Cadasil;Cadasil

Fortschritte der Neurologie Psychiatrie

Volumn 67, Issue 9, 1999, Pages 426-433

  Calabrese, P ^b   Roth, H ^b   Gehlen, W ^b   Mellies, Jörg Konrad ^a  

^a RUHR UNIVERSITY BOCHUM   (Germany)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

AFFECTIVE NEUROSIS; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; BRAIN DEGENERATION; BRAIN INFARCTION; CEREBROVASCULAR DISEASE; CHROMOSOME 19P; DEMENTIA; GENE MUTATION; HUMAN; LEUKOENCEPHALOPATHY; MIGRAINE; NUCLEAR MAGNETIC RESONANCE IMAGING; SEIZURE; GENETICS; MULTIINFARCT DEMENTIA; PEDIGREE; PSYCHOLOGICAL ASPECT; RADIOGRAPHY; REVIEW;

DEMENTIA, MULTI-INFARCT; HUMANS; PEDIGREE;

EID: 0033197281     PISSN: 07204299     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2007-994992     Document Type: Article

References (49)

1. Adair JC, Hart BL, Kornfeld M, et al. Autosomal Dominant Cerebral Arteriopathy: Neuropsychiatric Syndrome in a Family. Neuropsych Neuropsychol Behav Neurol 1998; 11: 31-39
2. Amberia K, Mononen H, Repo M, Viitanen M. Cognitive decline in members of a Finnish CADASIL family. Neurobiol Aging 1998; 19: 86 (Abstract)
3. Baudrimont M, Dubas F, Joutel A, Tournier-Lasserve E, Bousser MG. Autosomal Dominant Leukoencephalopathy and Subcortical Ischemic Stroke. A Clinicopathological Study. Stroke 1993; 24: 122-125
4. Bennett C, Crawford F, Osborne A, et al. Evidence that the APOE locus influences rate of disease progression in late onset familial Alzheimer's Disease but is not causative. Am J Med Genet 1995; 60: 1-6
5. Caronti B, Calandriello L, Francia Aet al. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL). Neuropathological and in vitro studies of abnormal elastogenesis. Acta Neurol Scand 10-1998; 98: 259-267
6. Chabriat H, Bousser MG, Pappata S. Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leucoencephalopathy: A Positron Emission Tomography Study in Two Affected Family Members. Stroke 1995; 26: 1729-1730
7. Chabriat H, Iba-Zizen MT, Joutel A, et al. Clinical spectrum of CADASIL: a study of 7 families. Lancet 1995; 346: 934-938
8. Chabriat H, Joutel A, Iba-Zizen MT, Tournier-Lasserve E, Bousser MG. CADASIL Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy. Rev Neurol (Paris) 1997; 153: 376-385
9. Chabriat H, Levy C, Taillia H, et al. Patterns of MRI lesions in CADASIL. Neurology 1998; 51: 452-457
10. Chabriat H, Tournier-Lasserve E, Vahedi K, et al. Autosomal dominant migraine with MRI white-matter abnormalities mapping to the CADASIL locus. Neurology 1995; 45: 1086-1091
11. Chimowitz MI, Awad IA, Furlan AJ. Periventricular lesions on MRI. Facts and theories. Stroke 1989; 20: 963-967
12. Davous P, Bequet D. CADASIL - A new model of subcortical dementia. Rev Neurol (Paris) 1996; 151: 634-639
13. Davous P, Ballett-Bianco C. Familial subcortical dementia with arteriopathic leukoencephalopathy: a clinicopathological study. Rev Neurol (Paris) 1991; 147: 376-384
14. Desmond DW, Moroney JT, Lynch T, et al. CADASIL in a North American family: clinical, pathologic, and radiologic findings. Neurology 1998; 51: 844-849
15. Dichgans M, Mayer M, Uttner I, et al. The phenotypic spectrum of CADASIL. Clinical findings in 102 cases. Ann Neurol 1998; 44: 731-739
16. Dichgans M, Müller-Myhsok B, Gasser T. Haplotype Analysis in 15 unrelated CADASIL pedigrees. J Neurol 1997; 244: S 83
17. Ducros A, Nagy T, Alamowitch S, et al. Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy. Genetic Homogeneity and Mapping of the Locus within a 2-cM Interval. Am J Hum Genet 1996; 58: 171-181
18. Ebke M, Dichgans M, Bergmann M, et al. CADASIL: skin biopsy allows diagnosis in early stages. Acta Neurol Scand 1997; 95: 351-357
19. Filley CM. The behavioral neurology of cerebral white matter. Neurology 1998; 50: 1535-1540
20. Furby A, Vahedi K, Force M, et al. Differential diagnosis of a vascular leukoencephalopathy within a CADASIL family: use of skin biopsy electron microscopy study and direct genotypic screening. J Neurol 1998; 245: 734-740
21. Goebel HH, Meyermann R, Rosin R, Schlote W. Characteristic morphologic manifestation of CADASIL, cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy, in skeletal muscle and skin. Muscle Nerve 1997; 20: 625-627
