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Volumn 55, Issue 1, 2009, Pages 19-21

Neurocariogenic syncope and hereditarity;A predispodição genética na síncope vasovagal

Author keywords

Genetic predisposition; Hereditariety; Syncope vasovagal

Indexed keywords


EID: 67650302131     PISSN: 01044230     EISSN: None     Source Type: Journal    
DOI: 10.1590/s0104-42302009000100009     Document Type: Article
Times cited : (2)

References (20)
  • 3
  • 4
    • 0019943760 scopus 로고
    • Evaluation and outcome of emergency room patients with transiet loss of consciousness
    • Day SC Evaluation and outcome of emergency room patients with transiet loss of consciousness. Am J Med. 1992;73:15-23
    • (1992) Am J Med , vol.73 , pp. 15-23
    • Day, S.C.1
  • 7
    • 0024512921 scopus 로고
    • Provocation of bradycardia and hypotension by isoproterol and upright posture in patientes with unexplained syncope
    • Alquimist A, Goldenberg IF, Miltein S, Chen MY, Chen XC, Hansen R, et al. Provocation of bradycardia and hypotension by isoproterol and upright posture in patientes with unexplained syncope. N Engl J Med. 1989;320:346-51.
    • (1989) N Engl J Med , vol.320 , pp. 346-351
    • Alquimist, A.1    Goldenberg, I.F.2    Miltein, S.3    Chen, M.Y.4    Chen, X.C.5    Hansen, R.6
  • 8
    • 0025996144 scopus 로고
    • Impairment of psycosocial function in recurrent syncope
    • Linzer M, Pontinem M, Gold DT, et al.Impairment of psycosocial function in recurrent syncope. J Gin Epidemiol. 1991;44:1037-43
    • (1991) J Gin Epidemiol , vol.44 , pp. 1037-1043
    • Linzer, M.1    Pontinem, M.2    Gold, D.T.3
  • 9
    • 0030077631 scopus 로고    scopus 로고
    • Síncope neurocardiogênica: Patogenia, diagnóstico e tratamento
    • Freitas J, Puig J, Cunha D, Costa O, Freitas A. Síncope neurocardiogênica: patogenia, diagnóstico e tratamento.Rev Port Cardiol. 1996;15:103-9.
    • (1996) Rev Port Cardiol , vol.15 , pp. 103-109
    • Freitas, J.1    Puig, J.2    Cunha, D.3    Costa, O.4    Freitas, A.5
  • 12
    • 0032750873 scopus 로고    scopus 로고
    • Tilt table testing in the diagnosis of unexplainec syncope
    • Parry SW, Kenny RA. Tilt table testing in the diagnosis of unexplainec syncope.Q J Med. 1999;92:623-9.
    • (1999) Q J Med , vol.92 , pp. 623-629
    • Parry, S.W.1    Kenny, R.A.2
  • 13
    • 0038369764 scopus 로고    scopus 로고
    • Prevalence of family history in vasovagal syncope and haemodynamic response to head up tilt in first degree relatives
    • Newton J, Kenny R, Lawson J, Kenny R, Freadson R, Donaldson P. Prevalence of family history in vasovagal syncope and haemodynamic response to head up tilt in first degree relatives. Clin Auton Res. 2003;13:22-6.
    • (2003) Clin Auton Res , vol.13 , pp. 22-26
    • Newton, J.1    Kenny, R.2    Lawson, J.3    Kenny, R.4    Freadson, R.5    Donaldson, P.6
  • 15
    • 0034464803 scopus 로고    scopus 로고
    • Familial vasovagal syncope and pseudosyncope: Observations in a case of a both natural and adopted siblings
    • Mathias CJ, Deguchi K, Bleasdale-Barr K, Smit S. Familial vasovagal syncope and pseudosyncope: observations in a case of a both natural and adopted siblings. Clin Auton Res. 2000; 10:43-5.
    • (2000) Clin Auton Res , vol.10 , pp. 43-45
    • Mathias, C.J.1    Deguchi, K.2    Bleasdale-Barr, K.3    Smit, S.4
  • 16
    • 0010338580 scopus 로고
    • Familial fainting- Observations in three families, including one with adopted children
    • Mathias CJ, Bleasdale-Baar K, Alam M. Familial fainting- observations in three families, including one with adopted children.Clin Autonom Res. 1995;5:105.
    • (1995) Clin Autonom Res , vol.5 , pp. 105
    • Mathias, C.J.1    Bleasdale-Baar, K.2    Alam, M.3
  • 17
    • 0024986332 scopus 로고
    • Syncope in childhood: A case controlstudy of the familial tendency to faint
    • Camfield PR, Camfield CS. Syncope in childhood: a case controlstudy of the familial tendency to faint. Can J Neurol Sci. 1990; 17:306-8.
    • (1990) Can J Neurol Sci , vol.17 , pp. 306-308
    • Camfield, P.R.1    Camfield, C.S.2
  • 19
    • 0035033623 scopus 로고    scopus 로고
    • Association study of the 5HT-2A receptor gene polymorphism, T102C and essencial hyperthension
    • Liolitsa D, Powwel JF, Prince M, Lovestone S. Association study of the 5HT-2A receptor gene polymorphism, T102C and essencial hyperthension.J Hum Hypetens. 2001;15:335-9.
    • (2001) J Hum Hypetens , vol.15 , pp. 335-339
    • Liolitsa, D.1    Powwel, J.F.2    Prince, M.3    Lovestone, S.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.