-
1
-
-
0017750160
-
Hereditary multi-infarct dementia. Morphological and clinical studies of a new disease
-
Sourander P, Walinder J. Hereditary multi-infarct dementia. Morphological and clinical studies of a new disease. Acta Neuropathol (Berl). 1977;39:247-254.
-
(1977)
Acta Neuropathol (Berl)
, vol.39
, pp. 247-254
-
-
Sourander, P.1
Walinder, J.2
-
2
-
-
0027479304
-
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12
-
Tournier-Lasserve E, Joutel A, Melki J, et al. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12. Nat Genet. 1993;3:256-259.
-
(1993)
Nat Genet
, vol.3
, pp. 256-259
-
-
Tournier-Lasserve, E.1
Joutel, A.2
Melki, J.3
-
3
-
-
16044362074
-
Notch 3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia
-
Joutel A, Corpechot C, Ducros A, et al. Notch 3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia. Nature. 1996;383:707-710.
-
(1996)
Nature
, vol.383
, pp. 707-710
-
-
Joutel, A.1
Corpechot, C.2
Ducros, A.3
-
4
-
-
0033617522
-
Notch signaling: Cell fate control and signal integration in development
-
Artavanis-Tsakonas S, Rand MD, Lake RJ. Notch signaling: cell fate control and signal integration in development. Science. 1999;284: 770-776.
-
(1999)
Science
, vol.284
, pp. 770-776
-
-
Artavanis-Tsakonas, S.1
Rand, M.D.2
Lake, R.J.3
-
5
-
-
0029089247
-
Clinical spectrum of CADASIL: A study of 7 families. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
-
Chabriat H, Vahedi K, Iba-Zizen MT, et al. Clinical spectrum of CADASIL: a study of 7 families. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. Lancet. 1995; 346:934-939.
-
(1995)
Lancet
, vol.346
, pp. 934-939
-
-
Chabriat, H.1
Vahedi, K.2
Iba-Zizen, M.T.3
-
6
-
-
16344394175
-
The natural history of CADASIL
-
Davous P. The natural history of CADASIL. Stroke 1999;30:22-47.
-
(1999)
Stroke
, vol.30
, pp. 22-47
-
-
Davous, P.1
-
7
-
-
0033036190
-
The natural history of CADASIL: A pooled analysis of previously published cases
-
Desmond DW, Moroney JT, Lynch T, et al. The natural history of CADASIL: a pooled analysis of previously published cases. Stroke. 1999; 30:1230-1233.
-
(1999)
Stroke
, vol.30
, pp. 1230-1233
-
-
Desmond, D.W.1
Moroney, J.T.2
Lynch, T.3
-
8
-
-
0031784085
-
Patterns of MRI lesions in CADASIL
-
Chabriat H, Levy C, Taillia H, et al. Patterns of MRI lesions in CADASIL. Neurology. 1998;51:452-457.
-
(1998)
Neurology
, vol.51
, pp. 452-457
-
-
Chabriat, H.1
Levy, C.2
Taillia, H.3
-
9
-
-
0032909815
-
Brain stem MRI signal abnormalities in CADASIL
-
Chabriat H. Mrissa R, Levy C, et al. Brain stem MRI signal abnormalities in CADASIL. Stroke. 1999;30:457-459.
-
(1999)
Stroke
, vol.30
, pp. 457-459
-
-
Chabriat, H.1
Mrissa, R.2
Levy, C.3
-
10
-
-
0033499725
-
Characteristic MR lesion pattern and correlation of T1 and T2 lesion volume with neurologic and neuropsychological findings in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)
-
Yousry TA, Seelos K, Mayer M, et al. Characteristic MR lesion pattern and correlation of T1 and T2 lesion volume with neurologic and neuropsychological findings in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). AJNR Am J Neuroradiol. 1999;20:91-100.
