CADASIL: Presenting as a mood disorder

Scottish Medical Journal

Volumn 47, Issue 2, 2002, Pages 36-37

  Thomas, Naveena ^a,d   Mathews', Thomas ^b   Loganathan, Arunan ^c  

^a UNIVERSITY OF DUNDEE   (United Kingdom)

^b Department of Neurology   (United States)

^c BORDERS GENERAL HOSPITAL   (United Kingdom)

^d NONE   (United Kingdom)

Author keywords

CADASIL; Notch 3 gene; Vascular dementia

Indexed keywords

NOTCH RECEPTOR;

ADULT; AFFECTIVE NEUROSIS; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BRAIN INFARCTION; CASE REPORT; CEREBROVASCULAR DISEASE; CHROMOSOME 19; CLINICAL FEATURE; COMPUTER ASSISTED TOMOGRAPHY; DEATH; DEMYELINATING DISEASE; GENE LOCUS; GENE MUTATION; GENETIC ANALYSIS; GENETIC LINKAGE; HUMAN; LEUKOENCEPHALOPATHY; MALE; MENTAL DISEASE; MIGRAINE; MULTIINFARCT DEMENTIA; NUCLEAR MAGNETIC RESONANCE IMAGING; SKIN BIOPSY; SYMPTOM; WHITE MATTER; DEPRESSION; GENETICS; MIDDLE AGED;

DEMENTIA, MULTI-INFARCT; DEPRESSIVE DISORDER; HUMANS; MALE; MIDDLE AGED;

EID: 0036014868     PISSN: 00369330     EISSN: None     Source Type: Journal    
DOI: 10.1177/003693300204700204     Document Type: Article

References (7)

1. Autosomal dominant syndrome with stroke-like episodes and leukoencephalopathy
2. The phenotypic spectrum of CADASIL; clinical findings in 102 cases
3. Patterns of MRI lesions in CADASIL
4. CADASIL: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
5. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)
6. The human Notch 3 mutations in CADASIL