-
1
-
-
0018073135
-
Familial and acquired paroxysmal dyskinesias. A proposed classification with delineation of clinical features
-
718486 10.1001/archneur.1978.00500360051010 1:STN:280: DyaE1M%2FmtFGhsg%3D%3D
-
Goodenough DJ, Fariello RG, Annis BL, Chun RW (1978) Familial and acquired paroxysmal dyskinesias. a proposed classification with delineation of clinical features. Arch Neurol 35:827-831
-
(1978)
Arch Neurol
, vol.35
, pp. 827-831
-
-
Goodenough, D.J.1
Fariello, R.G.2
Annis, B.L.3
Chun, R.W.4
-
2
-
-
19944402859
-
Clinical evaluation of idiopathic paroxysmal kinesigenic dyskinesia: New diagnostic criteria
-
15623687 10.1212/01.WNL.0000147298.05983.50 1:STN:280: DC%2BD2cnkslWjug%3D%3D
-
Bruno MK, Hallett M, Gwinn-Hardy K, Sorensen B, Considine E, Tucker S, Lynch DR, Mathews KD, Swoboda KJ, Harris J, Soong BW, Ashizawa T, Jankovic J, Renner D, Fu YH, Ptacek LJ (2004) Clinical evaluation of idiopathic paroxysmal kinesigenic dyskinesia: new diagnostic criteria. Neurology 63:2280-2287
-
(2004)
Neurology
, vol.63
, pp. 2280-2287
-
-
Bruno, M.K.1
Hallett, M.2
Gwinn-Hardy, K.3
Sorensen, B.4
Considine, E.5
Tucker, S.6
Lynch, D.R.7
Mathews, K.D.8
Swoboda, K.J.9
Harris, J.10
Soong, B.W.11
Ashizawa, T.12
Jankovic, J.13
Renner, D.14
Fu, Y.H.15
Ptacek, L.J.16
-
3
-
-
82255186531
-
Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia
-
22101681 10.1038/ng.1008 1:CAS:528:DC%2BC3MXhsV2gt7rN
-
Chen WJ, Lin Y, Xiong ZQ, Wei W, Ni W, Tan GH, Guo SL, He J, Chen YF, Zhang QJ, Li HF, Lin Y, Murong SX, Xu J, Wang N, Wu ZY (2011) Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia. Nat Genet 43:1252-1255
-
(2011)
Nat Genet
, vol.43
, pp. 1252-1255
-
-
Chen, W.J.1
Lin, Y.2
Xiong, Z.Q.3
Wei, W.4
Ni, W.5
Tan, G.H.6
Guo, S.L.7
He, J.8
Chen, Y.F.9
Zhang, Q.J.10
Li, H.F.11
Lin, Y.12
Murong, S.X.13
Xu, J.14
Wang, N.15
Wu, Z.Y.16
-
4
-
-
83755205987
-
Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesias
-
22120146 10.1093/brain/awr289
-
Wang JL, Cao L, Li XH, Hu ZM, Li JD, Zhang JG, Liang Y, San A, Li N, Chen SQ, Guo JF, Jiang H, Shen L, Zheng L, Mao X, Yan WQ, Zhou Y, Shi YT, Ai SX, Dai MZ, Zhang P, Xia K, Chen SD, Tang BS (2011) Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesias. Brain 134:3493-3501
-
(2011)
Brain
, vol.134
, pp. 3493-3501
-
-
Wang, J.L.1
Cao, L.2
Li, X.H.3
Hu, Z.M.4
Li, J.D.5
Zhang, J.G.6
Liang, Y.7
San, A.8
Li, N.9
Chen, S.Q.10
Guo, J.F.11
Jiang, H.12
Shen, L.13
Zheng, L.14
Mao, X.15
Yan, W.Q.16
Zhou, Y.17
Shi, Y.T.18
Ai, S.X.19
Dai, M.Z.20
Zhang, P.21
Xia, K.22
Chen, S.D.23
Tang, B.S.24
more..
