Hereditary haemorrhagic telangiectasia in children. Endovascular treatment of neurovascular malformations. Results in 31 patients

Interventional Neuroradiology

Volumn 11, Issue 1, 2005, Pages 13-23

  Krings, T ^a   Chng, S M ^c   Ozanne, A ^c   Alvarez, H ^c   Rodesch, G ^b   Lasjaunias, P L ^c  

^a UNIVERSITY HOSPITAL RWTH AACHEN   (Germany)

^b FOCH HOSPITAL   (France)

^c BICÊTRE HOSPITAL   (France)

Author keywords

Cerebral arteriovenous fistulae; Cerebral arteriovenous malformations; Embolization; Hereditary haemorrhagic telangiectasia; Rendu Osler Weber disease

Indexed keywords

ENBUCRILATE; GLUE;

ADOLESCENT; AGE DISTRIBUTION; ARTERIOVENOUS FISTULA; ARTIFICIAL EMBOLISM; BRAIN ARTERIOVENOUS MALFORMATION; CHILD; CLINICAL ARTICLE; COIL EMBOLIZATION; FEMALE; HUMAN; INFANT; INTERVENTIONAL RADIOLOGY; MALE; NEUROLOGIC DISEASE; PHENOTYPE; RENDU OSLER WEBER DISEASE; REVIEW; SPINAL CORD MALFORMATION; TREATMENT OUTCOME;

EID: 20944438357     PISSN: 11239344     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

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