-
1
-
-
0021476278
-
The varied clinical expressions of dystonia
-
Fahn S. The varied clinical expressions of dystonia. Neurol Clin 1984;2:541-54
-
(1984)
Neurol Clin
, vol.2
, pp. 541-554
-
-
Fahn, S.1
-
2
-
-
0023675531
-
Concept and classification of dystonia
-
Fahn S. Concept and classification of dystonia. Adv Neurol 1988;50:1-8
-
(1988)
Adv Neurol
, vol.50
, pp. 1-8
-
-
Fahn, S.1
-
3
-
-
0141868763
-
Dystonia: Phenotypes and genotypes
-
Bressman SB. Dystonia: phenotypes and genotypes. Rev Neurol 2003;159:849-56
-
(2003)
Rev Neurol
, vol.159
, pp. 849-856
-
-
Bressman, S.B.1
-
4
-
-
0036212214
-
The genetics of primary dystonias and related disorders
-
Nemeth AH. The genetics of primary dystonias and related disorders. Brain 2002;125:695-721
-
(2002)
Brain
, vol.125
, pp. 695-721
-
-
Nemeth, A.H.1
-
6
-
-
85057436097
-
-
Defazio G. Epidemiology of primary and secondary dystonia. In: Handbook of Dystonia. Stacey ME (Ed.), New York, USA: Informa Healthcare; 2007. p. 11-20
-
Defazio G. Epidemiology of primary and secondary dystonia. In: Handbook of Dystonia. Stacey ME (Ed.), New York, USA: Informa Healthcare; 2007. p. 11-20
-
-
-
-
7
-
-
33751545897
-
Dystonia in Parkinson's disease
-
Tolosa E, Compta Y. Dystonia in Parkinson's disease. J Neurol 2006;253(Suppl 7):7-13
-
(2006)
J Neurol
, vol.253
, Issue.SUPPL. 7
, pp. 7-13
-
-
Tolosa, E.1
Compta, Y.2
-
9
-
-
4544345754
-
Classification and definition of disorders causing hypertonia in childhood
-
Sanger TD, Delgado MR, Gaebler-Spira D, et al. Classification and definition of disorders causing hypertonia in childhood. Pediatrics 2003;111:89-97
-
(2003)
Pediatrics
, vol.111
, pp. 89-97
-
-
Sanger, T.D.1
Delgado, M.R.2
Gaebler-Spira, D.3
-
10
-
-
0020052267
-
Dyskinetic cerebral palsy. I. Clinical categories, associated neurological abnormalities and incidences
-
Kyllerman M, Bager B, Bensch J, et al. Dyskinetic cerebral palsy. I. Clinical categories, associated neurological abnormalities and incidences. Acta Pediatr Scand 1982;71:543-50
-
(1982)
Acta Pediatr Scand
, vol.71
, pp. 543-550
-
-
Kyllerman, M.1
Bager, B.2
Bensch, J.3
-
12
-
-
33750583772
-
Treatment of dystonia
-
Jankovic J. Treatment of dystonia. Lancet Neurol 2006;5:864-72
-
(2006)
Lancet Neurol
, vol.5
, pp. 864-872
-
-
Jankovic, J.1
-
13
-
-
33744728066
-
A systematic review on the diagnosis and treatment of primary (idiopathic) dystonia and dystonia plus syndromes: Repor of an EFNS/MDS-ES task force
-
Albanese A, Barnes MP, Bhatia KP, et al. A systematic review on the diagnosis and treatment of primary (idiopathic) dystonia and dystonia plus syndromes: repor of an EFNS/MDS-ES task force. Eur J Neurol 2006; 13:433-44
-
(2006)
Eur J Neurol
, vol.13
, pp. 433-444
-
-
Albanese, A.1
Barnes, M.P.2
Bhatia, K.P.3
-
14
-
-
0026778221
-
Baclofen in the treatment of dystonia
-
Greene P. Baclofen in the treatment of dystonia. Clin Neuropharmacol 1992;15:276-88
-
(1992)
Clin Neuropharmacol
