-
1
-
-
33750984197
-
Olivopontocerebellar atrophy: toward a better nosological definition
-
Berciano J., Boesch S., Perez-Ramos J., et al. Olivopontocerebellar atrophy: toward a better nosological definition. Movement Disorders 2006, 21:1607-1613.
-
(2006)
Movement Disorders
, vol.21
, pp. 1607-1613
-
-
Berciano, J.1
Boesch, S.2
Perez-Ramos, J.3
-
2
-
-
0029611008
-
Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies). Clinical and neuropathological analysis of 53 patients from three unrelated SCA 2 families
-
Durr A., Smadja D., Cancel G., et al. Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies). Clinical and neuropathological analysis of 53 patients from three unrelated SCA 2 families. Brain 1995, 118:1573-1581.
-
(1995)
Brain
, vol.118
, pp. 1573-1581
-
-
Durr, A.1
Smadja, D.2
Cancel, G.3
-
3
-
-
9244225693
-
Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular and neuropathological features
-
Durr A., Stevanin G., Cancel G., et al. Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular and neuropathological features. Ann Neurol 1996, 39:490-499.
-
(1996)
Ann Neurol
, vol.39
, pp. 490-499
-
-
Durr, A.1
Stevanin, G.2
Cancel, G.3
-
4
-
-
0345391031
-
Nuclear inclusions in spinocerebellar ataxia type 1
-
Duyckaerts C., Durr A., Cancel G., et al. Nuclear inclusions in spinocerebellar ataxia type 1. Acta Neuropathol 1999, 97:201-207.
-
(1999)
Acta Neuropathol
, vol.97
, pp. 201-207
-
-
Duyckaerts, C.1
Durr, A.2
Cancel, G.3
-
5
-
-
0033046989
-
Spinocerebellar ataxia 2 (SCA 2): morphometric analyses of 11 autopsies
-
Estrada R., Galarraga J., Orozco G., et al. Spinocerebellar ataxia 2 (SCA 2): morphometric analyses of 11 autopsies. Acta Neuropathol 1999, 97:306-310.
-
(1999)
Acta Neuropathol
, vol.97
, pp. 306-310
-
-
Estrada, R.1
Galarraga, J.2
Orozco, G.3
-
6
-
-
0028819081
-
Clinical, neuropathologic, and genetic studies of a large spinocerebellar ataxia type 1 (SCA 1) kindred: (CAG)n expansion and early premonitory signs and symptoms
-
Genis D., Matilla T., Volpini V., et al. Clinical, neuropathologic, and genetic studies of a large spinocerebellar ataxia type 1 (SCA 1) kindred: (CAG)n expansion and early premonitory signs and symptoms. Neurology 1995, 45:24-30.
-
(1995)
Neurology
, vol.45
, pp. 24-30
-
-
Genis, D.1
Matilla, T.2
Volpini, V.3
-
7
-
-
22144453212
-
Involvement of the cranial nerves and their nuclei in spinocerebellar ataxia type 2 (SCA 2)
-
Gierga K., Burk K., Bauer M., et al. Involvement of the cranial nerves and their nuclei in spinocerebellar ataxia type 2 (SCA 2). Acta Neuropathol 2005, 109:617-631.
-
(2005)
Acta Neuropathol
, vol.109
, pp. 617-631
-
-
Gierga, K.1
Burk, K.2
Bauer, M.3
-
8
-
-
0030040304
-
Spinocerebellar ataxia type 1 with multiple system degeneration and glial cytoplasmic inclusions
-
Gilman S., Sima A.A.F., Junck L., et al. Spinocerebellar ataxia type 1 with multiple system degeneration and glial cytoplasmic inclusions. Ann Neurol 1996, 39:241-255.
-
(1996)
Ann Neurol
, vol.39
, pp. 241-255
-
-
Gilman, S.1
Sima, A.A.F.2
Junck, L.3
-
9
-
-
0033837087
-
Evolution of sporadic olivopontocerebellar atrophy into multiple system atrophy
-
Gilman S., Little R., Johanns J., et al. Evolution of sporadic olivopontocerebellar atrophy into multiple system atrophy. Neurology 2000, 55:527-532.
