-
1
-
-
16044362074
-
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 1996;383:707-710
-
(1996)
Nature
, vol.383
, pp. 707-710
-
-
Joutel, A.1
Corpechot, C.2
Ducros, A.3
-
2
-
-
0033036190
-
The natural history of CADASIL
-
Desmond D, Moroney J, Lynch T, Chan S, Chin S, Mohr JP. The natural history of CADASIL. Stroke 1999;30:1230-1233
-
(1999)
Stroke
, vol.30
, pp. 1230-1233
-
-
Desmond, D.1
Moroney, J.2
Lynch, T.3
Chan, S.4
Chin, S.5
Mohr, J.P.6
-
4
-
-
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
-
5
-
-
4043177097
-
Migraine with aura and brain magnetic resonance imaging abnormalities in patients with CADASIL
-
Vahedi K, Chabriat H, Levy C, Joutel A, Tournier-Lasserve E, Bousser MG. Migraine with aura and brain magnetic resonance imaging abnormalities in patients with CADASIL. Arch Neurol 2004;61:1237-1240
-
(2004)
Arch Neurol
, vol.61
, pp. 1237-1240
-
-
Vahedi, K.1
Chabriat, H.2
Levy, C.3
Joutel, A.4
Tournier-Lasserve, E.5
Bousser, M.G.6
-
6
-
-
0347003556
-
Retinal migraine as unusual feature of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)
-
Ravaglia S, Costa A, Santorelli FM, Nappi G, Moglia A. Retinal migraine as unusual feature of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). Cephalalgia 2004;24:74-77
-
(2004)
Cephalalgia
, vol.24
, pp. 74-77
-
-
Ravaglia, S.1
Costa, A.2
Santorelli, F.M.3
Nappi, G.4
Moglia, A.5
-
8
-
-
16344379266
-
Early diagnosis in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL): The role of MRI
-
Fattapposta F, Restuccia R, Pirro C et al. Early diagnosis in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL): the role of MRI. Funct Neurol 2004;19:239-242
-
(2004)
Funct Neurol
, vol.19
, pp. 239-242
-
-
Fattapposta, F.1
Restuccia, R.2
Pirro, C.3
-
9
-
-
0035852975
-
MRI hyperintensities of the temporal lobe and external capsule in patients with CADASIL
-
O'Sullivan M, Jarosz J, Martin RJ, Deasy N, Powell JF, Markus HS. MRI hyperintensities of the temporal lobe and external capsule in patients with CADASIL. Neurology 2001;56:628-634
-
(2001)
Neurology
, vol.56
, pp. 628-634
-
-
O'Sullivan, M.1
Jarosz, J.2
Martin, R.J.3
Deasy, N.4
Powell, J.F.5
Markus, H.S.6
-
10
-
-
0035140388
-
Differential lesion patterns in CADASIL and sporadic subcortical arteriosclerotic encephalopathy: MR imaging study with statistical parametric group comparison
-
Auer D, Putz B, Gossl C, Elbel G, Gasser T, Dichgans M. Differential lesion patterns in CADASIL and sporadic subcortical arteriosclerotic encephalopathy: MR imaging study with statistical parametric group comparison. Radiology 2001;218:443-451
-
(2001)
Radiology
, vol.218
, pp. 443-451
-
-
Auer, D.1
Putz, B.2
Gossl, C.3
Elbel, G.4
Gasser, T.5
Dichgans, M.6
-
11
-
-
33644835560
-
The spatial distribution of MR imaging abnormalities in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy and their relationship to age and clinical features
-
Singhal S, Rich P, Markus HS. The spatial distribution of MR imaging abnormalities in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy and their relationship to age and clinical features. Am J Neuroradiol 2005;26:2481-2487
-
(2005)
Am J Neuroradiol
, vol.26
, pp. 2481-2487
-
-
Singhal, S.1
Rich, P.2
Markus, H.S.3
-
12
-
-
0025735586
-
Familial subcortical dementia with arteriopathic leucoencephalopathy. A clinico-pathological case
-
Davous P, Fallet Bianco C. Familial subcortical dementia with arteriopathic leucoencephalopathy. A clinico-pathological case. Rev Neurol (Paris) 1991;147:376-384
-
(1991)
Rev Neurol (Paris)
, vol.147
, pp. 376-384
-
-
Davous, P.1
Fallet Bianco, C.2
-
13
-
-
0030884876
-
CADASIL: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
-
Ruchoux MM, Mange 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
Mange, C.A.2
-
14
-
-
0029050447
-
Systemic vascular smooth muscle cell impairment in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
-
Ruchoux MM, Guerouaou D, Vandenhaute B, Pruvo JP, Vermersch P, Leys D. 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
Pruvo, J.P.4
Vermersch, P.5
Leys, D.6
-
15
-
-
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
-
16
-
-
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
-
17
-
-
0031590602
-
Strong clustering and stereotyped nature of Notch 3 mutations in CADASIL patients
-
Joutel A, Vahedi K, Corpechot C et al. Strong clustering and stereotyped nature of Notch 3 mutations in CADASIL patients. Lancet 1997;350:1511-1515
-
(1997)
Lancet
, vol.350
, pp. 1511-1515
-
-
Joutel, A.1
Vahedi, K.2
Corpechot, C.3
-
19
-
-
22844446634
-
Spectrum of mutations in biopsy-proven CADASIL: Implications for diagnostic strategies
