A citation-based method for searching scientific literature

T Lotze, J Jankovic. Semin Pediatr Neurol 2003
Times Cited: 31







List of co-cited articles
235 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Clinical evaluation of idiopathic paroxysmal kinesigenic dyskinesia: new diagnostic criteria.
M K Bruno, M Hallett, K Gwinn-Hardy, B Sorensen, E Considine, S Tucker, D R Lynch, K D Mathews, K J Swoboda, J Harris,[...]. Neurology 2004
254
54



Secondary paroxysmal dyskinesias.
Jaishri Blakeley, Joseph Jankovic. Mov Disord 2002
92
29

Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1.
Arvid Suls, Peter Dedeken, Karolien Goffin, Hilde Van Esch, Patrick Dupont, David Cassiman, Judith Kempfle, Thomas V Wuttke, Yvonne Weber, Holger Lerche,[...]. Brain 2008
208
25


A locus for paroxysmal kinesigenic dyskinesia maps to human chromosome 16.
L B Bennett, E S Roach, A M Bowcock. Neurology 2000
95
22

Classification of paroxysmal dyskinesias and ataxias.
Joseph Jankovic, Meltem Demirkiran. Adv Neurol 2002
35
22

Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia.
Wan-Jin Chen, Yu Lin, Zhi-Qi Xiong, Wei Wei, Wang Ni, Guo-He Tan, Shun-Ling Guo, Jin He, Ya-Fang Chen, Qi-Jie Zhang,[...]. Nat Genet 2011
313
22

Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesias.
Jun-Ling Wang, Li Cao, Xun-Hua Li, Zheng-Mao Hu, Jia-Da Li, Jian-Guo Zhang, Yu Liang, San-A, Nan Li, Su-Qin Chen,[...]. Brain 2011
204
22

Paroxysmal kinesigenic dyskinesia and infantile convulsions: clinical and linkage studies.
K J Swoboda, B Soong, C McKenna, E R Brunt, M Litt, J F Bale, T Ashizawa, L B Bennett, A M Bowcock, E S Roach,[...]. Neurology 2000
94
19

Genetic and clinical heterogeneity in paroxysmal kinesigenic dyskinesia: evidence for a third EKD gene.
Sian D Spacey, Enza-Maria Valente, Gurusidheshwar M Wali, Thomas T Warner, Paul R Jarman, Anthony H V Schapira, Peter H Dixon, Mary B Davis, Kailash P Bhatia, Nicholas W Wood. Mov Disord 2002
45
19

The paroxysmal dyskinesias.
K P Bhatia. J Neurol 1999
82
19

The gene for paroxysmal non-kinesigenic dyskinesia encodes an enzyme in a stress response pathway.
Hsien-Yang Lee, Ying Xu, Yong Huang, Andrew H Ahn, Georg W J Auburger, Massimo Pandolfo, Hubert Kwiecinski, David A Grimes, Anthony E Lang, Jorgen E Nielsen,[...]. Hum Mol Genet 2004
106
19

GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak.
Yvonne G Weber, Alexander Storch, Thomas V Wuttke, Knut Brockmann, Judith Kempfle, Snezana Maljevic, Lucia Margari, Christoph Kamm, Susanne A Schneider, Stephan M Huber,[...]. J Clin Invest 2008
234
19


Paroxysmal kinesigenic choreoathetosis locus maps to chromosome 16p11.2-q12.1.
H a Tomita, S Nagamitsu, K Wakui, Y Fukushima, K Yamada, M Sadamatsu, A Masui, T Konishi, T Matsuishi, M Aihara,[...]. Am J Hum Genet 1999
122
16

A systematic review on the diagnosis and treatment of primary (idiopathic) dystonia and dystonia plus syndromes: report of an EFNS/MDS-ES Task Force.
A Albanese, M P Barnes, K P Bhatia, E Fernandez-Alvarez, G Filippini, T Gasser, J K Krauss, A Newton, I Rektor, M Savoiardo,[...]. Eur J Neurol 2006
165
16

Genotype-phenotype correlation of paroxysmal nonkinesigenic dyskinesia.
M K Bruno, H-Y Lee, G W J Auburger, A Friedman, J E Nielsen, A E Lang, E Bertini, P Van Bogaert, Y Averyanov, M Hallett,[...]. Neurology 2007
91
16

Paroxysmal kinesigenic choreoathetosis (PKC): confirmation of linkage to 16p11-q21, but unsuccessful detection of mutations among 157 genes at the PKC-critical region in seven PKC families.
Taeko Kikuchi, Masayo Nomura, Hiroaki Tomita, Naoki Harada, Kazuaki Kanai, Tohru Konishi, Ayako Yasuda, Masato Matsuura, Nobumasa Kato, Koh-Ichiro Yoshiura,[...]. J Hum Genet 2007
33
16


Paroxysmal kinesigenic choreoathetosis: a report of 26 patients.
M K Houser, V L Soland, K P Bhatia, N P Quinn, C D Marsden. J Neurol 1999
83
16

Myofibrillogenesis regulator 1 gene mutations cause paroxysmal dystonic choreoathetosis.
Shirley Rainier, Donald Thomas, Debra Tokarz, Lei Ming, Melanie Bui, Erin Plein, Xinping Zhao, Rosemary Lemons, Roger Albin, Colin Delaney,[...]. Arch Neurol 2004
110
16

Genetic and phenotypic heterogeneity in sporadic and familial forms of paroxysmal dyskinesia.
Alexander J A Groffen, Thom Klapwijk, Anne-Fleur van Rootselaar, Justus L Groen, Marina A J Tijssen. J Neurol 2013
38
16

PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome.
Sarah E Heron, Bronwyn E Grinton, Sara Kivity, Zaid Afawi, Sameer M Zuberi, James N Hughes, Clair Pridmore, Bree L Hodgson, Xenia Iona, Lynette G Sadleir,[...]. Am J Hum Genet 2012
181
16


Ictal (99m)Tc ECD SPECT in paroxysmal kinesigenic choreoathetosis.
C H Ko, C K Kong, W T Ngai, K M Ma. Pediatr Neurol 2001
34
12

Calcium-sensitive potassium channelopathy in human epilepsy and paroxysmal movement disorder.
Wei Du, Jocelyn F Bautista, Huanghe Yang, Ana Diez-Sampedro, Sun-Ah You, Lejin Wang, Prakash Kotagal, Hans O Lüders, Jingyi Shi, Jianmin Cui,[...]. Nat Genet 2005
385
12

Abnormal cortical and spinal inhibition in paroxysmal kinesigenic dyskinesia.
Pablo Mir, Ying-Zu Huang, Francesca Gilio, Mark J Edwards, Alfredo Berardelli, John C Rothwell, Kailash P Bhatia. Brain 2005
38
12


Increased ictal perfusion of the thalamus in paroxysmal kinesigenic dyskinesia.
S Shirane, M Sasaki, D Kogure, H Matsuda, T Hashimoto. J Neurol Neurosurg Psychiatry 2001
36
12

Mutations in PRRT2 responsible for paroxysmal kinesigenic dyskinesias also cause benign familial infantile convulsions.
Shinji Ono, Koh-ichiro Yoshiura, Akira Kinoshita, Taeko Kikuchi, Yoshibumi Nakane, Nobumasa Kato, Miyuki Sadamatsu, Tohru Konishi, Shinichiro Nagamitsu, Masato Matsuura,[...]. J Hum Genet 2012
67
12

Mutations in PRRT2 result in paroxysmal dyskinesias with marked variability in clinical expression.
Qing Liu, Zhan Qi, Xin-Hua Wan, Jing-Yun Li, Lei Shi, Qiang Lu, Xiang-Qin Zhou, Lei Qiao, Li-Wen Wu, Xiu-Qin Liu,[...]. J Med Genet 2012
75
12

Mutations in the gene PRRT2 cause paroxysmal kinesigenic dyskinesia with infantile convulsions.
Hsien-Yang Lee, Yong Huang, Nadine Bruneau, Patrice Roll, Elisha D O Roberson, Mark Hermann, Emily Quinn, James Maas, Robert Edwards, Tetsuo Ashizawa,[...]. Cell Rep 2012
178
12

Targeted genomic sequencing identifies PRRT2 mutations as a cause of paroxysmal kinesigenic choreoathetosis.
Jingyun Li, Xilin Zhu, Xin Wang, Wei Sun, Bing Feng, Te Du, Bei Sun, Fenghe Niu, Hua Wei, Xiaopan Wu,[...]. J Med Genet 2012
75
12

The clinical and genetic heterogeneity of paroxysmal dyskinesias.
Alice R Gardiner, Fatima Jaffer, Russell C Dale, Robyn Labrum, Roberto Erro, Esther Meyer, Georgia Xiromerisiou, Maria Stamelou, Matthew Walker, Dimitri Kullmann,[...]. Brain 2015
81
12



Electrical stimulation of the globus pallidus internus in patients with primary generalized dystonia: long-term results.
Philippe Coubes, Laura Cif, Hassan El Fertit, Simone Hemm, Nathalie Vayssiere, Stephanie Serrat, Marie Christine Picot, Sylvie Tuffery, Mireille Claustres, Bernard Echenne,[...]. J Neurosurg 2004
286
9

Long-term botulinum toxin efficacy, safety, and immunogenicity.
Nicte I Mejia, Kevin Dat Vuong, Joseph Jankovic. Mov Disord 2005
131
9


Intrathecal baclofen for dystonia.
J G Hou, W Ondo, J Jankovic. Mov Disord 2001
22
13

Comparison of botulinum toxin serotypes A and B for the treatment of cervical dystonia.
C L Comella, J Jankovic, K M Shannon, J Tsui, M Swenson, S Leurgans, W Fan. Neurology 2005
144
9


Botulinum toxin in clinical practice.
J Jankovic. J Neurol Neurosurg Psychiatry 2004
245
9

Bilateral deep-brain stimulation of the globus pallidus in primary generalized dystonia.
Marie Vidailhet, Laurent Vercueil, Jean-Luc Houeto, Pierre Krystkowiak, Alim-Louis Benabid, Philippe Cornu, Christelle Lagrange, Sophie Tézenas du Montcel, Didier Dormont, Sylvie Grand,[...]. N Engl J Med 2005
704
9

Botulinum toxin in the treatment of blepharospasm and hemifacial spasm.
C Kenney, J Jankovic. J Neural Transm (Vienna) 2008
69
9

Treatment of dystonia.
Joseph Jankovic. Lancet Neurol 2006
190
9

Management of status dystonicus: our experience and review of the literature.
Paolo Mariotti, Alfonso Fasano, M Fiorella Contarino, Giacomo Della Marca, Marco Piastra, Orazio Genovese, Silvia Pulitanò, Antonio Chiaretti, Anna Rita Bentivoglio. Mov Disord 2007
67
9

Bilateral, pallidal, deep-brain stimulation in primary generalised dystonia: a prospective 3 year follow-up study.
Marie Vidailhet, Laurent Vercueil, Jean-Luc Houeto, Pierre Krystkowiak, Christelle Lagrange, Jerôme Yelnik, Eric Bardinet, Alim-Louis Benabid, Soledad Navarro, Didier Dormont,[...]. Lancet Neurol 2007
265
9


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.