-
1
-
-
0031898673
-
Autosomal dominant cerebral arteriopathy: Neuropsychiatric syndrome in a family
-
Adair JC, Hart BR, Kornfeld M, Graham GD, Swanda RM, Ptacek LJ, Davis LE: Autosomal dominant cerebral arteriopathy: neuropsychiatric syndrome in a family. Neuropsych Neuropsychol Beh Neurol, 1998, 11, 31-39.
-
(1998)
Neuropsych Neuropsychol Beh Neurol
, vol.11
, pp. 31-39
-
-
Adair, J.C.1
Hart, B.R.2
Kornfeld, M.3
Graham, G.D.4
Swanda, R.M.5
Ptacek, L.J.6
Davis, L.E.7
-
2
-
-
0027390357
-
Autosomal dominant leukoencephalopathy and subcortical ischemic stroke. A clinico- pathological study
-
Baudrimont M, Dubas F, Joutel A, Toumier-Lasserve E, Bousser MG: Autosomal dominant leukoencephalopathy and subcortical ischemic stroke. A clinico-pathological study. Stroke, 1993, 24, 122-125.
-
(1993)
Stroke
, vol.24
, pp. 122-125
-
-
Baudrimont, M.1
Dubas, F.2
Joutel, A.3
Toumier-Lasserve, E.4
Bousser, M.G.5
-
3
-
-
0029834598
-
Cerebral autosmal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL): A morphological study of a German family
-
Berl
-
Bergmann M, Ebke M, Yuan Y, Bruck W, Mugler M, Schwendemann G: Cerebral autosmal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL): a morphological study of a German family. Acta Neuropathol (Berl), 1996, 92, 341-350.
-
(1996)
Acta Neuropathol
, vol.92
, pp. 341-350
-
-
Bergmann, M.1
Ebke, M.2
Yuan, Y.3
Bruck, W.4
Mugler, M.5
Schwendemann, G.6
-
4
-
-
0031469486
-
Mortality from hereditary cerebral haemorrhage with amyloidosis - Dutch type. The impact of sex, parental transmission and year of birth
-
Bornebroek M, Westendorp RGJ, Haan J, Bakker E, Timmers WF, Van Broeckhovev C, Roos RAC: Mortality from hereditary cerebral haemorrhage with amyloidosis - Dutch type. The impact of sex, parental transmission and year of birth. Brain, 1997, 120, 2243-2249.
-
(1997)
Brain
, vol.120
, pp. 2243-2249
-
-
Bornebroek, M.1
Westendorp, R.G.J.2
Haan, J.3
Bakker, E.4
Timmers, W.F.5
Van Broeckhovev, C.6
Roos, R.A.C.7
-
5
-
-
0031661678
-
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL). Neuropathological and in vitro studies of abnormal elastogenesis
-
Caronti B, Calandriello LTA, Francia B, Scorretti L, Manfredi M, Sansolini T, Pennisi EM, Calderaro C, Palladini G: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL). Neuropathological and in vitro studies of abnormal elastogenesis. Acta Neurol Scand, 1998, 98, 259-267.
-
(1998)
Acta Neurol Scand
, vol.98
, pp. 259-267
-
-
Caronti, B.1
Calandriello, L.T.A.2
Francia, B.3
Scorretti, L.4
Manfredi, M.5
Sansolini, T.6
Pennisi, E.M.7
Calderaro, C.8
Palladini, G.9
-
6
-
-
0029040890
-
Autosomal dominant migraine with MRI white matter abnormalities mapping to the CADASIL locus
-
Chabrait H, Tournier-Lasserve E, Vahedi K, Leys D, Joutel A, Nibbio A, Escaillas JP, Iba-Zizen MT, Bracard S, Tehindrazanarivelo A, Gastaut JL, Bousser MG: Autosomal dominant migraine with MRI white matter abnormalities mapping to the CADASIL locus. Neurology, 1995A, 45, 1086-1091.
