A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


ILAE official report: a practical clinical definition of epilepsy.
Robert S Fisher, Carlos Acevedo, Alexis Arzimanoglou, Alicia Bogacz, J Helen Cross, Christian E Elger, Jerome Engel, Lars Forsgren, Jacqueline A French, Mike Glynn,[...]. Epilepsia 2014
29

Recent advances in epilepsy genetics.
Alessandro Orsini, Federico Zara, Pasquale Striano. Neurosci Lett 2018
38
11

Association between SCN1A gene polymorphisms and drug resistant epilepsy in pediatric patients.
Lucia Margari, Anna R Legrottaglie, Alessandra Vincenti, Giangennaro Coppola, Francesca F Operto, Maura Buttiglione, Amalia Cassano, Nicola Bartolomeo, Maria A Mariggiò. Seizure 2018
10
20


Blood brain barrier: the role of calcium homeostasis.
Atmaram Yarlagadda, Shaifali Kaushik, Anita H Clayton. Psychiatry (Edgmont) 2007
13
15

Calcium and ROS: A mutual interplay.
Agnes Görlach, Katharina Bertram, Sona Hudecova, Olga Krizanova. Redox Biol 2015
520
11

Phospholipase C signaling and calcium influx.
James W Putney, Takuro Tomita. Adv Biol Regul 2012
83
11

Neuronal calcium signaling: function and dysfunction.
Marisa Brini, Tito Calì, Denis Ottolini, Ernesto Carafoli. Cell Mol Life Sci 2014
235
11

Calcium-Binding Proteins as Determinants of Central Nervous System Neuronal Vulnerability to Disease.
Richard Fairless, Sarah K Williams, Ricarda Diem. Int J Mol Sci 2019
29
11

Calcium/calmodulin-dependent protein kinase II links ER stress with Fas and mitochondrial apoptosis pathways.
Jenelle M Timmins, Lale Ozcan, Tracie A Seimon, Gang Li, Cristina Malagelada, Johannes Backs, Thea Backs, Rhonda Bassel-Duby, Eric N Olson, Mark E Anderson,[...]. J Clin Invest 2009
297
11

Calcium signaling in neurodegeneration.
Philippe Marambaud, Ute Dreses-Werringloer, Valérie Vingtdeux. Mol Neurodegener 2009
162
11

Neuronal calcium homeostasis and dysregulation.
Marc Gleichmann, Mark P Mattson. Antioxid Redox Signal 2011
147
11

Secretagogin is a Ca2+-binding protein specifying subpopulations of telencephalic neurons.
Jan Mulder, Misha Zilberter, Lauren Spence, Giuseppe Tortoriello, Mathias Uhlén, Yuchio Yanagawa, Fabienne Aujard, Tomas Hökfelt, Tibor Harkany. Proc Natl Acad Sci U S A 2009
52
11

Epileptic seizures and epilepsy: definitions proposed by the International League Against Epilepsy (ILAE) and the International Bureau for Epilepsy (IBE).
Robert S Fisher, Walter van Emde Boas, Warren Blume, Christian Elger, Pierre Genton, Phillip Lee, Jerome Engel. Epilepsia 2005
11

The neurobiology of epilepsy.
Helen E Scharfman. Curr Neurol Neurosci Rep 2007
210
11


The consequences of refractory epilepsy and its treatment.
Kenneth D Laxer, Eugen Trinka, Lawrence J Hirsch, Fernando Cendes, John Langfitt, Norman Delanty, Trevor Resnick, Selim R Benbadis. Epilepsy Behav 2014
268
11

A definition and classification of status epilepticus--Report of the ILAE Task Force on Classification of Status Epilepticus.
Eugen Trinka, Hannah Cock, Dale Hesdorffer, Andrea O Rossetti, Ingrid E Scheffer, Shlomo Shinnar, Simon Shorvon, Daniel H Lowenstein. Epilepsia 2015
788
11



Trafficking patterns of NMDA and GABAA receptors in a Mg2+-free cultured hippocampal neuron model of status epilepticus.
Yang-Je Cho, Hyunjeong Kim, Won-Joo Kim, Seungsoo Chung, Young-Hwan Kim, Inja Cho, Byung In Lee, Kyoung Heo. Epilepsy Res 2017
10
20

Hippocampal TNFα Signaling Contributes to Seizure Generation in an Infection-Induced Mouse Model of Limbic Epilepsy.
Dipan C Patel, Glenna Wallis, E Jill Dahle, Pallavi B McElroy, Kyle E Thomson, Raymond J Tesi, David E Szymkowski, Peter J West, Roy M Smeal, Manisha Patel,[...]. eNeuro 2017
42
11

Status epilepticus increases the intracellular accumulation of GABAA receptors.
Howard P Goodkin, Jwu-Lai Yeh, Jaideep Kapur. J Neurosci 2005
186
11


The Role of Calcium Channels in Epilepsy.
Sanjeev Rajakulendran, Michael G Hanna. Cold Spring Harb Perspect Med 2016
29
11

Calcium-dependent blood-brain barrier breakdown by NOX5 limits postreperfusion benefit in stroke.
Ana I Casas, Pamela Wm Kleikers, Eva Geuss, Friederike Langhauser, Thure Adler, Dirk H Busch, Valerie Gailus-Durner, Martin Hrabê de Angelis, Javier Egea, Manuela G Lopez,[...]. J Clin Invest 2019
29
11

Delayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine.
E E Kors, G M Terwindt, F L Vermeulen, R B Fitzsimons, P E Jardine, P Heywood, S Love, A M van den Maagdenberg, J Haan, R R Frants,[...]. Ann Neurol 2001
232
11

Dysfunction of the brain calcium channel CaV2.1 in absence epilepsy and episodic ataxia.
Paola Imbrici, Stephen L Jaffe, Louise H Eunson, Nicholas P Davies, Colin Herd, Robert Robertson, Dimitri M Kullmann, Michael G Hanna. Brain 2004
148
11

CACNA1A R1347Q: a frequent recurrent mutation in hemiplegic migraine.
A H Stam, K R J Vanmolkot, H P H Kremer, J Gärtner, J Brown, E Leshinsky-Silver, R Gilad, E E Kors, W S Frankhuizen, H B Ginjaar,[...]. Clin Genet 2008
13
15

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
11

New CACNA1A gene mutation in a case of familial hemiplegic migraine with status epilepticus.
Katell Beauvais, Florence Cavé-Riant, Claire De Barace, Marc Tardieu, Elisabeth Tournier-Lasserve, Alain Furby. Eur Neurol 2004
36
11

Clinical spectrum of episodic ataxia type 2.
J Jen, G W Kim, R W Baloh. Neurology 2004
177
11

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
11


Neuronal P/Q-type calcium channel dysfunction in inherited disorders of the CNS.
Sanjeev Rajakulendran, Diego Kaski, Michael G Hanna. Nat Rev Neurol 2012
86
11

De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraine.
F Riant, A Ducros, C Ploton, C Barbance, C Depienne, E Tournier-Lasserve. Neurology 2010
80
11

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

Early seizures and cerebral oedema after trivial head trauma associated with the CACNA1A S218L mutation.
A H Stam, G-J Luijckx, B T Poll-Thé, I B Ginjaar, R R Frants, J Haan, M D Ferrari, G M Terwindt, A M J M van den Maagdenberg. J Neurol Neurosurg Psychiatry 2009
62
11


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
11

Large scale calcium channel gene rearrangements in episodic ataxia and hemiplegic migraine: implications for diagnostic testing.
R W Labrum, S Rajakulendran, T D Graves, L H Eunson, R Bevan, M G Sweeney, S R Hammans, N Tubridy, T Britton, L J Carr,[...]. J Med Genet 2009
37
11

Phenotypic variability of episodic ataxia type 2 mutations: a family study.
Julien Jung, Hervé Testard, Elisabeth Tournier-Lasserve, Florence Riant, Anne-Evelyne Vallet, Stéphane Berroir, Emmanuel Broussolle. Eur Neurol 2010
16
12

Eye movement disorders are an early manifestation of CACNA1A mutations in children.
Esther M Tantsis, Deepak Gill, Lyn Griffiths, Sachin Gupta, John Lawson, Neven Maksemous, Robert Ouvrier, Florence Riant, Robert Smith, Christopher Troedson,[...]. Dev Med Child Neurol 2016
36
11

Association of A Novel Splice Site Mutation in P/Q-Type Calcium Channels with Childhood Epilepsy and Late-Onset Slowly Progressive Non-Episodic Cerebellar Ataxia.
Claudia Stendel, Maria Cristina D'Adamo, Manuela Wiessner, Marina Dusl, Marta Cenciarini, Silvia Belia, Ehsan Nematian-Ardestani, Peter Bauer, Jan Senderek, Thomas Klopstock,[...]. Int J Mol Sci 2020
6
33

The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel.
A Ducros, C Denier, A Joutel, M Cecillon, C Lescoat, K Vahedi, F Darcel, E Vicaut, M G Bousser, E Tournier-Lasserve. N Engl J Med 2001
359
11

Episodic ataxia type 2: phenotype characteristics of a novel CACNA1A mutation and review of the literature.
Wolfgang Nachbauer, Michael Nocker, Elfriede Karner, Iva Stankovic, Iris Unterberger, Andreas Eigentler, Rainer Schneider, Werner Poewe, Margarete Delazer, Sylvia Boesch. J Neurol 2014
33
11

Sporadic hemiplegic migraine and delayed cerebral oedema after minor head trauma: a novel de novo CACNA1A gene mutation.
Timothy J Malpas, Florence Riant, Elisabeth Tournier-Lasserve, Katayoun Vahedi, Brian G R Neville. Dev Med Child Neurol 2010
19
11

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
11

Congenital ataxia, mental retardation, and dyskinesia associated with a novel CACNA1A mutation.
Lubov Blumkin, Marina Michelson, Esther Leshinsky-Silver, Sara Kivity, Dorit Lev, Tally Lerman-Sagie. J Child Neurol 2010
34
11

Exercise-induced downbeat nystagmus in a Korean family with a nonsense mutation in CACNA1A.
Jae-Hwan Choi, Jae-Deuk Seo, Yu Ri Choi, Min-Ji Kim, Jin-Hong Shin, Ji Soo Kim, Kwang-Dong Choi. Neurol Sci 2015
7
28


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.