22. Hedera P, Friedland RP. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: study of two American families with predominant dementia. J Neurol Sci 1997; 146: 27-33
23. Jen J, Cohen AH, Yue Q, et al. Hereditary endotheliopathy with retinopathy, nephropathy and stroke (HERNS). Neurology 1997; 49: 1322-1330
24. Joutel A, Corpechot Ch, Ducros A, et al. Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia. Nature 1996; 383: 707-710
25. Joutel A, Ducros A, Vahedi K, et al. Genetic heterogeneity of familial hemiplegic migraine. Am J Hum Genet 1994; 55: 1166-1172
26. Joutel A, Vahedi K, Corpechot C, et al. Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients. Lancet 1997; 350: 1511-1515
27. Kumar SK, Mahr G. CADASIL presenting as bipolar disorder. Psychosomatics 1997; 38: 397-398
28. Malandrini A, Carrera P, Ciacci G, et al. Unusual clinical features and early brain MRI lesions in a family with cerebral autosomal dominant arteriopathy. Neurology 1997; 48: 1200-1203
29. Mas JL, Dilouya A, deRecondo J. Familial disorder with subcortical ischemic strokes, dementia and leukoencephalopathy. Neurology 1992; 42: 1015-1019
30. Mellies JK, Bäumer T, Müller JA, et al. SPECT study of German CADASIL family. A phenotype with migraine and progressive dementia only. Neurology 1998; 50: 1715-1721
31. Nishio T, Arima K, Eto K, Ogawa M, Sunohara N. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy - report of an autopsied Japanese case. Rinsho Skinkeigaku 1997; 37: 910-916
32. Nyholt DR, Lea RA, Goadsby PJ, Brimage PJ, Griffiths LR. Familial typical migraine. Linkage to chromosome 19p13 and evidence for genetic heterogeneity. Neurology 1998; 50: 1428-1432
33. Otto V, Kaps M, Burgmann T, Kompf D. CADASIL: 2 case reports of hereditary multiinfarct dementia. Fortschr Neurol Psychiat 1997; 65: 90-95
34. Robbins L, Friedman H. MRI in migraineurs. Headache 1992; 32: 507-508
35. Rubio A, Rifkin D, Powers JM, et al. Phenotypic variability of CADASIL and novel morphologic findings. Acta Neuropathol 1997; 94: 247-254
36. Ruchoux MM, Chabriat H, Bousser MG, Baudrimont M, Tournier-Lasserve E. Presence of ultrastructural arterial lesions in muscle and skin vessels of patients with CADASIL. Stroke 1994; 25: 2291-2292
37. Ruchoux MM, Maurage CA. Endothelial changes in muscle and skin biopsies in patients with CADASIL. Neuropathol Appl Neurobiol 1998; 24: 60-65
38. Sabbadini G, Francia A, Calandriello L, et al. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). Clinical, neuroimaging, pathological and genetic study of a large Italian family. Brain 1995; 118: 207-215
39. Schröder JM, Sellhaus B, Jörg J. Identifications of the characteristic vascular changes in a sural nerve biopsy of a case with cerebral autosomal arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). Acta Neuropathol 1995; 89: 116-121
40. Skehan SJ, Hutchinson M, MacErlaine DP. Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy: MR Findings. Am J Neuroradiol 1995; 16: 2115-2119
41. Sourander P, Walinder J. Hereditary multi-infarct dementia: morphological and clinical studies of a new disease. Acta Neuropathol 1977; 39: 247-254
42. St. Clair D, Bolt J, Morris S, Doyle D. Hereditary multi-infarct dementia unlinked to chromosome 19q12 in a large Scottish pedigree: evidence of probable locus heterogeneity. J Med Genet 1995; 32: 57-60
43. Taillia H, Chabriat H, Kurtz A, et al. Cognitive alterations in non-demented CADASlL patients. Cerebrovasc Dis 1998; 8: 97-101
44. Tournier-Lasserve E. Personal communication. 1997
45. Tournier-Lasserve E, Joutel A, Melki J, et al. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12. Nature Genetics 1993; 3: 256-259
46. Trojano L, Ragno M, Manca A, Caruso G. A kindred affected by cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). A 2-year neuropsychological follow-up. J Neurol 1998; 245: 217-222
47. Vahedi K, Joutel A, Bogaert Van P, et al. A gene for hereditary paroxysmal cerebellar ataxia maps to chromosome 19p. Ann Neurol 1995; 37: 289-293
48. Vérin M, Rolland Y, Landgraf F, et al. New phenotype of the cerebral autosomal dominant arteriopathy mapped to chromosome 19: migraine as the prominent clinical feature. J Neurol Neurosurg Psychiatry 1995; 59: 579-585
49. Weller M, Dichgans J, Klockgether T. Acetazolamide-responsive migraine in CADASIL Neurology 1998; 50: 1505