-
(1995)
Neurology
, vol.45
, pp. 1086-1091
-
-
Chabrait, H.1
Tournier-Lasserve, E.2
Vahedi, K.3
Leys, D.4
Joutel, A.5
Nibbio, A.6
Escaillas, J.P.7
Iba-Zizen, M.T.8
Bracard, S.9
Tehindrazanarivelo, A.10
Gastaut, J.L.11
Bousser, M.G.12
-
7
-
-
0029089247
-
Clinical spectrum of CADASIL: A study of 7 families
-
Chabrait H, Vahedi K, Iba-Zizen MT, Joutel A, Nibbio A, Nagy TG, Krebs MO, Julien J, Dubois B, Ducrocq X, Levasseur M, Homeyer P, Mas JL, Lyon-Caen O, Tournier-Lasserve E, Bousser MG: Clinical spectrum of CADASIL: a study of 7 families. Lancet, 1995B, 346, 934-939.
-
(1995)
Lancet
, vol.346
, pp. 934-939
-
-
Chabrait, H.1
Vahedi, K.2
Iba-Zizen, M.T.3
Joutel, A.4
Nibbio, A.5
Nagy, T.G.6
Krebs, M.O.7
Julien, J.8
Dubois, B.9
Ducrocq, X.10
Levasseur, M.11
Homeyer, P.12
Mas, J.L.13
Lyon-Caen, O.14
Tournier-Lasserve, E.15
Bousser, M.G.16
-
8
-
-
0031784085
-
Patterns of MRI lesions in CADASIL
-
Chabriat H. Levy C, Taillia H, Iba-Zizen MT, Vahedi K, Joutel A, Tournier-Lasserve E, Bousser MG: 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
Iba-Zizen, M.T.4
Vahedi, K.5
Joutel, A.6
Tournier-Lasserve, E.7
Bousser, M.G.8
-
9
-
-
44049123201
-
Workshop pseudoxanthoma elasticum. Molecular biology and pathology of elastic fibers
-
Christiano AM, Lebwohl MG, Boyd ChD, Uitto J: Workshop pseudoxanthoma elasticum. Molecular biology and pathology of elastic fibers. J Invest Derm, 1992, 99, 660-663.
-
(1992)
J Invest Derm
, vol.99
, pp. 660-663
-
-
Christiano, A.M.1
Lebwohl, M.G.2
Boyd, Ch.D.3
Uitto, J.4
-
10
-
-
84901305077
-
CADASIL in an African-American family
-
Abst P06067
-
Cohen BA, Quinn B, Meeks JJ, Kaplan J, Han-Xiang Deng, Siddique T: CADASIL in an African-American family. Neurology, 1999, 52, Suppl 2, Abst P06067.
-
(1999)
Neurology
, vol.52
, Issue.2 SUPPL.
-
-
Cohen, B.A.1
Quinn, B.2
Meeks, J.J.3
Kaplan, J.4
Deng, H.-X.5
Siddique, T.6
-
11
-
-
0025735586
-
Demence sous-corticale familiale avec leucoencephalopathie arteriopathique. Observation clinico-pathologiqué
-
Paris
-
Davous P, Fallet-Bianco C: Demence sous-corticale familiale avec leucoencephalopathie arteriopathique. Observation clinico-pathologiqué. Rev Neurol (Paris), 1991, 147, 376-384.
-
(1991)
Rev Neurol
, vol.147
, pp. 376-384
-
-
Davous, P.1
Fallet-Bianco, C.2
-
12
-
-
0031751315
-
CADASIL in a North American family. Clinical, pathologic and radiologie findings
-
Desmond DW, Moroney JT, Lynch T, Chan S, Chin SS, Shungu DC, Naini AB, Mohr JP: CADASIL in a North American family. Clinical, pathologic and radiologie findings. Neurology, 1998, 51, 844-849.
-
(1998)
Neurology
, vol.51
, pp. 844-849
-
-
Desmond, D.W.1
Moroney, J.T.2
Lynch, T.3
Chan, S.4
Chin, S.S.5
Shungu, D.C.6
Naini, A.B.7
Mohr, J.P.8
-
13
-
-
0031738054
-
The phenotypic spectrum of CADASIL: Clinical findings in 102 cases
-
Dichgans M, Mayer M, Uttner I, Bruning R, Muller-Hocker J, Rungger G, Ebke M, Klockgether T, Gasser T: 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
Bruning, R.4
Muller-Hocker, J.5
Rungger, G.6
Ebke, M.7
Klockgether, T.8
Gasser, T.9
-
14
-
-
0031695156
-
Differential diagnosis of a vascular leukoencephalopathy within a CADASIL family: Use of skin biopsy electron microscopy study and direct genotypic screening
-
Furby A, Vahedi K, Force M, Larrouy S, Ruchoux MM, Joutel A, Tournier-Lasserve E: 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.