-
(2000)
Neurology
, vol.55
, pp. 527-532
-
-
Gilman, S.1
Little, R.2
Johanns, J.3
-
10
-
-
0025073902
-
Immunohistochemical evidence for the selective involvement of dorsal root fibers in Friedreich's ataxia
-
Goto S., Hirano A. Immunohistochemical evidence for the selective involvement of dorsal root fibers in Friedreich's ataxia. Neuropathol Appl Neurobiol 1990, 16:365-370.
-
(1990)
Neuropathol Appl Neurobiol
, vol.16
, pp. 365-370
-
-
Goto, S.1
Hirano, A.2
-
13
-
-
0031739224
-
Hereditary dentatorubral-pallidoluysian atrophy: detection of widespread ubiquitinated neuronal and glial intranuclear inclusions in the brain
-
Hayashi Y., Kakita A., Yamada M., et al. Hereditary dentatorubral-pallidoluysian atrophy: detection of widespread ubiquitinated neuronal and glial intranuclear inclusions in the brain. Acta Neuropathol 1998, 96:547-552.
-
(1998)
Acta Neuropathol
, vol.96
, pp. 547-552
-
-
Hayashi, Y.1
Kakita, A.2
Yamada, M.3
-
14
-
-
7144229376
-
Spinocerebellar ataxia type 7 (SCA7): a neurodegenerative disorder with neuronal intranuclear inclusions
-
Holmberg M., Duyckaerts C., Dürr A., et al. Spinocerebellar ataxia type 7 (SCA7): a neurodegenerative disorder with neuronal intranuclear inclusions. Hum Mol Genet 1998, 7:913-918.
-
(1998)
Hum Mol Genet
, vol.7
, pp. 913-918
-
-
Holmberg, M.1
Duyckaerts, C.2
Dürr, A.3
-
15
-
-
0033811788
-
Nuclear localization or inclusion body formation of ataxin-2 are not necessary for SCA 2 pathogenesis in mouse or human
-
Huynh D.P., Figueroa K., Hoang N., et al. Nuclear localization or inclusion body formation of ataxin-2 are not necessary for SCA 2 pathogenesis in mouse or human. Nat Genet 2000, 26:44-50.
-
(2000)
Nat Genet
, vol.26
, pp. 44-50
-
-
Huynh, D.P.1
Figueroa, K.2
Hoang, N.3
-
16
-
-
0035954366
-
Cytoplasmic and nuclear polyglutamine aggregates in SCA 6 Purkinje cells
-
Ishikawa K., Owada K., Ishida K., et al. Cytoplasmic and nuclear polyglutamine aggregates in SCA 6 Purkinje cells. Neurology 2001, 56:1753-1756.
-
(2001)
Neurology
, vol.56
, pp. 1753-1756
-
-
Ishikawa, K.1
Owada, K.2
Ishida, K.3
-
17
-
-
0025275242
-
Idiopathic cerebellar ataxia of late onset: natural history and MRI morphology
-
Klockgether T., Schroth G., Diener H.-C., et al. Idiopathic cerebellar ataxia of late onset: natural history and MRI morphology. J Neurol Neurosurg Psychiatry 1990, 53:297-305.
-
(1990)
J Neurol Neurosurg Psychiatry
, vol.53
, pp. 297-305
-
-
Klockgether, T.1
Schroth, G.2
Diener, H.-C.3
-
18
-
-
0002654217
-
Neuropathology of inherited ataxias
-
Cambridge University Press, Cambridge, M.-U. Manto, M. Pandolfo (Eds.)
-
Koeppen A.H. Neuropathology of inherited ataxias. The Cerebellum and its Disorders 2002, Cambridge University Press, Cambridge. M.-U. Manto, M. Pandolfo (Eds.).
