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Volumn 37, Issue 10, 1997, Pages 910-916

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy - Report of an autopsied Japanese case

Author keywords

Autopsy case; Autosomal dominant; CADASIL; Leukoencephalopathy; Migraine attacks

Indexed keywords

COMPLEMENT COMPONENT C1Q; COMPLEMENT COMPONENT C3; COMPLEMENT COMPONENT C4;

EID: 0031410819     PISSN: 0009918X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (21)

References (27)
  • 1
    • 0025947095 scopus 로고
    • Autosomal dominant syndrome with strokelike episodes and leukoencephalopathy
    • Tournier-Lasserve E, Iba-Zizen M-T, Romero N, et al : Autosomal dominant syndrome with strokelike episodes and leukoencephalopathy. Stroke 22 : 1297-1302, 1991
    • (1991) Stroke , vol.22 , pp. 1297-1302
    • Tournier-Lasserve, E.1    Iba-Zizen, M.-T.2    Romero, N.3
  • 2
    • 0026664380 scopus 로고
    • A familial disorder with subcortical ischemic strokes, dementia and leukoencephalopathy
    • Mas JL, Dilouya A, de Rocondo J : A familial disorder with subcortical ischemic strokes, dementia and leukoencephalopathy. Neurology 42 : 1015-1019, 1992
    • (1992) Neurology , vol.42 , pp. 1015-1019
    • Mas, J.L.1    Dilouya, A.2    De Rocondo, J.3
  • 3
    • 0027390357 scopus 로고
    • Autosomal dominant leukoencephalopathy and subcortical ischemic stroke. A clinico-pathological study
    • Baudrimont M, Dubas F, Joutel A, et al : Autosomal dominant leukoencephalopathy and subcortical ischemic stroke. A clinico-pathological study. Stroke 24 122-125, 1993
    • (1993) Stroke , vol.24 , pp. 122-125
    • Baudrimont, M.1    Dubas, F.2    Joutel, A.3
  • 4
    • 0029040890 scopus 로고
    • Autosomal dominant migraine with MRI white-matter abnormalities mapping to the CADASIL locus
    • Chabriat H, Tournier LE, Vahedi K, et al : Autosomal dominant migraine with MRI white-matter abnormalities mapping to the CADASIL locus. Neurology 45 : 1086-1091, 1995
    • (1995) Neurology , vol.45 , pp. 1086-1091
    • Chabriat, H.1    Tournier, L.E.2    Vahedi, K.3
  • 5
    • 0029089247 scopus 로고
    • Clinical spectrum of CADASIL : A study of 7 families. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
    • Chabriat H, Vahedi K, Iba ZM, et al : Clinical spectrum of CADASIL : a study of 7 families. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. Lancet 346 : 934-939, 1995
    • (1995) Lancet , vol.346 , pp. 934-939
    • Chabriat, H.1    Vahedi, K.2    Iba, Z.M.3
  • 6
    • 0029092525 scopus 로고
    • An Italian kindred with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)
    • Ragno M, Tournier LE, Fiori MG, et al : An Italian kindred with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). Ann Neurol 38 : 231-236, 1995
    • (1995) Ann Neurol , vol.38 , pp. 231-236
    • Ragno, M.1    Tournier, L.E.2    Fiori, M.G.3
  • 7
    • 0029620204 scopus 로고
    • Cerebral autosomal dominant arteriopathy (CADASIL). Description of a German family
    • Mayer M, Dichgans M, Gasser T, et al : Cerebral autosomal dominant arteriopathy (CADASIL). Description of a German family. Nervenarzt 66 : 927-932, 1995
    • (1995) Nervenarzt , vol.66 , pp. 927-932
    • Mayer, M.1    Dichgans, M.2    Gasser, T.3
  • 8
    • 0028871460 scopus 로고
    • A four-generation Dutch family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leuko-encephalopathy (CADASIL), linked to chromosome 19p13
    • Wielaard R, Bornebroek M, Ophoff RA, et al : A four-generation Dutch family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leuko-encephalopathy (CADASIL), linked to chromosome 19p13. Clin Neurol Neurosurg 97 : 307-313, 1995
    • (1995) Clin Neurol Neurosurg , vol.97 , pp. 307-313
    • Wielaard, R.1    Bornebroek, M.2    Ophoff, R.A.3
  • 9
    • 0028785253 scopus 로고
    • Familial hemiplegic migraine and autosomal dominant arteriopathy with leukoencephalopathy (CADASIL)
