-
1
-
-
0027390357
-
Autosomal dominant leukoencephalopathy and subcortical ischemic stroke
-
Baudrimont M, Dubas F, Joutel A, Tournier-Lasserve E, Bousser MG (1993) Autosomal dominant leukoencephalopathy and subcortical ischemic stroke. Stroke 24:122-125
-
(1993)
Stroke
, vol.24
, pp. 122-125
-
-
Baudrimont, M.1
Dubas, F.2
Joutel, A.3
Tournier-Lasserve, E.4
Bousser, M.G.5
-
2
-
-
0029834598
-
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL): A morphological study of a German family
-
Bergmann M, Ebke M, Yuan Y, Brück W, Mugler M, Schwendemann G (1996) Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL): a morphological study of a German family. Acta Neuropathol 92:341-350
-
(1996)
Acta Neuropathol
, vol.92
, pp. 341-350
-
-
Bergmann, M.1
Ebke, M.2
Yuan, Y.3
Brück, W.4
Mugler, M.5
Schwendemann, G.6
-
3
-
-
0026455377
-
Leukoencéphalopathie artériopatique juvénile: Étude anatomoclinique d'un cas
-
Paris
-
Berthier E, Broussolle E, Garcia-Jacquier M, Tommasi M, Chazot G (1992) Leukoencéphalopathie artériopatique juvénile: étude anatomoclinique d'un cas. Rev Neurol (Paris) 148:146-149
-
(1992)
Rev Neurol
, vol.148
, pp. 146-149
-
-
Berthier, E.1
Broussolle, E.2
Garcia-Jacquier, M.3
Tommasi, M.4
Chazot, G.5
-
4
-
-
0029040890
-
Autosomal dominant migraine with MRI white-matter abnormalities mapping to the CADASIL locus
-
Chabriat H, Tournier-Lasserve E, Vahedi K, et al (1995) Autosomal dominant migraine with MRI white-matter abnormalities mapping to the CADASIL locus. Neurology 45:1086-1091
-
(1995)
Neurology
, vol.45
, pp. 1086-1091
-
-
Chabriat, H.1
Tournier-Lasserve, E.2
Vahedi, K.3
-
5
-
-
0029089247
-
Clinical spectrum of CADASIL: A study of 7 families
-
Chabriat H, Vahedi K, Iba-Zizen MT, et al (1995) Clinical spectrum of CADASIL: a study of 7 families. Lancet 346:934-939
-
(1995)
Lancet
, vol.346
, pp. 934-939
-
-
Chabriat, H.1
Vahedi, K.2
Iba-Zizen, M.T.3
-
6
-
-
0028986010
-
Hereditary multi-infarct dementia unlinked to chromosome 19q12 in a large scottish pedigree: Evidence of probable locus heterogeneity
-
Clair St D, Bolt J, Morris S, Doyle D (1995) Hereditary multi-infarct dementia unlinked to chromosome 19q12 in a large scottish pedigree: evidence of probable locus heterogeneity. J Med Genet 32:57-60
-
(1995)
J Med Genet
, vol.32
, pp. 57-60
-
-
St. Clair, D.1
Bolt, J.2
Morris, S.3
Doyle, D.4
-
7
-
-
0025735586
-
Démence sous-corticale familiale avec leucoencéphalopathie artériopatique: Observation clinico-pathologique
-
Paris
-
Davous P, Fallet-Bianco C (1991) Démence sous-corticale familiale avec leucoencéphalopathie artériopatique: observation clinico-pathologique. Rev Neurol (Paris) 5:376-384
-
(1991)
Rev Neurol
, vol.5
, pp. 376-384
-
-
Davous, P.1
Fallet-Bianco, C.2
-
8
-
-
0029932262
-
Identification of a key recombinant narrow the CADASIL gene region to 8 cM and argues against allelism of CADASIL and familial hemiplegic migraine
-
Dichgans M, Mayer M, Müller-Myhsok B, Straube A, Gasser T (1996) Identification of a key recombinant narrow the CADASIL gene region to 8 cM and argues against allelism of CADASIL and familial hemiplegic migraine. Genomics 32:151-154
-
(1996)
Genomics
, vol.32
, pp. 151-154
-
-
Dichgans, M.1
Mayer, M.2
Müller-Myhsok, B.3
Straube, A.4
Gasser, T.5
-
9
-
-
0021247932
-
Diagnostic electron microscopy on reembedded "popped off" areas of large Spurr epoxy sections
-
Di Sant'Agnese PA, Mesy Jensen KL de (1984) Diagnostic electron microscopy on reembedded "popped off" areas of large Spurr epoxy sections. Ultrastruct Pathol 6:247-253
-
(1984)
