-
2
-
-
0026314680
-
A new type of complicated form of hereditary spastic paraplegia showing mental deterioration, quadriplegia with muscular atrophy, sensory disturbance, extrapyramidal disorders, and epilepsy
-
Iwabuchi K, Yagishita S, Amano N, Kosaka K. A new type of complicated form of hereditary spastic paraplegia showing mental deterioration, quadriplegia with muscular atrophy, sensory disturbance, extrapyramidal disorders, and epilepsy. Rinsho Shinkeigaku 1991;31:945-952.
-
(1991)
Rinsho Shinkeigaku
, vol.31
, pp. 945-952
-
-
Iwabuchi, K.1
Yagishita, S.2
Amano, N.3
Kosaka, K.4
-
3
-
-
0029003729
-
Hereditary spastic paraparesis with dementia, amyotrophy and peripheral neuropathy. A neuropathological study
-
Ferrer I, Olive M, Rivera R, Pou A, Narberhaus B, Ugarte A. Hereditary spastic paraparesis with dementia, amyotrophy and peripheral neuropathy. A neuropathological study. Neuropathol Appl Neurobiol 1995;21:255-261.
-
(1995)
Neuropathol Appl Neurobiol
, vol.21
, pp. 255-261
-
-
Ferrer, I.1
Olive, M.2
Rivera, R.3
Pou, A.4
Narberhaus, B.5
Ugarte, A.6
-
4
-
-
0035144658
-
Autosomal recessive spastic paraplegia with hypoplastic corpus callosum, multisystem degeneration and ubiquitinated eosinophilic granules
-
Berl
-
Wakabayashi K, Kobayashi H, Kawasaki S, Kondo H, Takahashi H. Autosomal recessive spastic paraplegia with hypoplastic corpus callosum, multisystem degeneration and ubiquitinated eosinophilic granules. Acta Neuropathol (Berl) 2001;101:69-73.
-
(2001)
Acta Neuropathol
, vol.101
, pp. 69-73
-
-
Wakabayashi, K.1
Kobayashi, H.2
Kawasaki, S.3
Kondo, H.4
Takahashi, H.5
-
5
-
-
0033930099
-
Linkage of autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum to chromosome 15q13-15
-
Shibasaki Y, Tanaka H, Iwabuchi K, et al. Linkage of autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum to chromosome 15q13-15. Ann Neurol 2000;48:108-112.
-
(2000)
Ann Neurol
, vol.48
, pp. 108-112
-
-
Shibasaki, Y.1
Tanaka, H.2
Iwabuchi, K.3
-
6
-
-
0034163576
-
Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia
-
Fonknechten N, Mavel D, Byrne P, et al. Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia. Hum Mol Genet 2000;9:637-644.
-
(2000)
Hum Mol Genet
, vol.9
, pp. 637-644
-
-
Fonknechten, N.1
Mavel, D.2
Byrne, P.3
-
7
-
-
0033782943
-
Mutation analysis of the spastin gene (SPG4) in patients with hereditary spastic paraparesis
-
Lindsey JC, Lusher ME, McDermott CJ, et al. Mutation analysis of the spastin gene (SPG4) in patients with hereditary spastic paraparesis. J Med Genet 2000;37:759-765.
-
(2000)
J Med Genet
, vol.37
, pp. 759-765
-
-
Lindsey, J.C.1
Lusher, M.E.2
McDermott, C.J.3
-
8
-
-
0031949628
-
A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1
-
Crook R, Verkkoniemi A, Perez-Tur J, et al. A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1. Nat Med 1998;4:452-455.
-
(1998)
Nat Med
, vol.4
, pp. 452-455
-
-
Crook, R.1
Verkkoniemi, A.2
Perez-Tur, J.3
-
9
-
-
0036704933
-
Frontal-subcortical neuronal circuits and clinical neuropsychiatry: An update
-
Tekin S, Cummings JL. Frontal-subcortical neuronal circuits and clinical neuropsychiatry: an update. J Psychosom Res 2002;53:647-654.
-
(2002)
J Psychosom Res
, vol.53
, pp. 647-654
-
-
Tekin, S.1
Cummings, J.L.2
-
10
-
-
0025802079
-
Widespread functional effects of discrete thalamic infarction
-
Szelies B, Herholz K, Pawlik G, Karbe H, Hebold I, Heiss WD. Widespread functional effects of discrete thalamic infarction. Arch Neurol 1991;48:178-182.
-
(1991)
Arch Neurol
, vol.48
, pp. 178-182
-
-
Szelies, B.1
Herholz, K.2
Pawlik, G.3
Karbe, H.4
Hebold, I.5
Heiss, W.D.6
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