, vol.15
, pp. 276-288
-
-
Greene, P.1
-
15
-
-
0033724391
-
Intrathecal baclofen for dystonia: Benefits and complications during six years of experience
-
Walker RH, Danisi FO, Swope DM, et al. Intrathecal baclofen for dystonia: benefits and complications during six years of experience. Mov Disord 2000; 15:1242-7
-
(2000)
Mov Disord
, vol.15
, pp. 1242-1247
-
-
Walker, R.H.1
Danisi, F.O.2
Swope, D.M.3
-
16
-
-
41249093716
-
-
Arce CA. Selective denervation in cervical dystonia. In: Handbook of dystonia. Stacey MA (Ed.), New York, USA: Informa Healthcare; 2007. p. 381-92
-
Arce CA. Selective denervation in cervical dystonia. In: Handbook of dystonia. Stacey MA (Ed.), New York, USA: Informa Healthcare; 2007. p. 381-92
-
-
-
-
17
-
-
41249097376
-
-
Marks WJJ. Brain surgery for dystonia. In: Handbook of Dystonia. Stacey MA (Ed.), New York, USA: Informa Healthcare; 2007. p. 393-406
-
Marks WJJ. Brain surgery for dystonia. In: Handbook of Dystonia. Stacey MA (Ed.), New York, USA: Informa Healthcare; 2007. p. 393-406
-
-
-
-
18
-
-
18144430546
-
Rodent models for dystonia research: Characteristics, evaluation, and utility
-
Jinnah HA, Hess EJ, Ledoux MS, et al. Rodent models for dystonia research: characteristics, evaluation, and utility. Mov Disord 2005;20:283-92
-
(2005)
Mov Disord
, vol.20
, pp. 283-292
-
-
Jinnah, H.A.1
Hess, E.J.2
Ledoux, M.S.3
-
19
-
-
16944366666
-
The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein
-
Ozelius LJ, Hewett JW, Page CE, et al. The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein. Nat Genet 1997;17:408
-
(1997)
Nat Genet
, vol.17
, pp. 408
-
-
Ozelius, L.J.1
Hewett, J.W.2
Page, C.E.3
-
20
-
-
0034702033
-
Mutant torsinA, responsible for early-onset torsion dystonia, forms membrane inclusions in cultured neural cells
-
Hewett JW, Gonzalez-Agosti C, Slater D, et al. Mutant torsinA, responsible for early-onset torsion dystonia, forms membrane inclusions in cultured neural cells. Hum Mol Genet 2000;9:1403-13
-
(2000)
Hum Mol Genet
, vol.9
, pp. 1403-1413
-
-
Hewett, J.W.1
Gonzalez-Agosti, C.2
Slater, D.3
-
21
-
-
29144460260
-
Loss of the dystonia-associated protein torsinA selectively disrupts the neuronal nuclear envelope
-
Goodchild RE, Kim CE, Dauer WT. Loss of the dystonia-associated protein torsinA selectively disrupts the neuronal nuclear envelope. Neuron 2005;48:923-32
-
(2005)
Neuron
, vol.48
, pp. 923-932
-
-
Goodchild, R.E.1
Kim, C.E.2
Dauer, W.T.3
-
22
-
-
19944429223
-
Transgenic mouse model of early-onset dyt1 dystonia
-
Shashidharan P, Sandu D, Potla U, et al. Transgenic mouse model of early-onset dyt1 dystonia. Hum Mol Genet 2005;14(1):125-33
-
(2005)
Hum Mol Genet
, vol.14
, Issue.1
, pp. 125-133
-
-
Shashidharan, P.1
Sandu, D.2
Potla, U.3
-
23
-
-
20044374519
-
Impaired motor learning in mice expressing torsinA with the dyt1 dystonia mutation
-
Sharma N, Baxter MG, Petravicz J, et al. Impaired motor learning in mice expressing torsinA with the dyt1 dystonia mutation. J Neurosci 2005;25(22):5351-5
