-
1
-
-
0036790909
-
Myoclonus-dystonia syndrome: epsilon-sarcoglycan mutations and phenotype
-
Asmus F, Zimprich A, Tezenas Du Montcel S, et al. Myoclonus-dystonia syndrome: epsilon-sarcoglycan mutations and phenotype. Ann Neurol 2002;52:489-492.
-
(2002)
Ann Neurol
, vol.52
, pp. 489-492
-
-
Asmus, F.1
Zimprich, A.2
Tezenas Du Montcel, S.3
-
2
-
-
67651183916
-
Myoclonus-dystonia: an update
-
Kinugawa K, Vidailhet M, Clot F, Apartis E, Grabli D, Roze E. Myoclonus-dystonia: an update. Mov Disord 2009;24:479-489.
-
(2009)
Mov Disord
, vol.24
, pp. 479-489
-
-
Kinugawa, K.1
Vidailhet, M.2
Clot, F.3
Apartis, E.4
Grabli, D.5
Roze, E.6
-
3
-
-
17944378309
-
Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome
-
Zimprich A, Grabowski M, Asmus F, et al. Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome. Nat Genet 2001;29:66-69.
-
(2001)
Nat Genet
, vol.29
, pp. 66-69
-
-
Zimprich, A.1
Grabowski, M.2
Asmus, F.3
-
4
-
-
33847322639
-
SGCE missense mutations that cause myoclonus-dystonia syndrome impair epsilon-sarcoglycan trafficking to the plasma membrane: modulation by ubiquitination and torsinA
-
Esapa CT, Waite A, Locke M, et al. SGCE missense mutations that cause myoclonus-dystonia syndrome impair epsilon-sarcoglycan trafficking to the plasma membrane: modulation by ubiquitination and torsinA. Hum Mol Genet 2007;16:327-342.
-
(2007)
Hum Mol Genet
, vol.16
, pp. 327-342
-
-
Esapa, C.T.1
Waite, A.2
Locke, M.3
-
5
-
-
84875237077
-
Prominent psychiatric comorbidity in the dominantly inherited movement disorder myoclonus-dystonia
-
Weissbach A, Kasten M, Grunewald A, et al. Prominent psychiatric comorbidity in the dominantly inherited movement disorder myoclonus-dystonia. Parkinsonism Relat Disord 2013;19:422-425.
-
(2013)
Parkinsonism Relat Disord
, vol.19
, pp. 422-425
-
-
Weissbach, A.1
Kasten, M.2
Grunewald, A.3
-
6
-
-
80052294248
-
Psychiatric disorders, myoclonus dystonia, and the epsilon-sarcoglycan gene: a systematic review
-
Peall KJ, Waite AJ, Blake DJ, Owen MJ, Morris HR. Psychiatric disorders, myoclonus dystonia, and the epsilon-sarcoglycan gene: a systematic review. Mov Disord 2011;26:1939-1942.
-
(2011)
Mov Disord
, vol.26
, pp. 1939-1942
-
-
Peall, K.J.1
Waite, A.J.2
Blake, D.J.3
Owen, M.J.4
Morris, H.R.5
-
7
-
-
84873359706
-
SGCE mutations cause psychiatric disorders: clinical and genetic characterization
-
Peall KJ, Smith DJ, Kurian MA, et al. SGCE mutations cause psychiatric disorders: clinical and genetic characterization. Brain 2013;136:294-303.
-
(2013)
Brain
, vol.136
, pp. 294-303
-
-
Peall, K.J.1
Smith, D.J.2
Kurian, M.A.3
-
9
-
-
33847029189
-
Myoclonus-dystonia, obsessive-compulsive disorder, and alcohol dependence in SGCE mutation carriers
-
Hess CW, Raymond D, de Aguiar PC, et al. Myoclonus-dystonia, obsessive-compulsive disorder, and alcohol dependence in SGCE mutation carriers. Neurology 2007;68:522-524.
-
(2007)
Neurology
, vol.68
, pp. 522-524
-
-
Hess, C.W.1
Raymond, D.2
de Aguiar, P.C.3
-
10
-
-
79961209745
-
Familial 7q21.3 microdeletion involving epsilon-sarcoglycan causing myoclonus dystonia, cognitive impairment, and psychosis
-
Dale RC, Nasti JJ, Peters GB. Familial 7q21.3 microdeletion involving epsilon-sarcoglycan causing myoclonus dystonia, cognitive impairment, and psychosis. Mov Disord 2011;26:1774-1775.
-
(2011)
Mov Disord
, vol.26
, pp. 1774-1775
-
-
Dale, R.C.1
Nasti, J.J.2
Peters, G.B.3
-
11
-
-
77951944550
-
Hereditary myoclonus dystonia (DYT11): a novel SGCE gene mutation with intrafamilial phenotypic heterogeneity
-
Wong SH, Steiger MJ, Larner AJ, Fletcher NA. Hereditary myoclonus dystonia (DYT11): a novel SGCE gene mutation with intrafamilial phenotypic heterogeneity. Mov Disord 2010;25:956-957.
