Silent threat? A retrospective study of screening practices for pulmonary arteriovenous malformations in patients with hereditary haemorrhagic telangiectasia

Rhinology

Volumn 50, Issue 3, 2012, Pages

  Verkerk, Misha M ^a   Shovlin, Claire L ^b   Lund, Valerie J ^c  

^a ROYAL FREE AND UNIVERSITY COLLEGE MEDICAL SCHOOL   (United Kingdom)

^b NATIONAL HEART AND LUNG INSTITUTE   (United Kingdom)

^c ROYAL NATIONAL THROAT NOSE AND EAR HOSPITAL   (United Kingdom)

Author keywords

Arteriovenous malformations; Embolization; Epistaxis; Hereditary hemorrhagic telangiectasia; Migraine; Shortness of breath; Therapeutic

Indexed keywords

ADOLESCENT; ADULT; AGE; AGED; ARTERIOVENOUS MALFORMATION; ARTICLE; CHILD; CLINICAL PRACTICE; COMPUTER ASSISTED TOMOGRAPHY; EPISTAXIS; FEMALE; HUMAN; LUNG; MALE; MASS SCREENING; MIDDLE AGED; PATIENT SELECTION; PRESCHOOL CHILD; RENDU OSLER WEBER DISEASE; RETROSPECTIVE STUDY; SPIROMETRY; VASCULARIZATION;

ADOLESCENT; ADULT; AGE FACTORS; AGED; AGED, 80 AND OVER; ARTERIOVENOUS MALFORMATIONS; CHILD; CHILD, PRESCHOOL; EPISTAXIS; FEMALE; HUMANS; LUNG; MALE; MASS SCREENING; MIDDLE AGED; PATIENT SELECTION; PHYSICIAN'S PRACTICE PATTERNS; RETROSPECTIVE STUDIES; SPIROMETRY; TELANGIECTASIA, HEREDITARY HEMORRHAGIC; TOMOGRAPHY, X-RAY COMPUTED; YOUNG ADULT;

EID: 84865316813     PISSN: 03000729     EISSN: None     Source Type: Journal    
DOI: 10.4193/Rhino12.043     Document Type: Article

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