Ultrastruct Pathol
, vol.6
, pp. 247-253
-
-
Di Sant'Agnese, P.A.1
De Mesy Jensen, K.L.2
-
10
-
-
0029655609
-
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, genetic homogeneity, and mapping of the locus within a 2-cM interval
-
Ducros A, Nagy T, Alamowitch S, et al (1996) 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 58:171-181
-
(1996)
Am J Hum Genet
, vol.58
, pp. 171-181
-
-
Ducros, A.1
Nagy, T.2
Alamowitch, S.3
-
11
-
-
0025817198
-
Sclerosing vasculopathy of the central nervous system in non-elderly demented patients
-
Estes ML, Chimowitz ML, Awad IA, McMahon JT, Furlan AJ, Ratliff NB (1991) Sclerosing vasculopathy of the central nervous system in non-elderly demented patients. Arch Neurol 48: 631-636
-
(1991)
Arch Neurol
, vol.48
, pp. 631-636
-
-
Estes, M.L.1
Chimowitz, M.L.2
Awad, I.A.3
McMahon, J.T.4
Furlan, A.J.5
Ratliff, N.B.6
-
13
-
-
0006897564
-
Extracerebral biopsy in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)
-
Goebel HH, Meyermann R, Schlote W, Rosin R (1996) Extracerebral biopsy in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). J Neuropathol Exp Neurol 55:648
-
(1996)
J Neuropathol Exp Neurol
, vol.55
, pp. 648
-
-
Goebel, H.H.1
Meyermann, R.2
Schlote, W.3
Rosin, R.4
-
14
-
-
0028271418
-
Autosomal dominant arteriopathic leukoencephalopathy and Alzheimer's disease
-
Gray F, Robert F, Labrecque R, Chrétien F, Baudrimont M, Fallet-Bianco C, Mikol J, Vinters HV (1994) Autosomal dominant arteriopathic leukoencephalopathy and Alzheimer's disease. Neuropathol Appl Neurobiol 20:22-30
-
(1994)
Neuropathol Appl Neurobiol
, vol.20
, pp. 22-30
-
-
Gray, F.1
Robert, F.2
Labrecque, R.3
Chrétien, F.4
Baudrimont, M.5
Fallet-Bianco, C.6
Mikol, J.7
Vinters, H.V.8
-
16
-
-
1842296090
-
Schweizer Familie mit CADASIL-syndrome (Cerebrale autosomal dominante Arteriopathie mit subcorticalen Infarkten und Leukoenzephalopathie) und assoziiertem Protein-S-Mangel
-
Güntert D, Hungerbühler H, Gessaga E, Schäfer H, Hess K (1994) Schweizer Familie mit CADASIL-syndrome (Cerebrale autosomal dominante Arteriopathie mit subcorticalen Infarkten und Leukoenzephalopathie) und assoziiertem Protein-S-Mangel. Verh Dtsch Ges Neurol 8:353-356
-
(1994)
Verh Dtsch Ges Neurol
, vol.8
, pp. 353-356
-
-
Güntert, D.1
Hungerbühler, H.2
Gessaga, E.3
Schäfer, H.4
Hess, K.5
-
17
-
-
0028008517
-
Small arterial granular degeneration in familiar Binswanger's syndrome
-
Gutierrez-Molina M, Rodriguez AC, García CM, Gutierrez JA, Bastos CM, Amer G (1994) Small arterial granular degeneration in familiar Binswanger's syndrome. Acta Neuropathol 87: 98-105
-
(1994)
Acta Neuropathol
, vol.87
, pp. 98-105
-
-
Gutierrez-Molina, M.1
Rodriguez, A.C.2
García, C.M.3
Gutierrez, J.A.4
Bastos, C.M.5
Amer, G.6
-
18
-
-
0346031709
-
Classification and diagnostic criteria for headache disorders, cranial neuralgias and facial pain
-
Headache Classification Committee of the International Headache Society (1988) Classification and diagnostic criteria for headache disorders, cranial neuralgias and facial pain. Cephalalgia 8:1-96
-
(1988)
Cephalalgia
, vol.8
, pp. 1-96
-
-
-
19
-
-
0028785253
-
Familial hemiplegic migraine and autosomal dominant arteriopathy with leukoencephalopathy (CADASIL)
-
Hutchinson M, O'Riordan J, Javed M, Quin E, Macerlaine D, Willcox T, Parfrey N, Nagy TG, Tournier-Lasserve E (1995) Familial hemiplegic migraine and autosomal dominant arteriopathy with leukoencephalopathy (CADASIL). Ann Neurol 38:817-824
-
(1995)
Ann Neurol
, vol.38
, pp. 817-824
-
-
Hutchinson, M.1
O'Riordan, J.2
Javed, M.3