-
(2005)
J Neurosci
, vol.25
, Issue.22
, pp. 5351-5355
-
-
Sharma, N.1
Baxter, M.G.2
Petravicz, J.3
-
24
-
-
34447641630
-
Overexpression of human wildtype torsinA and human deltaGAG torsinA in a transgenic mousemodel causes phenotypic abnormalities
-
Grundmann M, Reischmann B, Vanhoutte G, et al. Overexpression of human wildtype torsinA and human deltaGAG torsinA in a transgenic mousemodel causes phenotypic abnormalities. Neurobiol Dis 2007;27:19-206
-
(2007)
Neurobiol Dis
, vol.27
, pp. 19-206
-
-
Grundmann, M.1
Reischmann, B.2
Vanhoutte, G.3
-
25
-
-
27744567561
-
Generation and characterization of Dyt1 deltaGAG knock-in mouse as a model for early-onset dystonia
-
Dang MT, Yokoi F, McNaught KS, et al. Generation and characterization of Dyt1 deltaGAG knock-in mouse as a model for early-onset dystonia. Exp Neurol 2005;196:452-63
-
(2005)
Exp Neurol
, vol.196
, pp. 452-463
-
-
Dang, M.T.1
Yokoi, F.2
McNaught, K.S.3
-
26
-
-
0016914818
-
Dystonia musculorum - an inherited disease of the nervous system in the mouse
-
Duchen LW. Dystonia musculorum - an inherited disease of the nervous system in the mouse. Adv Neurol 1976;14:353-65
-
(1976)
Adv Neurol
, vol.14
, pp. 353-365
-
-
Duchen, L.W.1
-
27
-
-
0021222931
-
Characterization of the rat mutant dystonic (dt): A new animal model of dystonia musculorum deformans
-
Lorden JF, McKeon TW, Baker HJ, et al. Characterization of the rat mutant dystonic (dt): a new animal model of dystonia musculorum deformans. J Neurosci 1984;4:1925-32
-
(1984)
J Neurosci
, vol.4
, pp. 1925-1932
-
-
Lorden, J.F.1
McKeon, T.W.2
Baker, H.J.3
-
28
-
-
0024365484
-
The sz mutant hamster: A genetic model of epilepsy or of paroxysmal dystonia?
-
Loscher W, Fisher JE, Schmidt D, et al. The sz mutant hamster: a genetic model of epilepsy or of paroxysmal dystonia? Mov Disord 1989;4:219-32
-
(1989)
Mov Disord
, vol.4
, pp. 219-232
-
-
Loscher, W.1
Fisher, J.E.2
Schmidt, D.3
-
29
-
-
0032040365
-
Pathology of idiopathic dystonia: Findings from genetic animal models
-
Richter A, Loscher W. Pathology of idiopathic dystonia: findings from genetic animal models. Prog Neurobiol 1998;54:633-77
-
(1998)
Prog Neurobiol
, vol.54
, pp. 633-677
-
-
Richter, A.1
Loscher, W.2
-
30
-
-
0037104726
-
Altered discharge pattern of basal ganglia output neurons in an animal model of idiopathic dystonia
-
Gernert M, Bennay M, Fedrowitz M, et al. Altered discharge pattern of basal ganglia output neurons in an animal model of idiopathic dystonia. J Neurosci 2002;22:7244-53
-
(2002)
J Neurosci
, vol.22
, pp. 7244-7253
-
-
Gernert, M.1
Bennay, M.2
Fedrowitz, M.3
-
31
-
-
0030584085
-
Absence epilepsy in tottering mutant mice is associated with calcium channel defects
-
Fletcher CF, Lutz CM, O'Sullivan TN, et al. Absence epilepsy in tottering mutant mice is associated with calcium channel defects. Cell 1996;87:607-17
-
(1996)
