-
1
-
-
0032835166
-
Autosomal dominant cerebellar ataxia type I: oculomotor abnormalities in families with SCA1, SCA2, and SCA3
-
Bürk K., Fetter M., Abele M., Laccone F., Brice A., Dichgans J., and Klockgether T. Autosomal dominant cerebellar ataxia type I: oculomotor abnormalities in families with SCA1, SCA2, and SCA3. J. Neurol. 246 (1999) 789-797
-
(1999)
J. Neurol.
, vol.246
, pp. 789-797
-
-
Bürk, K.1
Fetter, M.2
Abele, M.3
Laccone, F.4
Brice, A.5
Dichgans, J.6
Klockgether, T.7
-
2
-
-
0030989388
-
Saccade velocity in idiopathic and autosomal dominant cerebellar ataxia
-
Bürk K., Fetter M., Skalej M., Laccone F., Stevanin G., Dichgans J., and Klockgether T. Saccade velocity in idiopathic and autosomal dominant cerebellar ataxia. J. Neurol. Neurosurg. Psychiat. 62 (1997) 662-664
-
(1997)
J. Neurol. Neurosurg. Psychiat.
, vol.62
, pp. 662-664
-
-
Bürk, K.1
Fetter, M.2
Skalej, M.3
Laccone, F.4
Stevanin, G.5
Dichgans, J.6
Klockgether, T.7
-
3
-
-
0031661913
-
Oculomotor phenotypes in autosomal dominant ataxias
-
Buttner N., Geschwind D., Jen J.C., Perlman S., Pulst S.M., and Baloh R.W. Oculomotor phenotypes in autosomal dominant ataxias. Arch. Neurol. 55 (1998) 1353-1357
-
(1998)
Arch. Neurol.
, vol.55
, pp. 1353-1357
-
-
Buttner, N.1
Geschwind, D.2
Jen, J.C.3
Perlman, S.4
Pulst, S.M.5
Baloh, R.W.6
-
4
-
-
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., Bellance R., Buisson G.G., Chneiweiss H., Dellanave J., et al. 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 (1995) 101-109
-
(1995)
Brain
, vol.118
, pp. 101-109
-
-
Dürr, A.1
Smadja, D.2
Cancel, G.3
Lezin, A.4
Stevanin, G.5
Mikol, J.6
Bellance, R.7
Buisson, G.G.8
Chneiweiss, H.9
Dellanave J.10
-
5
-
-
49349102234
-
-
Duvoisin R.C., and Plaitakis A. (Eds), Raven press, New York
-
In: Duvoisin R.C., and Plaitakis A. (Eds). The Olivopontocerebellar Atrophies (1984), Raven press, New York
-
(1984)
The Olivopontocerebellar Atrophies
-
-
-
6
-
-
49349110111
-
-
Geiner, S. (1995) Bestimmung der synaptischen Dichte an identifizierten praemotorischen Neuronen des okulomotorischen Systems des Menschen und vergleichende Untersuchung eines Falles mit Augenbewegungsstörungen. Doctoral Thesis. Ludwig-Maximilian University, Munich.
-
Geiner, S. (1995) Bestimmung der synaptischen Dichte an identifizierten praemotorischen Neuronen des okulomotorischen Systems des Menschen und vergleichende Untersuchung eines Falles mit Augenbewegungsstörungen. Doctoral Thesis. Ludwig-Maximilian University, Munich.
-
-
-
-
7
-
-
0022530791
-
The role of glutamate in neurotransmission and in neurologic disease
-
Greenamyre J.T. The role of glutamate in neurotransmission and in neurologic disease. Arch. Neurol. 43 (1986) 1058-1062
-
(1986)
Arch. Neurol.
, vol.43
, pp. 1058-1062
-
-
Greenamyre, J.T.1
-
8
-
-
0020641096
-
Classification of the hereditary ataxias and paraplegias
-
Harding A.E. Classification of the hereditary ataxias and paraplegias. The Lancet 1 (1983) 1151-1155
-
(1983)
The Lancet
, vol.1
, pp. 1151-1155
-
-
Harding, A.E.1
-
9
-
-
0029101426
-
Histological identification of premotor neurons for horizontal saccades in monkey and man by parvalbumin immunostaining
-
Horn A.K.E., Büttner-Ennever J.A., Suzuki Y., and Henn V. Histological identification of premotor neurons for horizontal saccades in monkey and man by parvalbumin immunostaining. J. Comp. Neurol. 359 (1995) 350-363
-
(1995)
