CADASIL: Hereditary disease of arteries causing brain infarcts and dementia

Neuropathology and Applied Neurobiology

Volumn 25, Issue 4, 1999, Pages 257-265

  Kalimo, H ^a,e   Viitanen, M ^e   Amberla, K ^e   Juvonen, V ^b   Marttila, R ^a   Poyhonen M ^c   Rinne, J O ^a   Savontaus, M L ^b   Tuisku, S ^d   Winblad, B ^e  

^a TURKU UNIVERSITY HOSPITAL   (Finland)

^b UNIVERSITY OF TURKU   (Finland)

^c Vaestoliitto   (Finland)

^d Keski Pohjanmaan Erikoissairaanhoito Ja Peruspalvelukuntayhtyma   (Finland)

^e KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

Author keywords

Arteriopathy; Brain infarct; CADASIL; Leukoencephalopathy; Migraine; Notch3; Stroke; Vascular dementia

Indexed keywords

CYSTEINE; MEMBRANE PROTEIN; RECEPTOR PROTEIN;

ADULT; AMINO TERMINAL SEQUENCE; ARTERY DISEASE; AUTOSOMAL DOMINANT DISORDER; BASAL GANGLION; BRAIN INFARCTION; DEMENTIA; FIBROSIS; HUMAN; IMAGE ANALYSIS; LEUKOENCEPHALOPATHY; MIGRAINE; MISSENSE MUTATION; NUCLEAR MAGNETIC RESONANCE IMAGING; PATHOGENESIS; POINT MUTATION; PRIORITY JOURNAL; REVIEW; SMOOTH MUSCLE FIBER; STROKE; THROMBOSIS; WHITE MATTER;

CEREBRAL ARTERIAL DISEASES; CEREBRAL INFARCTION; DEMENTIA; HUMANS; LEUKOENCEPHALOPATHY, PROGRESSIVE MULTIFOCAL; SYNDROME;

EID: 0032781403     PISSN: 03051846     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2990.1999.00198.x     Document Type: Review

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