Cell
, vol.87
, pp. 607-617
-
-
Fletcher, C.F.1
Lutz, C.M.2
O'Sullivan, T.N.3
-
32
-
-
0032567437
-
Single tottering mutations responsible for the neuropathic phenotype of the P-type calcium channel
-
Wakamori M, Yamazaki K, Matsunodaira H. Single tottering mutations responsible for the neuropathic phenotype of the P-type calcium channel. J Biol Chem 1998;52:34857-67
-
(1998)
J Biol Chem
, vol.52
, pp. 34857-34867
-
-
Wakamori, M.1
Yamazaki, K.2
Matsunodaira, H.3
-
33
-
-
0031949521
-
Cerebellar circuitry is activated during convulsive episodes in the tottering (tg/tg) mutant mouse
-
Campbell DB, Hess EJ. Cerebellar circuitry is activated during convulsive episodes in the tottering (tg/tg) mutant mouse. Neuroscience 1998;85:773-83
-
(1998)
Neuroscience
, vol.85
, pp. 773-783
-
-
Campbell, D.B.1
Hess, E.J.2
-
34
-
-
0032710832
-
Tottering mouse motor dysfunction is abolished on the Purkinje cell degeneration (pcd) mutant background
-
Campbell DB, North JB, Hess EJ. Tottering mouse motor dysfunction is abolished on the Purkinje cell degeneration (pcd) mutant background. Exp Neurol 1999; 160:268-78
-
(1999)
Exp Neurol
, vol.160
, pp. 268-278
-
-
Campbell, D.B.1
North, J.B.2
Hess, E.J.3
-
35
-
-
0142103763
-
Focal hand dystonia may result from aberrant neuroplasticity
-
Byl NN. Focal hand dystonia may result from aberrant neuroplasticity. Adv Neurol 1994;94:19-28
-
(1994)
Adv Neurol
, vol.94
, pp. 19-28
-
-
Byl, N.N.1
-
36
-
-
0026100745
-
Basal ganglia motor control. III. Pallidal ablation: Normal reaction time, muscle cocontraction, and slow movement
-
Mink JW, Thach WT. Basal ganglia motor control. III. Pallidal ablation: normal reaction time, muscle cocontraction, and slow movement. J Neurophysiol 1991;65:330-51
-
(1991)
J Neurophysiol
, vol.65
, pp. 330-351
-
-
Mink, J.W.1
Thach, W.T.2
-
37
-
-
0028890583
-
Selective putaminal excitotoxic lesions in non-human primates model the movement disorder of Huntington disease
-
Burns LH, Pakzaban P, Deacon TW, et al. Selective putaminal excitotoxic lesions in non-human primates model the movement disorder of Huntington disease. Neuroscience 1995;64:1007-17
-
(1995)
Neuroscience
, vol.64
, pp. 1007-1017
-
-
Burns, L.H.1
Pakzaban, P.2
Deacon, T.W.3
-
39
-
-
0020453355
-
Frontal torticollis (head tilt) induced by electrolytic lesion and kainic acid injection in monkeys and cats
-
Malouin F, Bedard PJ. Frontal torticollis (head tilt) induced by electrolytic lesion and kainic acid injection in monkeys and cats. Exp Neurol 1982;78:551-60
-
(1982)
Exp Neurol
, vol.78
, pp. 551-560
-
-
Malouin, F.1
Bedard, P.J.2
-
41
-
-
0021826543
-
The anatomical basis of symptomatic dystonia
-
Marsden CD, Obeso JA, Zarranz JJ. The anatomical basis of symptomatic dystonia. Brain 1985;108:463-83
-
(1985)
Brain
, vol.108
, pp. 463-483
-
-
Marsden, C.D.1
Obeso, J.A.2
Zarranz, J.J.3
-
42
-
-
0030659028
-
MPTP induces dystonia and parkinsonism. Clues to the pathophysiology of dystonia