-
5
-
-
84856144700
-
Mutations in the novel protein PRRT2 cause paroxysmal kinesigenic dyskinesia with infantile convulsions
-
10.1016/j.celrep.2011.11.001 1:CAS:528:DC%2BC38XjtVSksbs%3D
-
Lee HY, Huang Y, Bruneau N, Roll P, Roberson ED, Hermann M, Quinn E, Maas J, Edwards R, Ashizawa T, Baykan B, Bhatia K, Bressman S, Bruno MK, Brunt ER, Caraballo R, Echenne B, Fejerman N, Frucht S, Gurnett CA, Hirsch E, Houlden H, Jankovic J, Lee WL, Lynch DR, Mohamed S, Muller U, Nespeca MP, Renner D, Rochette J, Rudolf G, Saiki S, Soong BW, Swoboda KJ, Tucker S, Wood N, Hanna M, Bowcock A, Szepetowski P, Fu YH, Ptacek LJ (2012) Mutations in the novel protein PRRT2 cause paroxysmal kinesigenic dyskinesia with infantile convulsions. Cell Rep 1:2-12
-
(2012)
Cell Rep
, vol.1
, pp. 2-12
-
-
Lee, H.Y.1
Huang, Y.2
Bruneau, N.3
Roll, P.4
Roberson, E.D.5
Hermann, M.6
Quinn, E.7
Maas, J.8
Edwards, R.9
Ashizawa, T.10
Baykan, B.11
Bhatia, K.12
Bressman, S.13
Bruno, M.K.14
Brunt, E.R.15
Caraballo, R.16
Echenne, B.17
Fejerman, N.18
Frucht, S.19
Gurnett, C.A.20
Hirsch, E.21
Houlden, H.22
Jankovic, J.23
Lee, W.L.24
Lynch, D.R.25
Mohamed, S.26
Muller, U.27
Nespeca, M.P.28
Renner, D.29
Rochette, J.30
Rudolf, G.31
Saiki, S.32
Soong, B.W.33
Swoboda, K.J.34
Tucker, S.35
Wood, N.36
Hanna, M.37
Bowcock, A.38
Szepetowski, P.39
Fu, Y.H.40
Ptacek, L.J.41
more..
-
6
-
-
84855827661
-
PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome
-
22243967 10.1016/j.ajhg.2011.12.003 1:CAS:528:DC%2BC38XovFGhtQ%3D%3D
-
Heron SE, Grinton BE, Kivity S, Afawi Z, Zuberi SM, Hughes JN, Pridmore C, Hodgson BL, Iona X, Sadleir LG, Pelekanos J, Herlenius E, Goldberg-Stern H, Bassan H, Haan E, Korczyn AD, Gardner AE, Corbett MA, Gecz J, Thomas PQ, Mulley JC, Berkovic SF, Scheffer IE, Dibbens LM (2012) PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome. Am J Hum Genet 90:152-160
-
(2012)
Am J Hum Genet
, vol.90
, pp. 152-160
-
-
Heron, S.E.1
Grinton, B.E.2
Kivity, S.3
Afawi, Z.4
Zuberi, S.M.5
Hughes, J.N.6
Pridmore, C.7
Hodgson, B.L.8
Iona, X.9
Sadleir, L.G.10
Pelekanos, J.11
Herlenius, E.12
Goldberg-Stern, H.13
Bassan, H.14
Haan, E.15
Korczyn, A.D.16
Gardner, A.E.17
Corbett, M.A.18
Gecz, J.19
Thomas, P.Q.20
Mulley, J.C.21
Berkovic, S.F.22
Scheffer, I.E.23
Dibbens, L.M.24
more..
-
7
-
-
84866251560
-
PRRT2 mutations: A major cause of paroxysmal kinesigenic dyskinesia in the European population
-
22744660 10.1212/WNL.0b013e31825f06c3 1:CAS:528:DC%2BC38XhtVWgt7fP
-
Meneret A, Grabli D, Depienne C, Gaudebout C, Picard F, Durr A, Lagroua I, Bouteiller D, Mignot C, Doummar D, Anheim M, Tranchant C, Burbaud P, Jedynak CP, Gras D, Steschenko D, Devos D, Billette de Villemeur T, Vidailhet M, Brice A, Roze E (2012) PRRT2 mutations: a major cause of paroxysmal kinesigenic dyskinesia in the European population. Neurology 79:170-174
-
(2012)
Neurology
, vol.79
, pp. 170-174
-
-
Meneret, A.1
Grabli, D.2
Depienne, C.3
Gaudebout, C.4
Picard, F.5
Durr, A.6
Lagroua, I.7
Bouteiller, D.8
Mignot, C.9
Doummar, D.10
Anheim, M.11
Tranchant, C.12
Burbaud, P.13
Jedynak, C.P.14
Gras, D.15
Steschenko, D.16
Devos, D.17
Billette De Villemeur, T.18
Vidailhet, M.19
Brice, A.20
Roze, E.21
more..