-
(2002)
The Cerebellum and its Disorders
-
-
Koeppen, A.H.1
-
19
-
-
34547119562
-
The dentate nucleus in Friedreich's ataxia: the role of iron-responsive proteins
-
Koeppen A.H., Michael S.C., Knutson M.D., et al. The dentate nucleus in Friedreich's ataxia: the role of iron-responsive proteins. Acta Neuropathol 2007, 114:163-173.
-
(2007)
Acta Neuropathol
, vol.114
, pp. 163-173
-
-
Koeppen, A.H.1
Michael, S.C.2
Knutson, M.D.3
-
20
-
-
71449093193
-
The dorsal root ganglion in Friedreich's ataxia
-
Koeppen A.H., Morral J.A., Davis A.N., et al. The dorsal root ganglion in Friedreich's ataxia. Acta Neuropathol 2009, 118:763-776.
-
(2009)
Acta Neuropathol
, vol.118
, pp. 763-776
-
-
Koeppen, A.H.1
Morral, J.A.2
Davis, A.N.3
-
21
-
-
0014787658
-
The olivopontocerebellar atrophies: a review
-
Konigsmark B.W., Weiner L.P. The olivopontocerebellar atrophies: a review. Medicine (Baltimore) 1970, 49:227-241.
-
(1970)
Medicine (Baltimore)
, vol.49
, pp. 227-241
-
-
Konigsmark, B.W.1
Weiner, L.P.2
-
22
-
-
0032840052
-
Neuronal intranuclear inclusions in spinocerebellar ataxia type 2: triple-labeling immunofluorescent study
-
Koyano S., Uchihara T., Fujigasaki H., et al. Neuronal intranuclear inclusions in spinocerebellar ataxia type 2: triple-labeling immunofluorescent study. Neurosci Lett 1999, 273:117-120.
-
(1999)
Neurosci Lett
, vol.273
, pp. 117-120
-
-
Koyano, S.1
Uchihara, T.2
Fujigasaki, H.3
-
23
-
-
0033964603
-
Cerebellar degeneration in hereditary dentatorubral-pallidoluysian atrophy and Machado-Joseph disease
-
Kumada S., Hayashi M., Mizuguchi M., et al. Cerebellar degeneration in hereditary dentatorubral-pallidoluysian atrophy and Machado-Joseph disease. Acta Neuropathol 2000, 99:48-54.
-
(2000)
Acta Neuropathol
, vol.99
, pp. 48-54
-
-
Kumada, S.1
Hayashi, M.2
Mizuguchi, M.3
-
24
-
-
0036050825
-
Peripheral neuropathy of Machado-Joseph disease in Taiwan: a morphometric and genetic study
-
Lin K.P., Soong B.W. Peripheral neuropathy of Machado-Joseph disease in Taiwan: a morphometric and genetic study. Eur Neurol 2002, 48:210-217.
-
(2002)
Eur Neurol
, vol.48
, pp. 210-217
-
-
Lin, K.P.1
Soong, B.W.2
-
25
-
-
0028067442
-
On an autosomal dominant form of retino-cerebellar degeneration: an autopsy study of 5 patients in one family
-
Martin J.-J., Van Regemorter N., Kros L., et al. On an autosomal dominant form of retino-cerebellar degeneration: an autopsy study of 5 patients in one family. Acta Neuropathol 1994, 88:277-286.
-
(1994)
Acta Neuropathol
, vol.88
, pp. 277-286
-
-
Martin, J.-J.1
Van Regemorter, N.2
Kros, L.3
-
26
-
-
0032751030
-
Dentatorubropallidoluysian atrophy in a Spanish family: a clinical, radiological, pathological and genetic study
-
Munoz E., Mila M., Sanchez A., et al. Dentatorubropallidoluysian atrophy in a Spanish family: a clinical, radiological, pathological and genetic study. J Neurol Neurosurg Psychiatry 1999, 67:811-814.