-
Perlmutter JS, Tempel LW, Black KJ, et al. MPTP induces dystonia and parkinsonism. Clues to the pathophysiology of dystonia. Neurology 1997;49:1432-8
-
(1997)
Neurology
, vol.49
, pp. 1432-1438
-
-
Perlmutter, J.S.1
Tempel, L.W.2
Black, K.J.3
-
43
-
-
33746419587
-
-
Tabbal SD, Mink JW, Antenor JAV, et al. 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced acute transient dystonia in monkeys with low striatal dopamine. Neuroscience 2006; 141:1281-7
-
Tabbal SD, Mink JW, Antenor JAV, et al. 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced acute transient dystonia in monkeys with low striatal dopamine. Neuroscience 2006; 141:1281-7
-
-
-
-
44
-
-
0025266077
-
Induction of chorea and dystonia in Parkinsonian primates
-
Boyce S, Clarke CE, Luguin R, et al. Induction of chorea and dystonia in Parkinsonian primates. Mov Disord 1990;5:3-7
-
(1990)
Mov Disord
, vol.5
, pp. 3-7
-
-
Boyce, S.1
Clarke, C.E.2
Luguin, R.3
-
45
-
-
0029937779
-
Manganese intoxication in the rhesus monkey: A clinical, imaging, pathologic, and biochemical study
-
Olanow CW, Good PF, Shinotoh H, et al. Manganese intoxication in the rhesus monkey: a clinical, imaging, pathologic, and biochemical study. Neurology 1996;46:492-8
-
(1996)
Neurology
, vol.46
, pp. 492-498
-
-
Olanow, C.W.1
Good, P.F.2
Shinotoh, H.3
-
46
-
-
0037137498
-
-
Ghorayeb I, Fernagut PO, Stefanova N, et al. Dystonia is predictive of subsequent altered dopaminergic responsiveness in a chronic 1-methyl4-phenyl-1,2,3,6-tetrahydropyridine + 3-nitropropionic acid model of striatonigral degeneration in monkeys. Neurosci Lett 2002;335:34-8
-
Ghorayeb I, Fernagut PO, Stefanova N, et al. Dystonia is predictive of subsequent altered dopaminergic responsiveness in a chronic 1-methyl4-phenyl-1,2,3,6-tetrahydropyridine + 3-nitropropionic acid model of striatonigral degeneration in monkeys. Neurosci Lett 2002;335:34-8
-
-
-
-
47
-
-
0029118136
-
Chronic mitochondrial energy impairment produces selective striatal degeneration and abnormal choreiform movements in primates
-
Brouillet E, Hantraye P, Ferrante RJ, et al. Chronic mitochondrial energy impairment produces selective striatal degeneration and abnormal choreiform movements in primates. Proc Natl Acad Sci USA 1995;92:7105-9
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 7105-7109
-
-
Brouillet, E.1
Hantraye, P.2
Ferrante, R.J.3
-
48
-
-
34248598584
-
Invertebrate animal models of diseases as screening tools in drug discovery. ACS
-
Segalat L. Invertebrate animal models of diseases as screening tools in drug discovery. ACS Chem Biol 2007;2:231-6
-
(2007)
Chem Biol
, vol.2
, pp. 231-236
-
-
Segalat, L.1
-
49
-
-
84882401716
-
-
Caldwell GA, Cao S, Izevbaye I, Caldwell KA. Use of C. elegans to model human movement disorders. In: Animal Models of Movement Disorders. LeDoux MS (Ed.), Burlington, USA: Elsevier; 2005. p. 111-26
-