-
(1998)
J Neurol
, vol.245
, pp. 734-740
-
-
Furby, A.1
Vahedi, K.2
Force, M.3
Larrouy, S.4
Ruchoux, M.M.5
Joutel, A.6
Tournier-Lasserve, E.7
-
15
-
-
0030931256
-
Characteristic morphologic manifestation of CADASIL, cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy, in skeletal muscle and skin
-
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.
-
(1997)
Muscle Nerve
, vol.20
, pp. 625-627
-
-
Goebel, H.H.1
Meyermann, R.2
Rosin, R.3
Schlote, W.4
-
16
-
-
0028008517
-
Small arterial granular degeneration in familial Binswanger's syndrome
-
Berl
-
Guitierrez-Molina M, Caminero RA, Martinez GC, Arpa GI, Morales BC, Amer G: Small arterial granular degeneration in familial Binswanger's syndrome. Acta Neuropathol (Berl), 1994, 87, 98-105.
-
(1994)
Acta Neuropathol
, vol.87
, pp. 98-105
-
-
Guitierrez-Molina, M.1
Caminero, R.A.2
Martinez, G.C.3
Arpa, G.I.4
Morales, B.C.5
Amer, G.6
-
17
-
-
0029347120
-
The role of beta-amyloid in the development of Alzheimer's disease
-
Ii-K: The role of beta-amyloid in the development of Alzheimer's disease. Drugs-Aging, 1995, 7, 97-109.
-
(1995)
Drugs-Aging
, vol.7
, pp. 97-109
-
-
Ii-K1
-
18
-
-
0030712287
-
Hereditary endotheliopathy with retinopathy, nephropathy, and stroke (HERNS)
-
Jen J, Cohen AH, Yue Q, Stout JT, Vinters HV, Nelson S, Baloh RW: Hereditary endotheliopathy with retinopathy, nephropathy, and stroke (HERNS). Neurology, 1997, 49, 1322-1330.
-
(1997)
Neurology
, vol.49
, pp. 1322-1330
-
-
Jen, J.1
Cohen, A.H.2
Yue, Q.3
Stout, J.T.4
Vinters, H.V.5
Nelson, S.6
Baloh, R.W.7
-
19
-
-
16044362074
-
Notch 3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia
-
Joutel A, Corpechot C, Ducros A, Vahedi K, Chabriat H, Mouton P, Alamowitch S, Domenga V, Cecillon M, Marechal E, Maciazek J, Vayssiere C, Cruaud C, Cabanis EA, Ruchoux MM, Weissenbach J, Bach JF, Bousser MG, Tournier-Lasserve E: 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
Vahedi, K.4
Chabriat, H.5
Mouton, P.6
Alamowitch, S.7
Domenga, V.8
Cecillon, M.9
Marechal, E.10
Maciazek, J.11
Vayssiere, C.12
Cruaud, C.13
Cabanis, E.A.14
Ruchoux, M.M.15
Weissenbach, J.16
Bach, J.F.17
Bousser, M.G.18
Tournier-Lasserve, E.19
-
20
-
-
0031590602
-
Strong clustering and stereotyped nature of Notch 3 mutations in CADASIL patients
-
Joutel A, Vahedi K, Corpechot C, Troesch A, Chabriat H, Vayssiere C, Cruaud C, Maciazek J, Weissenbach J, Bousser MG, Bach JF, Toumier-Lasserve E: 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
Troesch, A.4
Chabriat, H.5
Vayssiere, C.6
Cruaud, C.7
Maciazek, J.8
Weissenbach, J.9
Bousser, M.G.10
Bach, J.F.11
Toumier-Lasserve, E.12
-
21
-
-
0001018886
-
Vascular disease
-
DI Graham, PL Lantos (eds). Arnold, London, Sydney, Auckland
-
Kalimo H, Kaste M, Haltia M: Vascular disease. In Greenfield Neuropathology. DI Graham, PL Lantos (eds). Arnold, London, Sydney, Auckland, 1997, I, 315-353.
