|
Volumn 11, Issue , 2011, Pages
|
Stroke in hereditary hemorrhagic telangiectasia patients. New evidence for repeated screening and early treatment of pulmonary vascular malformations: Two case reports
|
Author keywords
[No Author keywords available]
|
Indexed keywords
SMAD4 PROTEIN;
WARFARIN;
CELL SURFACE RECEPTOR;
ENG PROTEIN, HUMAN;
LEUKOCYTE ANTIGEN;
SMAD4 PROTEIN, HUMAN;
ADULT;
ARTERY DIAMETER;
ARTICLE;
BRAIN INFARCTION;
CASE REPORT;
COIL EMBOLIZATION;
COMPUTER ASSISTED TOMOGRAPHY;
CORTICAL SENSORY APHASIA;
DEEP VEIN THROMBOSIS;
DIFFUSION WEIGHTED IMAGING;
DYSPNEA;
EARLY INTERVENTION;
FEEDING ARTERY;
FEMALE;
FOLLOW UP;
GAIT DISORDER;
GENE MUTATION;
HEMOPTYSIS;
HUMAN;
LUNG ANGIOGRAPHY;
LUNG ARTERY;
MALE;
PARADOXICAL EMBOLISM;
PRACTICE GUIDELINE;
PULMONARY ARTERIOVENOUS FISTULA;
RENDU OSLER WEBER DISEASE;
RESCREENING;
STROKE;
THORAX RADIOGRAPHY;
THROMBOPHILIA;
TRANSTHORACIC ECHOCARDIOGRAPHY;
WEAKNESS;
ARTERIOVENOUS MALFORMATION;
ARTIFICIAL EMBOLISM;
CONGENITAL MALFORMATION;
GENETICS;
MASS SCREENING;
MUTATION;
PULMONARY ARTERY;
PULMONARY VEIN;
ADULT;
ANTIGENS, CD;
ARTERIOVENOUS MALFORMATIONS;
EMBOLIZATION, THERAPEUTIC;
FEMALE;
HUMANS;
MALE;
MASS SCREENING;
MUTATION;
PRACTICE GUIDELINES AS TOPIC;
PULMONARY ARTERY;
PULMONARY VEINS;
RECEPTORS, CELL SURFACE;
SMAD4 PROTEIN;
STROKE;
TELANGIECTASIA, HEREDITARY HEMORRHAGIC;
TOMOGRAPHY, X-RAY COMPUTED;
|
EID: 79959987447
PISSN: None
EISSN: 14712377
Source Type: Journal
DOI: 10.1186/1471-2377-11-54 Document Type: Article |
Times cited : (7)
|
References (5)
|