CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leucoencephalopathy): An Australian perspective

Journal of Clinical Neuroscience

Volumn 8, Issue 5, 2001, Pages 404-406

  Chuah, T L ^a   Tan, K M ^a   Flanagan, S ^a   Hyland, V ^a   Sullivan, A A ^a   Henderson, R ^a   MacMillan, J ^a   Lander, C ^a  

^a ROYAL BRISBANE AND WOMEN'S HOSPITAL   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

NOTCH RECEPTOR;

ADULT; AGED; ARTICLE; AUSTRALIA; BRAIN INFARCTION; CADASIL; CEREBROVASCULAR DISEASE; CHROMOSOME 19P; CLINICAL ARTICLE; CLINICAL EXAMINATION; DIAGNOSTIC IMAGING; EXON; GENE MUTATION; HUMAN; LEUKOENCEPHALOPATHY; PRIORITY JOURNAL; SIBLING; STROKE;

EID: 0034843769     PISSN: 09675868     EISSN: None     Source Type: Journal    
DOI: 10.1054/jocn.2000.0848     Document Type: Article

References (21)

1. CADASIL: Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leucoencephalopathy
2. New phenotype of the cerebral autosomal dominant arteriopathy mapped to chromosome 19: Migraine as the prominent clinical feature
3. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy: Study of two American families with predominant dementia
4. CADASIL presenting as bipolar disorder
5. Unusual clinical features and early brain MRI lesions in a family with cerebral autosomal dominant arteriopathy
6. Autosomal dominant syndrome with stroke-like episodes and leucoencephalopathy
7. Démence sous corticale familiale avec leucoencéphalopathie artériopathique: Observation clinico-pathologique
8. Patterns of MRI lesions in CADASIL
9. Summary of the Proceedings of the First International Workshop on CADASIL
10. Clinical spectrum of CADASIL: A study of 7 families
11. Identification of the characteristic vascular changes in a sural nerve biopsy of a case with cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL)
12. CADASIL: Skin biopsy allows diagnosis in early stages
13. Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia
14. Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients
15. Epidermal growth factor-like modules
16. Notch Signaling
17. Human ligands of the notch receptor
18. CADASIL: A review with proposed diagnostic criteria
19. Notch3 mutations and the potential for diagnostic testing for CADASIL
20. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy
21. The phenotypic spectrum of CADASIL: Clinical findings in 102 cases