-
(1997)
Greenfield Neuropathology
, vol.1
, pp. 315-353
-
-
Kalimo, H.1
Kaste, M.2
Haltia, M.3
-
22
-
-
0029065542
-
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASlL) - Confirmation by cerebral biopsy in 2 cases
-
Lammie GA, Rakshi J, Rossor MN, Harding AE, Scaravilli F: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASlL) - confirmation by cerebral biopsy in 2 cases. Clin Neuropathol, 1995, 14, 210-206.
-
(1995)
Clin Neuropathol
, vol.14
, pp. 210-1206
-
-
Lammie, G.A.1
Rakshi, J.2
Rossor, M.N.3
Harding, A.E.4
Scaravilli, F.5
-
23
-
-
8944257612
-
Clinicopathological and genetic studies of two further Italian families with cerebral autosomal dominant arteriopathy
-
Berl
-
Malandrini A, Carrera P, Palmeri S, Cavallaro T, Fabrizi GM, Villanova M, Fattaposta M, Vismara L, Brancollini V, Tanganelli P, Cali A, Morocutti C, Zeviani M, Ferrari M, Guazzi GC: Clinicopathological and genetic studies of two further Italian families with cerebral autosomal dominant arteriopathy. Acta Neuropathol (Berl), 1996, 92, 115-122.
-
(1996)
Acta Neuropathol
, vol.92
, pp. 115-122
-
-
Malandrini, A.1
Carrera, P.2
Palmeri, S.3
Cavallaro, T.4
Fabrizi, G.M.5
Villanova, M.6
Fattaposta, M.7
Vismara, L.8
Brancollini, V.9
Tanganelli, P.10
Cali, A.11
Morocutti, C.12
Zeviani, M.13
Ferrari, M.14
Guazzi, G.C.15
-
24
-
-
0026664380
-
A familial disorder with subcortical ischemic strokes, dementia, and leukoencephalopathy
-
Mas JL, Dilouya A, de Recondo J: A familial disorder with subcortical ischemic strokes, dementia, and leukoencephalopathy. Neurology, 1992, 42, 1015-1019.
-
(1992)
Neurology
, vol.42
, pp. 1015-1019
-
-
Mas, J.L.1
Dilouya, A.2
De Recondo, J.3
-
25
-
-
0345367425
-
SPECT study of a German CADASIL family. A phenotype with migraine and progressive dementia only
-
Mellies JK, Baumer T, Muller JA, Toumier-Lasserve E, Chabriat H, Knobloch O, Hackeloer HJ, Goebel HH, Wetzig L, Haller P: SPECT study of a German CADASIL family. A phenotype with migraine and progressive dementia only. Neurology, 1998, 50, 1715-1721.
-
(1998)
Neurology
, vol.50
, pp. 1715-1721
-
-
Mellies, J.K.1
Baumer, T.2
Muller, J.A.3
Toumier-Lasserve, E.4
Chabriat, H.5
Knobloch, O.6
Hackeloer, H.J.7
Goebel, H.H.8
Wetzig, L.9
Haller, P.10
-
26
-
-
0014816024
-
Pseudoxanthoma elasticum. Report of an autopsied case with cerebral involvement
-
Messis ChP, Budzilovich GN: Pseudoxanthoma elasticum. Report of an autopsied case with cerebral involvement. Neurology, 1970, 20, 703-709.
-
(1970)
Neurology
, vol.20
, pp. 703-709
-
-
Messis, Ch.P.1
Budzilovich, G.N.2
-
27
-
-
13144261781
-
Familial internal carotid dissection
-
Perez-Errazquin F, Gil-Peralta A, Garzon FJ, Salinas E, Franco E: Familial internal carotid dissection. (in Spanish) Neurology, 1998, 13, 247-249.
