-
1
-
-
0020076144
-
Olivopontocerebellar atrophy. A review of 117 cases
-
Berciano J. Olivopontocerebellar atrophy. A review of 117 cases. J. Neurol. Sci. 1982, 53:253-272.
-
(1982)
J. Neurol. Sci.
, vol.53
, pp. 253-272
-
-
Berciano, J.1
-
2
-
-
0020641096
-
Classification of the hereditary ataxias and paraplegias
-
Harding A.E. Classification of the hereditary ataxias and paraplegias. Lancet 1983, i:1151-1155.
-
(1983)
Lancet
, vol.i
, pp. 1151-1155
-
-
Harding, A.E.1
-
3
-
-
11144356369
-
Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis
-
Schöls L., Bauer P., Schmidt T., Schulte T., Riess O. Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis. Lancet Neurol. 2004, 3:291-304.
-
(2004)
Lancet Neurol.
, vol.3
, pp. 291-304
-
-
Schöls, L.1
Bauer, P.2
Schmidt, T.3
Schulte, T.4
Riess, O.5
-
4
-
-
0043127451
-
Dominant ataxias and Friedreich ataxia: an update
-
Albin R.L. Dominant ataxias and Friedreich ataxia: an update. Curr. Opin. Neurol. 2003, 16:507-514.
-
(2003)
Curr. Opin. Neurol.
, vol.16
, pp. 507-514
-
-
Albin, R.L.1
-
5
-
-
20844458601
-
Glial cell cytoplasmic inclusions in SCA2 do not express α-synuclein
-
Berciano J., Ferrer I. Glial cell cytoplasmic inclusions in SCA2 do not express α-synuclein. J. Neurol. 2005, 252:742-744.
-
(2005)
J. Neurol.
, vol.252
, pp. 742-744
-
-
Berciano, J.1
Ferrer, I.2
-
6
-
-
0025876335
-
Hered-itary ataxias and paraplegias in Cantabria, Spain. An epidemiological and clinical study
-
Polo J.M., Calleja J., Combarros O., Berciano J. Hered-itary ataxias and paraplegias in Cantabria, Spain. An epidemiological and clinical study. Brain 1991, 114:855-866.
-
(1991)
Brain
, vol.114
, pp. 855-866
-
-
Polo, J.M.1
Calleja, J.2
Combarros, O.3
Berciano, J.4
-
7
-
-
0027742974
-
Autosomal dominant cerebellar ataxia type I is unrelated to genetic heterogeneity
-
Dürr A., Chneiweiss H., Kathi C., Stevanin G., Cancel G., Feingold J., Agid Y., Brice A. Autosomal dominant cerebellar ataxia type I is unrelated to genetic heterogeneity. Brain 1993, 116:1497-1508.
-
(1993)
Brain
, vol.116
, pp. 1497-1508
-
-
Dürr, A.1
Chneiweiss, H.2
Kathi, C.3
Stevanin, G.4
Cancel, G.5
Feingold, J.6
Agid, Y.7
Brice, A.8
-
8
-
-
0023719083
-
Motor dysfunction in olivopon-tocerebellar atrophy is related to cerebral metabolic rate with positron emission tomography
-
Roshenthal G., Gilman S., Koeppe R.A., Kluin K.J., Martel D.S., Junck L., Gebarski S.S. Motor dysfunction in olivopon-tocerebellar atrophy is related to cerebral metabolic rate with positron emission tomography. Ann. Neurol. 1988, 24:414-419.
-
(1988)
Ann. Neurol.
, vol.24
, pp. 414-419
-
-
Roshenthal, G.1
Gilman, S.2
Koeppe, R.A.3
Kluin, K.J.4
Martel, D.S.5
Junck, L.6
Gebarski, S.S.7
-
9
-
-
0026040351
-
Presynaptic parkinsonism in olivopontocerebellar atrophy: clinical, pathological and neurochemical evidence
-
Pascual J., Pazos A., Del Olmo E., Figols J., Leno C., Berciano J. Presynaptic parkinsonism in olivopontocerebellar atrophy: clinical, pathological and neurochemical evidence. Ann. Neurol. 1991, 30:425-428.
-
(1991)
Ann. Neurol.