-
(1999)
AJNR Am J Neuroradiol
, vol.20
, pp. 91-100
-
-
Yousry, T.A.1
Seelos, K.2
Mayer, M.3
-
11
-
-
0030884876
-
CADASIL: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
-
Ruchoux MM, Maurage CA. CADASIL: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. J Neuropathol Exp Neurol. 1997;56:947-964.
-
(1997)
J Neuropathol Exp Neurol
, vol.56
, pp. 947-964
-
-
Ruchoux, M.M.1
Maurage, C.A.2
-
12
-
-
0031930666
-
Endothelial changes in muscle and skin biopsies in patients with CADASIL
-
Ruchoux MM, Maurage CA. Endothelial changes in muscle and skin biopsies in patients with CADASIL. Neuropathol Appl Neurobiol. 1998; 24:60-65.
-
(1998)
Neuropathol Appl Neurobiol
, vol.24
, pp. 60-65
-
-
Ruchoux, M.M.1
Maurage, C.A.2
-
13
-
-
0028113875
-
Presence of ultrastructural arterial lesions in muscle and skin vessels of patients with CADASIL
-
Ruchoux MM, Chabriat H, Bousser MG, et al. Presence of ultrastructural arterial lesions in muscle and skin vessels of patients with CADASIL. Stroke. 1994;25:2291-2292.
-
(1994)
Stroke
, vol.25
, pp. 2291-2292
-
-
Ruchoux, M.M.1
Chabriat, H.2
Bousser, M.G.3
-
14
-
-
0029050447
-
Systemic vascular smooth muscle cell impairment in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
-
Ruchoux MM, Guerouaou D, Vandenhaute B. et al. Systemic vascular smooth muscle cell impairment in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. Acta Neuropathol (Berl). 1995;89:500-512.
-
(1995)
Acta Neuropathol (Berl)
, vol.89
, pp. 500-512
-
-
Ruchoux, M.M.1
Guerouaou, D.2
Vandenhaute, B.3
-
15
-
-
0028872678
-
Identification of the characteristic vascular changes in a sural nerve biopsy 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 nerve biopsy of a case with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). Acta Neuropathol (Berl). 1995;89:116-121.
-
(1995)
Acta Neuropathol (Berl)
, vol.89
, pp. 116-121
-
-
Schroder, J.M.1
Sellhaus, B.2
Jorg, J.3
-
16
-
-
0036942727
-
Morphometric analysis of ultrastructural vascular changes in CADASIL: Analysis of 50 skin biopsy specimens and pathogenic implications
-
Brulin P, Godfraind C, Leteurtre E, et al. Morphometric analysis of ultrastructural vascular changes in CADASIL: analysis of 50 skin biopsy specimens and pathogenic implications. Acta Neuropathol (Berl). 2002; 104:241-248.
-
(2002)
Acta Neuropathol (Berl)
, vol.104
, pp. 241-248
-
-
Brulin, P.1
Godfraind, C.2
Leteurtre, E.3
-
17
-
-
0036736182
-
CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy): A neurovascular disease diagnosed by ultrastructural examination of the skin
-
Kanitakis J, Thobois S, Claudy A, et al. CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy): a neurovascular disease diagnosed by ultrastructural examination of the skin. J Cutan Pathol. 2002;29:498-501.
-
(2002)
J Cutan Pathol
, vol.29
, pp. 498-501
-
-
Kanitakis, J.1
Thobois, S.2
Claudy, A.3
-
18
-
-
0033669757
-
CADASlL: The dermatologic diagnosis of a neurologic disease. Cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy
-
Rumbaugh JA, La DJ, Shan Y, et al. CADASlL: the dermatologic diagnosis of a neurologic disease. Cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy. J Am Acad Dermatol. 2000;43:1128-1130.