-
(2010)
Mov Disord
, vol.25
, pp. 956-957
-
-
Wong, S.H.1
Steiger, M.J.2
Larner, A.J.3
Fletcher, N.A.4
-
12
-
-
0037159182
-
Clinical findings of a myoclonus-dystonia family with two distinct mutations
-
Doheny D, Danisi F, Smith C, et al. Clinical findings of a myoclonus-dystonia family with two distinct mutations. Neurology 2002;59:1244-1246.
-
(2002)
Neurology
, vol.59
, pp. 1244-1246
-
-
Doheny, D.1
Danisi, F.2
Smith, C.3
-
13
-
-
39549102002
-
Myoclonus-dystonia syndrome: clinical presentation, disease course, and genetic features in 11 families
-
Nardocci N, Zorzi G, Barzaghi C, et al. Myoclonus-dystonia syndrome: clinical presentation, disease course, and genetic features in 11 families. Mov Disord 2008;23:28-34.
-
(2008)
Mov Disord
, vol.23
, pp. 28-34
-
-
Nardocci, N.1
Zorzi, G.2
Barzaghi, C.3
-
14
-
-
66149112424
-
Myoclonus-dystonia: clinical and genetic evaluation of a large cohort
-
Ritz K, Gerrits MC, Foncke EM, et al. Myoclonus-dystonia: clinical and genetic evaluation of a large cohort. J Neurol Neurosurg Psychiatry 2009;80:653-658.
-
(2009)
J Neurol Neurosurg Psychiatry
, vol.80
, pp. 653-658
-
-
Ritz, K.1
Gerrits, M.C.2
Foncke, E.M.3
-
15
-
-
0037154246
-
Myoclonus dystonia: possible association with obsessive-compulsive disorder and alcohol dependence
-
Saunders-Pullman R, Shriberg J, Heiman G, et al. Myoclonus dystonia: possible association with obsessive-compulsive disorder and alcohol dependence. Neurology 2002;58:242-245.
-
(2002)
Neurology
, vol.58
, pp. 242-245
-
-
Saunders-Pullman, R.1
Shriberg, J.2
Heiman, G.3
-
16
-
-
0003575871
-
-
New York: New York State Psychiatric Institute, Biometrics Research
-
First MB, Spitzer RL, Gibbon M, Williams JB: Structured Clinical Interview for DSM-IV Axis I Disorders-Non-Patient Edition (SCID-I/NP), version 2.0. New York: New York State Psychiatric Institute, Biometrics Research, 1996.
-
(1996)
Structured Clinical Interview for DSM-IV Axis I Disorders-Non-Patient Edition (SCID-I/NP), version 2.0
-
-
First, M.B.1
Spitzer, R.L.2
Gibbon, M.3
Williams, J.B.4
-
17
-
-
0032421570
-
The Mini-International Neuropsychiatric Interview (M.I.N.I.): the development and validation of a structured diagnostic psychiatric interview for DSM-IV and ICD-10
-
quiz 34-57.
-
Sheehan DV, Lecrubier Y, Sheehan KH, et al. The Mini-International Neuropsychiatric Interview (M.I.N.I.): the development and validation of a structured diagnostic psychiatric interview for DSM-IV and ICD-10. J Clin Psychiatry 1998;59(Suppl 20):22-33; quiz 34-57.
-
(1998)
J Clin Psychiatry
, vol.59
, pp. 22-33
-
-
Sheehan, D.V.1
Lecrubier, Y.2
Sheehan, K.H.3
-
18
-
-
0034320318
-
Case ascertainment: the Composite International Diagnostic Interview
-
Andrews G. Case ascertainment: the Composite International Diagnostic Interview. Aust N Z J Psychiatry 2000;34(Suppl):S161-163.
-
(2000)
Aust N Z J Psychiatry
, vol.34
, pp. S161-S163
-
-
Andrews, G.1
-
19
-
-
0028156958
-
Lifetime and 12-month prevalence of DSM-III-R psychiatric disorders in the United States. Results from the National Comorbidity Survey
-
Kessler RC, McGonagle KA, Zhao S, et al. Lifetime and 12-month prevalence of DSM-III-R psychiatric disorders in the United States. Results from the National Comorbidity Survey. Arch Gen Psychiatry 1994;51:8-19.
-
(1994)
Arch Gen Psychiatry
, vol.51
, pp. 8-19
-
-
Kessler, R.C.1
McGonagle, K.A.2
Zhao, S.3
-
20
-
-
0028858243
-
Obsessive-compulsive disorder in a birth cohort of 18-year-olds: prevalence and predictors
-
Douglass HM, Moffitt TE, Dar R, McGee R, Silva P. Obsessive-compulsive disorder in a birth cohort of 18-year-olds: prevalence and predictors. J Am Acad Child Adolesc Psychiatry 1995;34:1424-1431.
-
(1995)
J Am Acad Child Adolesc Psychiatry
, vol.34
, pp. 1424-1431
-
-
Douglass, H.M.1
Moffitt, T.E.2
Dar, R.3
McGee, R.4
Silva, P.5
-
21
-
-
0041822179
-
Myoclonus in a patient with a deletion of the epsilon-sarcoglycan locus on chromosome 7q21
-
DeBerardinis RJ, Conforto D, Russell K, et al. Myoclonus in a patient with a deletion of the epsilon-sarcoglycan locus on chromosome 7q21. Am J Med Genet A 2003;121A:31-36.