, vol.30
, pp. 425-428
-
-
Pascual, J.1
Pazos, A.2
Del, O.E.3
Figols, J.4
Leno, C.5
Berciano, J.6
-
10
-
-
0029053255
-
Positron emission tomography studies on the dopaminergic system and striatal opioid binding in the olivopon-tocerebellar atrophy variant of multiple system at
-
Rinne J.O., Burn D.J., Mathias C.J., Quinn N.P., Marsden C.D., Brooks D.J. Positron emission tomography studies on the dopaminergic system and striatal opioid binding in the olivopon-tocerebellar atrophy variant of multiple system at. Ann. Neurol. 1995, 37:568-573.
-
(1995)
Ann. Neurol.
, vol.37
, pp. 568-573
-
-
Rinne, J.O.1
Burn, D.J.2
Mathias, C.J.3
Quinn, N.P.4
Marsden, C.D.5
Brooks, D.J.6
-
11
-
-
0033046989
-
Spinocerebellar ataxia 2 (SCA2): morphometric analyses in 11 autopsies
-
Estrada R., Galarraga J., Orozco G., Nodarse A., Auburger G. Spinocerebellar ataxia 2 (SCA2): morphometric analyses in 11 autopsies. Acta Neuropathol. (Berl.) 1999, 97:303-311.
-
(1999)
Acta Neuropathol. (Berl.)
, vol.97
, pp. 303-311
-
-
Estrada, R.1
Galarraga, J.2
Orozco, G.3
Nodarse, A.4
Auburger, G.5
-
12
-
-
18944384702
-
Autosomal dominant cerebellar ataxias in Spain. Molecular and clinical correlations, prevalence estimation and survival analysis
-
Infante J., Combarros O., Volpini V., Corral J., Llorca J, Berciano J. Autosomal dominant cerebellar ataxias in Spain. Molecular and clinical correlations, prevalence estimation and survival analysis. Acta Neurol. Scand. 2005, 111:391-399.
-
(2005)
Acta Neurol. Scand.
, vol.111
, pp. 391-399
-
-
Infante, J.1
Combarros, O.2
Volpini, V.3
Corral, J.4
Llorca, J.5
Berciano, J.6
-
13
-
-
0028125274
-
Brainstem reflexes in patients with olivopontocerebellar atrophy
-
Valls-Solé J., Lou J., Hallet M. Brainstem reflexes in patients with olivopontocerebellar atrophy. Muscle Nerve 1994, 17:1439-1448.
-
(1994)
Muscle Nerve
, vol.17
, pp. 1439-1448
-
-
Valls-Solé, J.1
Lou, J.2
Hallet, M.3
-
14
-
-
0024464624
-
Non-Alzheimer type pattern of brain choline acetyltransferase reduction in dominantly inherited olivopontocerebellar atrophy
-
Kish S.J., Robitaille Y., El-Awar M., Deck J.H., Simmonds J., Schut J., Chang L.J., DiStefano L., Freeman M. Non-Alzheimer type pattern of brain choline acetyltransferase reduction in dominantly inherited olivopontocerebellar atrophy. Ann. Neurol. 1989, 26:362-367.
-
(1989)
Ann. Neurol.
, vol.26
, pp. 362-367
-
-
Kish, S.J.1
Robitaille, Y.2
El-Awar, M.3
Deck, J.H.4
Simmonds, J.5
Schut, J.6
Chang, L.J.7
DiStefano, L.8
Freeman, M.9
-
15
-
-
0021946356
-
Neuronal loss in the basal nucleus of Meynert in a patient with olivopontocerebellar atrophy
-
Tagliavini F., Pilleri G. Neuronal loss in the basal nucleus of Meynert in a patient with olivopontocerebellar atrophy. Acta Neuropathol. (Berl.) 1985, 66:127-133.
-
(1985)
Acta Neuropathol. (Berl.)
, vol.66
, pp. 127-133
-
-
Tagliavini, F.1
Pilleri, G.2
-
16
-
-
0028325407
-
Disease-specific patterns of neuronal loss in the spinal ventral horn in amyotrophic lateral sclerosis, multiple system atrophy and X-linked recessive bulbosp
-
Terao S., Sobue G., Hashizume Y., Mitsuma T., Takahashi A. Disease-specific patterns of neuronal loss in the spinal ventral horn in amyotrophic lateral sclerosis, multiple system atrophy and X-linked recessive bulbosp. J. Neurol. 1994, 241:196-203.