-
8
-
-
84866287779
-
PRRT2 Mutations are the major cause of benign familial infantile seizures
-
22623405 10.1002/humu.22126 1:CAS:528:DC%2BC38XhtlCjsLfM
-
Schubert J, Paravidino R, Becker F, Berger A, Bebek N, Bianchi A, Brockmann K, Capovilla G, Bernardina BD, Fukuyama Y, Hoffmann GF, Jurkat-Rott K, Anttonen AK, Kurlemann G, Lehesjoki AE, Lehmann-Horn F, Mastrangelo M, Mause U, Muller S, Neubauer B, Pust B, Rating D, Robbiano A, Ruf S, Schroeder C, Seidel A, Specchio N, Stephani U, Striano P, Teichler J, Turkdogan D, Vigevano F, Viri M, Bauer P, Zara F, Lerche H, Weber YG (2012) PRRT2 Mutations are the major cause of benign familial infantile seizures. Hum Mutat 33:1439-1443
-
(2012)
Hum Mutat
, vol.33
, pp. 1439-1443
-
-
Schubert, J.1
Paravidino, R.2
Becker, F.3
Berger, A.4
Bebek, N.5
Bianchi, A.6
Brockmann, K.7
Capovilla, G.8
Bernardina, B.D.9
Fukuyama, Y.10
Hoffmann, G.F.11
Jurkat-Rott, K.12
Anttonen, A.K.13
Kurlemann, G.14
Lehesjoki, A.E.15
Lehmann-Horn, F.16
Mastrangelo, M.17
Mause, U.18
Muller, S.19
Neubauer, B.20
Pust, B.21
Rating, D.22
Robbiano, A.23
Ruf, S.24
Schroeder, C.25
Seidel, A.26
Specchio, N.27
Stephani, U.28
Striano, P.29
Teichler, J.30
Turkdogan, D.31
Vigevano, F.32
Viri, M.33
Bauer, P.34
Zara, F.35
Lerche, H.36
Weber, Y.G.37
more..
-
9
-
-
84862776732
-
Targeted genomic sequencing identifies PRRT2 mutations as a cause of paroxysmal kinesigenic choreoathetosis
-
22131361 10.1136/jmedgenet-2011-100635 1:CAS:528:DC%2BC38XktFCisbs%3D
-
Li J, Zhu X, Wang X, Sun W, Feng B, Du T, Sun B, Niu F, Wei H, Wu X, Dong L, Li L, Cai X, Wang Y, Liu Y (2012) Targeted genomic sequencing identifies PRRT2 mutations as a cause of paroxysmal kinesigenic choreoathetosis. J Med Genet 49:76-78
-
(2012)
J Med Genet
, vol.49
, pp. 76-78
-
-
Li, J.1
Zhu, X.2
Wang, X.3
Sun, W.4
Feng, B.5
Du, T.6
Sun, B.7
Niu, F.8
Wei, H.9
Wu, X.10
Dong, L.11
Li, L.12
Cai, X.13
Wang, Y.14
Liu, Y.15
-
10
-
-
84862811273
-
Identification of a novel PRRT2 mutation in patients with paroxysmal kinesigenic dyskinesias and c.649dupC as a mutation hot-spot
-
22386217 10.1016/j.parkreldis.2012.02.006
-
Cao L, Huang XJ, Zheng L, Xiao Q, Wang XJ, Chen SD (2012) Identification of a novel PRRT2 mutation in patients with paroxysmal kinesigenic dyskinesias and c.649dupC as a mutation hot-spot. Parkinsonism Relat Disord 18:704-706
-
(2012)
Parkinsonism Relat Disord
, vol.18
, pp. 704-706
-
-
Cao, L.1
Huang, X.J.2
Zheng, L.3
Xiao, Q.4
Wang, X.J.5
Chen, S.D.6
-
11
-
-
84861640003
-
Mutations in PRRT2 responsible for paroxysmal kinesigenic dyskinesias also cause benign familial infantile convulsions
-
22399141 10.1038/jhg.2012.23 1:CAS:528:DC%2BC38Xns1yrtbk%3D
-
Ono S, Yoshiura K, Kinoshita A, Kikuchi T, Nakane Y, Kato N, Sadamatsu M, Konishi T, Nagamitsu S, Matsuura M, Yasuda A, Komine M, Kanai K, Inoue T, Osamura T, Saito K, Hirose S, Koide H, Tomita H, Ozawa H, Niikawa N, Kurotaki N (2012) Mutations in PRRT2 responsible for paroxysmal kinesigenic dyskinesias also cause benign familial infantile convulsions. J Hum Genet 57:338-341
-
(2012)
J Hum Genet
, vol.57
, pp. 338-341
-
-
Ono, S.1
Yoshiura, K.2
Kinoshita, A.3
Kikuchi, T.4
Nakane, Y.5
Kato, N.6
Sadamatsu, M.7
Konishi, T.8
Nagamitsu, S.9
Matsuura, M.10
Yasuda, A.11
Komine, M.12
Kanai, K.13
Inoue, T.14
Osamura, T.15
Saito, K.16
Hirose, S.17
Koide, H.18
Tomita, H.19
Ozawa, H.20
Niikawa, N.21
Kurotaki, N.22
more..
