A citation-based method for searching scientific literature

Kapil D Sethi, Joseph Jankovic. Mov Disord 2002
Times Cited: 37







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



Times Cited
  Times     Co-cited
Similarity


Extrapyramidal motor signs in degenerative ataxias.
L Schöls, S Peters, S Szymanski, R Krüger, S Lange, C Hardt, O Riess, H Przuntek. Arch Neurol 2000
66
29

Focal limb dystonia in a patient with a cerebellar mass.
F Alarcón, E Tolosa, E Muñoz. Arch Neurol 2001
45
27


Dystonia as a presenting sign of spinocerebellar ataxia type 1.
Yih-Ru Wu, Guey-Jen Lee-Chen, Anthony E Lang, Chiung-Mei Chen, Hsuan-Yuan Lin, Sien-Tsong Chen. Mov Disord 2004
21
47

Clinical features and genetic analysis of a Spanish family with spinocerebellar ataxia 6.
J Arpa, A Cuesta, A Cruz-Martínez, S Santiago, J Sarriá, F Palau. Acta Neurol Scand 1999
15
53

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel.
O Zhuchenko, J Bailey, P Bonnen, T Ashizawa, D W Stockton, C Amos, W B Dobyns, S H Subramony, H Y Zoghbi, C C Lee. Nat Genet 1997
21

Functional brain networks in DYT1 dystonia.
D Eidelberg, J R Moeller, A Antonini, K Kazumata, T Nakamura, V Dhawan, P Spetsieris, D deLeon, S B Bressman, S Fahn. Ann Neurol 1998
228
21

Focal dystonia as a presenting sign of spinocerebellar ataxia 17.
Johann M Hagenah, Christine Zühlke, Yorck Hellenbroich, Wolfgang Heide, Christine Klein. Mov Disord 2004
46
21

Movement disorders in spinocerebellar ataxias.
Judith van Gaalen, Paola Giunti, Bart P van de Warrenburg. Mov Disord 2011
97
21

Slowly progressive cerebellar ataxia and cervical dystonia: clinical presentation of a new form of spinocerebellar ataxia?
Mikko Kuoppamäki, Paula Giunti, Niall Quinn, Nicholas W Wood, Kailash P Bhatia. Mov Disord 2003
34
20


Task specific focal dystonia: a presentation of spinocerebellar ataxia type 6.
M B Muzaimi, C M Wiles, N P Robertson, D Ravine, D A S Compston. J Neurol Neurosurg Psychiatry 2003
17
41

Spinocerebellar ataxia type 3 presenting as an L-DOPA responsive dystonia phenotype in a Chinese family.
E Wilder-Smith, E K Tan, H Y Law, Y Zhao, I Ng, M C Wong. J Neurol Sci 2003
46
18



Abnormal cerebellar signaling induces dystonia in mice.
Carolyn E Pizoli, H A Jinnah, Melvin L Billingsley, Ellen J Hess. J Neurosci 2002
115
16

Spinocerebellar ataxia type 6: CAG repeat expansion in alpha1A voltage-dependent calcium channel gene and clinical variations in Japanese population.
T Ikeuchi, H Takano, R Koide, Y Horikawa, Y Honma, Y Onishi, S Igarashi, H Tanaka, N Nakao, K Sahashi,[...]. Ann Neurol 1997
110
16

Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese.
K Gwinn-Hardy, J Y Chen, H C Liu, T Y Liu, M Boss, W Seltzer, A Adam, A Singleton, W Koroshetz, C Waters,[...]. Neurology 2000
153
16

Molecular and clinical correlations in spinocerebellar ataxia 2: a study of 32 families.
G Cancel, A Dürr, O Didierjean, G Imbert, K Bürk, A Lezin, S Belal, A Benomar, M Abada-Bendib, C Vial,[...]. Hum Mol Genet 1997
194
16

Predominant dystonia with marked cerebellar atrophy: a rare phenotype in familial dystonia.
I Le Ber, F Clot, L Vercueil, A Camuzat, M Viémont, N Benamar, P De Liège, A M Ouvrard-Hernandez, P Pollak, G Stevanin,[...]. Neurology 2006
60
16

SCA-12: Tremor with cerebellar and cortical atrophy is associated with a CAG repeat expansion.
E O'Hearn, S E Holmes, P C Calvert, C A Ross, R L Margolis. Neurology 2001
84
13

Machado-Joseph disease presenting as severe generalised dystonia in a German patient.
A Münchau, D Dressler, K P Bhatia, P Vogel, C Zühlke. J Neurol 1999
17
29

Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuropathological features.
A Dürr, G Stevanin, G Cancel, C Duyckaerts, N Abbas, O Didierjean, H Chneiweiss, A Benomar, O Lyon-Caen, J Julien,[...]. Ann Neurol 1996
348
13

The metabolic topography of essential blepharospasm: a focal dystonia with general implications.
M Hutchinson, T Nakamura, J R Moeller, A Antonini, A Belakhlef, V Dhawan, D Eidelberg. Neurology 2000
111
13

Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds.
L Schöls, R Krüger, G Amoiridis, H Przuntek, J T Epplen, O Riess. J Neurol Neurosurg Psychiatry 1998
127
13

Benign paroxysmal torticollis of infancy: four new cases and linkage to CACNA1A mutation.
N J Giffin, S Benton, P J Goadsby. Dev Med Child Neurol 2002
99
13