-
(1999)
J Neurol Neurosurg Psychiatry
, vol.67
, pp. 811-814
-
-
Munoz, E.1
Mila, M.2
Sanchez, A.3
-
27
-
-
0034950232
-
Small fibers involvement in Friedreich's ataxia
-
Nolano M., Provitera V., Crisci C., et al. Small fibers involvement in Friedreich's ataxia. Ann Neurol 2001, 50:17-25.
-
(2001)
Ann Neurol
, vol.50
, pp. 17-25
-
-
Nolano, M.1
Provitera, V.2
Crisci, C.3
-
28
-
-
0018392248
-
Brain lesions in Friedreich's ataxia
-
Oppenheimer D.R. Brain lesions in Friedreich's ataxia. Can J Neurol Sci 1979, 6:173-176.
-
(1979)
Can J Neurol Sci
, vol.6
, pp. 173-176
-
-
Oppenheimer, D.R.1
-
29
-
-
0024422743
-
Dominantly inherited olivopontocerebellar atrophy from Eastern Cuba. Clinical, neuropathological, and biochemical findings
-
Orozco G., Estrada R., Perry T., et al. Dominantly inherited olivopontocerebellar atrophy from Eastern Cuba. Clinical, neuropathological, and biochemical findings. J Neurol Sci 1989, 93:37-50.
-
(1989)
J Neurol Sci
, vol.93
, pp. 37-50
-
-
Orozco, G.1
Estrada, R.2
Perry, T.3
-
30
-
-
0033772916
-
Hereditary dentatorubral-pallidoluysian atrophy
-
Oyanagi S. Hereditary dentatorubral-pallidoluysian atrophy. Neuropathology 2000, 20:S42-S46.
-
(2000)
Neuropathology
, vol.20
-
-
Oyanagi, S.1
-
31
-
-
0036185711
-
Neuronal intranuclear inclusions in SCA2: a genetic, morphological and immunohistochemical study of two cases
-
Pang J.T., Giunti P., Chamberlain S., et al. Neuronal intranuclear inclusions in SCA2: a genetic, morphological and immunohistochemical study of two cases. Brain 2002, 125:656-663.
-
(2002)
Brain
, vol.125
, pp. 656-663
-
-
Pang, J.T.1
Giunti, P.2
Chamberlain, S.3
-
32
-
-
0030847065
-
The neuropathology of CAG repeat diseases: review and update of genetic and molecular features
-
Robitaille Y., Lopes-Cendes I., Becher M., et al. The neuropathology of CAG repeat diseases: review and update of genetic and molecular features. Brain Pathol 1997, 7:901-926.
-
(1997)
Brain Pathol
, vol.7
, pp. 901-926
-
-
Robitaille, Y.1
Lopes-Cendes, I.2
Becher, M.3
-
33
-
-
0037327486
-
Guidelines for the pathoanatomical examination of the lower brain stem in ingestive and swallowing disorders and its application to a dysphagic spinocerebellar ataxia type 3 patient
-
Rüb U., Brunt E.R., Del Turco D., et al. Guidelines for the pathoanatomical examination of the lower brain stem in ingestive and swallowing disorders and its application to a dysphagic spinocerebellar ataxia type 3 patient. Neuropathol Appl Neurobiol 2003, 29:1-13.
-
(2003)
Neuropathol Appl Neurobiol
, vol.29
, pp. 1-13
-
-
Rüb, U.1
Brunt, E.R.2
Del Turco, D.3
-
34
-
-
4344644922
-
Degeneration of the central vestibular system in spinocerebellar ataxia type 3 (SCA3) patients and its possible clinical significance
-
Rüb U.E., Brunt E.R., de Vos R.A.I. Degeneration of the central vestibular system in spinocerebellar ataxia type 3 (SCA3) patients and its possible clinical significance. Neuropathol Appl Neurobiol 2004, 30:402-414.
