CADASIL : Clinical and neuro-imaging aspects;CADASIL (artériopathie cérébrale autosomique dominante avec infarctus sous-corticaux et leucoencéphalopathie) : Clinique et neuroimagerie

Bulletin de l'Academie Nationale de Medecine

Volumn 184, Issue 7, 2000, Pages 1523-1533

  Chabriat, Hugues ^a   Joutel, Anne ^a   Vahedi, Katayoun ^a   Iba Zizen, Marie Thérèse ^b   Tournier Lasserve, Elizabeth ^a   Bousser, Marie Germaine ^a  

^a HÔPITAL LARIBOISIÈRE   (France)

^b CENTRE HOSPITALIER NATIONAL D OPHTALMOLOGIE DES QUINZE VINGTS   (France)

Author keywords

[No Author keywords available]

Indexed keywords

HUMAN; MULTIINFARCT DEMENTIA; REVIEW;

DEMENTIA, MULTI-INFARCT; HUMANS;

EID: 0034569343     PISSN: 00014079     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (19)

1. TOURNIER-LASSERVE E., JOUTEL A., MELKI J., WEISSENBACH J., LATHROP G.M., CHABRIAT H., MAS J.L., CABANIS E.A., BAUDRIMONT M., MACIAZEK J., BACH M.A., BOUSSER M.G. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps on chromosome 19q12. Nature genetics. 1993, 3, 256-59.
2. BOUSSER M.G., TOURNIER-LASSERVEE., AYLWARD R., TOURBAH A., DORMONT D., ROMERO N., CABANIS E., FARDEAU M. Recurrent strokes in a family with diffuse white-matter abnormalities - a new mitochondrial cytopathy ? J Neurol, 1988, 235 (suppl 1), S4-S5,
3. TOURNIER-LASSERVE E., IBA-ZIZEN M.T., ROMERO N., BOUSSER M.G. - Autosomal dominant syndrome with stroke-like episodes and leukoencephalopathy. Stroke, 1991, 22, 1297-1302.
4. BAUDRIMONT M., DUBAS F., JOUTEL A., TOURNIER-LASSERVE E., BOUSSER M.G. - Autosomal dominant leukoencephalopathy and subcortical ischemic strokes : a clinicopathological study. Stroke, 1993, 24, 122-25.
5. VAN BOGAERT L. - Encéphalopathie sous-corticale progressive (Binswanger) à évolution rapide chez deux sœurs. Med Hellen, 1955, 24, 961-72.
6. JOUTEL A., CORPECHOT C., DUCROS A., VAHEDI K., CHABRIAT H., MOUTON P., ALAMOWITCH S., DOMENGA V., CECILLON M., MARECHAL E., MACIAZEK J., VAYSSIERE C., CRUAUD C., CABANIS E.A., RUCHOUX M.M., WEISSENBACH J., BACH J.F., BOUSSER M.G., TOURNIER-LASSERVE E. Notch 3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia. Nature, 1996, 383, 707-710.
7. CHABRIAT H., VAHEDI K., IBA-ZIZEN M.T., JOUTEL A., NIBBIO A., NAGY T.G., KREBS M.O., JULIEN J., DUBOIS B., DUCROCQ S., LEVASSEUR M., HOMEYER P., MAS J.L., LYON-CAEN O., TOURNIER-LASSERVE E., BOUSSER M.G. - Clinical spectrum of CADASIL : a study of 7 families. Lancet, 1995, 346, 934-39.
8. DICHGANS M., MAYER M., UTTNER I., BRUNING R., MULLER-HOCKER J., RUNGGER G., EBKE M., KLOCKGETHER T., GASSER T. - The phenotypic spectrum of CADASIL : clinical findings in 102 cases. Ann. Neurol., 1998, 44, 731-39.
9. CHABRIAT H., TOURNIER-LASSERVE E., VAHEDI K., LEYS D., JUTEL A., NIBBIO A., ESCAILLAS J.P., IBA-ZIZEN M.T., BRACARD S., TEHINDRAZANARIVELO A., GASTAUT J.L., BOUSSER M.G. -Autosomal dominant migraine with MRI abnormalities mapping to the CADASIL locus. Neurology, 1995, 45, 1086-1091.
10. VERIN M., ROLLAND Y., LANDGRAF, BOMPAIS B., CHABRIAT H., TOURMER-LASSERVE E., LEMAITRE M.H., EDAN G. - New phenotype of CADASIL with migraine as prominent clinical feature. J Neurol Neurosurg Psychiatr., 1995, 59, 579-585.
11. BOUSSER M.G., TOURNIER-LASSERVE E. - Summary of the first international workshop on CADASIL. Stroke, 1994, 25, 704-770.
12. TAILLIA H., CHABRIAT H., KURTZ A., LEVY C., VAHEDI K., JOUTEL A., TOURNIER-LASSERVE E., BOUSSER M.G. - Cognitive alterations in non demented CADASIL patients. Cerebrovasc Dis, 1998, 8, 97-101.
13. HUTCHINSON M., O'RIORDAN J., JAVED M., QUIN E., MARCELAINE D., WILLCOX T., PARFREY N., NAGY T.G., TOURNIER-LASSERVE E. Familial Hemiplegie migraine and autosomal dominant arteriopathy with leukoencephalopathy (CADASIL). Ann Neurol, 1995, 38, 817-24.
14. VAHEDI K., CHABRIAT H., DUCROS A., ALAMOVITCH S., JOUTEL A., IBA-ZIZEN M.T., CABANIS E.A., TOURNIER-LASSERVE E., BOUSSER M.G. - Analysis of CADASIL clinical and natural history in a series of 134 patients belonging to 17 families linked to chromosome 19. Neurology, 1996, 46, 211.
15. CHABRIAT H., LEVY C., TAILLIA H. Patterns of MRI lesions in CADASIL. Neurology, 1998, 51, 452-457.
16. CHABRIAT H., MRISSA T., LEVY C., IBA-ZIZEN M.T., JOUTEL A., TOURNIER-LASSERVE E., BOUSSER M.G. - Brain stem MRI signal abnormalities in CADASIL. Stroke, 1999, 30, 457-459.
17. CHABRIAT H., PAPPATA S., POUPON C., CLARCK C., VAHEDI K., POUPON F., MANGIN J., PACHOT-CLOUARD M., JOBERT A., LEBIHAN D., BOUSSER M. G. - Clinical severity in CADASIL related to ultrastructural damage in white matter, In vivo study with diffusion tensor MRI. Stroke, 1999, 30, 2637-43
18. JOUTEL A., DODICK D.D., PARISI J.E., CECILLON M., TOURNIER-LASSERVE E., BOUSSER M.G. -De novo mutation in the Notch 3 gene causing CADASIL. Ann. Neurol., 2000, 47, 388-391.
19. JOUTEL A., ANDREUX F., GAULIS S., DOMENGA V., CECILLON M., BATTAIL N., PIGA N., CHAPON F., GODFRAIN C., TOURNIER-LASSERVE E. The ectodomain of the Notch 3 receptor accumulates within the cerebrovasculaturc of CADASIL patients. J. Clin. Invest., 2000, 105, 597-605.