A citation-based method for searching scientific literature

Claudio M de Gusmao, Lucas Rogerio Garcia, Aaron Jesuthasan, Meaghan Muir, Alex Paciorkowski, Jonathan W Mink, Laura Silveira-Moriyama. Mov Disord Clin Pract 2020
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Parkin disease: a phenotypic study of a large case series.
Naheed L Khan, Elizabeth Graham, Peter Critchley, Anette E Schrag, Nicholas W Wood, Andrew J Lees, Kailash P Bhatia, Niall Quinn. Brain 2003
248
100

A novel SLC2A1 mutation linking hemiplegic migraine with alternating hemiplegia of childhood.
Claudia M Weller, Wilhelmina G Leen, Brian G R Neville, John S Duncan, Boukje de Vries, Marije A Geilenkirchen, Joost Haan, Erik-Jan Kamsteeg, Michel D Ferrari, Arn M J M van den Maagdenberg,[...]. Cephalalgia 2015
19
100

ATP1A3 spectrum disorders: A video-documented history of 7 genetically confirmed early onset cases.
Michela Stagnaro, Livia Pisciotta, Marcella Gherzi, Maja Di Rocco, Fiorella Gurrieri, Elena Parrini, Giulia Prato, Edvige Veneselli, Elisa De Grandis. Eur J Paediatr Neurol 2018
10
100

CACNA1A-related early-onset encephalopathy with myoclonic epilepsy: A case report.
Takuya Hayashida, Yoshiaki Saito, Atsushi Ishii, Hiroyuki Yamada, Ayako Itakura, Toshinori Minato, Tetsuhiro Fukuyama, Yoshihiro Maegaki, Shinichi Hirose. Brain Dev 2018
13
100

Early onset absence epilepsy: 1 in 10 cases is caused by GLUT1 deficiency.
Todor Arsov, Saul A Mullen, John A Damiano, Kate M Lawrence, Linda L Huh, Melinda Nolan, Helen Young, Anaïs Thouin, Hans-Henrik M Dahl, Samuel F Berkovic,[...]. Epilepsia 2012
64
100

From nocturnal paroxysmal dystonia to nocturnal frontal lobe epilepsy.
F Provini, G Plazzi, E Lugaresi. Clin Neurophysiol 2000
50
100

TBC1D24-TLDc-related epilepsy exercise-induced dystonia: rescue by antioxidants in a disease model.
Kevin Lüthy, Davide Mei, Baptiste Fischer, Maurizio De Fusco, Jef Swerts, Jone Paesmans, Elena Parrini, Naomi Lubarr, Inge A Meijer, Katherine M Mackenzie,[...]. Brain 2019
19
100

Reversible valproate-induced choreiform movements.
Dilek Ince Gunal, Meliha Guleryuz, Canan Aykut Bingol. Seizure 2002
13
100

A homozygous missense variant in CACNB4 encoding the auxiliary calcium channel beta4 subunit causes a severe neurodevelopmental disorder and impairs channel and non-channel functions.
Pierre Coste de Bagneaux, Leonie von Elsner, Tatjana Bierhals, Marta Campiglio, Jessika Johannsen, Gerald J Obermair, Maja Hempel, Bernhard E Flucher, Kerstin Kutsche. PLoS Genet 2020
6
100

Dominant-negative mutation p.Arg324Thr in KCNA1 impairs Kv1.1 channel function in episodic ataxia.
Enriqueta Tristán-Clavijo, Francisco G Scholl, Alfons Macaya, Gemma Iglesias, Ana M Rojas, Miguel Lucas, Antonio Castellano, Amalia Martinez-Mir. Mov Disord 2016
13
100

The expanding spectrum of ATP1A3 related disease.
Cecilia Fernandes, Mohamad A Mikati. Eur J Paediatr Neurol 2019
10
100

Clinical phenotypes of infantile onset CACNA1A-related disorder.
Tamar Gur-Hartman, Oren Berkowitz, Keren Yosovich, Agathe Roubertie, Ginevra Zanni, Alfons Macaya, Gali Heimer, Belén Pérez Dueñas, Deborah A Sival, Ben Pode-Shakked,[...]. Eur J Paediatr Neurol 2021
2
100