Caldwell GA, Cao S, Izevbaye I, Caldwell KA. Use of C. elegans to model human movement disorders. In: Animal Models of Movement Disorders. LeDoux MS (Ed.), Burlington, USA: Elsevier; 2005. p. 111-26
-
-
-
-
51
-
-
0141940628
-
Animal models of Parkinson's disease in rodents induced by toxins: An update
-
Hirsch EC, Hoglinger G, Rousselet E, et al. Animal models of Parkinson's disease in rodents induced by toxins: an update. Neural Transm Suppl 2003;65:89-100
-
(2003)
Neural Transm Suppl
, vol.65
, pp. 89-100
-
-
Hirsch, E.C.1
Hoglinger, G.2
Rousselet, E.3
-
53
-
-
22244442489
-
The biochemistry of Parkinson's disease
-
Cookson MR. The biochemistry of Parkinson's disease. Annu Rev Biochem 2005;74:29-52
-
(2005)
Annu Rev Biochem
, vol.74
, pp. 29-52
-
-
Cookson, M.R.1
-
54
-
-
33947323759
-
-
Benatar M. Lost in translation: treatment trials in the SOD1 mouse and in human ALS. Neurobiol Dis 2007;26:1-13
-
Benatar M. Lost in translation: treatment trials in the SOD1 mouse and in human ALS. Neurobiol Dis 2007;26:1-13
-
-
-
-
55
-
-
33747887690
-
The value of animal models for drug development in multiple sclerosis
-
Friese MA, Montalban X, Willcox N, et al. The value of animal models for drug development in multiple sclerosis. Brain 2006; 129:1940-52
-
(2006)
Brain
, vol.129
, pp. 1940-1952
-
-
Friese, M.A.1
Montalban, X.2
Willcox, N.3
-
56
-
-
19544376511
-
Neuroprotection for ischemic stroke: Two decades of success and failure
-
Cheng YD, Al-Khoury L, Zivin JA. Neuroprotection for ischemic stroke: two decades of success and failure. NeuroRx 2004; 1:36-45
-
(2004)
NeuroRx
, vol.1
, pp. 36-45
-
-
Cheng, Y.D.1
Al-Khoury, L.2
Zivin, J.A.3
-
57
-
-
0036330007
-
Toward wisdom from failure: Lessons from neuroprotective stroke trials and new therapeutic directions
-
Gladstone DJ, Black SE, Hakim AM. Toward wisdom from failure: lessons from neuroprotective stroke trials and new therapeutic directions. Stroke 2002;33:2123-36
-
(2002)
Stroke
, vol.33
, pp. 2123-2136
-
-
Gladstone, D.J.1
Black, S.E.2
Hakim, A.M.3
-
58
-
-
0041659304
-
Animal models of stroke: Do they have value for discovering neuroprotective agents?
-
Green AR, Odergren T, Ashwood T. Animal models of stroke: do they have value for discovering neuroprotective agents? Trends Pharmacol Sci 2003;24:402-8
-
(2003)
Trends Pharmacol Sci
, vol.24
, pp. 402-408
-
-
Green, A.R.1
Odergren, T.2
Ashwood, T.3
-
59
-
-
33644818304
-
1,026 experimental treatments in acute stroke
-
O'Collins VE, MacLeod MR, Donnan GA, et al. 1,026 experimental treatments in acute stroke. Ann Neurol 2006;59:467-77
-
(2006)
Ann Neurol
, vol.59
, pp. 467-477
-
-
O'Collins, V.E.1
MacLeod, M.R.2
Donnan, G.A.3
-
60
-
-
30144443464
-
Molecular targest versus modesl for new antiepileptic drug discovery
-
Rogawski MA. Molecular targest versus modesl for new antiepileptic drug discovery. Epilepsy Res 2006;68:22-8
-
(2006)
Epilepsy Res
, vol.68
, pp. 22-28
-
-
Rogawski, M.A.1
-
61
-
-
27744533560
-
