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Volumn 104, Issue 8, 2010, Pages 1218-1224

Experience of the Irish National Centre for hereditary haemorrhagic telangiectasia 2003-2008

Author keywords

Cerebral arteriovenous malformation; Embolisation; Hereditary haemorrhagic telangiectasia; Pulmonary arteriovenous malformation; Rendu Osler Weber syndrome

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; ARTIFICIAL EMBOLISM; BRAIN ARTERIOVENOUS MALFORMATION; CHILD; CLINICAL FEATURE; COMPUTER ASSISTED TOMOGRAPHY; CONTRAST ECHOCARDIOGRAPHY; DEMOGRAPHY; EPISTAXIS; EXPERIENCE; FEMALE; GENOTYPE; HUMAN; IRELAND; MAJOR CLINICAL STUDY; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; PHENOTYPE; PREVALENCE; PRIORITY JOURNAL; PULMONARY ARTERIOVENOUS FISTULA; RENDU OSLER WEBER DISEASE; SCHOOL CHILD; SCREENING; TELANGIECTASIA;

EID: 77953896987     PISSN: 09546111     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.rmed.2010.03.003     Document Type: Article
Times cited : (9)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.