregnancy for women with hereditary haemorrhagic telangiectasia (Osler- Weber-Rendu syndrome): suggested approach for obstetric services. BJOG 2008;115:1108-15.
    • (2008) BJOG , vol.115 , pp. 1108-1115
    • Shovlin, C.L.1    Sodhi, V.2    McCarthy, A.3
  • 13
    • 1642332403 scopus 로고    scopus 로고
    • Hepatic involvement in hereditary hemorrhagic telangiectasia: CT findings
    • Memeo M, Stabile Ianora AA, Scardapane A, et al. Hepatic involvement in hereditary hemorrhagic telangiectasia: CT findings. Abdom Imaging2004;29:211-20.
    • (2004) Abdom Imaging , vol.29 , pp. 211-220
    • Memeo, M.1    Stabile Ianora, A.A.2    Scardapane, A.3
  • 14
    • 0038016648 scopus 로고    scopus 로고
    • Should asymptomatic patients with hereditary haemorrhagic telangiectasia (HHT) be screened for cerebral vascular malformations? Data from 22,061 years of HHT patient life
    • Easey AJ, Wallace GM, Hughes JM, et al. Should asymptomatic patients with hereditary haemorrhagic telangiectasia (HHT) be screened for cerebral vascular malformations? Data from 22,061 years of HHT patient life. J Neurol Neurosurg Psychiatry 2003;74:743-8.
    • (2003) J Neurol Neurosurg Psychiatry , vol.74 , pp. 743-748
    • Easey, A.J.1    Wallace, G.M.2    Hughes, J.M.3
  • 15
    • 3442883144 scopus 로고    scopus 로고
    • Hereditary hemorrhagic telangiectasia: An overview of diagnosis and management in the molecular era for clinicians
    • Bayrak-Toydemir P, Mao R, Lewin S, et al. Hereditary hemorrhagic telangiectasia: an overview of diagnosis and management in the molecular era for clinicians. Genet Med2004;6:175-91.
    • (2004) Genet Med , vol.6 , pp. 175-191
    • Bayrak-Toydemir, P.1    Mao, R.2    Lewin, S.3
  • 16
    • 0030663612 scopus 로고    scopus 로고
    • Embolotherapy of large pulmonary arteri- ovenous malformations: Long-term results
    • Lee DW, White RI Jr, Egglin TK, et al. Embolotherapy of large pulmonary arteri- ovenous malformations: long-term results. Ann Thorac Surg 1997;64:930-9.
    • (1997) Ann Thorac Surg , vol.64 , pp. 930-939
    • Lee, D.W.1    White Jr, R.I.2    Egglin, T.K.3
  • 17
    • 2142703735 scopus 로고    scopus 로고
    • Pulmonary arteriovenous malformations in patients with hereditary hemorrhagic telangiectasia
    • Cottin V, Plauchu H, Bayle JY, et al. Pulmonary arteriovenous malformations in patients with hereditary hemorrhagic telangiectasia. Am J Respir Crit Care Med 2004;169:994-1000.
    • (2004) Am J Respir Crit Care Med , vol.169 , pp. 994-1000
    • Cottin, V.1    Plauchu, H.2    Bayle, J.Y.3
  • 18
    • 0028851489 scopus 로고
    • Screening family members of patients with hereditary hemorrhagic telangiectasia
    • Haitjema T, Disch F, Overtoom TT, et al. Screening family members of patients with hereditary hemorrhagic telangiectasia. Am J Med 1995;99:519-24.
    • (1995) Am J Med , vol.99 , pp. 519-524
    • Haitjema, T.1    Disch, F.2    Overtoom, T.T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.