Triggers of paroxysmal dyskinesia in the calcium channel mouse mutant tottering.
Brandy E Fureman, H A Jinnah, Ellen J Hess. Pharmacol Biochem Behav 2002
45
13

Dystonia and cerebellar atrophy in Cacna1a null mice lacking P/Q calcium channel activity.
C F Fletcher, A Tottene, V A Lennon, S M Wilson, S J Dubel, R Paylor, D A Hosford, L Tessarollo, M W McEnery, D Pietrobon,[...]. FASEB J 2001
138
13

Clinical and molecular features of spinocerebellar ataxia type 6.
G Stevanin, A Dürr, G David, O Didierjean, G Cancel, S Rivaud, A Tourbah, J M Warter, Y Agid, A Brice. Neurology 1997
100
13

Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4.
R A Ophoff, G M Terwindt, M N Vergouwe, R van Eijk, P J Oefner, S M Hoffman, J E Lamerdin, H W Mohrenweiser, D E Bulman, M Ferrari,[...]. Cell 1996
13


Two novel CACNA1A gene mutations associated with episodic ataxia type 2 and interictal dystonia.
Sian D Spacey, Luke A Materek, Blajez I Szczygielski, Thomas D Bird. Arch Neurol 2005
43
13

Cerebellothalamocortical connectivity regulates penetrance in dystonia.
Miklos Argyelan, Maren Carbon, Martin Niethammer, Aziz M Ulug, Henning U Voss, Susan B Bressman, Vijay Dhawan, David Eidelberg. J Neurosci 2009
209
13

The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 gene.
Allison Brashear, William B Dobyns, Patricia de Carvalho Aguiar, Michel Borg, C J M Frijns, Seema Gollamudi, Andrew Green, João Guimaraes, Bret C Haake, Christine Klein,[...]. Brain 2007
167
13

Autosomal dominant cerebellar ataxia type I clinical features and MRI in families with SCA1, SCA2 and SCA3.
K Bürk, M Abele, M Fetter, J Dichgans, M Skalej, F Laccone, O Didierjean, A Brice, T Klockgether. Brain 1996
180
10

Characteristic magnetic resonance imaging findings in spinocerebellar ataxia 6.
Y Murata, H Kawakami, S Yamaguchi, M Nishimura, T Kohriyama, F Ishizaki, Z Matsuyama, Y Mimori, S Nakamura. Arch Neurol 1998
54
10

Autosomal dominant cerebellar ataxia: phenotypic differences in genetically defined subtypes?
L Schöls, G Amoiridis, T Büttner, H Przuntek, J T Epplen, O Riess. Ann Neurol 1997
248
10

Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies). Clinical and neuropathological analysis of 53 patients from three unrelated SCA2 families.
A Dürr, D Smadja, G Cancel, A Lezin, G Stevanin, J Mikol, R Bellance, G G Buisson, H Chneiweiss, J Dellanave. Brain 1995
169
10


Characterization of the rat mutant dystonic (dt): a new animal model of dystonia musculorum deformans.
J F Lorden, T W McKeon, H J Baker, N Cox, S U Walkley. J Neurosci 1984
69
10

Spinocerebellar ataxia type 6. Frequency of the mutation and genotype-phenotype correlations.
D H Geschwind, S Perlman, K P Figueroa, J Karrim, R W Baloh, S M Pulst. Neurology 1997
134
10

Movement disorders in hereditary ataxias.
Pedro J Garcia Ruiz, David Mayo, Jaime Hernandez, Susana Cantarero, Carmen Ayuso. J Neurol Sci 2002
25
16

Cervical dystonia in spinocerebellar ataxia type 2: clinical and polymyographic findings.
S M Boesch, J Müller, G K Wenning, W Poewe. J Neurol Neurosurg Psychiatry 2007
20
20

Identification of a novel SCA14 mutation in a Dutch autosomal dominant cerebellar ataxia family.
B P C van de Warrenburg, D S Verbeek, S J Piersma, F A M Hennekam, P L Pearson, N V A M Knoers, H P H Kremer, R J Sinke. Neurology 2003
78
10

Paroxysmal torticollis and blepharospasm following bilateral cerebellar infarction.
Killian O'Rourke, Sean O'Riordan, Jean Gallagher, Michael Hutchinson. J Neurol 2006
31
12

The basal ganglia and cerebellum interact in the expression of dystonic movement.
Vladimir K Neychev, Xueliang Fan, V I Mitev, Ellen J Hess, H A Jinnah. Brain 2008
201
10

Animal models of generalized dystonia.
Robert S Raike, H A Jinnah, Ellen J Hess. NeuroRx 2005
47
10

Subthalamic-thalamic DBS in a case with spinocerebellar ataxia type 2 and severe tremor-A unusual clinical benefit.
Hans-Joachim Freund, Utako B Barnikol, Dagmar Nolte, Harald Treuer, Georg Auburger, Peter A Tass, Madjid Samii, Volker Sturm. Mov Disord 2007
49
10

Spinocerebellar ataxia type 17 (SCA17): oculomotor phenotype and clinical characterization of 15 Italian patients.
Caterina Mariotti, Dario Alpini, Roberto Fancellu, Paola Soliveri, Marina Grisoli, Sabrina Ravaglia, Carlo Lovati, Vincenza Fetoni, Giorgio Giaccone, Alessia Castucci,[...]. J Neurol 2007
39
10


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.