-
(2000)
J Am Acad Dermatol
, vol.43
, pp. 1128-1130
-
-
Rumbaugh, J.A.1
La, D.J.2
Shan, Y.3
-
19
-
-
0033674339
-
CADASlL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy): Diagnostic skin biopsy changes determined by electron microscopy
-
Walsh JS, Perniciaro C, Meschia JF. CADASlL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy): diagnostic skin biopsy changes determined by electron microscopy. J Am Acad Dermatol. 2000;43:1125-1127.
-
(2000)
J Am Acad Dermatol
, vol.43
, pp. 1125-1127
-
-
Walsh, J.S.1
Perniciaro, C.2
Meschia, J.F.3
-
20
-
-
0031738054
-
The phenotypic spectrum of CADASIL: Clinical findings in 102 cases
-
Dichgans M, Mayer M, Uttner I, et al. The phenotypic spectrum of CADASIL: clinical findings in 102 cases. Ann Neurol. 1998:44:731-739.
-
(1998)
Ann Neurol
, vol.44
, pp. 731-739
-
-
Dichgans, M.1
Mayer, M.2
Uttner, I.3
-
21
-
-
0034010024
-
De novo mutation in the Notch3 gene causing CADASIL
-
Joutel A, Dodick DD, Parisi JE, et al. De novo mutation in the Notch3 gene causing CADASIL. Ann Neurol. 2000;47:388-391.
-
(2000)
Ann Neurol
, vol.47
, pp. 388-391
-
-
Joutel, A.1
Dodick, D.D.2
Parisi, J.E.3
-
22
-
-
17644438177
-
The ectodomain of the Notch3 receptor accumulates within the cerebrovasculature of CADASIL patients
-
Joutel A, Andreux F, Gaulis S, et al. The ectodomain of the Notch3 receptor accumulates within the cerebrovasculature of CADASIL patients. J Clin Invest. 2000;105:597-605.
-
(2000)
J Clin Invest
, vol.105
, pp. 597-605
-
-
Joutel, A.1
Andreux, F.2
Gaulis, S.3
-
23
-
-
0032781960
-
Muscle and skin biopsies are a sensitive diagnostic tool in the diagnosis of CADASIL
-
Mayer M, Straube A, Bruening R, et al. Muscle and skin biopsies are a sensitive diagnostic tool in the diagnosis of CADASIL. J Neurol. 1999;246:526-532.
-
(1999)
J Neurol
, vol.246
, pp. 526-532
-
-
Mayer, M.1
Straube, A.2
Bruening, R.3
-
24
-
-
0031695156
-
Differential diagnosis of a vascular leukoencephalopathy within a CADASlL family: Use of skin biopsy electron microscopy study and direct genotypic screening
-
Furby A, Vahedi K, Force M, et al. Differential diagnosis of a vascular leukoencephalopathy within a CADASlL family: use of skin biopsy electron microscopy study and direct genotypic screening. J Neurol. 1998;245:734-740.
-
(1998)
J Neurol
, vol.245
, pp. 734-740
-
-
Furby, A.1
Vahedi, K.2
Force, M.3
-
25
-
-
0030854861
-
CADASIL: Skin biopsy allows diagnosis in early stages
-
Ebke M, Dichgans M, Bergmann M, et al. CADASIL: skin biopsy allows diagnosis in early stages. Acta Neurol Scand. 1997;95:351-357.
-
(1997)
Acta Neurol Scand
, vol.95
, pp. 351-357
-
-
Ebke, M.1
Dichgans, M.2
Bergmann, M.3
-
26
-
-
0037221480
-
Transgenic mice expressing mutant Notch3 develop vascular alterations characteristic of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
-
Ruchoux MM, Domenga V, Brulin P, et al. Transgenic mice expressing mutant Notch3 develop vascular alterations characteristic of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. Am J Pathol. 2003;162:329-342.
-
(2003)
Am J Pathol
, vol.162
, pp. 329-342
-
-
Ruchoux, M.M.1
Domenga, V.2
Brulin, P.3
|