Silencing primary dystonia: Lentiviral-mediated RNA interference therapy for DYT1 dystonia
-
Gonzalez-Alegre P, Bode N, Davidson BL, Paulson HL. Silencing primary dystonia: lentiviral-mediated RNA interference therapy for DYT1 dystonia. J Neurosci 2005;25:10502-9
-
(2005)
J Neurosci
, vol.25
, pp. 10502-10509
-
-
Gonzalez-Alegre, P.1
Bode, N.2
Davidson, B.L.3
Paulson, H.L.4
-
62
-
-
0037319121
-
Suppression of polyglutamine-induced protein aggregation in Caenorhabditis elegans by torsin proteins
-
Caldwell GA, Cao S, Sexton EG, et al. Suppression of polyglutamine-induced protein aggregation in Caenorhabditis elegans by torsin proteins. Hum Mol Genet 2003;12:307-19
-
(2003)
Hum Mol Genet
, vol.12
, pp. 307-319
-
-
Caldwell, G.A.1
Cao, S.2
Sexton, E.G.3
-
63
-
-
33750999596
-
Antidystonic effects of Kv7 (KCNA) channel openers in the dt sz mutant, an animal model of primary paroxsymal dystonia
-
Richter A, Sander SE, Rundfeldt C. Antidystonic effects of Kv7 (KCNA) channel openers in the dt sz mutant, an animal model of primary paroxsymal dystonia. Br J Pharmacol 2006; 149:747-53
-
(2006)
Br J Pharmacol
, vol.149
, pp. 747-753
-
-
Richter, A.1
Sander, S.E.2
Rundfeldt, C.3
-
64
-
-
30844453816
-
Mouse models of dystonia
-
Le Doux MS Ed, San Diego, USA: Elsevier;
-
Hess EJ, Jinnah HA. Mouse models of dystonia. In: Animal Models of Movement Disorders. Le Doux MS (Ed.), San Diego, USA: Elsevier; 2005. p. 265-77
-
(2005)
Animal Models of Movement Disorders
, pp. 265-277
-
-
Hess, E.J.1
Jinnah, H.A.2
-
65
-
-
0036077774
-
Benign paroxysmal torticollis of infancy: Four new cases and linkage m CACNA1A mutation
-
Giffin NJ, Benton S, Goadsby PJ. Benign paroxysmal torticollis of infancy: four new cases and linkage m CACNA1A mutation. Dev Med Child Neurol 2002;44:490-3
-
(2002)
Dev Med Child Neurol
, vol.44
, pp. 490-493
-
-
Giffin, N.J.1
Benton, S.2
Goadsby, P.J.3
-
66
-
-
13444249849
-
Two novel CACNA1A gene mutations associated with episodic ataxia type 2 and interictal dystonia
-
Spacey SD, Materek LA, Szczygielski BI, Bird TD. Two novel CACNA1A gene mutations associated with episodic ataxia type 2 and interictal dystonia. Arch Neurol 2005;62:314-16
-
(2005)
Arch Neurol
, vol.62
, pp. 314-316
-
-
Spacey, S.D.1
Materek, L.A.2
Szczygielski, B.I.3
Bird, T.D.4
-
67
-
-
0034034781
-
Calcium channel agonists and dystonia in the mouse
-
Jinnah HA, Sepkuty JP, Ho T, et al. Calcium channel agonists and dystonia in the mouse. Mov Disord 2000;15:542-51
-
(2000)
Mov Disord
, vol.15
, pp. 542-551
-
-
Jinnah, H.A.1
Sepkuty, J.P.2
Ho, T.3
-
68
-
-
0031021124
-
The type 1 inositol triphosphate receptor gene is altered in the opisthotonus mouse
-
Street VA, Bosma MM, Demas VP, et al. The type 1 inositol triphosphate receptor gene is altered in the opisthotonus mouse. J Neurosci 1997;17:635-47
-
(1997)
J Neurosci
, vol.17
, pp. 635-647
-
-
Street, V.A.1
Bosma, M.M.2
Demas, V.P.3
-
69
-
-
13344250473
-
