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Archives of Disease in Childhood: Fetal and Neonatal Edition
Volumn 87, Issue 3, 2002, Pages
Neonatal pulmonary arteriovenous malformation in hereditary haemorrhagic telangiectasia
Author keywords

[No Author keywords available]
Indexed keywords

APNEA; ARTERIOVENOUS MALFORMATION; ARTICLE; ARTIFICIAL EMBOLISM; CASE REPORT; CLINICAL FEATURE; COUGHING; DISEASE ASSOCIATION; DISEASE COURSE; ECHOGRAPHY; FEMALE; HEART CATHETERIZATION; HUMAN; HYPOXEMIA; LUNG ANGIOGRAPHY; NEWBORN; NEWBORN CARE; PHYSICAL EXAMINATION; PRIORITY JOURNAL; RENDU OSLER WEBER DISEASE; TREATMENT OUTCOME; TREATMENT PLANNING;
EID: 0036829373     PISSN: 13592998     EISSN: 14682052     Source Type: Journal    
DOI: 10.1136/fn.87.3.f226     Document Type: Article
Times cited : (11)
References (10)
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  • 4
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    • Pulmonary arteriovenous malformations: Therapeutic options
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  • 5
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    • Pulmonary arteriovenous fistula: Presentation, diagnosis and treatment
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    • Pick, A.1    Deschamps, C.2    Stanson, A.W.3
  • 6
    • 0033968624 scopus 로고    scopus 로고
    • Diffuse pulmonary arteriovenous malformations
    • Faughnan ME, Lui YW, Wirth JA, et al. Diffuse pulmonary arteriovenous malformations. Chest 2000;117:31-3.
    • (2000) Chest , vol.117 , pp. 31-33
    • Faughnan, M.E.1    Lui, Y.W.2    Wirth, J.A.3
  • 7
    • 0033906469 scopus 로고    scopus 로고
    • Two common endoglin mutations in families with hereditary hemorrhagic telangiectasia in the Netherlands Antilles: Evidence for a founder effect
    • Gallione CJ, Scheessele EA, Reinhardt D, et al. Two common endoglin mutations in families with hereditary hemorrhagic telangiectasia in the Netherlands Antilles: Evidence for a founder effect. Hum Genet 2000;107:40-4.
    • (2000) Hum Genet , vol.107 , pp. 40-44
    • Gallione, C.J.1    Scheessele, E.A.2    Reinhardt, D.3
  • 8
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    • 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
    • 0029986771 scopus 로고    scopus 로고
    • Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu disease): New insights in pathogenesis, complications and treatment
    • Haitjema T, Westermann CJ, Overtoom TC, et al. Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu disease): New insights in pathogenesis, complications and treatment. Arch Intern Med 1996;156:714-19.
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    • Haitjema, T.1    Westermann, C.J.2    Overtoom, T.C.3
  • 10
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    • Transcatheter coil embolisation of a pulmonary arteriovenous malformation in a neonate
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    • Grady, R.M.1    Sharkey, A.M.2    Bridges, N.D.3

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.