-
1
-
-
0037435546
-
A new cause of hereditary small vessel disease: Angiopathy of retina and brain
-
Dichgans M (2003) A new cause of hereditary small vessel disease: angiopathy of retina and brain. Neurology 60:8-9
-
(2003)
Neurology
, vol.60
, pp. 8-9
-
-
Dichgans, M.1
-
2
-
-
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
-
3
-
-
0028100021
-
Treatment of radiation-induced nervous system injury with heparin and warfarin
-
Glantz MJ, Burger PC, Friedman AH et al. (1994) Treatment of radiation-induced nervous system injury with heparin and warfarin. Neurology 44:2020-2027
-
(1994)
Neurology
, vol.44
, pp. 2020-2027
-
-
Glantz, M.J.1
Burger, P.C.2
Friedman, A.H.3
-
4
-
-
0023923348
-
Cerebroretinal vasculopathy. A new hereditary syndrome
-
Grand MG, Kaine J, Fulling K et al. (1988) Cerebroretinal vasculopathy. A new hereditary syndrome. Ophthalmology 95:649-659
-
(1988)
Ophthalmology
, vol.95
, pp. 649-659
-
-
Grand, M.G.1
Kaine, J.2
Fulling, K.3
-
5
-
-
0030712287
-
Hereditary endotheliopathy with retinopathy, nephropathy, and stroke (HERNS)
-
Jen J, Cohen AH, Yue Q et al. (1997) Hereditary endotheliopathy with retinopathy, nephropathy, and stroke (HERNS). Neurology 49:1322-1330
-
(1997)
Neurology
, vol.49
, pp. 1322-1330
-
-
Jen, J.1
Cohen, A.H.2
Yue, Q.3
-
6
-
-
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
-
7
-
-
0033768116
-
Cerebroretinal vasculopathy and leukoencephalopathy mimicking a brain tumor. Report of two early-onset cases with Fanconi's anemia-like phenotypes suggesting an autosomal-recessive inheritance pattern
-
Niedermayer I, Reiche W, Graf N et al. (2000) Cerebroretinal vasculopathy and leukoencephalopathy mimicking a brain tumor. Report of two early-onset cases with Fanconi's anemia-like phenotypes suggesting an autosomal-recessive inheritance pattern. Clin Neuropathol 19:285-295
-
(2000)
Clin Neuropathol
, vol.19
, pp. 285-295
-
-
Niedermayer, I.1
Reiche, W.2
Graf, N.3
-
8
-
-
0034920305
-
Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3
-
Ophoff RA, DeYoung J, Service SK et al. (2001) Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3. Am J Hum Genet 69:447-453
-
(2001)
Am J Hum Genet
, vol.69
, pp. 447-453
-
-
Ophoff, R.A.1
DeYoung, J.2
Service, S.K.3
-
11
-
-
0037435523
-
Hereditary infantile hemiparesis, retinal arteriolar tortuosity, and leukoencephalopathy
-
Vahedi K, Massin P, Guichard JP et al. (2003) Hereditary infantile hemiparesis, retinal arteriolar tortuosity, and leukoencephalopathy. Neurology 60:57-63
-
(2003)
Neurology
, vol.60
, pp. 57-63
-
-
Vahedi, K.1
Massin, P.2
Guichard, J.P.3
-
12
-
-
0033546629
-
Cerebroretinal vasculopathy mimicking a brain tumor: A case of a rare hereditary syndrome
-
Weil S, Reifenberger G, Dudel C et al. (1999) Cerebroretinal vasculopathy mimicking a brain tumor: a case of a rare hereditary syndrome. Neurology 53:629-631
-
(1999)
Neurology
, vol.53
, pp. 629-631
-
-
Weil, S.1
Reifenberger, G.2
Dudel, C.3
-
13
-
-
0037066143
-
Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
-
Yanagawa S, Ito N, Arima K et al. (2002) Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy. Neurology 58:817-820
-
(2002)
Neurology
, vol.58
, pp. 817-820
-
-
Yanagawa, S.1
Ito, N.2
Arima, K.3
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