Retinal findings in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)

Survey of Ophthalmology

Volumn 45, Issue 5, 2001, Pages 445-448

  Robinson, Wendy ^a   Galetta, Steven L ^b,c   McCluskey, Leo ^b   Forman, Mark S ^b   Balcer, Laura J ^b  

^a MICHIGAN STATE UNIVERSITY   (United States)

^b UNIVERSITY OF PENNSYLVANIA   (United States)

^c NONE   (United States)

Author keywords

CADASIL; Cerebral autosomal dominant arteriopathy with subscortical infarcts and leukoencephalopathy; Electron microscopy; Granular osmiophilic material; Retina

Indexed keywords

NOTCH RECEPTOR;

ADULT; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; BASEMENT MEMBRANE; CADASIL; CASE REPORT; CEREBROVASCULAR DISEASE; CHROMOSOME 19; CHROMOSOME MUTATION; CLINICAL FEATURE; DISEASE COURSE; ELECTRON MICROSCOPY; FLUORESCENCE ANGIOGRAPHY; GENETIC ANALYSIS; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; HUMAN TISSUE; MALE; PRIORITY JOURNAL; RETINA ARTERY; SKIN BIOPSY; SMOOTH MUSCLE FIBER; VISUAL FIELD;

BIOPSY; CEREBRAL CORTEX; CEREBRAL INFARCTION; DEMENTIA, MULTI-INFARCT; DIAGNOSIS, DIFFERENTIAL; FLUORESCEIN ANGIOGRAPHY; FUNDUS OCULI; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; MIDDLE AGED; NUCLEAR FAMILY; RETINA; SEVERITY OF ILLNESS INDEX; SKIN;

EID: 0035077197     PISSN: 00396257     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0039-6257(00)00206-X     Document Type: Article

References (21)

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16. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL). Clinical, neuroimaging, pathological and genetic study of a large Italian family
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18. Hereditary multi-infarct dementia. Morphological and clinical studies of a new disease
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