-
12
-
-
84866105879
-
PRRT2 phenotypes and penetrance of paroxysmal kinesigenic dyskinesia and infantile convulsions
-
van Vliet R, Breedveld G, van de Rijk AJ, Brilstra E, Verbeek N, Verschuuren-Bemelmans C, Boon M, Samijn J, Diderich K, van de Laar I, Oostra B, Bonifati V, Maat-Kievit A (2012) PRRT2 phenotypes and penetrance of paroxysmal kinesigenic dyskinesia and infantile convulsions. Am Acad Neurol 79:777-784
-
(2012)
Am Acad Neurol
, vol.79
, pp. 777-784
-
-
Van Vliet, R.1
Breedveld, G.2
Van De Rijk, A.J.3
Brilstra, E.4
Verbeek, N.5
Verschuuren-Bemelmans, C.6
Boon, M.7
Samijn, J.8
Diderich, K.9
Van De Laar, I.10
Oostra, B.11
Bonifati, V.12
Maat-Kievit, A.13
-
13
-
-
84864762353
-
PRRT2 mutations in paroxysmal kinesigenic dyskinesia with infantile convulsions in a Taiwanese cohort
-
22870186 10.1371/journal.pone.0038543 1:CAS:528:DC%2BC38XhtFKlurvO
-
Lee Y-C, Lee M-J, Yu HY, Chen C, Hsu CH, Lin KP, Liao KK, Chang MH, Liao YC, Soong BW (2012) PRRT2 mutations in paroxysmal kinesigenic dyskinesia with infantile convulsions in a Taiwanese cohort. PLoS One 7:e38543
-
(2012)
PLoS One
, vol.7
, pp. 38543
-
-
Lee, Y.-C.1
Lee, M.-J.2
Yu, H.Y.3
Chen, C.4
Hsu, C.H.5
Lin, K.P.6
Liao, K.K.7
Chang, M.H.8
Liao, Y.C.9
Soong, B.W.10
-
14
-
-
2342586800
-
Interpreting the BOLD signal
-
14977420 10.1146/annurev.physiol.66.082602.092845 1:CAS:528: DC%2BD2cXjt1emtL4%3D
-
Logothetis NK, Wandell BA (2004) Interpreting the BOLD signal. Annu Rev Physiol 66:735-769
-
(2004)
Annu Rev Physiol
, vol.66
, pp. 735-769
-
-
Logothetis, N.K.1
Wandell, B.A.2
-
15
-
-
0034903209
-
Frequencies contributing to functional connectivity in the cerebral cortex in "resting-state" data
-
11498421 1:STN:280:DC%2BD3Mvlt1Sluw%3D%3D
-
Cordes D, Haughton VM, Arfanakis K, Carew JD, Turski PA, Moritz CH, Quigley MA, Meyerand ME (2001) Frequencies contributing to functional connectivity in the cerebral cortex in "resting-state" data. Am J Neuroradiol 22:1326-1333
-
(2001)
Am J Neuroradiol
, vol.22
, pp. 1326-1333
-
-
Cordes, D.1
Haughton, V.M.2
Arfanakis, K.3
Carew, J.D.4
Turski, P.A.5
Moritz, C.H.6
Quigley, M.A.7
Meyerand, M.E.8
-
16
-
-
24144436151
-
Spontaneous low-frequency BOLD signal fluctuations: An fMRI investigation of the resting-state default mode of brain function hypothesis
-
15852468 10.1002/hbm.20113
-
Fransson P (2005) Spontaneous low-frequency BOLD signal fluctuations: an fMRI investigation of the resting-state default mode of brain function hypothesis. Hum Brain Mapp 26:15-29
-
(2005)
Hum Brain Mapp
, vol.26
, pp. 15-29
-
-
Fransson, P.1
-
17
-
-
0029166541
-
Functional connectivity in the motor cortex of resting human brain using echo-planar MRI
-
8524021 10.1002/mrm.1910340409 1:STN:280:DyaK287gslKrsg%3D%3D
-
Biswal B, Yetkin FZ, Haughton VM, Hyde JS (1995) Functional connectivity in the motor cortex of resting human brain using echo-planar MRI. Magn Reson Med 34:537-541
-
(1995)
Magn Reson Med
, vol.34
, pp. 537-541
-
-
Biswal, B.1
Yetkin, F.Z.2
Haughton, V.M.3
Hyde, J.S.4
-
18
-
-
33846485017
-
Altered baseline brain activity in children with ADHD revealed by resting-state functional MRI
-