Quin, E.4
Macerlaine, D.5
Willcox, T.6
Parfrey, N.7
Nagy, T.G.8
Tournier-Lasserve, E.9
-
20
-
-
0027256756
-
αB-crystallin in oxidative muscle fibers and its accumulation in ragged-red fibers: A comparative immunohistochemical and histochemical study in human skeletal muscle
-
Iwaki T, Iwaki A, Goldman JE (1993) αB-crystallin in oxidative muscle fibers and its accumulation in ragged-red fibers: a comparative immunohistochemical and histochemical study in human skeletal muscle. Acta Neuropathol 85:475-480
-
(1993)
Acta Neuropathol
, vol.85
, pp. 475-480
-
-
Iwaki, T.1
Iwaki, A.2
Goldman, J.E.3
-
21
-
-
0027306090
-
A gene for familial hemiplegic migraine maps to chromosome 19
-
Joutel A, Bousser MG, Biousse V, et al (1993) A gene for familial hemiplegic migraine maps to chromosome 19. Nature Genet 5:40-45
-
(1993)
Nature Genet
, vol.5
, pp. 40-45
-
-
Joutel, A.1
Bousser, M.G.2
Biousse, V.3
-
22
-
-
16044362074
-
Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia
-
Joutel A, Corpechot C, Ducros A. et al (1996) Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia. Nature 383:707-710
-
(1996)
Nature
, vol.383
, pp. 707-710
-
-
Joutel, A.1
Corpechot, C.2
Ducros, A.3
-
23
-
-
0029096518
-
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: A clinicopathological and genetic study of a Swiss family
-
Jung HH, Bassetti C, Tournier-Lasserve E, Vahedi K, Arnaboldi M, Blatter Arifi V, Burgunder JM (1995) 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)
J Neurol Neurosurg Psychiatry
, vol.59
, pp. 138-143
-
-
Jung, H.H.1
Bassetti, C.2
Tournier-Lasserve, E.3
Vahedi, K.4
Arnaboldi, M.5
Blatter Arifi, V.6
Burgunder, J.M.7
-
24
-
-
0029065542
-
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) - Confirmation by cerebral biopsy in two cases
-
Lammie GA, Rakshi J, Rossor MN, Harding AE, Scaravilli F (1995) Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) - confirmation by cerebral biopsy in two cases. Clin Neuropathol 14: 201-206
-
(1995)
Clin Neuropathol
, vol.14
, pp. 201-206
-
-
Lammie, G.A.1
Rakshi, J.2
Rossor, M.N.3
Harding, A.E.4
Scaravilli, F.5
-
25
-
-
0020026639
-
Subcortical arteriosclerotic encephalopathy (Binswanger's type) and cortical infarcts in a young normotensive patient
-
Loizou LA, Jefferson JM, Smith WT (1982) Subcortical arteriosclerotic encephalopathy (Binswanger's type) and cortical infarcts in a young normotensive patient. J Neurol Neurosurg Psychiatry 45:409-417
-
(1982)
J Neurol Neurosurg Psychiatry
, vol.45
, pp. 409-417
-
-
Loizou, L.A.1
Jefferson, J.M.2
Smith, W.T.3
-
26
-
-
0026541969
-
αB-crystallin expression in non-lenticular tissues and selective presence in ubiquitinated inclusion bodies in human disease
-
Lowe J, McDermott H, Pike I, Spendlove I, Landon M, Mayer RJ (1992) αB-crystallin expression in non-lenticular tissues and selective presence in ubiquitinated inclusion bodies in human disease. J Pathol 166:61-68
-
(1992)
J Pathol
, vol.166
, pp. 61-68
-
-
Lowe, J.1
McDermott, H.2
Pike, I.3
Spendlove, I.4
Landon, M.5
Mayer, R.J.6
-
27
-
-
0028891783
-
Apoptosis, oncosis, and necrosis: An overview of cell death
-
Majno G, Joris I (1995) Apoptosis, oncosis, and necrosis: an overview of cell death. Am J Pathol 146:3-15
-
(1995)
Am J Pathol
, vol.146
, pp. 3-15
-
-
Majno, G.1
Joris, I.2
-
28
-
-
0026664380
-
A familial disorder with subcortical ischemic strokes, dementia and leukoencephalopathy
-
Mas JL, Dilouya A, Recondo J (1992) A familial disorder with subcortical ischemic strokes, dementia and leukoencephalopathy. Neurology 42:1015-1019
-
(1992)
