A citation-based method for searching scientific literature

Mari Akiyama, Katsuhiro Kobayashi, Harumi Yoshinaga, Yoko Ohtsuka. Epilepsia 2010
Times Cited: 111







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



Times Cited
  Times     Co-cited
Similarity


Dravet syndrome: the long-term outcome.
Pierre Genton, Reana Velizarova, Charlotte Dravet. Epilepsia 2011
139
53

De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy.
L Claes, J Del-Favero, B Ceulemans, L Lagae, C Van Broeckhoven, P De Jonghe. Am J Hum Genet 2001
785
34

Dravet syndrome as epileptic encephalopathy: evidence from long-term course and neuropathology.
Claudia B Catarino, Joan Y W Liu, Ioannis Liagkouras, Vaneesha S Gibbons, Robyn W Labrum, Rachael Ellis, Cathy Woodward, Mary B Davis, Shelagh J Smith, J Helen Cross,[...]. Brain 2011
119
33

Prognostic, clinical and demographic features in SCN1A mutation-positive Dravet syndrome.
A Brunklaus, R Ellis, E Reavey, G H Forbes, S M Zuberi. Brain 2012
173
33

Severe myoclonic epilepsy of infancy (Dravet syndrome): recognition and diagnosis in adults.
F E Jansen, L G Sadleir, L A Harkin, L Vadlamudi, J M McMahon, J C Mulley, I E Scheffer, S F Berkovic. Neurology 2006
87
36

The core Dravet syndrome phenotype.
Charlotte Dravet. Epilepsia 2011
262
30

Reduced sodium current in GABAergic interneurons in a mouse model of severe myoclonic epilepsy in infancy.
Frank H Yu, Massimo Mantegazza, Ruth E Westenbroek, Carol A Robbins, Franck Kalume, Kimberly A Burton, William J Spain, G Stanley McKnight, Todd Scheuer, William A Catterall. Nat Neurosci 2006
643
28

Severe myoclonic epilepsy of infants (Dravet syndrome): natural history and neuropsychological findings.
Markus Wolff, Catherine Cassé-Perrot, Charlotte Dravet. Epilepsia 2006
174
28

Stiripentol in severe myoclonic epilepsy in infancy: a randomised placebo-controlled syndrome-dedicated trial. STICLO study group.
C Chiron, M C Marchand, A Tran, E Rey, P d'Athis, J Vincent, O Dulac, G Pons. Lancet 2000
327
25

Long-term course of Dravet syndrome: a study from an epilepsy center in Japan.
Rumiko Takayama, Tateki Fujiwara, Hideo Shigematsu, Katsumi Imai, Yukitoshi Takahashi, Kazuhiro Yamakawa, Yushi Inoue. Epilepsia 2014
45
55

Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patients.
C Depienne, O Trouillard, C Saint-Martin, I Gourfinkel-An, D Bouteiller, W Carpentier, B Keren, B Abert, A Gautier, S Baulac,[...]. J Med Genet 2009
225
23


The spectrum of SCN1A-related infantile epileptic encephalopathies.
Louise A Harkin, Jacinta M McMahon, Xenia Iona, Leanne Dibbens, James T Pelekanos, Sameer M Zuberi, Lynette G Sadleir, Eva Andermann, Deepak Gill, Kevin Farrell,[...]. Brain 2007
345
22

Encephalopathy in children with Dravet syndrome is not a pure consequence of epilepsy.
Rima Nabbout, Nicole Chemaly, Mathilde Chipaux, Giulia Barcia, Charles Bouis, Celia Dubouch, Dorothee Leunen, Isabelle Jambaqué, Olivier Dulac, Georges Dellatolas,[...]. Orphanet J Rare Dis 2013
88
23

Cognitive development in Dravet syndrome: a retrospective, multicenter study of 26 patients.
Francesca Ragona, Tiziana Granata, Bernardo Dalla Bernardina, Francesca Offredi, Francesca Darra, Domenica Battaglia, Monica Morbi, Daniela Brazzo, Simona Cappelletti, Daniela Chieffo,[...]. Epilepsia 2011
74
27

Dravet syndrome: early clinical manifestations and cognitive outcome in 37 Italian patients.
Francesca Ragona, Daniela Brazzo, Ilaria De Giorgi, Monica Morbi, Elena Freri, Federica Teutonico, Elena Gennaro, Federico Zara, Simona Binelli, Pierangelo Veggiotti,[...]. Brain Dev 2010
69
27