16919409 10.1016/j.braindev.2006.10.001
-
Zang YF, He Y, Zhu CZ, Cao QJ, Sui MQ, Liang M, Tian LX, Jiang TZ, Wang YF (2007) Altered baseline brain activity in children with ADHD revealed by resting-state functional MRI. Brain Dev 29:83-91
-
(2007)
Brain Dev
, vol.29
, pp. 83-91
-
-
Zang, Y.F.1
He, Y.2
Zhu, C.Z.3
Cao, Q.J.4
Sui, M.Q.5
Liang, M.6
Tian, L.X.7
Jiang, T.Z.8
Wang, Y.F.9
-
19
-
-
74149094868
-
Localization of cerebral functional deficits in treatment-naive, first-episode schizophrenia using resting-state fMRI
-
19963069 10.1016/j.neuroimage.2009.11.072
-
Huang XQ, Lui S, Deng W, Chan RC, Wu QZ, Jiang LJ, Zhang JR, Jia ZY, Li XL, Li F, Chen L, Li T, Gong QY (2010) Localization of cerebral functional deficits in treatment-naive, first-episode schizophrenia using resting-state fMRI. Neuroimage 49:2901-2906
-
(2010)
Neuroimage
, vol.49
, pp. 2901-2906
-
-
Huang, X.Q.1
Lui, S.2
Deng, W.3
Chan, R.C.4
Wu, Q.Z.5
Jiang, L.J.6
Zhang, J.R.7
Jia, Z.Y.8
Li, X.L.9
Li, F.10
Chen, L.11
Li, T.12
Gong, Q.Y.13
-
20
-
-
75749126490
-
Amplitude of low-frequency oscillations in schizophrenia a resting state fMRI study
-
19854028 10.1016/j.schres.2009.09.030
-
Hoptman MJ (2010) Amplitude of low-frequency oscillations in schizophrenia a resting state fMRI study. Schizophr Res 117:13-20
-
(2010)
Schizophr Res
, vol.117
, pp. 13-20
-
-
Hoptman, M.J.1
-
21
-
-
80051812489
-
Abnormal spontaneous brain activity in medication-naive ADHD children: A resting state fMRI study
-
21810451 10.1016/j.neulet.2011.07.028 1:CAS:528:DC%2BC3MXhtVGkurjF
-
Yang H, Wu QZ, Guo LT, Li QQ, Long XY, Huang XQ, Chan RC, Gong QY (2011) Abnormal spontaneous brain activity in medication-naive ADHD children: a resting state fMRI study. Neurosci Lett 502:89-93
-
(2011)
Neurosci Lett
, vol.502
, pp. 89-93
-
-
Yang, H.1
Wu, Q.Z.2
Guo, L.T.3
Li, Q.Q.4
Long, X.Y.5
Huang, X.Q.6
Chan, R.C.7
Gong, Q.Y.8
-
22
-
-
80052666163
-
Spatial patterns of intrinsic brain activity in mild cognitive impairment and alzheimer's disease: A resting-state functional MRI study
-
21077137 10.1002/hbm.21140
-
Wang Z, Yan C, Zhao C, Qi Z, Zhou W, Lu J, He Y, Li K (2011) Spatial patterns of intrinsic brain activity in mild cognitive impairment and alzheimer's disease: a resting-state functional MRI study. Hum Brain Mapp 32:1720-1740
-
(2011)
Hum Brain Mapp
, vol.32
, pp. 1720-1740
-
-
Wang, Z.1
Yan, C.2
Zhao, C.3
Qi, Z.4
Zhou, W.5
Lu, J.6
He, Y.7
Li, K.8
-
23
-
-
77955071290
-
Hyperactive putamen in patients with paroxysmal kinesigenic choreoathetosis: A resting-state functional magnetic resonance imaging study
-
20629125 10.1002/mds.22967
-
Zhou B, Chen Q, Zhang Q, Chen L, Gong Q, Shang H, Tang H, Zhou D (2010) Hyperactive putamen in patients with paroxysmal kinesigenic choreoathetosis: a resting-state functional magnetic resonance imaging study. Mov Disord 25:1226-1231
-
(2010)
Mov Disord
, vol.25
, pp. 1226-1231
-
-
Zhou, B.1
Chen, Q.2
Zhang, Q.3
Chen, L.4
Gong, Q.5
Shang, H.6
Tang, H.7
Zhou, D.8
-
24
-
-
80052944191
-
REST: A toolkit for resting-state functional magnetic resonance imaging data processing
-
21949842 10.1371/journal.pone.0025031 1:CAS:528:DC%2BC3MXht12ns7nK
