A citation-based method for searching scientific literature

Anna Latorre, Kailash P Bhatia. Neurol Clin 2020
Times Cited: 9







List of co-cited articles
68 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
252
55

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
55


Psychogenic paroxysmal movement disorders--clinical features and diagnostic clues.
Christos Ganos, Maria Aguirregomozcorta, Amit Batla, Maria Stamelou, Petra Schwingenschuh, Alexander Münchau, Mark J Edwards, Kailash P Bhatia. Parkinsonism Relat Disord 2014
51
44

Unravelling of the paroxysmal dyskinesias.
Roberto Erro, Kailash P Bhatia. J Neurol Neurosurg Psychiatry 2019
35
44

Paroxysmal movement disorders: An update.
A Méneret, E Roze. Rev Neurol (Paris) 2016
36
33

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
33

Biallelic mutations of TBC1D24 in exercise-induced paroxysmal dystonia.
Dora Steel, Jennifer Heim, Michael C Kruer, Alba Sanchis-Juan, Lucy F Raymond, Paul Eunson, Manju A Kurian. Mov Disord 2020
6
50

Triheptanoin dramatically reduces paroxysmal motor disorder in patients with GLUT1 deficiency.
Fanny Mochel, Elodie Hainque, Domitille Gras, Isaac M Adanyeguh, Samantha Caillet, Bénédicte Héron, Agathe Roubertie, Elsa Kaphan, Romain Valabregue, Daisy Rinaldi,[...]. J Neurol Neurosurg Psychiatry 2016
58
33

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
115
33

Pyruvate dehydrogenase complex-E2 deficiency causes paroxysmal exercise-induced dyskinesia.
Jennifer Friedman, Annette Feigenbaum, Nathaniel Chuang, Jennifer Silhavy, Joseph G Gleeson. Neurology 2017
16
33

Movement disorders in GLUT1 deficiency syndrome respond to the modified Atkins diet.
Wilhelmina G Leen, Leena Mewasingh, Marcel M Verbeek, Erik-Jan Kamsteeg, Bart P van de Warrenburg, Michel A Willemsen. Mov Disord 2013
32
33

Familial paroxysmal exercise-induced dystonia: atypical presentation of autosomal dominant GTP-cyclohydrolase 1 deficiency.
Russell C Dale, Anna Melchers, Victor S C Fung, Padraic Grattan-Smith, Henry Houlden, John Earl. Dev Med Child Neurol 2010
34
33

Clinical and Genetic Overview of Paroxysmal Movement Disorders and Episodic Ataxias.
Giacomo Garone, Alessandro Capuano, Lorena Travaglini, Federica Graziola, Fabrizia Stregapede, Ginevra Zanni, Federico Vigevano, Enrico Bertini, Francesco Nicita. Int J Mol Sci 2020
18
33

The evolving spectrum of PRRT2-associated paroxysmal diseases.
Darius Ebrahimi-Fakhari, Afshin Saffari, Ana Westenberger, Christine Klein. Brain 2015
149
33

Paroxysmal kinesigenic dyskinesia: Clinical and genetic analyses of 110 patients.
Xiao-Jun Huang, Tian Wang, Jun-Ling Wang, Xiao-Li Liu, Xiang-Qian Che, Jin Li, Xiao Mao, Mei Zhang, Guang-Hui Bi, Li Wu,[...]. Neurology 2015
44
33

Paroxysmal dyskinesias: clinical features and classification.
M Demirkiran, J Jankovic. Ann Neurol 1995
356
33

Severe phenotypic spectrum of biallelic mutations in PRRT2 gene.
Marion Delcourt, Florence Riant, Josette Mancini, Mathieu Milh, Vincent Navarro, Emmanuel Roze, Véronique Humbertclaude, Christian Korff, Vincent Des Portes, Pierre Szepetowski,[...]. J Neurol Neurosurg Psychiatry 2015
50
22

Movement disorders in multiple sclerosis and neuromyelitis optica: A clinical marker of neurological disability.
Carolina Candeias da Silva, Denis Bernardi Bichuetti, Sonia Maria Cesar de Azevedo Silva, Henrique Ballalai Ferraz, Enedina Maria Lobato de Oliveira, Vanderci Borges. Parkinsonism Relat Disord 2018
5
40

Transition from ketogenic diet to triheptanoin in patients with GLUT1 deficiency syndrome.
Elodie Hainque, Aurélie Meneret, Domitille Gras, Mariana Atencio, Marie-Pierre Luton, Magali Barbier, Anne De Saint Martin, Thierry Billette de Villemeur, Chris Ottolenghi, Emmanuel Roze,[...]. J Neurol Neurosurg Psychiatry 2020
6
33

Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 gene.
Xiao-Meng Yin, Jing-Han Lin, Li Cao, Tong-Mei Zhang, Sheng Zeng, Kai-Lin Zhang, Wo-Tu Tian, Zheng-Mao Hu, Nan Li, Jun-Ling Wang,[...]. Hum Mol Genet 2018
29
22

Paroxysmal Asymmetric Dystonic Arm Posturing-A Less Recognized but Characteristic Manifestation of ATP1A3-related disease.
Bettina Balint, Christopher D Stephen, Vrajesh Udani, Charulata Savant Sankhla, Narendrakumar H Barad, Anthony E Lang, Kailash P Bhatia. Mov Disord Clin Pract 2019
9
22

Perfusion abnormality of the caudate nucleus in patients with paroxysmal kinesigenic choreoathetosis.
Eun Yeon Joo, Seung Bong Hong, Woo Suk Tae, Jee Hyun Kim, Sun Jung Han, Dae Won Seo, Kyung-Han Lee, Myoung-Hee Kim, Seunghwan Kim, Mann Hyung Lee,[...]. Eur J Nucl Med Mol Imaging 2005
37
22

GNAO1-related movement disorder with life-threatening exacerbations: movement phenomenology and response to DBS.
Michaela Waak, Shekeeb S Mohammad, David Coman, Kate Sinclair, Lisa Copeland, Peter Silburn, Terry Coyne, Jim McGill, Mary O'Regan, Richard Selway,[...]. J Neurol Neurosurg Psychiatry 2018
34
22

Current Concepts in Diagnosis and Treatment of Functional Neurological Disorders.
Alberto J Espay, Selma Aybek, Alan Carson, Mark J Edwards, Laura H Goldstein, Mark Hallett, Kathrin LaFaver, W Curt LaFrance, Anthony E Lang, Tim Nicholson,[...]. JAMA Neurol 2018
228
22

Hyperactive putamen in patients with paroxysmal kinesigenic choreoathetosis: a resting-state functional magnetic resonance imaging study.
Bo Zhou, Qin Chen, Qin Zhang, Lei Chen, Qiyong Gong, Huifang Shang, Hehan Tang, Dong Zhou. Mov Disord 2010
28
22

Clinical Course of Six Children With GNAO1 Mutations Causing a Severe and Distinctive Movement Disorder.
Amitha L Ananth, Amy Robichaux-Viehoever, Young-Min Kim, Andrea Hanson-Kahn, Rachel Cox, Gregory M Enns, Jonathan Strober, Marcia Willing, Bradley L Schlaggar, Yvonne W Wu,[...]. Pediatr Neurol 2016
52
22

De Novo mutations in GNAO1, encoding a Gαo subunit of heterotrimeric G proteins, cause epileptic encephalopathy.
Kazuyuki Nakamura, Hirofumi Kodera, Tenpei Akita, Masaaki Shiina, Mitsuhiro Kato, Hideki Hoshino, Hiroshi Terashima, Hitoshi Osaka, Shinichi Nakamura, Jun Tohyama,[...]. Am J Hum Genet 2013
127
22

Paroxysmal eye-head movements in Glut1 deficiency syndrome.
Toni S Pearson, Roser Pons, Kristin Engelstad, Steven A Kane, Michael E Goldberg, Darryl C De Vivo. Neurology 2017
23
22

ADCY5 mutation carriers display pleiotropic paroxysmal day and nighttime dyskinesias.
Jennifer R Friedman, Aurélie Méneret, Dong-Hui Chen, Oriane Trouillard, Marie Vidailhet, Wendy H Raskind, Emmanuel Roze. Mov Disord 2016
35
22

A randomized, controlled, double-blind, crossover trial of zonisamide in myoclonus-dystonia.
Elodie Hainque, Marie Vidailhet, Nathalie Cozic, Fanny Charbonnier-Beaupel, Stéphane Thobois, Christine Tranchant, Vanessa Brochard, Gérald Glibert, Sophie Drapier, Eugénie Mutez,[...]. Neurology 2016
34
22

Secondary paroxysmal dyskinesia in multiple sclerosis: Clinical-radiological features and treatment. Case report of seven patients.
Ethel Ciampi, Reinaldo Uribe-San-Martín, Jaime Godoy-Santín, Juan Pablo Cruz, Claudia Cárcamo-Rodríguez, Carlos Juri. Mult Scler 2017
10
22


Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder.
Wilhelmina G Leen, Joerg Klepper, Marcel M Verbeek, Maike Leferink, Tom Hofste, Baziel G van Engelen, Ron A Wevers, Todd Arthur, Nadia Bahi-Buisson, Diana Ballhausen,[...]. Brain 2010
224
22