-
Peters N, Opherk C, Bergmann T, Castro M, Herzog J, Dichgans M. Spectrum of mutations in biopsy-proven CADASIL: implications for diagnostic strategies. Arch Neurol 2005;62:1091-1094
-
(2005)
Arch Neurol
, vol.62
, pp. 1091-1094
-
-
Peters, N.1
Opherk, C.2
Bergmann, T.3
Castro, M.4
Herzog, J.5
Dichgans, M.6
-
20
-
-
22144484846
-
The spectrum of mutations for CADASIL diagnosis
-
Federico A, Bianchi S, Dotti MT. The spectrum of mutations for CADASIL diagnosis. Neurol Sci 2005;26:117-124
-
(2005)
Neurol Sci
, vol.26
, pp. 117-124
-
-
Federico, A.1
Bianchi, S.2
Dotti, M.T.3
-
21
-
-
0035856449
-
NOTCH3 mutation involving three cysteine residues in a family with typical CADASIL
-
Dichgans M, Herzog J, Gasser T. NOTCH3 mutation involving three cysteine residues in a family with typical CADASIL. Neurology 2001;57:1714-1717
-
(2001)
Neurology
, vol.57
, pp. 1714-1717
-
-
Dichgans, M.1
Herzog, J.2
Gasser, T.3
-
22
-
-
0034624904
-
Splice site mutation causing a seven amino acid notch3 in-frame deletion in CADASIL
-
Joutel A, Chabriat H, Vahedi K et al. Splice site mutation causing a seven amino acid notch3 in-frame deletion in CADASIL. Neurology 2000;54:1874-1875
-
(2000)
Neurology
, vol.54
, pp. 1874-1875
-
-
Joutel, A.1
Chabriat, H.2
Vahedi, K.3
-
23
-
-
4344574903
-
The influence of genetic and cardiovascular risk factors on the CADASIL phenotype
-
Singhal S, Bevan S, Barrick T, Rich P, Markus HS. The influence of genetic and cardiovascular risk factors on the CADASIL phenotype. Brain 2004;127:2031-2038
-
(2004)
Brain
, vol.127
, pp. 2031-2038
-
-
Singhal, S.1
Bevan, S.2
Barrick, T.3
Rich, P.4
Markus, H.S.5
-
24
-
-
0028008517
-
Small arterial granular degeneration in familial Binswanger's syndrome
-
Gutierrez-Molina M, Caminero Rodriguez A, Martinez Garcia C, Arpa Gutierrez J, Morales Bastos C, Amer G. Small arterial granular degeneration in familial Binswanger's syndrome. Acta Neuropathol (Berl) 1994;87:98-105
-
(1994)
Acta Neuropathol (Berl)
, vol.87
, pp. 98-105
-
-
Gutierrez-Molina, M.1
Caminero Rodriguez, A.2
Martinez Garcia, C.3
Arpa Gutierrez, J.4
Morales Bastos, C.5
Amer, G.6
-
25
-
-
0030580175
-
An additional monogenic disorder that masquerades as multiple sclerosis
-
[letter]
-
Vahedi K, Tournier-Lasserve E, Vahedi K, Chabriat H, Bousser MG. An additional monogenic disorder that masquerades as multiple sclerosis. [letter] Am J Med Genet 1996;65:357-358
-
(1996)
Am J Med Genet
, vol.65
, pp. 357-358
-
-
Vahedi, K.1
Tournier-Lasserve, E.2
Vahedi, K.3
Chabriat, H.4
Bousser, M.G.5
-
26
-
-
0033502642
-
Distinguishing primary angiitis of the central nervous system from cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: The importance of family history
-
Williamson EE, Chukwudelunzu FE, Meschia JF, Witte RJ, Dickson DW, Cohen MD. Distinguishing primary angiitis of the central nervous system from cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: the importance of family history. Arthritis Rheum 1999;42:2243-2248
-
(1999)
Arthritis Rheum
, vol.42
, pp. 2243-2248
-
-
Williamson, E.E.1
Chukwudelunzu, F.E.2
Meschia, J.F.3
Witte, R.J.4
Dickson, D.W.5
Cohen, M.D.6
-
27
-
-
0033843087
-
Genetics and ischemic stroke
-
Hassan A, Markus HS. Genetics and ischemic stroke. Brain 2000;123:1784-1811
-
(2000)
Brain
, vol.123
, pp. 1784-1811
-
-
Hassan, A.1
Markus, H.S.2
-
28
-
-
27444432634
-
Is inadequate family history a barrier to diagnosis in CADASIL?
-
Razvi SS, Davidson R, Bone I, Muir KW. Is inadequate family history a barrier to diagnosis in CADASIL? Acta Neurol Scand 2005;112:323-326
-
(2005)
Acta Neurol Scand
, vol.112
, pp. 323-326
-
-
Razvi, S.S.1
Davidson, R.2
Bone, I.3
Muir, K.W.4
-
29
-
-
17644376503
-
The prevalence of cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) in the west of Scotland
-
Razvi SS, Davidson R, Bone I, Muir KW. The prevalence of cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) in the west of Scotland. J Neurol Neurosurg Psychiatry 2005;76: 739-741
-
(2005)
J Neurol Neurosurg Psychiatry
, vol.76
, pp. 739-741
-
-
Razvi, S.S.1
Davidson, R.2
Bone, I.3
Muir, K.W.4
-
30
-
-
3042690581
-
A two-year clinical follow-up study in 80 CADASIL subjects. Progression patterns and implications for clinical trials
-
Peters N, Herzog J, Opherk C, Dichgans M. A two-year clinical follow-up study in 80 CADASIL subjects. Progression patterns and implications for clinical trials. Stroke 2004; 35:1603-1608
-
(2004)
Stroke
, vol.35
, pp. 1603-1608
-
-
Peters, N.1
Herzog, J.2
Opherk, C.3
Dichgans, M.4
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