-
(2004)
Neuropathol Appl Neurobiol
, vol.30
, pp. 402-414
-
-
Rüb, U.E.1
Brunt, E.R.2
de Vos, R.A.I.3
-
35
-
-
27144467422
-
Spinocerebellar ataxias types 2 and 3:degeneration of the precerebellar nuclei isolates the three phylogenetically defined regions of the cerebellum
-
Rüb U., Gierga K., Brunt E.R., et al. Spinocerebellar ataxias types 2 and 3:degeneration of the precerebellar nuclei isolates the three phylogenetically defined regions of the cerebellum. J Neural Transm 2005, 112:1523-1545.
-
(2005)
J Neural Transm
, vol.112
, pp. 1523-1545
-
-
Rüb, U.1
Gierga, K.2
Brunt, E.R.3
-
36
-
-
27944503345
-
Spinocerebellar ataxia type 7 (SCA7): first report of a systematic neuropathological study of the brain of a patient with a very short expanded CAG-repeat
-
Rüb U., Brunt E.R., Gierga K., et al. Spinocerebellar ataxia type 7 (SCA7): first report of a systematic neuropathological study of the brain of a patient with a very short expanded CAG-repeat. Brain Pathol 2005, 15:287-295.
-
(2005)
Brain Pathol
, vol.15
, pp. 287-295
-
-
Rüb, U.1
Brunt, E.R.2
Gierga, K.3
-
37
-
-
33746859957
-
Degeneration of ingestion-related brainstem nuclei in spinocerebellar ataxia type 2, 3, 6 and 7
-
Rüb U., Brunt E.R., Petrasch-Parwez E., et al. Degeneration of ingestion-related brainstem nuclei in spinocerebellar ataxia type 2, 3, 6 and 7. Neuropathol Appl Neurobiol 2006, 32:635-649.
-
(2006)
Neuropathol Appl Neurobiol
, vol.32
, pp. 635-649
-
-
Rüb, U.1
Brunt, E.R.2
Petrasch-Parwez, E.3
-
38
-
-
33846635034
-
Consistent affection of the central somatosensory system in spinocerebellar ataxia type 2 and type 3 and its significance for clinical symptoms and rehabilitative therapy
-
Rüb U., Seidela K., Özerden I., et al. Consistent affection of the central somatosensory system in spinocerebellar ataxia type 2 and type 3 and its significance for clinical symptoms and rehabilitative therapy. Brain Res Rev 2007, 53:235-249.
-
(2007)
Brain Res Rev
, vol.53
, pp. 235-249
-
-
Rüb, U.1
Seidela, K.2
Özerden, I.3
-
39
-
-
42649118505
-
New insights into the pathoanatomy of spinocerebellar ataxia type 3 (Machado-Joseph disease)
-
Rüb U., Brunt E.R., Deller T. New insights into the pathoanatomy of spinocerebellar ataxia type 3 (Machado-Joseph disease). Curr Opin Neurol 2008, 21:111-116.
-
(2008)
Curr Opin Neurol
, vol.21
, pp. 111-116
-
-
Rüb, U.1
Brunt, E.R.2
Deller, T.3
-
40
-
-
0031883338
-
Neuropathological and molecular studies of spinocerebellar ataxia type 6 (SCA 6)
-
Sasaki H., Kojima H., Yabe I., et al. Neuropathological and molecular studies of spinocerebellar ataxia type 6 (SCA 6). Acta Neuropathol 1998, 95:199-204.
-
(1998)
Acta Neuropathol
, vol.95
, pp. 199-204
-
-
Sasaki, H.1
Kojima, H.2
Yabe, I.3
-
41
-
-
0027356605
-
Epidemiology and clinical aspects of Machado-Joseph disease
-
Raven Press, New York
-
Sequeiros J., Coutinho P. Epidemiology and clinical aspects of Machado-Joseph disease. Advances in Neurology 1993, Vol. 61. Raven Press, New York.
