CADASIL: Clinical and diagnostic;CADASIL: Klinik und diagnostik

Deutsche Medizinische Wochenschrift

Volumn 123, Issue 33, 1998, Pages 979-981

  Dichgans, M ^a   Gasser, T ^a  

^a LUDWIG MAXIMILIANS UNIVERSITY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BRAIN ANGIOGRAPHY; BRAIN INFARCTION; CEREBROVASCULAR DISEASE; CLINICAL FEATURE; COGNITIVE DEFECT; GENETICS; HUMAN; LEUKOENCEPHALOPATHY; MIGRAINE;

EID: 0032516795     PISSN: 00120472     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2007-1024107     Document Type: Article

References (8)

1. Bergmann, M. M., Ebke, Y. Yuan, W. Bruck, M. Mugler, G. Schwendemann: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). A morphological study of a German family. Acta Neuropathol. 92 (1996), 341-350.
2. Chabriat, H., K. Vahedi, M. T. Iba Zizen, A. Joutel, A. Nibbio, T. G. Nagy, M. O. Krebs, J. Julien, B. Dubois, X. Ducrocq, M. Levasseur, P. Homeyer, J. Mas, O. Lyon-Caen, E. Tournier-Lasserve, M. G. Bousser: Clinical spectrum of CADASIL. A study of 7 families. Lancet 346 (1995), 934-939.
3. Dichgans, M., M. Mayer, I. Uttner, R. Brüning, J. Müller-Höcker, G. Rungger, M. Ebke, T. Klockgether, T. Gasser: The phenotypic spectrum of CADASIL Clinical finding in 102 cases. Ann. Neurol. (in press).
4. Dichgans, M., D. Petersen: Angiographic complications in CADASIL Lancet 349 (1997), 776-777.
5. Joutel, A., C. Corpechot, A. Ducros, K. Vahedi, H. Chabriat, P. Mouton, S. Alamowitch, V. Domenga, M. Cecillion, E. Marechal, J. Maciazek, C. Vayssiere, C. Cruaud, E. A. Cabanis, M. M. Ruchoux, J. Weissenbach, J. F. Bach, M. G. Bousser, E. Tournier-Lasserve: Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia. Nature 383 (1996), 707-710.
6. Joutel, A., K. Vahedi, C. Corpechot, A. Troesch, H. Chabriat, C. Vayssiere, C. Cruaud, J. Maciazek, J. Weissenbach, M. G. Bousser, J. F. Bach, E. Tournier-Lasserve: Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients. Lancet 350 (1997), 1511-1515.
7. Ruchoux, M. M., C. A. Maurage: CADASIL. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. J. Neuropathol. Exp. Neurol. 56 (1997), 947-964.
8. Tournier-Lasserve, E., A. Joutel, J. Melki, J. Weissenbach, G. M. Lathrop, H. Chabriat, J. L. Mas, E. A. Cabanis, M. Baudrimont. J. Maciazek, M. A. Bach, M. G. Bousser: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12. Nat. Genet. 3 (1993), 256-259.