Lesion correlates of secondary paroxysmal dyskinesia in multiple sclerosis.
Kilian Fröhlich, Klemens Winder, Ralf A Linker, Konstantin Huhn, Tobias Engelhorn, Arnd Dörfler, De-Hyung Lee, Stefan Schwab, Frank Seifert. J Neurol 2018
6
33

Paroxysmal exercise-induced dystonia within the phenotypic spectrum of ECHS1 deficiency.
Simone Olgiati, Matej Skorvanek, Marialuisa Quadri, Michelle Minneboo, Josja Graafland, Guido J Breedveld, Ramon Bonte, Zeliha Ozgur, Mirjam C G N van den Hout, Kees Schoonderwoerd,[...]. Mov Disord 2016
38
22

Phenomenology of psychogenic movement disorders in children.
Carlotta Canavese, Claudia Ciano, Federica Zibordi, Giovanna Zorzi, Vanessa Cavallera, Nardo Nardocci. Mov Disord 2012
26
22

Infantile-Onset Paroxysmal Movement Disorder and Episodic Ataxia Associated with a TBC1D24 Mutation.
Vincent Zimmern, Florence Riant, Emmanuel Roze, Emmanuelle Ranza, Frank Lehmann-Horn, Julitta de Bellescize, Dorothée Ville, Gaetan Lesca, Christian M Korff. Neuropediatrics 2019
8
25

Deep brain stimulation reduces (nocturnal) dyskinetic exacerbations in patients with ADCY5 mutation: a case series.
Ana Luísa de Almeida Marcelino, Tina Mainka, Patricia Krause, Werner Poewe, Christos Ganos, Andrea A Kühn. J Neurol 2020
10
22

Pallidal neurostimulation in patients with medication-refractory cervical dystonia: a randomised, sham-controlled trial.
Jens Volkmann, Joerg Mueller, Günther Deuschl, Andrea A Kühn, Joachim K Krauss, Werner Poewe, Lars Timmermann, Daniela Falk, Andreas Kupsch, Anatol Kivi,[...]. Lancet Neurol 2014
191
22


Medical treatment of dystonia.
Pichet Termsarasab, Thananan Thammongkolchai, Steven J Frucht. J Clin Mov Disord 2016
23
22

Treatable inherited rare movement disorders.
H A Jinnah, Alberto Albanese, Kailash P Bhatia, Francisco Cardoso, Gustavo Da Prat, Tom J de Koning, Alberto J Espay, Victor Fung, Pedro J Garcia-Ruiz, Oscar Gershanik,[...]. Mov Disord 2018
50
22

Distinct neurological disorders with ATP1A3 mutations.
Erin L Heinzen, Alexis Arzimanoglou, Allison Brashear, Steven J Clapcote, Fiorella Gurrieri, David B Goldstein, Sigurður H Jóhannesson, Mohamad A Mikati, Brian Neville, Sophie Nicole,[...]. Lancet Neurol 2014
156
22

Paroxysmal dyskinesias.
Kailash P Bhatia. Mov Disord 2011
109
22


PRRT2 controls neuronal excitability by negatively modulating Na+ channel 1.2/1.6 activity.
Floriana Fruscione, Pierluigi Valente, Bruno Sterlini, Alessandra Romei, Simona Baldassari, Manuela Fadda, Cosimo Prestigio, Giorgia Giansante, Jacopo Sartorelli, Pia Rossi,[...]. Brain 2018
60
22

Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutation.
Elena Gardella, Felicitas Becker, Rikke S Møller, Julian Schubert, Johannes R Lemke, Line H G Larsen, Hans Eiberg, Michael Nothnagel, Holger Thiele, Janine Altmüller,[...]. Ann Neurol 2016
112
22

Proline-rich transmembrane protein 2-negative paroxysmal kinesigenic dyskinesia: Clinical and genetic analyses of 163 patients.
Wo-Tu Tian, Xiao-Jun Huang, Xiao Mao, Qing Liu, Xiao-Li Liu, Sheng Zeng, Xia-Nan Guo, Jun-Yi Shen, Yang-Qi Xu, Hui-Dong Tang,[...]. Mov Disord 2018
25
22

PRRT2 phenotypes and penetrance of paroxysmal kinesigenic dyskinesia and infantile convulsions.
Rianne van Vliet, Guido Breedveld, Johanneke de Rijk-van Andel, Eva Brilstra, Nienke Verbeek, Corien Verschuuren-Bemelmans, Maartje Boon, Johnny Samijn, Karin Diderich, Ingrid van de Laar,[...]. Neurology 2012
63
22


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.