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Volumn 11, Issue 5, 2009, Pages 356-358

Transillumination of the fingers for vascular anomalies: A novel method for evaluating hereditary hemorrhagic telangiectasia

Author keywords

Congenital vascular anomaly; Finger; Hereditary hemorrhagic telangiectasia; Telangiectases; Transillumination

Indexed keywords

ADULT; AGED; ARTICLE; CLINICAL ARTICLE; CONGENITAL BLOOD VESSEL MALFORMATION; CONTROLLED STUDY; DIAGNOSTIC IMAGING; FEMALE; FINGER; HUMAN; MALE; OTOSCOPE; RENDU OSLER WEBER DISEASE;

EID: 67249096183     PISSN: 10983600     EISSN: None     Source Type: Journal    
DOI: 10.1097/GIM.0b013e31819b245a     Document Type: Article
Times cited : (5)

References (10)
  • 1
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    • On a family form of recurring epistaxis, associated with multiple telangiectases of the skin and mucous membranes
    • Osler W. On a family form of recurring epistaxis, associated with multiple telangiectases of the skin and mucous membranes. Bull Johns Hopkins Hosp 1901;12:333-337.
    • (1901) Bull Johns Hopkins Hosp , vol.12 , pp. 333-337
    • Osler, W.1
  • 2
    • 55949129900 scopus 로고    scopus 로고
    • Hereditary hemorrhagic telangiectasia
    • Rimoin DL, Connor JM, Pyeritz RE, Korf BR, editors. Philadelphia: Churchill Livingstone
    • Guttmacher A, Marchuck D, Pyeritz RE. Hereditary hemorrhagic telangiectasia. In: Rimoin DL, Connor JM, Pyeritz RE, Korf BR, editors. Principles and practice of medical genetics, 5th ed. Philadelphia: Churchill Livingstone, 2007:1200-1213.
    • (2007) Principles and Practice of Medical Genetics, 5th Ed. , pp. 1200-1213
    • Guttmacher, A.1    Marchuck, D.2    Pyeritz, R.E.3
  • 3
    • 0001506230 scopus 로고
    • Epistaxis as an indication of impaired nutrition, and of degeneration of the vascular system
    • Sutton HG. Epistaxis as an indication of impaired nutrition, and of degeneration of the vascular system. Med Mirror 1864;1:769.
    • (1864) Med Mirror , vol.1 , pp. 769
    • Sutton, H.G.1
  • 4
    • 0013427627 scopus 로고
    • Hereditary hemorrhagic telangiectasia; nine cases in one Negro family, with special reference to hepatic lesions
    • Smith JL, Lineback MI. Hereditary hemorrhagic telangiectasia; nine cases in one Negro family, with special reference to hepatic lesions. Am J Med 1954;17:41-49.
    • (1954) Am J Med , vol.17 , pp. 41-49
    • Smith, J.L.1    Lineback, M.I.2
  • 7
    • 0017821361 scopus 로고
    • Neurological manifestations of hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber disease): Report of 2 cases and review of the literature
    • Roman G, Fisher M, Perl DP, Poser CM. Neurological manifestations of hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber disease): report of 2 cases and review of the literature. Ann Neurol 1978;4:130-144. (Pubitemid 8392040)
    • (1978) Annals of Neurology , vol.4 , Issue.2 , pp. 130-144
    • Roman, G.1    Fisher, M.2    Perl, D.P.3    Poser, C.M.4
  • 8
    • 0025800105 scopus 로고
    • Cerebral abscess associated with dental procedure in hereditary haemorrhagic telangiectasia
    • Mohler ER, Monahan B, Canty MD, Flockhart DA. Cerebral abscess associated with dental procedure in hereditary haemorrhagic telangiectasia. Lancet 1991;338:508-509.
    • (1991) Lancet , vol.338 , pp. 508-509
    • Mohler, E.R.1    Monahan, B.2    Canty, M.D.3    Flockhart, D.A.4
  • 9
    • 0034130826 scopus 로고    scopus 로고
    • Value of capillary microscopy in the diagnosis of hereditary hemorrhagic telangiectasia
    • Mager JJ, Westermann CJ. Value of capillary microscopy in the diagnosis of hereditary hemorrhagic telangiectasia. Arch Dermatol 2000;136:732-734. (Pubitemid 30407428)
    • (2000) Archives of Dermatology , vol.136 , Issue.6 , pp. 732-734
    • Mager, J.J.1    Westermann, C.J.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.