-
1
-
-
19344374422
-
Spinocerebellar ataxia type 2 (SCA2) with white matter involvement
-
Armstrong J, Bonaventura I, Rojo A, González G, Corral J, Nadal N, et al (2005) Spinocerebellar ataxia type 2 (SCA2) with white matter involvement. Neurosci Lett 381: 247-251.
-
(2005)
Neurosci Lett
, vol.381
, pp. 247-251
-
-
Armstrong, J.1
Bonaventura, I.2
Rojo, A.3
González, G.4
Corral, J.5
Nadal, N.6
-
2
-
-
7244236320
-
Inclusion body formation reduces levels of mutant Huntington and the risk of neuronal death
-
Arrasate M, Mitra S, Schweitzer ES, Segal MR, Finkbeiner S, (2004) Inclusion body formation reduces levels of mutant Huntington and the risk of neuronal death. Nature 431: 805-810.
-
(2004)
Nature
, vol.431
, pp. 805-810
-
-
Arrasate, M.1
Mitra, S.2
Schweitzer, E.S.3
Segal, M.R.4
Finkbeiner, S.5
-
3
-
-
0029611008
-
Autosomal dominant cerebellar ataxia type i in Martinique (French West Indies). Clinical and neuropathological analysis of 53 patients from three unrelated SCA2 families
-
Dürr A, Smadja D, Cancel G, Lezin A, Stevanin G, Mikol J, et al (1995) Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies). Clinical and neuropathological analysis of 53 patients from three unrelated SCA2 families. Brain 118: 1573-1581.
-
(1995)
Brain
, vol.118
, pp. 1573-1581
-
-
Dürr, A.1
Smadja, D.2
Cancel, G.3
Lezin, A.4
Stevanin, G.5
Mikol, J.6
-
4
-
-
0033802841
-
Ataxin-3 is translocated into the nucleus for the formation of intranuclear inclusions in normal and Machado-Joseph disease brains
-
Fujigasaki H, Uchihara T, Koyano S, Iwabuchi K, Yagishita S, Makifuchi T, et al (2000) Ataxin-3 is translocated into the nucleus for the formation of intranuclear inclusions in normal and Machado-Joseph disease brains. Exp Neurol 165: 248-256.
-
(2000)
Exp Neurol
, vol.165
, pp. 248-256
-
-
Fujigasaki, H.1
Uchihara, T.2
Koyano, S.3
Iwabuchi, K.4
Yagishita, S.5
Makifuchi, T.6
-
5
-
-
22144453212
-
Involvement of the cranial nerves and their nuclei in spinocerebellar ataxia type 2 (SCA2)
-
Gierga K, Bürk K, Bauer M, Orozco Diaz G, Auburger G, Schultz C, et al (2005) Involvement of the cranial nerves and their nuclei in spinocerebellar ataxia type 2 (SCA2). Acta Neuropathol 109: 617-631.
-
(2005)
Acta Neuropathol
, vol.109
, pp. 617-631
-
-
Gierga, K.1
Bürk, K.2
Bauer, M.3
Orozco Diaz, G.4
Auburger, G.5
Schultz, C.6
-
6
-
-
84871577955
-
Changes in Purkinje cell firing and gene expression precede behavioral pathology in a mouse model of SCA2
-
Hansen ST, Meera P, Otis TS, Pulst SM, (2013) Changes in Purkinje cell firing and gene expression precede behavioral pathology in a mouse model of SCA2. Hum Mol Genet 22: 271-283.
-
(2013)
Hum Mol Genet
, vol.22
, pp. 271-283
-
-
Hansen, S.T.1
Meera, P.2
Otis, T.S.3
Pulst, S.M.4
-
7
-
-
77955973878
-
Current understanding on the pathogenesis of polyglutamine diseases
-
He XH, Lin F, Qin ZH, (2010) Current understanding on the pathogenesis of polyglutamine diseases. Neurosci Bull 26: 247-256.
-
(2010)
Neurosci Bull
, vol.26
, pp. 247-256
-
-
He, X.H.1
Lin, F.2
Qin, Z.H.3
-
8
-
-
0033811788
-
Nuclear localization or inclusion body formation of ataxin-2 are not necessary for SCA2 pathogenesis in mouse or human
-
Huynh DP, Figueroa K, Hoang N, Pulst SM, (2000) Nuclear localization or inclusion body formation of ataxin-2 are not necessary for SCA2 pathogenesis in mouse or human. Nat Genet 26: 44-50.