-
(1998)
Neurology
, vol.13
, pp. 247-249
-
-
Perez-Errazquin, F.1
Gil-Peralta, A.2
Garzon, F.J.3
Salinas, E.4
Franco, E.5
-
28
-
-
0016249745
-
Autosomal dominant pseudoxanthoma elasticum
-
Pope FM: Autosomal dominant pseudoxanthoma elasticum. J Med Gen, 1974, 11, 152-157.
-
(1974)
J Med Gen
, vol.11
, pp. 152-157
-
-
Pope, F.M.1
-
29
-
-
0030875945
-
Phenotypic variability of CADASIL and novel morphologic findings
-
Berl
-
Rubio A, Rifkin D, Powers JM, Patel U, Stewart I, Faust P, Goldman JE, Mohr JP, Numaguchi Y, Jensen K: Phenotypic variability of CADASIL and novel morphologic findings. Acta Neuropathol (Berl), 1997, 94, 247-254.
-
(1997)
Acta Neuropathol
, vol.94
, pp. 247-254
-
-
Rubio, A.1
Rifkin, D.2
Powers, J.M.3
Patel, U.4
Stewart, I.5
Faust, P.6
Goldman, J.E.7
Mohr, J.P.8
Numaguchi, Y.9
Jensen, K.10
-
30
-
-
0029050447
-
Systemic vascular smooth muscle cell imairment in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
-
Berl
-
Ruchoux MM, Guerouaou D, Vandenhaute B, Pruvo JP, Vermersch P, Leys D: Systemic vascular smooth muscle cell imairment in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. Acta Neuropathol (Berl), 1995, 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
-
31
-
-
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
-
32
-
-
0031930666
-
Endothelial changes in muscle and skin bipsies in patient with CADASIL
-
Ruchoux MM, Maurage CA: Endothelial changes in muscle and skin bipsies in patient with CADASIL. Neuropathol Appl Neurobiol, 1998, 23, 60-65.
-
(1998)
Neuropathol Appl Neurobiol
, vol.23
, pp. 60-65
-
-
Ruchoux, M.M.1
Maurage, C.A.2
-
33
-
-
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: 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.
-
(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
-
34
-
-
84901352408
-
Objective study the pathological and radiological findings in a 58 year old woman with familial history of subcortical dementia, mood and behavioral disorder
-
San Francisco, Abstr S2808
-
Salloway SR, Stopa E: Objective study the pathological and radiological findings in a 58 year old woman with familial history of subcortical dementia, mood and behavioral disorder. AAN 48th Annual Meeting, San Francisco, 1996, Abstr S2808.
-
(1996)
AAN 48th Annual Meeting
-
-
Salloway, S.R.1
Stopa, E.2
-
35
-
-
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)
-
Berl
-
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
, vol.89
, pp. 116-121
-
-
Schroder, J.M.1
Sellhaus, B.2
Jorg, J.3
-
36
-
-
0030878067
-
Molecular defects in rare bleeding disorders: Hereditary haemorrhagic teleangiectasia
-
Shovlin CL: Molecular defects in rare bleeding disorders: hereditary haemorrhagic teleangiectasia. Thromb Haemost, 1997, 78, 145-150.
-
(1997)
Thromb Haemost
, vol.78
, pp. 145-150
-
-
Shovlin, C.L.1
-
37
-
-
0023621324
-
Hereditary multi-infarct dementia
-
Sonninen V, Savontaus ML: Hereditary multi-infarct dementia. Eur Neurol, 1987, 27, 209-215.
-
(1987)
Eur Neurol
, vol.27
, pp. 209-215
-
-
Sonninen, V.1
Savontaus, M.L.2
-
38
-
-
0017750160
-
Hereditary multi-infarct dementia. Morphological and clinical studies of a new disease
-
Berl
-
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
, vol.39
, pp. 247-254
-
-
Sourander, P.1
Walinder, J.2
-
39
-
-
0014477593
-
Cerebrovascular "moyamaya" disease. Disease showing abnormal net-like vessels in base of brain
-
Suzuki I, Takaku A: Cerebrovascular "moyamaya" disease. Disease showing abnormal net-like vessels in base of brain. Arch Neurol, 1969, 20, 288-289.