-
Song XW, Dong ZY, Long XY, Li SF, Zuo XN, Zhu CZ, He Y, Yan CG, Zang YF (2011) REST: a toolkit for resting-state functional magnetic resonance imaging data processing. PLoS One 6:e25031
-
(2011)
PLoS One
, vol.6
, pp. 25031
-
-
Song, X.W.1
Dong, Z.Y.2
Long, X.Y.3
Li, S.F.4
Zuo, X.N.5
Zhu, C.Z.6
He, Y.7
Yan, C.G.8
Zang, Y.F.9
-
25
-
-
34547399211
-
Integrating VBM into the General Linear Model with voxelwise anatomical covariates
-
17113790 10.1016/j.neuroimage.2006.10.007
-
Oakes TR, Fox AS, Johnstone T, Chung MK, Kalin N, Davidson RJ (2007) Integrating VBM into the General Linear Model with voxelwise anatomical covariates. Neuroimage 34:500-508
-
(2007)
Neuroimage
, vol.34
, pp. 500-508
-
-
Oakes, T.R.1
Fox, A.S.2
Johnstone, T.3
Chung, M.K.4
Kalin, N.5
Davidson, R.J.6
-
26
-
-
33751111992
-
Biological parametric mapping: A statistical toolbox for multimodality brain image analysis
-
17070709 10.1016/j.neuroimage.2006.09.011
-
Casanova R, Srikanth R, Baer A, Laurienti PJ, Burdette JH, Hayasaka S, Flowers L, Wood F, Maldjian JA (2007) Biological parametric mapping: a statistical toolbox for multimodality brain image analysis. Neuroimage 34:137-143
-
(2007)
Neuroimage
, vol.34
, pp. 137-143
-
-
Casanova, R.1
Srikanth, R.2
Baer, A.3
Laurienti, P.J.4
Burdette, J.H.5
Hayasaka, S.6
Flowers, L.7
Wood, F.8
Maldjian, J.A.9
-
27
-
-
0027401153
-
The role of premotor cortex and the supplementary motor area in the temporal control of movement in man
-
8453461 10.1093/brain/116.1.243
-
Halsband U, Ito N, Tanji J, Freund HJ (1993) The role of premotor cortex and the supplementary motor area in the temporal control of movement in man. Brain 116(Pt 1):243-266
-
(1993)
Brain
, vol.116
, Issue.PART 1
, pp. 243-266
-
-
Halsband, U.1
Ito, N.2
Tanji, J.3
Freund, H.J.4
-
28
-
-
0037039469
-
Dorsal anterior cingulate cortex: A role in reward-based decision making
-
11756669 10.1073/pnas.012470999 1:CAS:528:DC%2BD38Xlt1Cqtg%3D%3D
-
Bush G, Vogt BA, Holmes J, Dale AM, Greve D, Jenike MA, Rosen BR (2002) Dorsal anterior cingulate cortex: a role in reward-based decision making. Proc Natl Acad Sci USA 99:523-528
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, pp. 523-528
-
-
Bush, G.1
Vogt, B.A.2
Holmes, J.3
Dale, A.M.4
Greve, D.5
Jenike, M.A.6
Rosen, B.R.7
-
29
-
-
54549125698
-
Increased basal-ganglia activation performing a non-dystonia-related task in focal dystonia
-
18557921 10.1111/j.1468-1331.2008.02196.x 1:STN:280: DC%2BD1crgtFenuw%3D%3D
-
Obermann M, Yaldizli O, de Greiff A, Konczak J, Lachenmayer ML, Tumczak F, Buhl AR, Putzki N, Vollmer-Haase J, Gizewski ER, Diener HC, Maschke M (2008) Increased basal-ganglia activation performing a non-dystonia-related task in focal dystonia. Eur J Neurol 15:831-838
-
(2008)
Eur J Neurol
, vol.15
, pp. 831-838
-
-
Obermann, M.1
Yaldizli, O.2
De Greiff, A.3
Konczak, J.4
Lachenmayer, M.L.5
Tumczak, F.6
Buhl, A.R.7
Putzki, N.8
Vollmer-Haase, J.9
Gizewski, E.R.10
Diener, H.C.11
Maschke, M.12
-
30
-
-
0022930826
-
Parallel organization of functionally segregated circuits linking basal ganglia and cortex
-