Mapping the gene for acetazolamide responsive hereditary paryoxysmal cerebellar ataxia to chromosome 19p.
B von Brederlow, A F Hahn, W J Koopman, G C Ebers, D E Bulman. Hum Mol Genet 1995
78
100

Paroxysmal movement disorders: An update.
A Méneret, E Roze. Rev Neurol (Paris) 2016
32
100

Acetazolamide in treatment of epilepsy.
J G Millichap. Lancet 1987
5
100

The expanding spectrum of movement disorders in genetic epilepsies.
Apostolos Papandreou, Federica Rachele Danti, Robert Spaull, Vincenzo Leuzzi, Amy Mctague, Manju A Kurian. Dev Med Child Neurol 2020
10
100

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
112
100

Treatment of Paroxysmal Dyskinesia.
Anna Latorre, Kailash P Bhatia. Neurol Clin 2020
9
100

Novel E815K knock-in mouse model of alternating hemiplegia of childhood.
Ashley R Helseth, Arsen S Hunanyan, Syed Adil, Molly Linabarger, Monisha Sachdev, Elie Abdelnour, Eric Arehart, Marlee Szabo, Jordan Richardson, William C Wetsel,[...]. Neurobiol Dis 2018
22
100

Late-onset episodic ataxia associated with SLC1A3 mutation.
Kwang-Dong Choi, Joanna C Jen, Seo Young Choi, Jin-Hong Shin, Hyang-Sook Kim, Hyo-Jung Kim, Ji-Soo Kim, Jae-Hwan Choi. J Hum Genet 2017
27
100

Targeted gene sequencing in 6994 individuals with neurodevelopmental disorder with epilepsy.
Henrike O Heyne, Mykyta Artomov, Florian Battke, Claudia Bianchini, Douglas R Smith, Nora Liebmann, Vasisht Tadigotla, Christine M Stanley, Dennis Lal, Heidi Rehm,[...]. Genet Med 2019
21
100


Episodic neurologic disorders: syndromes, genes, and mechanisms.
Jonathan F Russell, Ying-Hui Fu, Louis J Ptáček. Annu Rev Neurosci 2013
13
100

Anticonvulsants-induced chorea: a role for pharmacodynamic drug interaction?
M Zaatreh, M Tennison, O D'Cruz, R L Beach. Seizure 2001
30
100

Microdeletions detected using chromosome microarray in children with suspected genetic movement disorders: a single-centre study.
Russell C Dale, Padraic Grattan-Smith, Michelle Nicholson, Greg B Peters. Dev Med Child Neurol 2012
56
100

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
207
100

[Dose-dependent relationship of chronic use of phenytoin and cerebellar atrophy in patients with epilepsy].
A Del Negro, C D Dantas, V Zanardi, M A Montenegro, F Cendes. Arq Neuropsiquiatr 2000
8
100

Paroxysmal kinesigenic dyskinesia: cortical or non-cortical origin.
Teun W van Strien, Anne-Fleur van Rootselaar, Anthony A J Hilgevoord, Wim H J P Linssen, Alexander J A Groffen, Marina A J Tijssen. Parkinsonism Relat Disord 2012
14
100

Direct evidence of impaired neuronal Na/K-ATPase pump function in alternating hemiplegia of childhood.
Christine Q Simmons, Christopher H Thompson, Bryan E Cawthon, Grant Westlake, Kathryn J Swoboda, Evangelos Kiskinis, Kevin C Ess, Alfred L George. Neurobiol Dis 2018
14
100

Drug-induced movement disorders.
Dénes Zádori, Gábor Veres, Levente Szalárdy, Péter Klivényi, László Vécsei. Expert Opin Drug Saf 2015
14
100

Paroxysmal motor disorders: expanding phenotypes lead to coalescing genotypes.
Laura Zima, Sophia Ceulemans, Gail Reiner, Serena Galosi, Dillon Chen, Michelle Sahagian, Richard H Haas, Keith Hyland, Jennifer Friedman. Ann Clin Transl Neurol 2018
7
100


Clinical Spectrum of KCNA1 Mutations: New Insights into Episodic Ataxia and Epilepsy Comorbidity.
Kelsey Paulhus, Lauren Ammerman, Edward Glasscock. Int J Mol Sci 2020
21
100

