A citation-based method for searching scientific literature

F Riant, K Vahedi, E Tournier-Lasserve. Rev Neurol (Paris) 2011
Times Cited: 9







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



Times Cited
  Times     Co-cited
Similarity


Primary episodic ataxias: diagnosis, pathogenesis and treatment.
J C Jen, T D Graves, E J Hess, M G Hanna, R C Griggs, R W Baloh. Brain 2007
198
55

Identification of novel and recurrent CACNA1A gene mutations in fifteen patients with episodic ataxia type 2.
Elide Mantuano, Silvia Romano, Liana Veneziano, Cinzia Gellera, Barbara Castellotti, Sara Caimi, Daniela Testa, Margherita Estienne, Giovanna Zorzi, Marianna Bugiani,[...]. J Neurol Sci 2010
48
33

Consensus paper: pathological mechanisms underlying neurodegeneration in spinocerebellar ataxias.
A Matilla-Dueñas, T Ashizawa, A Brice, S Magri, K N McFarland, M Pandolfo, S M Pulst, O Riess, D C Rubinsztein, J Schmidt,[...]. Cerebellum 2014
75
33

Episodic Ataxias: Clinical and Genetic Features.
Kwang-Dong Choi, Jae-Hwan Choi. J Mov Disord 2016
38
33

Internuclear ophthalmoparesis in episodic ataxia type 2.
Janet C Rucker, Joanna Jen, John S Stahl, Nandhitha Natesan, Robert W Baloh, R John Leigh. Ann N Y Acad Sci 2005
8
25

Novel CACNA1A mutation causes febrile episodic ataxia with interictal cerebellar deficits.
S H Subramony, Kelly Schott, Robert S Raike, Joel Callahan, Leigh R Langford, Peka S Christova, John H Anderson, Christopher M Gomez. Ann Neurol 2003
30
22


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
22

Genetic and functional characterisation of the P/Q calcium channel in episodic ataxia with epilepsy.
Sanjeev Rajakulendran, Tracey D Graves, Robyn W Labrum, Dimitrios Kotzadimitriou, Louise Eunson, Mary B Davis, Rosalyn Davies, Nicholas W Wood, Dimitri M Kullmann, Michael G Hanna,[...]. J Physiol 2010
52
22

Consensus paper: management of degenerative cerebellar disorders.
W Ilg, A J Bastian, S Boesch, R G Burciu, P Celnik, J Claaßen, K Feil, R Kalla, I Miyai, W Nachbauer,[...]. Cerebellum 2014
88
22

Clinical and molecular features of Joubert syndrome and related disorders.
Melissa A Parisi. Am J Med Genet C Semin Med Genet 2009
123
22

PRRT2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine.
Alice R Gardiner, Kailash P Bhatia, Maria Stamelou, Russell C Dale, Manju A Kurian, Susanne A Schneider, G M Wali, Tim Counihan, Anthony H Schapira, Sian D Spacey,[...]. Neurology 2012
109
22


Paroxysmal movement disorders.
Olga Waln, Joseph Jankovic. Neurol Clin 2015
35
22

Toxic agents causing cerebellar ataxias.
Mario Manto. Handb Clin Neurol 2012
36
22

Clinical presentation of immune-mediated cerebellar ataxia.
G Demarquay, J Honnorat. Rev Neurol (Paris) 2011
10
22

Joubert syndrome: congenital cerebellar ataxia with the molar tooth.
Marta Romani, Alessia Micalizzi, Enza Maria Valente. Lancet Neurol 2013
186
22

Cerebellar and afferent ataxias.
Massimo Pandolfo, Mario Manto. Continuum (Minneap Minn) 2013
21
22

Ataxia.
Umar Akbar, Tetsuo Ashizawa. Neurol Clin 2015
30
22

Fragile X-associated tremor/ataxia syndrome.
Paul J Hagerman, Randi J Hagerman. Ann N Y Acad Sci 2015
88
22