-
(1993)
Advances in Neurology
, vol.61
-
-
Sequeiros, J.1
Coutinho, P.2
-
42
-
-
0029882009
-
Dominant cerebello-olivary atrophy is not due to a mutation at the spinocerebellar ataxia 1, Machado-Joseph disease or dentato-rubro-pallido-luysian atrophy locus
-
Subramony S.H., Manyam B.N., Currier R.D., et al. Dominant cerebello-olivary atrophy is not due to a mutation at the spinocerebellar ataxia 1, Machado-Joseph disease or dentato-rubro-pallido-luysian atrophy locus. Mov Disord 1996, 11:174-180.
-
(1996)
Mov Disord
, vol.11
, pp. 174-180
-
-
Subramony, S.H.1
Manyam, B.N.2
Currier, R.D.3
-
43
-
-
0031934596
-
Autosomal dominant cerebellar ataxia (SCA 6): clinical, genetic and neuropathological study in a family
-
Takahashi H., Ikeuchi T., Houma Y., et al. Autosomal dominant cerebellar ataxia (SCA 6): clinical, genetic and neuropathological study in a family. Acta Neuropathol 1998, 95:333-337.
-
(1998)
Acta Neuropathol
, vol.95
, pp. 333-337
-
-
Takahashi, H.1
Ikeuchi, T.2
Houma, Y.3
-
44
-
-
0028141691
-
A clinical and pathologic study of a large Japanese family with Machado-Joseph disease tightly linked to the DNA markers on chromosome 14q
-
Takiyama Y., Oynagi S., Kawashima S., et al. A clinical and pathologic study of a large Japanese family with Machado-Joseph disease tightly linked to the DNA markers on chromosome 14q. Neurology 1994, 44:1302-1308.
-
(1994)
Neurology
, vol.44
, pp. 1302-1308
-
-
Takiyama, Y.1
Oynagi, S.2
Kawashima, S.3
-
45
-
-
0030056030
-
Decreased parvalbumin immunoreactivity in surviving Purkinje cells of patients with spinocerebellar ataxia-1
-
Vig P.J.S., Fratkin J.D., Desaiah D., et al. Decreased parvalbumin immunoreactivity in surviving Purkinje cells of patients with spinocerebellar ataxia-1. Neurology 1996, 47:249-253.
-
(1996)
Neurology
, vol.47
, pp. 249-253
-
-
Vig, P.J.S.1
Fratkin, J.D.2
Desaiah, D.3
-
46
-
-
0039803708
-
Evidence of peripheral neuropathy in a variety of heredo-familial olivo-ponto-cerebellar degenerations frequently seen in India
-
University of Tokyo Press, Tokyo, I. Sobue (Ed.)
-
Wadia N., Irani P., Mehta L., et al. Evidence of peripheral neuropathy in a variety of heredo-familial olivo-ponto-cerebellar degenerations frequently seen in India. Spinocerebellar Degenerations 1980, University of Tokyo Press, Tokyo. I. Sobue (Ed.).
-
(1980)
Spinocerebellar Degenerations
-
-
Wadia, N.1
Irani, P.2
Mehta, L.3
-
47
-
-
33746117919
-
Polyglutamine disease: recent advances in the neuropathology of dentatorubral-pallidoluysian atrophy
-
Yamada M., Shimohata M., Sato T., et al. Polyglutamine disease: recent advances in the neuropathology of dentatorubral-pallidoluysian atrophy. Neuropathology 2006, 26:346-351.
-
(2006)
Neuropathology
, vol.26
, pp. 346-351
-
-
Yamada, M.1
Shimohata, M.2
Sato, T.3
-
48
-
-
36949022900
-
CAG repeat disorder models and human neuropathology: similarities and differences
-
Yamada M., Sato T., Tsuji S., et al. CAG repeat disorder models and human neuropathology: similarities and differences. Acta Neuropathol 2008, 115:71-86.
-
(2008)
Acta Neuropathol
, vol.115
, pp. 71-86
-
-
Yamada, M.1
Sato, T.2
Tsuji, S.3
|