-
(2000)
Nat Genet
, vol.26
, pp. 44-50
-
-
Huynh, D.P.1
Figueroa, K.2
Hoang, N.3
Pulst, S.M.4
-
9
-
-
80053095998
-
An autopsy case of an aged patient with spinocerebellar ataxia type 2
-
Ishida C, Komai K, Yonezawa K, Sakajiri K, Nitta E, Kawashima A, Yamada M, (2011) An autopsy case of an aged patient with spinocerebellar ataxia type 2. Neuropathology 31: 510-518.
-
(2011)
Neuropathology
, vol.31
, pp. 510-518
-
-
Ishida, C.1
Komai, K.2
Yonezawa, K.3
Sakajiri, K.4
Nitta, E.5
Kawashima, A.6
Yamada, M.7
-
10
-
-
0033111229
-
Autosomal dominant spinocerebellar degenerations. Clinical, pathological, and genetic correlations
-
Iwabuchi K, Tsuchiya K, Uchihara T, Yagishita S, (1999) Autosomal dominant spinocerebellar degenerations. Clinical, pathological, and genetic correlations. Rev Neurol (Paris) 155: 255-270.
-
(1999)
Rev Neurol (Paris)
, vol.155
, pp. 255-270
-
-
Iwabuchi, K.1
Tsuchiya, K.2
Uchihara, T.3
Yagishita, S.4
-
11
-
-
0036786139
-
Paradoxical absence of nuclear inclusion in cerebellar Purkinje cells of hereditary ataxias linked to CAG expansion
-
Koyano S, Iwabuchi K, Yagishita S, Kuroiwa Y, Uchihara T, (2002) Paradoxical absence of nuclear inclusion in cerebellar Purkinje cells of hereditary ataxias linked to CAG expansion. J Neurol Neurosurg Psychiatry 73: 450-452.
-
(2002)
J Neurol Neurosurg Psychiatry
, vol.73
, pp. 450-452
-
-
Koyano, S.1
Iwabuchi, K.2
Yagishita, S.3
Kuroiwa, Y.4
Uchihara, T.5
-
12
-
-
0032840052
-
Neuronal intranuclear inclusions in spinocerebellar ataxia type 2: Triple-labeling immunofluorescent study
-
Koyano S, Uchihara T, Fujigasaki H, Nakamura A, Yagishita S, Iwabuchi K, (1999) Neuronal intranuclear inclusions in spinocerebellar ataxia type 2: triple-labeling immunofluorescent study. Neurosci Lett 273: 117-120.
-
(1999)
Neurosci Lett
, vol.273
, pp. 117-120
-
-
Koyano, S.1
Uchihara, T.2
Fujigasaki, H.3
Nakamura, A.4
Yagishita, S.5
Iwabuchi, K.6
-
14
-
-
17744414905
-
CAG repeat expansion in an Italian family with spinocerebellar ataxia type 2 (SCA2): A clinical and genetic study
-
Malandrini A, Galli L, Villanova M, Palmeri S, Parrotta E, DeFalco D, et al (1998) CAG repeat expansion in an Italian family with spinocerebellar ataxia type 2 (SCA2): a clinical and genetic study. Eur Neurol 40: 164-168.
-
(1998)
Eur Neurol
, vol.40
, pp. 164-168
-
-
Malandrini, A.1
Galli, L.2
Villanova, M.3
Palmeri, S.4
Parrotta, E.5
Defalco, D.6
-
15
-
-
0024422743
-
Dominantly inherited olivopontocerebellar atrophy from eastern Cuba. Clinical, neuropathological, and biochemical findings
-
Orozco G, Estrada R, Perry TL, Araña J, Fernandez R, Gonzalez-Quevedo A, et al (1989) Dominantly inherited olivopontocerebellar atrophy from eastern Cuba. Clinical, neuropathological, and biochemical findings. J Neurol Sci 93: 37-50.
-
(1989)
J Neurol Sci
, vol.93
, pp. 37-50
-
-
Orozco, G.1
Estrada, R.2
Perry, T.L.3
Araña, J.4
Fernandez, R.5
Gonzalez-Quevedo, A.6
-
16
-
-
0036185711
-
Neuronal intranuclear inclusions in SCA2: A genetic, morphological and immunohistochemical study of two cases
-
Pang JT, Giunti P, Chamberlain S, An SF, Vitaliani R, Scaravilli T, et al (2002) Neuronal intranuclear inclusions in SCA2: a genetic, morphological and immunohistochemical study of two cases. Brain 125: 656-663.