3085570 10.1146/annurev.ne.09.030186.002041 1:STN:280: DyaL283htlKksw%3D%3D
-
Alexander GE, DeLong MR, Strick PL (1986) Parallel organization of functionally segregated circuits linking basal ganglia and cortex. Annu Rev Neurosci 9:357-381
-
(1986)
Annu Rev Neurosci
, vol.9
, pp. 357-381
-
-
Alexander, G.E.1
Delong, M.R.2
Strick, P.L.3
-
31
-
-
0037246226
-
Frontal-striatal circuit functions: Context, sequence, and consequence
-
12570364
-
Saint-Cyr JA (2003) Frontal-striatal circuit functions: context, sequence, and consequence. J Int Neuropsychol Soc 9:103-127
-
(2003)
J Int Neuropsychol Soc
, vol.9
, pp. 103-127
-
-
Saint-Cyr, J.A.1
-
32
-
-
0031920886
-
Proton MR spectroscopic findings in paroxysmal kinesigenic dyskinesia
-
9613757 10.1002/mds.870130334 1:STN:280:DyaK1c3ntlyisQ%3D%3D
-
Kim MO, Im JH, Choi CG, Lee MC (1998) Proton MR spectroscopic findings in paroxysmal kinesigenic dyskinesia. Mov Disord 13:570-575
-
(1998)
Mov Disord
, vol.13
, pp. 570-575
-
-
Kim, M.O.1
Im, J.H.2
Choi, C.G.3
Lee, M.C.4
-
33
-
-
0034776283
-
Regression of ventral striatum hypometabolism after calcium/calcitriol therapy in paroxysmal kinesigenic choreoathetosis due to idiopathic primary hypoparathyroidism
-
11606688 10.1136/jnnp.71.5.691 1:STN:280:DC%2BD3MrmtVyluw%3D%3D
-
Volonte MA, Perani D, Lanzi R, Poggi A, Anchisi D, Balini A, Comi G, Fazio F (2001) Regression of ventral striatum hypometabolism after calcium/calcitriol therapy in paroxysmal kinesigenic choreoathetosis due to idiopathic primary hypoparathyroidism. J Neurol Neurosurg Psychiatry 71:691-695
-
(2001)
J Neurol Neurosurg Psychiatry
, vol.71
, pp. 691-695
-
-
Volonte, M.A.1
Perani, D.2
Lanzi, R.3
Poggi, A.4
Anchisi, D.5
Balini, A.6
Comi, G.7
Fazio, F.8
-
34
-
-
25144491062
-
Perfusion abnormality of the caudate nucleus in patients with paroxysmal kinesigenic choreoathetosis
-
15948007 10.1007/s00259-005-1814-z
-
Joo EY, Hong SB, Tae WS, Kim JH, Han SJ, Seo DW, Lee KH, Kim MH, Kim S, Lee MH, Kim BT (2005) Perfusion abnormality of the caudate nucleus in patients with paroxysmal kinesigenic choreoathetosis. Eur J Nucl Med Mol Imaging 32:1205-1209
-
(2005)
Eur J Nucl Med Mol Imaging
, vol.32
, pp. 1205-1209
-
-
Joo, E.Y.1
Hong, S.B.2
Tae, W.S.3
Kim, J.H.4
Han, S.J.5
Seo, D.W.6
Lee, K.H.7
Kim, M.H.8
Kim, S.9
Lee, M.H.10
Kim, B.T.11
-
35
-
-
0020575522
-
Paroxysmal kinesigenic choreoathetosis and abnormal contingent negative variation. A case report
-
6847446 10.1001/archneur.1983.04050060081016 1:STN:280: DyaL3s3gtlGmuw%3D%3D
-
Franssen H, Fortgens C, Wattendorff AR, van Woerkom TC (1983) Paroxysmal kinesigenic choreoathetosis and abnormal contingent negative variation. a case report. Arch Neurol 40:381-385
-
(1983)
Arch Neurol
, vol.40
, pp. 381-385
-
-
Franssen, H.1
Fortgens, C.2
Wattendorff, A.R.3
Van Woerkom, T.C.4
-
36
-
-
0021720988
-
Autosomal dominant paroxysmal kinesigenic choreoathetosis. An electroneurophysiological study
-
6096061 10.1016/0303-8467(84)90290-7 1:STN:280:DyaL2M%2FnsFaruw%3D%3D
-
Busard HL, Renier WO, Gabreels FJ, Vos AJ, Declerck AC, Verhey FH (1984) Autosomal dominant paroxysmal kinesigenic choreoathetosis. an electroneurophysiological study. Clin Neurol Neurosurg 86:281-289