-
(1969)
Arch Neurol
, vol.20
, pp. 288-289
-
-
Suzuki, I.1
Takaku, A.2
-
40
-
-
0027479304
-
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12
-
Tournier-Lasserve E, Joutel A, Melki J, Weissenbach J, Lathrop GM, Chabriat H, Mas JL. Cabanis EA, Baudrimont M, Maciazek J, Bach MA, Bousser MG: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12. Nature Genet, 1993, 3, 256-259.
-
(1993)
Nature Genet
, vol.3
, pp. 256-259
-
-
Tournier-Lasserve, E.1
Joutel, A.2
Melki, J.3
Weissenbach, J.4
Lathrop, G.M.5
Chabriat, H.6
Mas, J.L.7
Cabanis, E.A.8
Baudrimont, M.9
Maciazek, J.10
Bach, M.A.11
Bousser, M.G.12
-
41
-
-
19244375510
-
Autosomal dominant early onset dementia and leukoencephalopathy in a Japanese family: Clinical, neurimaging and genetic studies
-
Utatsu Y, Takashima H, Michizono J, Kanda N, Endou K, Mitsuyama Y, Fujimoto T, Nagai M, Umehara F, Higuchi I, Arimura K, Nakagawa M, Osame M: Autosomal dominant early onset dementia and leukoencephalopathy in a Japanese family: clinical, neurimaging and genetic studies. J Neurol Sci, 1997, 147, 55-62.
-
(1997)
J Neurol Sci
, vol.147
, pp. 55-62
-
-
Utatsu, Y.1
Takashima, H.2
Michizono, J.3
Kanda, N.4
Endou, K.5
Mitsuyama, Y.6
Fujimoto, T.7
Nagai, M.8
Umehara, F.9
Higuchi, I.10
Arimura, K.11
Nakagawa, M.12
Osame, M.13
-
42
-
-
0029039146
-
Hereditary cerebral haemorrhage with amyloidosis. Dutch type (HCHWA-D): Clinicopathological studies
-
Wattendorff AR, Frangione B, Luyendijk W, Bots GT: Hereditary cerebral haemorrhage with amyloidosis. Dutch type (HCHWA-D): clinicopathological studies. J Neurol Neurosurg Psychiatr, 1997, 58, 699-705.
-
(1997)
J Neurol Neurosurg Psychiatr
, vol.58
, pp. 699-705
-
-
Wattendorff, A.R.1
Frangione, B.2
Luyendijk, W.3
Bots, G.T.4
-
43
-
-
0027976226
-
Miscovascular changes in cases of hereditary multi-infarct disease of the brain
-
Berl
-
Wei Zhang, Ma K Ch, Andersen O, Sourander P, Tollesson PO, Olsson Y: Miscovascular changes in cases of hereditary multi-infarct disease of the brain. Acta Neuropathol (Berl), 1994, 87, 317-324.
-
(1994)
Acta Neuropathol
, vol.87
, pp. 317-324
-
-
Zhang, W.1
Ma, K.Ch.2
Andersen, O.3
Sourander, P.4
Tollesson, P.O.5
Olsson, Y.6
-
44
-
-
84901362980
-
Vascular alteration in different organs in CADASIL. Light and EM studies on biopsy and autopsy specimens
-
Budapst, 18-20 March Abstr L61
-
Viragh Sz, Nagy Z, Ovary Cs: Vascular alteration in different organs in CADASIL. Light and EM studies on biopsy and autopsy specimens. First Conference of the Central and Eastern Europaean Society, Budapst, 18-20 March 1999, Abstr L61, p 21.
-
(1999)
First Conference of the Central and Eastern Europaean Society
, pp. 21
-
-
Viragh, Sz.1
Nagy, Z.2
Ovary, Cs.3
-
45
-
-
0023147465
-
Subcortical encephalopathy in a normotensive, young adult with premature baldness and spondylitis deformans. A clinicopathological study and review of the literature
-
Yamamura T, Nishimura M, Shirabe T, Fujita M: Subcortical encephalopathy in a normotensive, young adult with premature baldness and spondylitis deformans. A clinicopathological study and review of the literature. J Neurol Sci, 1987, 78, 175-188.
-
(1987)
J Neurol Sci
, vol.78
, pp. 175-188
-
-
Yamamura, T.1
Nishimura, M.2
Shirabe, T.3
Fujita, M.4
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