Neurology
, vol.42
, pp. 1015-1019
-
-
Mas, J.L.1
Dilouya, A.2
Recondo, J.3
-
29
-
-
0029092525
-
An italian kindred with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)
-
Ragno M, Tournier-Lasserve E, Fiori M, et al (1995) An italian kindred with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). Ann Neurol 38:231-236
-
(1995)
Ann Neurol
, vol.38
, pp. 231-236
-
-
Ragno, M.1
Tournier-Lasserve, E.2
Fiori, M.3
-
30
-
-
0028113875
-
Presence of ultrastructural arterial lesions in muscle and skin vessels of patients with CADASIL
-
Ruchoux MM, Chabriat H, Bousser MG, Baudrimont M, Tournier-Lasserve E (1994) Presence of ultrastructural arterial lesions in muscle and skin vessels of patients with CADASIL. Stroke 25:2291-2292
-
(1994)
Stroke
, vol.25
, pp. 2291-2292
-
-
Ruchoux, M.M.1
Chabriat, H.2
Bousser, M.G.3
Baudrimont, M.4
Tournier-Lasserve, E.5
-
31
-
-
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 (1995) Systemic vascular smooth muscle cell impairment in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. Acta Neuropathol 89:500-512
-
(1995)
Acta Neuropathol
, 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
-
32
-
-
0028943944
-
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, Di Biasi C, Trasimeni G, Gualdi GF, Palladini G, Manfredi M, Frontali M (1995) 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)
Brain
, vol.118
, pp. 207-215
-
-
Sabbadini, G.1
Francia, A.2
Calandriello, L.3
Di Biasi, C.4
Trasimeni, G.5
Gualdi, G.F.6
Palladini, G.7
Manfredi, M.8
Frontali, M.9
-
33
-
-
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)
-
Schröder JM, Sellhaus B, Jörg J (1995) 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 89:116-121
-
(1995)
Acta Neuropathol
, vol.89
, pp. 116-121
-
-
Schröder, J.M.1
Sellhaus, B.2
Jörg, J.3
-
34
-
-
0017750160
-
Hereditary multi-infarct dementia. Morphological and clinical studies of a new disease
-
Berl
-
Sourander P, Walinder J (1977) Hereditary multi-infarct dementia. Morphological and clinical studies of a new disease. Acta Neuropathol (Berl) 39:247-254
-
(1977)
Acta Neuropathol
, vol.39
, pp. 247-254
-
-
Sourander, P.1
Walinder, J.2
-
35
-
-
0017782948
-
Chronic familiar vascular encephalopathy
-
Stevens DL, Hewlett RH, Brownell B (1977) Chronic familiar vascular encephalopathy. Lancet II:1364-1365
-
(1977)
Lancet
, vol.2
, pp. 1364-1365
-
-
Stevens, D.L.1
Hewlett, R.H.2
Brownell, B.3
-
36
-
-
0025947095
-
Autosomal dominant syndrome with stroke like episodes and leukoencephalopathy
-
Tournier-Lasserve E, Iba-Zizen MT, Romero N, Bousser MG (1991) Autosomal dominant syndrome with stroke like episodes and leukoencephalopathy. Stroke 22:1297-1302
-
(1991)
Stroke
, vol.22
, pp. 1297-1302
-
-
Tournier-Lasserve, E.1
Iba-Zizen, M.T.2
Romero, N.3
Bousser, M.G.4
-
37
-
-
0019851945
-
Formation of "ghost" bodies and calcification in experimental atherosclerosis in nonhuman primates: An ultrastructural study
-
Trillo AA (1981) Formation of "ghost" bodies and calcification in experimental atherosclerosis in nonhuman primates: an ultrastructural study. Virchows Arch [B] 38:127-139
-
(1981)
Virchows Arch [B]
, vol.38
, pp. 127-139
-
-
Trillo, A.A.1
-
38
-
-
0016776463
-
Elektronmikroskopische Untersuchungen zur Entstehung von 'ghost bodies' in Aorten
-
Veltmann E, Backwinkel KP, Themann H, Hauss WH (1975) Elektronmikroskopische Untersuchungen zur Entstehung von 'ghost bodies' in Aorten. Virchows Arch [A] 367:281-288
-
(1975)
Virchows Arch [A]
, vol.367
, pp. 281-288
-
-
Veltmann, E.1
Backwinkel, K.P.2
Themann, H.3
Hauss, W.H.4
|