-
1
-
-
0029882099
-
Essential myoclonus and myoclonic dystonia
-
Quinn NP: Essential myoclonus and myoclonic dystonia. Mov Disord 1996;11:119-124.
-
(1996)
Mov Disord
, vol.11
, pp. 119-124
-
-
Quinn, N.P.1
-
2
-
-
0031604087
-
Inherited myoclonus-dystonia syndrome
-
Gasser T: Inherited myoclonus-dystonia syndrome. Adv Neurol 1998;78:325-334.
-
(1998)
Adv Neurol
, vol.78
, pp. 325-334
-
-
Gasser, T.1
-
3
-
-
0037159102
-
Phenotypic features of myoclonus-dystonia in three kindreds
-
Doheny DO, Brin MF, Morrison CE, Smith CJ, Walker RH, Abbasi S, et al: Phenotypic features of myoclonus-dystonia in three kindreds. Neurology 2002;59:1187-1196.
-
(2002)
Neurology
, vol.59
, pp. 1187-1196
-
-
Doheny, D.O.1
Brin, M.F.2
Morrison, C.E.3
Smith, C.J.4
Walker, R.H.5
Abbasi, S.6
-
4
-
-
0036916437
-
Evidence that paternal expression of the epsilon-sarcoglycan gene accounts for reduced penetrance in myoclonus-dystonia
-
Muller B, Hedrich K, Kock N, Dragasevic N, Svetel M, Garrels J, et al: Evidence that paternal expression of the epsilon-sarcoglycan gene accounts for reduced penetrance in myoclonus-dystonia. Am J Hum Genet 2002;71:1303-1311.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 1303-1311
-
-
Muller, B.1
Hedrich, K.2
Kock, N.3
Dragasevic, N.4
Svetel, M.5
Garrels, J.6
-
5
-
-
51649104741
-
-
Michael B, Spitzer RL, Gibbon M, Williams BWJ: Structured Clinical Interview for DSM-IV-TR Axis I Disorders, Research Version, Patient Edition (SCID-I/P). New York, Biometrics Research, New York State Psychiatric Institute, 2002.
-
Michael B, Spitzer RL, Gibbon M, Williams BWJ: Structured Clinical Interview for DSM-IV-TR Axis I Disorders, Research Version, Patient Edition (SCID-I/P). New York, Biometrics Research, New York State Psychiatric Institute, 2002.
-
-
-
-
6
-
-
51649096718
-
-
Wechsler D: Wechsler Adult Intelligence Scale-Revised. Manual. Cleveland, Psychological Corporation, 1981.
-
Wechsler D: Wechsler Adult Intelligence Scale-Revised. Manual. Cleveland, Psychological Corporation, 1981.
-
-
-
-
7
-
-
0036382009
-
European Association of Nuclear Medicine procedure guidelines for brain perfusion SPET using (99m)Tc-labelled radiopharmaceuticals
-
Tatsch K, Asenbaum S, Bartenstein P, Catafau A, Halldin C, Pilowsky LS, et al: European Association of Nuclear Medicine procedure guidelines for brain perfusion SPET using (99m)Tc-labelled radiopharmaceuticals. Eur J Nucl Med Mol Imaging 2002;29:BP36-BP42.
-
(2002)
Eur J Nucl Med Mol Imaging
, vol.29
-
-
Tatsch, K.1
Asenbaum, S.2
Bartenstein, P.3
Catafau, A.4
Halldin, C.5
Pilowsky, L.S.6
-
8
-
-
0033754411
-
A major locus for myoclonus-dystonia maps to chromosome 7q in eight families
-
Klein C, Schilling K, Saunders-Pullman RJ, et al: A major locus for myoclonus-dystonia maps to chromosome 7q in eight families. Am J Hum Genet 2000;67:1314-1319.
-
(2000)
Am J Hum Genet
, vol.67
, pp. 1314-1319
-
-
Klein, C.1
Schilling, K.2
Saunders-Pullman, R.J.3
-
9
-
-
0035826884
-
A major locus for several phenotypes of myoclonus-dystonia on chromosome 7q
-
Vidailhet M, Tassin J, Durif F, et al: A major locus for several phenotypes of myoclonus-dystonia on chromosome 7q. Neurology 2001;56:1213-1216.
-
(2001)
Neurology
, vol.56
, pp. 1213-1216
-
-
Vidailhet, M.1
Tassin, J.2
Durif, F.3
-
11
-
-
0035112509
-
Inherited myoclonus-dystonia syndrome: Narrowing the 7q21-q31 locus in German families
-
Asmus F, Zimprich A, Naumann M, et al: Inherited myoclonus-dystonia syndrome: narrowing the 7q21-q31 locus in German families. Ann Neurol 2001;49:121-124.
-
(2001)
Ann Neurol
, vol.49
, pp. 121-124
-
-
Asmus, F.1
Zimprich, A.2
Naumann, M.3
-
12
-
-
0032705097
-
Localization of a gene for myoclonus-dystonia to chromosome 7q21-q31
-
Nygaard TG, Raymond D, Chen C, et al: Localization of a gene for myoclonus-dystonia to chromosome 7q21-q31. Ann Neurol 1999;46:794-798.