-
(1984)
Clin Neurol Neurosurg
, vol.86
, pp. 281-289
-
-
Busard, H.L.1
Renier, W.O.2
Gabreels, F.J.3
Vos, A.J.4
Declerck, A.C.5
Verhey, F.H.6
-
37
-
-
0038638023
-
Preprogramming motor dysfunction in paroxysmal kinesigenic choreoathetosis
-
12760411
-
Fattapposta F, My F, Valente D, Quadrini R, D'Alessio C, Amabile G (2003) Preprogramming motor dysfunction in paroxysmal kinesigenic choreoathetosis. Funct Neurol 18:29-34
-
(2003)
Funct Neurol
, vol.18
, pp. 29-34
-
-
Fattapposta, F.1
My, F.2
Valente, D.3
Quadrini, R.4
D'Alessio, C.5
Amabile, G.6
-
38
-
-
84862912899
-
Mutations in PRRT2 result in paroxysmal dyskinesias with marked variability in clinical expression
-
22209761 10.1136/jmedgenet-2011-100653 1:CAS:528:DC%2BC38XktFCisbY%3D
-
Liu Q, Qi Z, Wan XH, Li JY, Shi L, Lu Q, Zhou XQ, Qiao L, Wu LW, Liu XQ, Yang W, Liu Y, Cui LY, Zhang X (2012) Mutations in PRRT2 result in paroxysmal dyskinesias with marked variability in clinical expression. J Med Genet 49:79-82
-
(2012)
J Med Genet
, vol.49
, pp. 79-82
-
-
Liu, Q.1
Qi, Z.2
Wan, X.H.3
Li, J.Y.4
Shi, L.5
Lu, Q.6
Zhou, X.Q.7
Qiao, L.8
Wu, L.W.9
Liu, X.Q.10
Yang, W.11
Liu, Y.12
Cui, L.Y.13
Zhang, X.14
-
39
-
-
0037036416
-
The 25-kDa synaptosome-associated protein (SNAP-25) binds and inhibits delayed rectifier potassium channels in secretory cells
-
11925439 10.1074/jbc.M201034200 1:CAS:528:DC%2BD38XkslWgsb8%3D
-
Ji J, Tsuk S, Salapatek AM, Huang X, Chikvashvili D, Pasyk EA, Kang Y, Sheu L, Tsushima R, Diamant N, Trimble WS, Lotan I, Gaisano HY (2002) The 25-kDa synaptosome-associated protein (SNAP-25) binds and inhibits delayed rectifier potassium channels in secretory cells. J Biol Chem 277:20195-20204
-
(2002)
J Biol Chem
, vol.277
, pp. 20195-20204
-
-
Ji, J.1
Tsuk, S.2
Salapatek, A.M.3
Huang, X.4
Chikvashvili, D.5
Pasyk, E.A.6
Kang, Y.7
Sheu, L.8
Tsushima, R.9
Diamant, N.10
Trimble, W.S.11
Lotan, I.12
Gaisano, H.Y.13
-
40
-
-
0037033997
-
Vesicular restriction of synaptobrevin suggests a role for calcium in membrane fusion
-
11832947 10.1038/415646a 1:CAS:528:DC%2BD38XhsVCjsbY%3D
-
Hu K, Carroll J, Fedorovich S, Rickman C, Sukhodub A, Davletov B (2002) Vesicular restriction of synaptobrevin suggests a role for calcium in membrane fusion. Nature 415:646-650
-
(2002)
Nature
, vol.415
, pp. 646-650
-
-
Hu, K.1
Carroll, J.2
Fedorovich, S.3
Rickman, C.4
Sukhodub, A.5
Davletov, B.6
-
41
-
-
2642511690
-
Carbamazepine reduces memory induced activation of mesial temporal lobe structures: A pharmacological fMRI-study
-
11710962 10.1186/1471-2377-1-6 1:STN:280:DC%2BD3srnvVOktw%3D%3D
-
Jokeit H, Okujava M, Woermann FG (2001) Carbamazepine reduces memory induced activation of mesial temporal lobe structures: a pharmacological fMRI-study. BMC Neurol 1:6
-
(2001)
BMC Neurol
, vol.1
, pp. 6
-
-
Jokeit, H.1
Okujava, M.2
Woermann, F.G.3
-
42
-
-
79960078418
-
Gender and drug effects on neuroimaging in epilepsy
-
10.1111/j.1528-1167.2011.03150.x
-
Koepp MJ (2011) Gender and drug effects on neuroimaging in epilepsy. Epilepsia 4:35-37
-
(2011)
Epilepsia
, vol.4
, pp. 35-37
-
-
Koepp, M.J.1
|