-
(1994)
J. Neurol.
, vol.241
, pp. 196-203
-
-
Terao, S.1
Sobue, G.2
Hashizume, Y.3
Mitsuma, T.4
Takahashi, A.5
-
17
-
-
0022644448
-
Urethral dysfunction in progressive autonomic failure with multiple system atrophy
-
Kirby R., Fowler C., Gosling J., Bannister R. Urethral dysfunction in progressive autonomic failure with multiple system atrophy. J. Neurol. Neurosurg. Psychiatry 1986, 49:554-562.
-
(1986)
J. Neurol. Neurosurg. Psychiatry
, vol.49
, pp. 554-562
-
-
Kirby, R.1
Fowler, C.2
Gosling, J.3
Bannister, R.4
-
18
-
-
0034765061
-
Depletion of corticotrophin-releasing factor neurons in the pontine micturition area in multiple system atrophy
-
Benarroch E.E., Schmeichel A.M. Depletion of corticotrophin-releasing factor neurons in the pontine micturition area in multiple system atrophy. Ann. Neurol. 2001, 50:640-645.
-
(2001)
Ann. Neurol.
, vol.50
, pp. 640-645
-
-
Benarroch, E.E.1
Schmeichel, A.M.2
-
19
-
-
20844441602
-
Damage to the reticulotegmental nucleus of the pons in spinocerebellar ataxia type 1, 2, and 3
-
Rüb U., Bürk K., Schöls L., Brunt F.G., de Voss R.A., Diez G.O., Gierga K., Ghebremedhin E., Schultz C., Del Turco D., Mittelbronn M., Auburger G., Deller T., Braak H. Damage to the reticulotegmental nucleus of the pons in spinocerebellar ataxia type 1, 2, and 3. Neurology 2004, 63:1258-1263.
-
(2004)
Neurology
, vol.63
, pp. 1258-1263
-
-
Rüb, U.1
Bürk, K.2
Schöls, L.3
Brunt, F.G.4
de, V.R.A.5
Diez, G.O.6
Gierga, K.7
Ghebremedhin, E.8
Schultz, C.9
Del, T.D.10
Mittelbronn, M.11
Auburger, G.12
Deller, T.13
Braak, H.14
-
20
-
-
0031648543
-
Sleep disturbance in spinocerebellar ataxias. Is the SCA3 muta-tion a cause of restless legs syndrome?
-
Schöls L., Haan J., Riess O., Amoiridis G., Przuntek K.H. Sleep disturbance in spinocerebellar ataxias. Is the SCA3 muta-tion a cause of restless legs syndrome?. Neurology 1998, 51:1603-1607.
-
(1998)
Neurology
, vol.51
, pp. 1603-1607
-
-
Schöls, L.1
Haan, J.2
Riess, O.3
Amoiridis, G.4
Przuntek, K.H.5
-
21
-
-
15244341379
-
Recent advances in hereditary spinocerebellar ataxia
-
Van de Warrenburg B.P., Sinke R.J., Kremer B. Recent advances in hereditary spinocerebellar ataxia. JNEP 2005, 64:171-180.
-
(2005)
JNEP
, vol.64
, pp. 171-180
-
-
Van, D.W.B.P.1
Sinke, R.J.2
Kremer, B.3
-
22
-
-
0019484086
-
"Idiopathic" late onset cerebellar ataxia. A clinical and genetic study of 36 cases
-
Harding A.E. "Idiopathic" late onset cerebellar ataxia. A clinical and genetic study of 36 cases. J. Neurol. Sci. 1981, 51:259-271.
-
(1981)
J. Neurol. Sci.
, vol.51
, pp. 259-271
-
-
Harding, A.E.1
-
23
-
-
0033837087
-
Evolution of sporadic olivopontocerebellar atrophy into multiple system atrophy
-
Gilman S., Little R., Johanns J., Heumann M., Kluin K.J., Junck K.L., Koeppe R.A., An H. 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
Heumann, M.4
Kluin, K.J.5
Junck, K.L.6
Koeppe, R.A.7
An, H.8
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