PRRT2 phenotypic spectrum includes sporadic and fever-related infantile seizures.
Ingrid E Scheffer, Bronwyn E Grinton, Sarah E Heron, Sara Kivity, Zaid Afawi, Xenia Iona, Hadassa Goldberg-Stern, Maria Kinali, Ian Andrews, Renzo Guerrini,[...]. Neurology 2012
60
100

Paroxysmal hypnogenic dyskinesia is associated with mutations in the PRRT2 gene.
Xiao-Rong Liu, Dan Huang, Jie Wang, Yi-Fan Wang, Hui Sun, Bin Tang, Wen Li, Jin-Xing Lai, Na He, Mei Wu,[...]. Neurol Genet 2016
22
100

Dyskinesia induced by phenytoin.
M A Montenegro, A E Scotoni, F Cendes. Arq Neuropsiquiatr 1999
12
100

D-DEMØ, a distinct phenotype caused by ATP1A3 mutations.
Lyndsey Prange, Milton Pratt, Kristin Herman, Raphael Schiffmann, David M Mueller, Melissa McLean, Mary Moya Mendez, Nicole Walley, Erin L Heinzen, David Goldstein,[...]. Neurol Genet 2020
8
100

Glut1 deficiency is a rare but treatable cause of childhood absence epilepsy with atypical features.
Víctor Soto-Insuga, Rosa Guerrero López, Rebeca Losada-Del Pozo, María Rodrigo-Moreno, Elena Martínez Cayuelas, Beatriz G Giráldez, Ester Díaz-Gómez, Gema Sánchez-Martín, Laura Olivié García, José M Serratosa. Epilepsy Res 2019
2
100

Paroxysmal choreoathetosis and seizures induced by movement (reflex epilepsy).
C Perez-Borja, A C Tassinari, A G Swanson. Epilepsia 1967
21
100

Revising rapid-onset dystonia-parkinsonism: Broadening indications for ATP1A3 testing.
Ihtsham U Haq, Beverly M Snively, Kathleen J Sweadner, Cynthia K Suerken, Jared F Cook, Laurie J Ozelius, Charlotte Miller, William V McCall, Christopher T Whitlow, Allison Brashear. Mov Disord 2019
16
100

Genetic Evidence for Possible Involvement of the Calcium Channel Gene CACNA1A in Autism Pathogenesis in Chinese Han Population.
Jun Li, Yang You, Weihua Yue, Meixiang Jia, Hao Yu, Tianlan Lu, Zhiliu Wu, Yanyan Ruan, Lifang Wang, Dai Zhang. PLoS One 2015
10
100

Movement disorders associated with the use of gabapentin.
A L Reeves, E L So, F W Sharbrough, L E Krahn. Epilepsia 1996
59
100

Non-epilepsy uses of antiepilepsy drugs.
Paweł D Zaremba, Magdalena Białek, Barbara Błaszczyk, Piotr Cioczek, Stanisław J Czuczwar. Pharmacol Rep 2006
41
100

Sporadic and familial glut1ds Italian patients: A wide clinical variability.
Valentina De Giorgis, Federica Teutonico, Cristina Cereda, Umberto Balottin, Marika Bianchi, Lucio Giordano, Sara Olivotto, Francesca Ragona, Anna Tagliabue, Giovanna Zorzi,[...]. Seizure 2015
22
100

Phenotypic spectrum of glucose transporter type 1 deficiency syndrome (Glut1 DS).
Toni S Pearson, Cigdem Akman, Veronica J Hinton, Kristin Engelstad, Darryl C De Vivo. Curr Neurol Neurosci Rep 2013
112
100


Early-onset encephalopathy with paroxysmal movement disorders and epileptic seizures without hemiplegic attacks: About three children with novel ATP1A3 mutations.
Pauline Marzin, Cyril Mignot, Nathalie Dorison, Louis Dufour, Dorothée Ville, Anna Kaminska, Eleni Panagiotakaki, Anne-Sophie Dienpendaele, Marie-José Penniello, Marie-Christine Nougues,[...]. Brain Dev 2018
15
100


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
26
100

Mutation in the glutamate transporter EAAT1 causes episodic ataxia, hemiplegia, and seizures.
J C Jen, J Wan, T P Palos, B D Howard, R W Baloh. Neurology 2005
224
100


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.