Lamotrigine and seizure aggravation in severe myoclonic epilepsy.
R Guerrini, C Dravet, P Genton, A Belmonte, A Kaminska, O Dulac. Epilepsia 1998
311
19

Genotype-phenotype associations in SCN1A-related epilepsies.
S M Zuberi, A Brunklaus, R Birch, E Reavey, J Duncan, G H Forbes. Neurology 2011
142
19

NaV1.1 channels and epilepsy.
William A Catterall, Franck Kalume, John C Oakley. J Physiol 2010
238
18

Dravet syndrome and parent associations: the IDEA League experience with comorbid conditions, mortality, management, adaptation, and grief.
Joan V Skluzacek, Kathryn P Watts, Olivier Parsy, Beverly Wical, Peter Camfield. Epilepsia 2011
87
20

Optimizing the Diagnosis and Management of Dravet Syndrome: Recommendations From a North American Consensus Panel.
Elaine C Wirrell, Linda Laux, Elizabeth Donner, Nathalie Jette, Kelly Knupp, Mary Anne Meskis, Ian Miller, Joseph Sullivan, Michelle Welborn, Anne T Berg. Pediatr Neurol 2017
103
18

Electroencephalographic characteristics of Dravet syndrome.
Michelle Bureau, Bernardo Dalla Bernardina. Epilepsia 2011
52
30

Nav1.1 localizes to axons of parvalbumin-positive inhibitory interneurons: a circuit basis for epileptic seizures in mice carrying an Scn1a gene mutation.
Ikuo Ogiwara, Hiroyuki Miyamoto, Noriyuki Morita, Nafiseh Atapour, Emi Mazaki, Ikuyo Inoue, Tamaki Takeuchi, Shigeyoshi Itohara, Yuchio Yanagawa, Kunihiko Obata,[...]. J Neurosci 2007
499
16

Severe myoclonic epilepsy in infancy: Dravet syndrome.
Charlotte Dravet, Michelle Bureau, Hirokazu Oguni, Yukio Fukuyama, Ozlem Cokar. Adv Neurol 2005
181
15


Neuropsychological development in children with Dravet syndrome.
Daniela Chieffo, Domenica Battaglia, Donatella Lettori, Maria Del Re, Claudia Brogna, Charlotte Dravet, Eugenio Mercuri, Francesco Guzzetta. Epilepsy Res 2011
46
30

Stiripentol open study in Japanese patients with Dravet syndrome.
Yushi Inoue, Yoko Ohtsuka, Hirokazu Oguni, Jun Tohyama, Hiroshi Baba, Katsuyuki Fukushima, Hideyuki Ohtani, Yukitoshi Takahashi, Shunya Ikeda. Epilepsia 2009
58
24

The genetics of Dravet syndrome.
Carla Marini, Ingrid E Scheffer, Rima Nabbout, Arvid Suls, Peter De Jonghe, Federico Zara, Renzo Guerrini. Epilepsia 2011
152
14

Mortality in Dravet syndrome.
Monica S Cooper, Anne Mcintosh, Douglas E Crompton, Jacinta M McMahon, Amy Schneider, Kevin Farrell, Vijeya Ganesan, Deepak Gill, Sara Kivity, Tally Lerman-Sagie,[...]. Epilepsy Res 2016
105
14

Reduced sodium current in Purkinje neurons from Nav1.1 mutant mice: implications for ataxia in severe myoclonic epilepsy in infancy.
Franck Kalume, Frank H Yu, Ruth E Westenbroek, Todd Scheuer, William A Catterall. J Neurosci 2007
170
13

Overall management of patients with Dravet syndrome.
Berten Ceulemans. Dev Med Child Neurol 2011
30
43

Cognitive and adaptive evaluation of 21 consecutive patients with Dravet syndrome.
Nathalie Villeneuve, Virginie Laguitton, Marine Viellard, Anne Lépine, Brigitte Chabrol, Charlotte Dravet, Mathieu Milh. Epilepsy Behav 2014
43
30

A screening test for the prediction of Dravet syndrome before one year of age.
Junri Hattori, Mamoru Ouchida, Junko Ono, Susumu Miyake, Satoshi Maniwa, Nobuyoshi Mimaki, Yoko Ohtsuka, Iori Ohmori. Epilepsia 2008
64
18