-
(2002)
Brain
, vol.125
, pp. 656-663
-
-
Pang, J.T.1
Giunti, P.2
Chamberlain, S.3
An, S.F.4
Vitaliani, R.5
Scaravilli, T.6
-
17
-
-
0030850412
-
Intranuclear inclusions of expanded polyglutamine protein in spinocerebellar ataxia type 3
-
Paulson HL, Perez MK, Trottier Y, Trojanowski JQ, Subramony SH, Das SS, et al (1997) Intranuclear inclusions of expanded polyglutamine protein in spinocerebellar ataxia type 3. Neuron 19: 333-344.
-
(1997)
Neuron
, vol.19
, pp. 333-344
-
-
Paulson, H.L.1
Perez, M.K.2
Trottier, Y.3
Trojanowski, J.Q.4
Subramony, S.H.5
Das, S.S.6
-
18
-
-
4444274236
-
Accumulation of aberrant ubiquitin induces aggregate formation and cell death in polyglutamine diseases
-
Pril R, Fischer DF, Maat-Schieman ML, Hobo B, de Vos RA, Brunt ER, et al (2004) Accumulation of aberrant ubiquitin induces aggregate formation and cell death in polyglutamine diseases. Hum Mol Genet 13: 1803-1813.
-
(2004)
Hum Mol Genet
, vol.13
, pp. 1803-1813
-
-
Pril, R.1
Fischer, D.F.2
Maat-Schieman, M.L.3
Hobo, B.4
De Vos, R.A.5
Brunt, E.R.6
-
19
-
-
0242336434
-
Thalamic involvement in a spinocerebellar ataxia type2 (SCA2) and a spinocerebellar ataxia type 3 (SCA3) patient, and its clinical relevance
-
Rüb U, Del Turco D, Del Tredici K, de Vos RA, Brunt ER, Reifenberger G, et al (2003) Thalamic involvement in a spinocerebellar ataxia type2 (SCA2) and a spinocerebellar ataxia type 3 (SCA3) patient, and its clinical relevance. Brain 126: 2257-2272.
-
(2003)
Brain
, vol.126
, pp. 2257-2272
-
-
Rüb, U.1
Del Turco, D.2
Del Tredici, K.3
De Vos, R.A.4
Brunt, E.R.5
Reifenberger, G.6
-
20
-
-
34547155455
-
Inclusion formation by ataxins -1, -2, -3, and -7
-
Tarlac V, Turnbull V, Stefani D, Kelly L, Walsh R, Storey E, (2007) Inclusion formation by ataxins -1, -2, -3, and -7. Int J Neurosci 117: 1289-1314.
-
(2007)
Int J Neurosci
, vol.117
, pp. 1289-1314
-
-
Tarlac, V.1
Turnbull, V.2
Stefani, D.3
Kelly, L.4
Walsh, R.5
Storey, E.6
-
21
-
-
80051800168
-
A comprehensive review of spinocerebellar ataxia type 2 in Cuba
-
Velázquez-Pérez L, Rodríguez-Labrada R, García-Rodríguez JC, Almaguer-Mederos LE, Cruz-Mariño T, Laffita-Mesa JM, (2011) A comprehensive review of spinocerebellar ataxia type 2 in Cuba. Cerebellum 10: 184-198.
-
(2011)
Cerebellum
, vol.10
, pp. 184-198
-
-
Velázquez-Pérez, L.1
Rodríguez-Labrada, R.2
García-Rodríguez, J.C.3
Almaguer-Mederos, L.E.4
Cruz-Mariño, T.5
Laffita-Mesa, J.M.6
-
22
-
-
22144466522
-
Relative atrophy of the flocculus and ocular motor dysfunction in SCA2 and SCA6
-
Ying SH, Choi SI, Lee M, Perlman SL, Baloh RW, Toga AW, Zee DS, (2005) Relative atrophy of the flocculus and ocular motor dysfunction in SCA2 and SCA6. Ann N Y Acad Sci 1039: 430-435.
-
(2005)
Ann N y Acad Sci
, vol.1039
, pp. 430-435
-
-
Ying, S.H.1
Choi, S.I.2
Lee, M.3
Perlman, S.L.4
Baloh, R.W.5
Toga, A.W.6
Zee, D.S.7
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