-
(2003)
Am J Med Genet A
, pp. 31-36
-
-
DeBerardinis, R.J.1
Conforto, D.2
Russell, K.3
-
22
-
-
62949241249
-
Obsessions and compulsions in the community: prevalence, interference, help-seeking, developmental stability, and co-occurring psychiatric conditions
-
Fullana MA, Mataix-Cols D, Caspi A, et al. Obsessions and compulsions in the community: prevalence, interference, help-seeking, developmental stability, and co-occurring psychiatric conditions. Am J Psychiatry 2009;166:329-336.
-
(2009)
Am J Psychiatry
, vol.166
, pp. 329-336
-
-
Fullana, M.A.1
Mataix-Cols, D.2
Caspi, A.3
-
23
-
-
0031957806
-
Higher prevalence of obsessive-compulsive symptoms in patients with blepharospasm than in patients with hemifacial spasm
-
Broocks A, Thiel A, Angerstein D, Dressler D. Higher prevalence of obsessive-compulsive symptoms in patients with blepharospasm than in patients with hemifacial spasm. Am J Psychiatry 1998;155:555-557.
-
(1998)
Am J Psychiatry
, vol.155
, pp. 555-557
-
-
Broocks, A.1
Thiel, A.2
Angerstein, D.3
Dressler, D.4
-
24
-
-
80055077115
-
Obsessive-compulsive symptoms in primary focal dystonia: a controlled study
-
Barahona-Correa B, Bugalho P, Guimaraes J, Xavier M. Obsessive-compulsive symptoms in primary focal dystonia: a controlled study. Mov Disord 2011;26:2274-2278.
-
(2011)
Mov Disord
, vol.26
, pp. 2274-2278
-
-
Barahona-Correa, B.1
Bugalho, P.2
Guimaraes, J.3
Xavier, M.4
-
25
-
-
0037102006
-
Obsessive compulsive disorder among idiopathic focal dystonia patients: an epidemiological and family study
-
Cavallaro R, Galardi G, Cavallini MC, et al. Obsessive compulsive disorder among idiopathic focal dystonia patients: an epidemiological and family study. Biol Psychiatry 2002;52:356-361.
-
(2002)
Biol Psychiatry
, vol.52
, pp. 356-361
-
-
Cavallaro, R.1
Galardi, G.2
Cavallini, M.C.3
-
26
-
-
77949528748
-
Psychiatric disorders in adult-onset focal dystonia: a case-control study
-
Fabbrini G, Berardelli I, Moretti G, et al. Psychiatric disorders in adult-onset focal dystonia: a case-control study. Mov Disord 2010;25:459-465.
-
(2010)
Mov Disord
, vol.25
, pp. 459-465
-
-
Fabbrini, G.1
Berardelli, I.2
Moretti, G.3
-
27
-
-
7244257523
-
Examination of the SGCE gene in Tourette syndrome patients with obsessive-compulsive disorder
-
de Carvalho Aguiar P, Fazzari M, Jankovic J, Ozelius LJ. Examination of the SGCE gene in Tourette syndrome patients with obsessive-compulsive disorder. Mov Disord 2004;19:1237-1238.
-
(2004)
Mov Disord
, vol.19
, pp. 1237-1238
-
-
de Carvalho Aguiar, P.1
Fazzari, M.2
Jankovic, J.3
Ozelius, L.J.4
-
28
-
-
70349653653
-
Primary focal dystonia - a disease of brain and mind: motor and psychiatric manifestations have a common neurobiological basis
-
Ron MA. Primary focal dystonia - a disease of brain and mind: motor and psychiatric manifestations have a common neurobiological basis. J Neurol Neurosurg Psychiatry 2009;80:1059.
-
(2009)
J Neurol Neurosurg Psychiatry
, vol.80
, pp. 1059
-
-
Ron, M.A.1
-
29
-
-
70349673427
-
Primary focal dystonia: evidence for distinct neuropsychiatric and personality profiles
-
Lencer R, Steinlechner S, Stahlberg J, et al. Primary focal dystonia: evidence for distinct neuropsychiatric and personality profiles. J Neurol Neurosurg Psychiatry 2009;80:1176-1179.
-
(2009)
J Neurol Neurosurg Psychiatry
, vol.80
, pp. 1176-1179
-
-
Lencer, R.1
Steinlechner, S.2
Stahlberg, J.3
-
30
-
-
0031802234
-
Psychiatric comorbidity in patients with spasmodic torticollis
-
Wenzel T, Schnider P, Wimmer A, Steinhoff N, Moraru E, Auff E. Psychiatric comorbidity in patients with spasmodic torticollis. J Psychosom Res 1998;44:687-690.
-
(1998)
J Psychosom Res
, vol.44
, pp. 687-690
-
-
Wenzel, T.1
Schnider, P.2
Wimmer, A.3
Steinhoff, N.4
Moraru, E.5
Auff, E.6
|