Severe myoclonic epilepsy in infancy: a systematic review and a meta-analysis of individual patient data.
Behrouz Kassaï, Catherine Chiron, Ségolène Augier, Michel Cucherat, Elisabeth Rey, François Gueyffier, Renzo Guerrini, Julien Vincent, Olivier Dulac, Gérard Pons. Epilepsia 2008
89
13

Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2.
A Escayg, B T MacDonald, M H Meisler, S Baulac, G Huberfeld, I An-Gourfinkel, A Brice, E LeGuern, B Moulard, D Chaigne,[...]. Nat Genet 2000
693
12

Dravet syndrome: seizure control and gait in adults with different SCN1A mutations.
Jennifer J Rilstone, Fernando M Coelho, Berge A Minassian, Danielle M Andrade. Epilepsia 2012
39
30

Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE Commission on Classification and Terminology, 2005-2009.
Anne T Berg, Samuel F Berkovic, Martin J Brodie, Jeffrey Buchhalter, J Helen Cross, Walter van Emde Boas, Jerome Engel, Jacqueline French, Tracy A Glauser, Gary W Mathern,[...]. Epilepsia 2010
11

Dravet syndrome: a study of 53 patients.
Roberto Horacio Caraballo, Natalio Fejerman. Epilepsy Res 2006
59
18

Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy.
R Nabbout, E Gennaro, B Dalla Bernardina, O Dulac, F Madia, E Bertini, G Capovilla, C Chiron, G Cristofori, M Elia,[...]. Neurology 2003
186
11

Topiramate in the treatment of highly refractory patients with Dravet syndrome.
J Kröll-Seger, P Portilla, O Dulac, C Chiron. Neuropediatrics 2006
49
22

Unusual consequences of status epilepticus in Dravet syndrome.
M Chipaux, N Villeneuve, P Sabouraud, I Desguerre, N Boddaert, C Depienne, C Chiron, O Dulac, R Nabbout. Seizure 2010
38
28

Mutations of sodium channel alpha subunit type 1 (SCN1A) in intractable childhood epilepsies with frequent generalized tonic-clonic seizures.
Tateki Fujiwara, Takashi Sugawara, Emi Mazaki-Miyazaki, Yukitoshi Takahashi, Katsuyuki Fukushima, Masako Watanabe, Keita Hara, Tateki Morikawa, Kazuichi Yagi, Kazuhiro Yamakawa,[...]. Brain 2003
228
11

Sporadic infantile epileptic encephalopathy caused by mutations in PCDH19 resembles Dravet syndrome but mainly affects females.
Christel Depienne, Delphine Bouteiller, Boris Keren, Emmanuel Cheuret, Karine Poirier, Oriane Trouillard, Baya Benyahia, Chloé Quelin, Wassila Carpentier, Sophie Julia,[...]. PLoS Genet 2009
221
11

Topiramate as add-on drug in severe myoclonic epilepsy in infancy: an Italian multicenter open trial.
Giangennaro Coppola, Giuseppe Capovilla, Alessandra Montagnini, Antonino Romeo, Maria Spanò, Gaetano Tortorella, Pierangelo Veggiotti, Maurizio Viri, Antonio Pascotto. Epilepsy Res 2002
92
11

Early diagnosis of severe myoclonic epilepsy in infancy.
M Yakoub, O Dulac, I Jambaqué, C Chiron, P Plouin. Brain Dev 1992
75
14

The pharmacologic treatment of Dravet syndrome.
Catherine Chiron, Olivier Dulac. Epilepsia 2011
87
12


Early development in Dravet syndrome; visual function impairment precedes cognitive decline.
Daniela Chieffo, Daniela Ricci, Giovanni Baranello, Diego Martinelli, Chiara Veredice, Donatella Lettori, Domenica Battaglia, Charlotte Dravet, Eugenio Mercuri, Francesco Guzzetta. Epilepsy Res 2011
30
36

Stiripentol in Dravet syndrome: results of a retrospective U.S. study.
Elaine C Wirrell, Linda Laux, David N Franz, Joseph Sullivan, Russell P Saneto, Richard P Morse, Orrin Devinsky, Harry Chugani, Angel Hernandez, Lorie Hamiwka,[...]. Epilepsia 2013
56
19



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.