New subtype of spinocerebellar ataxia with altered vertical eye movements mapping to chromosome 1p32.
Carmen Serrano-Munuera, Marc Corral-Juan, Giovanni Stevanin, Hector San Nicolás, Carles Roig, Jordi Corral, Berta Campos, Laura de Jorge, Carlos Morcillo-Suárez, Arcadi Navarro,[...]. JAMA Neurol 2013
22
22

Drug-induced cerebellar ataxia: a systematic review.
J van Gaalen, F G Kerstens, R P P W M Maas, L Härmark, B P C van de Warrenburg. CNS Drugs 2014
27
22

Nonmotor and extracerebellar features in Machado-Joseph disease: a review.
José Luiz Pedroso, Marcondes C França, Pedro Braga-Neto, Anelyssa D'Abreu, Maria Luiza Saraiva-Pereira, Jonas A Saute, Hélio A Teive, Paulo Caramelli, Laura Bannach Jardim, Iscia Lopes-Cendes,[...]. Mov Disord 2013
61
22

Characterizing POLG ataxia: clinics, electrophysiology and imaging.
Matthis Synofzik, Karin Srulijes, Jana Godau, Daniela Berg, Ludger Schöls. Cerebellum 2012
43
22

Cerebellar ataxia and glutamic acid decarboxylase antibodies: immunologic profile and long-term effect of immunotherapy.
Helena Ariño, Nuria Gresa-Arribas, Yolanda Blanco, Eugenia Martínez-Hernández, Lidia Sabater, Mar Petit-Pedrol, Idoia Rouco, Luis Bataller, Josep O Dalmau, Albert Saiz,[...]. JAMA Neurol 2014
91
22

Autosomal dominant cerebellar ataxias: a systematic review of clinical features.
M Rossi, S Perez-Lloret, L Doldan, D Cerquetti, J Balej, P Millar Vernetti, H Hawkes, A Cammarota, M Merello. Eur J Neurol 2014
71
22

Acetazolamide-responsive ataxia.
Vikas Kotagal. Semin Neurol 2012
24
22

Clinical spectrum of episodic ataxia type 2.
J Jen, G W Kim, R W Baloh. Neurology 2004
177
22

Late-onset episodic ataxia type 2 due to an in-frame insertion in CACNA1A.
P Imbrici, L H Eunson, T D Graves, K P Bhatia, N H Wadia, D M Kullmann, M G Hanna. Neurology 2005
35
22

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
22

Coding and noncoding variation of the human calcium-channel beta4-subunit gene CACNB4 in patients with idiopathic generalized epilepsy and episodic ataxia.
A Escayg, M De Waard, D D Lee, D Bichet, P Wolf, T Mayer, J Johnston, R Baloh, T Sander, M H Meisler. Am J Hum Genet 2000
269
22

An autosomal dominant disorder with episodic ataxia, vertigo, and tinnitus.
J L Steckley, G C Ebers, M Z Cader, R S McLachlan. Neurology 2001
47
22

Hereditary paroxysmal ataxia: response to acetazolamide.
R C Griggs, R T Moxley, R A Lafrance, J McQuillen. Neurology 1978
159
22

A novel locus for episodic ataxia:UBR4 the likely candidate.
Judith Conroy, Paul McGettigan, Raymond Murphy, David Webb, Sinéad M Murphy, Blathnaid McCoy, Christine Albertyn, Dara McCreary, Cara McDonagh, Orla Walsh,[...]. Eur J Hum Genet 2014
40
22

Periodic vestibulocerebellar ataxia, an autosomal dominant ataxia with defective smooth pursuit, is genetically distinct from other autosomal dominant ataxias.
K F Damji, R R Allingham, S C Pollock, K Small, K E Lewis, J M Stajich, L H Yamaoka, J M Vance, M A Pericak-Vance. Arch Neurol 1996
59
22

Treatment of episodic ataxia type 2 with the potassium channel blocker 4-aminopyridine.
M Strupp, R Kalla, M Dichgans, T Freilinger, S Glasauer, T Brandt. Neurology 2004
145
22