    • Hutchinson M, O'Riordan J, Javed M, et al : Familial hemiplegic migraine and autosomal dominant arteriopathy with leukoencephalopathy (CADASIL). Ann Neurol 38 : 817-824, 1995
    • (1995) Ann Neurol , vol.38 , pp. 817-824
    • Hutchinson, M.1    O'Riordan, J.2    Javed, M.3
  • 10
    • 0029096518 scopus 로고
    • Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy : A clinicopathological and genetic study of a Swiss family
    • Jung HH, Bassetti C, Tournier LE, et al : Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy : a clinicopathological and genetic study of a Swiss family. J Neurol Neurosurg Psychiatry 59 : 138-143, 1995
    • (1995) J Neurol Neurosurg Psychiatry , vol.59 , pp. 138-143
    • Jung, H.H.1    Bassetti, C.2    Tournier, L.E.3
  • 11
    • 0028271418 scopus 로고
    • Autosomal dominant arteriopathic leuko-encephalopathy and Alzheimer's disease
    • Gray F, Robert F, Labrecque R, et al : Autosomal dominant arteriopathic leuko-encephalopathy and Alzheimer's disease. Neuropathol Appl Neurobiol 20 : 22-30, 1994
    • (1994) Neuropathol Appl Neurobiol , vol.20 , pp. 22-30
    • Gray, F.1    Robert, F.2    Labrecque, R.3
  • 12
    • 0029065542 scopus 로고
    • Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)-confirmation by cerebral biopsy in 2 cases
    • Lammie GA, Rakshi J, Rossor MN, et al : Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)-confirmation by cerebral biopsy in 2 cases. Clin Neuropathol 14 : 201-206, 1995
    • (1995) Clin Neuropathol , vol.14 , pp. 201-206
    • Lammie, G.A.1    Rakshi, J.2    Rossor, M.N.3
  • 13
    • 0028872678 scopus 로고
    • Identification of the characteristic vascular changes in a sural nervebiopsy of a case with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)
    • Schroder JM, Sellhaus B, Jorg J : Identification of the characteristic vascular changes in a sural nervebiopsy of a case with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). Acta Neuropathol 89 : 116-121, 1995
    • (1995) Acta Neuropathol , vol.89 , pp. 116-121
    • Schroder, J.M.1    Sellhaus, B.2    Jorg, J.3
  • 14
    • 0029050447 scopus 로고
    • Systemic vascular smooth muscle cell impairment in cerebral autosomal dominant arteriopathy with sub cortical infarcts and leukoencephalopathy
    • Ruchoux MM, Guerouaou D, Vandenhaute B, et al : Systemic vascular smooth muscle cell impairment in cerebral autosomal dominant arteriopathy with sub cortical infarcts and leukoencephalopathy. Acta Neuropathol 89 : 500-512, 1995
    • (1995) Acta Neuropathol , vol.89 , pp. 500-512
    • Ruchoux, M.M.1    Guerouaou, D.2    Vandenhaute, B.3
  • 15
    • 0028858163 scopus 로고
    • New phenotype of the cerebral autosomal dominant arteriopathy mapped to chromosome 19 : Migraine as the prominent clinical feature
    • Verin 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 Psychiat 59 : 579-585, 1995
    • (1995) J Neurol Neurosurg Psychiat , vol.59 , pp. 579-585
    • Verin, M.1    Rolland, Y.2    Landgraf, F.3
  • 16
    • 73849175819 scopus 로고
    • Subcortical arteriosclerotic encephalopathy : Review of the literature on the so-called Binswanger's disease and presentation of two cases
    • Olszewski J : Subcortical arteriosclerotic encephalopathy : review of the literature on the so-called Binswanger's disease and presentation of two cases. World Neurol 3 : 359-373, 1965
    • (1965) World Neurol , vol.3 , pp. 359-373
    • Olszewski, J.1
  • 17
    • 0018117605 scopus 로고
    • Clinical features of subcortical arteriosclerotic encephalopathy (Binswanger disease)
    • Caplan LR, Schoene WC : Clinical features of subcortical arteriosclerotic encephalopathy (Binswanger disease) Neurology 28 : 1206-1215, 1978
    • (1978) Neurology , vol.28 , pp. 1206-1215
    • Caplan, L.R.1    Schoene, W.C.2
  • 18
    • 0028901768 scopus 로고
    • Binswanger's disease-revisited
    • Caplan L R : Binswanger's disease-revisited. Neurology 45 : 626-633, 1995