Ataxia and epileptic seizures in mice lacking type 1 inositol 1,4,5-triphosphate receptor
-
Matsumoto M, Nakagawa T, Inoue T, et al. Ataxia and epileptic seizures in mice lacking type 1 inositol 1,4,5-triphosphate receptor. Nature 1996;379:168-71
-
(1996)
Nature
, vol.379
, pp. 168-171
-
-
Matsumoto, M.1
Nakagawa, T.2
Inoue, T.3
-
70
-
-
0032895055
-
L-type calcium channels contribute to the tottering mouse dystonic episodes
-
Campbell DB, Hess EJ. L-type calcium channels contribute to the tottering mouse dystonic episodes. Mol Pharmacol 1999;55:23-31
-
(1999)
Mol Pharmacol
, vol.55
, pp. 23-31
-
-
Campbell, D.B.1
Hess, E.J.2
-
71
-
-
3342924056
-
Abnormal motor behavior and vestibular dysfunction in the stargazer mouse mutant
-
Khan Z, Carey J, Park HJ, et al. Abnormal motor behavior and vestibular dysfunction in the stargazer mouse mutant. Neuroscience 2004;127:785-96
-
(2004)
Neuroscience
, vol.127
, pp. 785-796
-
-
Khan, Z.1
Carey, J.2
Park, H.J.3
-
72
-
-
0037107157
-
Paroxysmal dyskinesias in the lethargic mouse mutant
-
Khan Z, Jinnah HA. Paroxysmal dyskinesias in the lethargic mouse mutant. J Neurosci 2002;22:8193-200
-
(2002)
J Neurosci
, vol.22
, pp. 8193-8200
-
-
Khan, Z.1
Jinnah, H.A.2
-
73
-
-
0029880817
-
Antidystonic effects of L-type Ca2+ channel antagonists in a hamster model of idiopathic dystonia
-
Richter A, Loscher W. Antidystonic effects of L-type Ca2+ channel antagonists in a hamster model of idiopathic dystonia. Eur J Pharmacol 1996;300:197-202
-
(1996)
Eur J Pharmacol
, vol.300
, pp. 197-202
-
-
Richter, A.1
Loscher, W.2
-
74
-
-
0027513709
-
Are calcium-channel blockers effective in the treatment of tardive dyskinesia?
-
Cates M, Lusk K, Wells BG. Are calcium-channel blockers effective in the treatment of tardive dyskinesia? Ann Pharmacother 1993;27:191-6
-
(1993)
Ann Pharmacother
, vol.27
, pp. 191-196
-
-
Cates, M.1
Lusk, K.2
Wells, B.G.3
-
75
-
-
0142072112
-
Dysfunction of dopaminergic pathways in dystonia
-
Perlmutter JS, Mink JW. Dysfunction of dopaminergic pathways in dystonia. Adv Neurol 2004;94:163-70
-
(2004)
Adv Neurol
, vol.94
, pp. 163-170
-
-
Perlmutter, J.S.1
Mink, J.W.2
-
76
-
-
33750298341
-
Pathophysiology of dystonia
-
Hallett M. Pathophysiology of dystonia. J Neural Transm Suppl 2006;70:485-8
-
(2006)
J Neural Transm Suppl
, vol.70
, pp. 485-488
-
-
Hallett, M.1
-
77
-
-
33645963751
-
Task-specific hand dystonia: Can too much plasticity be bad for you?
-
Quartarone A, Siebner HR, Rothwell JC. Task-specific hand dystonia: can too much plasticity be bad for you? Trends Neurosci 2006;29:192-9
-
(2006)
Trends Neurosci
, vol.29
, pp. 192-199
-
-
Quartarone, A.1
Siebner, H.R.2
Rothwell, J.C.3
-
79
-
-
34447303772
-
Dopamine release is impaired in a mouse model of DYT1 dystonia
-
Balcioglu A, Kim MO, Sharma N, et al. Dopamine release is impaired in a mouse model of DYT1 dystonia. J Neurochem 2007;102:783-8
-
(2007)
J Neurochem
, vol.102
, pp. 783-788
-
-
Balcioglu, A.1
Kim, M.O.2
Sharma, N.3
|