J. Comp. Neurol.
, vol.359
, pp. 350-363
-
-
Horn, A.K.E.1
Büttner-Ennever, J.A.2
Suzuki, Y.3
Henn, V.4
-
10
-
-
0028353885
-
Neurotransmitter profile of saccadic omnipause neurons in nucleus raphe interpositus
-
Horn A.K.E., Büttner-Ennever J.A., Wahle P., and Reichenberger I. Neurotransmitter profile of saccadic omnipause neurons in nucleus raphe interpositus. J. Neurosci. 14 (1994) 2032-2046
-
(1994)
J. Neurosci.
, vol.14
, pp. 2032-2046
-
-
Horn, A.K.E.1
Büttner-Ennever, J.A.2
Wahle, P.3
Reichenberger, I.4
-
11
-
-
0029891884
-
Effect of ibotenic acid lesions of the omnipause neurons on saccadic eye movements in Rhesus macaques
-
Kaneko C.R.S. Effect of ibotenic acid lesions of the omnipause neurons on saccadic eye movements in Rhesus macaques. J. Neurophysiol. 75 (1996) 2229-2242
-
(1996)
J. Neurophysiol.
, vol.75
, pp. 2229-2242
-
-
Kaneko, C.R.S.1
-
12
-
-
0343526456
-
The molecular biology of the autosomal-dominant cerebellar ataxias
-
Klockgether T., Wüllner U., Spauschus A., and Evert B. The molecular biology of the autosomal-dominant cerebellar ataxias. Mov. Disord. 15 (2000) 604-612
-
(2000)
Mov. Disord.
, vol.15
, pp. 604-612
-
-
Klockgether, T.1
Wüllner, U.2
Spauschus, A.3
Evert, B.4
-
14
-
-
0030848204
-
Clinical aspects of CAG repeat diseases
-
Nance M.A. Clinical aspects of CAG repeat diseases. Brain Pathol. 7 (1997) 881-900
-
(1997)
Brain Pathol.
, vol.7
, pp. 881-900
-
-
Nance, M.A.1
-
15
-
-
0028859878
-
Autosomal dominant cerebellar phenotypes: the genotype has settled the issue
-
Rosenberg R.N. Autosomal dominant cerebellar phenotypes: the genotype has settled the issue. Neurol. 45 (1995) 1-5
-
(1995)
Neurol.
, vol.45
, pp. 1-5
-
-
Rosenberg, R.N.1
-
16
-
-
0021196320
-
A variety of olivopontocerebellar atrophy distinguished by slow eye movements and peripheral neuropathy
-
Duvoisin R.C., and Plaitakis A. (Eds), Raven press, New York
-
Wadia N. A variety of olivopontocerebellar atrophy distinguished by slow eye movements and peripheral neuropathy. In: Duvoisin R.C., and Plaitakis A. (Eds). The Olivopontocerebellar Atrophies (1984), Raven press, New York 149-177
-
(1984)
The Olivopontocerebellar Atrophies
, pp. 149-177
-
-
Wadia, N.1
-
17
-
-
0031797677
-
A clinicogenetic analysis of six Indian spinocerebellar ataxia (SCA2) pedigrees: the significance of slow saccades in diagnosis
-
Wadia N., Pang J., Desai J., Mankodi A., Desai M., and Chamberlain S. A clinicogenetic analysis of six Indian spinocerebellar ataxia (SCA2) pedigrees: the significance of slow saccades in diagnosis. Brain 121 (1998) 2341-2355
-
(1998)
Brain
, vol.121
, pp. 2341-2355
-
-
Wadia, N.1
Pang, J.2
Desai, J.3
Mankodi, A.4
Desai, M.5
Chamberlain, S.6
-
18
-
-
0014998732
-
A new form of heredo-familial spinocerebellar degeneration with slow eye movements (nine families)
-
Wadia N.H., and Swami R.K. A new form of heredo-familial spinocerebellar degeneration with slow eye movements (nine families). Brain 94 (1971) 359-374
-
(1971)
Brain
, vol.94
, pp. 359-374
-
-
Wadia, N.H.1
Swami, R.K.2
-
19
-
-
0017249903
-
Slow saccades in spinocerebellar degeneration
-
Zee D.S., Optican L.M., Cook J.D., Robinson D.A., and Engel W.K. Slow saccades in spinocerebellar degeneration. Arch. Neurol. 33 (1976) 243-251
-
(1976)
Arch. Neurol.
, vol.33
, pp. 243-251
-
-
Zee, D.S.1
Optican, L.M.2
Cook, J.D.3
Robinson, D.A.4
Engel, W.K.5
|