    • (1995) Neurology , vol.45 , pp. 626-633
    • Caplan, L.R.1
  • 19
    • 0025296269 scopus 로고
    • Mutation of the Alzheimer's disease amyloid gene in hereditary cerebral hemorrhage. Dutch type
    • Levy E, Carman MD, Fernandez-Madrid IJ, et al : Mutation of the Alzheimer's disease amyloid gene in hereditary cerebral hemorrhage. Dutch type. Science 248 : 1124-1128, 1990
    • (1990) Science , vol.248 , pp. 1124-1128
    • Levy, E.1    Carman, M.D.2    Fernandez-Madrid, I.J.3
  • 20
    • 0017140935 scopus 로고
    • Familial unusual encephalopathy of Binswanger's type without hypertension
    • Maeda S, Nakayama H, Isaka K, et al : Familial unusual encephalopathy of Binswanger's type without hypertension. Folia Psychiatr Neurol Jpn 30 : 165-177, 1976
    • (1976) Folia Psychiatr Neurol Jpn , vol.30 , pp. 165-177
    • Maeda, S.1    Nakayama, H.2    Isaka, K.3
  • 21
    • 0022363706 scopus 로고
    • Chronic progressive leukoencephalopathy with systemic arteriosclerosis in young adults
    • Yokoi S, Nakayama H : Chronic progressive leukoencephalopathy with systemic arteriosclerosis in young adults. Clin Neuropathol 4 : 165-173, 1985
    • (1985) Clin Neuropathol , vol.4 , pp. 165-173
    • Yokoi, S.1    Nakayama, H.2
  • 22
    • 0023147465 scopus 로고
    • Subcortical vascular encephalopathy in a normotensive, young adult with premature baldness and spondylitis deformans A clinicopathological study and review of literature
    • Yamamura T, Nishimura M, Shirabe T, et al : Subcortical vascular encephalopathy in a normotensive, young adult with premature baldness and spondylitis deformans A clinicopathological study and review of literature. J Neurol Sci 78 : 175-188, 1987
    • (1987) J Neurol Sci , vol.78 , pp. 175-188
    • Yamamura, T.1    Nishimura, M.2    Shirabe, T.3
  • 23
    • 0028905614 scopus 로고
    • Familial young-adult-onset arteriosclerotic leukoencephalopathy with alopecia and lumbago without hypertension
    • Fukutake T, Hirayama K : Familial young-adult-onset arteriosclerotic leukoencephalopathy with alopecia and lumbago without hypertension. Eur Neurol 35 : 69-79, 1995
    • (1995) Eur Neurol , vol.35 , pp. 69-79
    • Fukutake, T.1    Hirayama, K.2
  • 24
    • 19244375510 scopus 로고    scopus 로고
    • Autosomal dominant early onset dementia and leu koencephalopathy in a Japanese family : Clinical, neuroimaging and genetic studies
    • Utatsu Y, Takashima H, Michizono K, et al : Autosomal dominant early onset dementia and leu koencephalopathy in a Japanese family : clinical, neuroimaging and genetic studies. J Neurol Sci 147 : 55-62, 1997
    • (1997) J Neurol Sci , vol.147 , pp. 55-62
    • Utatsu, Y.1    Takashima, H.2    Michizono, K.3
  • 25
    • 0028943944 scopus 로고
    • Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). Clinical, neuroimaging, pathological and genetic study of a large Italian family
    • 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 118 : 207-215, 1995
    • (1995) Brain , vol.118 , pp. 207-215
    • Sabbadini, G.1    Francia, A.2    Calandriello, L.3
  • 26
    • 0029834598 scopus 로고    scopus 로고
    • Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) : A morphological study of a German family
    • Bergmann M, Ebke M, Yuan Y, et al : Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) : a morphological study of a German family. Acta Neuropathol 92 : 341-350, 1996
    • (1996) Acta Neuropathol , vol.92 , pp. 341-350
    • Bergmann, M.1    Ebke, M.2    Yuan, Y.3
  • 27
    • 16044362074 scopus 로고    scopus 로고
    • Notch3 mutations in CADASIL. a hereditary adult-onset condition causing stroke and dementia
    • Joutel A, Corpechot C, Ducros A, et al : Notch3 mutations in CADASIL. a hereditary adult-onset condition causing stroke and dementia. Nature 383 : 707-710, 1996
    • (1996) Nature , vol.383 , pp. 707-710
    • Joutel, A.1    Corpechot, C.2    Ducros, A.3


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