-
(1999)
Ann Neurol
, vol.46
, pp. 794-798
-
-
Nygaard, T.G.1
Raymond, D.2
Chen, C.3
-
14
-
-
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
-
15
-
-
0027259438
-
Early-onset dystonia decreasing with development. Case report of two children with familial myoclonic dystonia
-
Kyllerman M, Sanner G, Forsgren L, Holmgren G, Wahlstrom J: Early-onset dystonia decreasing with development. Case report of two children with familial myoclonic dystonia. Brain Dev 1993;15:295-298.
-
(1993)
Brain Dev
, vol.15
, pp. 295-298
-
-
Kyllerman, M.1
Sanner, G.2
Forsgren, L.3
Holmgren, G.4
Wahlstrom, J.5
-
17
-
-
0023035596
-
Psychological aspects of painful medical conditions in children. 2. Personality factors, family characteristics and treatment
-
Lavigne JV, Schulein MJ, Hahn YS: Psychological aspects of painful medical conditions in children. 2. Personality factors, family characteristics and treatment. Pain 1986;27:147-169.
-
(1986)
Pain
, vol.27
, pp. 147-169
-
-
Lavigne, J.V.1
Schulein, M.J.2
Hahn, Y.S.3
-
18
-
-
0034056156
-
Prevalence of DSM IV anxiety and affective disorders in a pediatric population of asthmatic children and adolescents
-
Vila G, Nollet-Clemencon C, de Blic J, Mouren-Simeoni MC, Scheinmann P: Prevalence of DSM IV anxiety and affective disorders in a pediatric population of asthmatic children and adolescents. J Affect Disord 2000;58:223-231.
-
(2000)
J Affect Disord
, vol.58
, pp. 223-231
-
-
Vila, G.1
Nollet-Clemencon, C.2
de Blic, J.3
Mouren-Simeoni, M.C.4
Scheinmann, P.5
-
19
-
-
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
-
20
-
-
0028151448
-
Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I gene
-
Ichinose H, Ohye T, Takahashi E, et al: Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I gene. Nat Genet 1994;8:236-242.
-
(1994)
Nat Genet
, vol.8
, pp. 236-242
-
-
Ichinose, H.1
Ohye, T.2
Takahashi, E.3
-
21
-
-
0034702033
-
Mutant torsin A, responsible for early-onset torsion dystonia, forms membrane inclusions in cultured neural cells
-
Hewett J, Gonzalez-Agosti C, Slater D, et al: Mutant torsin A, responsible for early-onset torsion dystonia, forms membrane inclusions in cultured neural cells. Hum Mol Genet 2000;9:1403-1413.
-
(2000)
Hum Mol Genet
, vol.9
, pp. 1403-1413
-
-
Hewett, J.1
Gonzalez-Agosti, C.2
Slater, D.3
-
22
-
-
0343932572
-
2 dopamine receptor gene in myoclonic dystonia and essential myoclonus
-
2 dopamine receptor gene in myoclonic dystonia and essential myoclonus. Ann Neurol 2000;48:127-128.
-
(2000)
Ann Neurol
, vol.48
, pp. 127-128
-
-
Durr, A.1
Tassin, J.2
Vidailhet, M.3
-
24
-
-
1542316163
-
Regional cerebral blood flow correlates of the severity of writer's cramp symptoms
-
Lerner A, Shill H, Hanakawa T, Bushara K, Goldfine A, Hallett M: Regional cerebral blood flow correlates of the severity of writer's cramp symptoms. Neuroimage 2004;21:904-913.
-
(2004)
Neuroimage
, vol.21
, pp. 904-913
-
-
Lerner, A.1
Shill, H.2
Hanakawa, T.3
Bushara, K.4
Goldfine, A.5
Hallett, M.6
-
25
-
-
34147110308
-
Local field potentials and oscillatory activity of the internal globus pallidus in myoclonus-dystonia
-
Foncke EM, Bour LJ, Speelman JD, Koelman JH, Tijssen MA: Local field potentials and oscillatory activity of the internal globus pallidus in myoclonus-dystonia. Mov Disord 2007;22:369-376.
-
(2007)
Mov Disord
, vol.22
, pp. 369-376
-
-
Foncke, E.M.1
Bour, L.J.2
Speelman, J.D.3
Koelman, J.H.4
Tijssen, M.A.5
-
26
-
-
0035139156
-
Unusual depression and Tc-99m ethyl cysteinate dimer SPECT brain uptake
-
Vander Borght T, De Coene B, Charlet S, Gilliard C, Reynaert C: Unusual depression and Tc-99m ethyl cysteinate dimer SPECT brain uptake. Clin Nucl Med 2001;26:160.
-
(2001)
Clin Nucl Med
, vol.26
, pp. 160
-
-
Vander Borght, T.1
De Coene, B.2
Charlet, S.3
Gilliard, C.4
Reynaert, C.5
|