Acute unilateral visual loss as the first symptom of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

Archives of Neurology

Volumn 61, Issue 4, 2004, Pages 577-580

  Rufa, Alessandra ^a   De Stefano, Nicola ^a   Dotti, Maria Teresa ^a   Bianchi, Silvia ^a   Sicurelli, Francesco ^a   Stromillo, Maria Laura ^a   D'Aniello, Bruno ^a   Federico, Antonio ^a  

^a UNIVERSITY OF SIENA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

NOTCH3 RECEPTOR; CELL SURFACE RECEPTOR; NOTCH RECEPTOR; NOTCH3 PROTEIN, HUMAN; ONCOPROTEIN;

ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BRAIN ELECTROPHYSIOLOGY; CADASIL; CARDIOVASCULAR RISK; CASE REPORT; CEREBROVASCULAR DISEASE; EVOKED VISUAL RESPONSE; EXON; FAMILY HISTORY; FLUORESCENCE ANGIOGRAPHY; GENE DELETION; GENE MUTATION; GENETIC SCREENING; HETEROZYGOSITY; HUMAN; MALE; MULTIINFARCT DEMENTIA; NEUROLOGIC DISEASE; NUCLEAR MAGNETIC RESONANCE IMAGING; OPTIC NERVE ATROPHY; OPTIC NERVE DISEASE; PHENOTYPE; PIGMENT EPITHELIUM; PRIORITY JOURNAL; QUADRIPLEGIA; STROKE; VISUAL ACUITY; VISUAL IMPAIRMENT; BLINDNESS; CHROMOSOME 19; DISEASE COURSE; GENETIC PREDISPOSITION; GENETICS; HEMISPHERIC DOMINANCE; HETEROZYGOTE DETECTION; ISCHEMIC OPTIC NEUROPATHY; MIDDLE AGED; NUCLEOTIDE SEQUENCE; PATHOLOGY; PATHOPHYSIOLOGY; PHYSIOLOGY; VISUAL CORTEX;

BLINDNESS; CHROMOSOMES, HUMAN, PAIR 19; DEMENTIA, MULTI-INFARCT; DISEASE PROGRESSION; DNA MUTATIONAL ANALYSIS; EVOKED POTENTIALS, VISUAL; EXONS; FLUORESCEIN ANGIOGRAPHY; FUNCTIONAL LATERALITY; GENETIC PREDISPOSITION TO DISEASE; HETEROZYGOTE DETECTION; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; MIDDLE AGED; OPTIC ATROPHY; OPTIC NEUROPATHY, ISCHEMIC; PHENOTYPE; PROTO-ONCOGENE PROTEINS; RECEPTORS, CELL SURFACE; RECEPTORS, NOTCH; VISUAL CORTEX;

EID: 2342587419     PISSN: 00039942     EISSN: None     Source Type: Journal    
DOI: 10.1001/archneur.61.4.577     Document Type: Article

References (16)

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