A randomized trial of 4-aminopyridine in EA2 and related familial episodic ataxias.
M Strupp, R Kalla, J Claassen, C Adrion, U Mansmann, T Klopstock, T Freilinger, H Neugebauer, R Spiegel, M Dichgans,[...]. Neurology 2011
109
22

Episodic ataxia type 2.
Michael Strupp, Andreas Zwergal, Thomas Brandt. Neurotherapeutics 2007
96
11

Neurological disorders caused by inherited ion-channel mutations.
Dimitri M Kullmann, Michael G Hanna. Lancet Neurol 2002
40
11

International Cooperative Ataxia Rating Scale for pharmacological assessment of the cerebellar syndrome. The Ataxia Neuropharmacology Committee of the World Federation of Neurology.
P Trouillas, T Takayanagi, M Hallett, R D Currier, S H Subramony, K Wessel, A Bryer, H C Diener, S Massaquoi, C M Gomez,[...]. J Neurol Sci 1997
877
11

Impaired eye movements in presymptomatic spinocerebellar ataxia type 6.
Peka Christova, John H Anderson, Christopher M Gomez. Arch Neurol 2008
29
11

Deficits in ocular and manual tracking due to episodic ataxia type 2.
Kevin C Engel, John H Anderson, Christopher M Gomez, John F Soechting. Mov Disord 2004
6
16

A wide spectrum of clinical, neurophysiological and neuroradiological abnormalities in a family with a novel CACNA1A mutation.
Romina Romaniello, Claudio Zucca, Alessandra Tonelli, Sara Bonato, Cinzia Baschirotto, Nicoletta Zanotta, Roberta Epifanio, Andrea Righini, Nereo Bresolin, Maria T Bassi,[...]. J Neurol Neurosurg Psychiatry 2010
34
11

Clinical neurophysiology of the episodic ataxias: insights into ion channel dysfunction in vivo.
Susan E Tomlinson, Michael G Hanna, Dimitri M Kullmann, S Veronica Tan, David Burke. Clin Neurophysiol 2009
27
11

Transglutaminase 6 antibodies in the diagnosis of gluten ataxia.
Marios Hadjivassiliou, Pascale Aeschlimann, David S Sanders, Markku Mäki, Katri Kaukinen, R A Grünewald, Oliver Bandmann, Nicola Woodroofe, Gail Haddock, Daniel P Aeschlimann. Neurology 2013
80
11

Spinocerebellar ataxia type 10 - A review.
Hélio A G Teive, Renato P Munhoz, Walter O Arruda, Salmo Raskin, Lineu César Werneck, Tetsuo Ashizawa. Parkinsonism Relat Disord 2011
57
11

RNA interference mitigates motor and neuropathological deficits in a cerebellar mouse model of Machado-Joseph disease.
Clévio Nóbrega, Isabel Nascimento-Ferreira, Isabel Onofre, David Albuquerque, Nicole Déglon, Luís Pereira de Almeida. PLoS One 2014
23
11

We cannot cure ataxia,we can only eradicate it.
Khalaf Bushara. JAMA Neurol 2013
4
25

PNPLA6 mutations cause Boucher-Neuhauser and Gordon Holmes syndromes as part of a broad neurodegenerative spectrum.
Matthis Synofzik, Michael A Gonzalez, Charles Marques Lourenco, Marie Coutelier, Tobias B Haack, Adriana Rebelo, Didier Hannequin, Tim M Strom, Holger Prokisch, Christoph Kernstock,[...]. Brain 2014
119
11

Clinical spectrum of ataxia-telangiectasia in adulthood.
M M M Verhagen, W F Abdo, M A A P Willemsen, F B L Hogervorst, D F C M Smeets, J A P Hiel, E R Brunt, M A van Rijn, D Majoor Krakauer, R A Oldenburg,[...]. Neurology 2009
103
11


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.