A citation-based method for searching scientific literature

S Guida, F Trettel, S Pagnutti, E Mantuano, A Tottene, L Veneziano, T Fellin, M Spadaro, K Stauderman, M Williams, S Volsen, R Ophoff, R Frants, C Jodice, M Frontali, D Pietrobon. Am J Hum Genet 2001
Times Cited: 108



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, J Haan, D Lindhout, G J van Ommen, M H Hofker, M D Ferrari, R R Frants. Cell 1996
Times Cited: 1724




List of shared articles



Times cited

Zebrafish as a Model System for the Study of Severe CaV2.1 (α1A) Channelopathies.
Sidharth Tyagi, Angeles B Ribera, Roger A Bannister. Front Mol Neurosci 2020
6

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

Targeting Alternative Splicing as a Potential Therapy for Episodic Ataxia Type 2.
Fanny Jaudon, Simona Baldassari, Ilaria Musante, Agnes Thalhammer, Federico Zara, Lorenzo A Cingolani. Biomedicines 2020
3


Keeping Our Calcium in Balance to Maintain Our Balance.
Melanie D Mark, Jan Claudius Schwitalla, Michelle Groemmke, Stefan Herlitze. Biochem Biophys Res Commun 2017
17

Genetic neurological channelopathies: molecular genetics and clinical phenotypes.
J Spillane, D M Kullmann, M G Hanna. J Neurol Neurosurg Psychiatry 2016
54

The Role of Calcium Channels in Epilepsy.
Sanjeev Rajakulendran, Michael G Hanna. Cold Spring Harb Perspect Med 2016
30

Pearls & Oy-sters: Episodic ataxia type 2: Case report and review of the literature.
Elan L Guterman, Brian Yurgionas, Alexandra B Nelson. Neurology 2016
11

RNAi silencing of P/Q-type calcium channels in Purkinje neurons of adult mouse leads to episodic ataxia type 2.
Julie Salvi, Federica Bertaso, Anne-Laure Mausset-Bonnefont, Alexandra Metz, Céline Lemmers, Fabrice Ango, Laurent Fagni, Philippe Lory, Alexandre Mezghrani. Neurobiol Dis 2014
13

CACNA1A variants may modify the epileptic phenotype of Dravet syndrome.
Iori Ohmori, Mamoru Ouchida, Katsuhiro Kobayashi, Yoshimi Jitsumori, Akiko Mori, Hiroyuki Michiue, Teiichi Nishiki, Yoko Ohtsuka, Hideki Matsui. Neurobiol Dis 2013
24

Episodic ataxias 1 and 2.
Robert W Baloh. Handb Clin Neurol 2012
22

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

Dramatically different levels of Cacna1a gene expression between pre-weaning wild type and leaner mice.
Liana Veneziano, Serena Albertosi, Daniela Pesci, Elide Mantuano, Marina Frontali, Carla Jodice. J Neurol Sci 2011
2

[Hereditary episodic ataxia].
F Riant, K Vahedi, E Tournier-Lasserve. Rev Neurol (Paris) 2011
9

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
111

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
49

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
53

CaV2.1 channelopathies.
Daniela Pietrobon. Pflugers Arch 2010
134

Neurological channelopathies.
Dimitri M Kullmann. Annu Rev Neurosci 2010
79

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

Genetics of headaches.
Arn M J M Van Den Maagdenberg, Gisela M Terwindt, Joost Haan, Rune R Frants, Michel D Ferrari. Handb Clin Neurol 2010
11

Dysfunction of the Ca(V)2.1 calcium channel in cerebellar ataxias.
Sanjeev Rajakulendran, Stephanie Schorge, Dimitri M Kullmann, Michael G Hanna. F1000 Biol Rep 2010
7

Newly characterised 5' and 3' regions of CACNA1A gene harbour mutations associated with Familial Hemiplegic Migraine and Episodic Ataxia.
Liana Veneziano, Serena Guida, Elide Mantuano, Paola Bernard, Patrizia Tarantino, Loredana Boccone, Fuki M Hisama, Paola Carrera, Carla Jodice, Marina Frontali. J Neurol Sci 2009
11

Low-frequency oscillations in the cerebellar cortex of the tottering mouse.
Gang Chen, Laurentiu S Popa, Xinming Wang, Wangcai Gao, Justin Barnes, Claudia M Hendrix, Ellen J Hess, Timothy J Ebner. J Neurophysiol 2009
41

Episodic ataxia associated with EAAT1 mutation C186S affecting glutamate reuptake.
Boukje de Vries, Hafsa Mamsa, Anine H Stam, Jijun Wan, Stef L M Bakker, Kaate R J Vanmolkot, Joost Haan, Gisela M Terwindt, Elles M J Boon, Bruce D Howard,[...]. Arch Neurol 2009
82

Late-onset episodic ataxia type 2 associated with a novel loss-of-function mutation in the CACNA1A gene.
Ester Cuenca-León, Isabel Banchs, Selma A Serra, Pilar Latorre, Noèlia Fernàndez-Castillo, Roser Corominas, Miguel A Valverde, Víctor Volpini, José M Fernández-Fernández, Alfons Macaya,[...]. J Neurol Sci 2009
24

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


Presynaptic calcium channels: structure, regulators, and blockers.
Alexandra E Kisilevsky, Gerald W Zamponi. Handb Exp Pharmacol 2008
22

Migraine: sex-influenced trait model?
Xiao-Ping Wang, Jian-Min Liu, Yong-Bo Zhao. Med Hypotheses 2008
11

Reduced ACh release at neuromuscular synapses of heterozygous leaner Ca(v)2.1-mutant mice.
Simon Kaja, Rob C G Van De Ven, Rune R Frants, Michel D Ferrari, Arn M J M Van Den Maagdenberg, Jaap J Plomp. Synapse 2008
10

Axonal function in a family with episodic ataxia type 2 due to a novel mutation.
Arun V Krishnan, Hugh Bostock, Jerome Ip, Michael Hayes, Shaun Watson, Matthew C Kiernan. J Neurol 2008
13

A destructive interaction mechanism accounts for dominant-negative effects of misfolded mutants of voltage-gated calcium channels.
Alexandre Mezghrani, Arnaud Monteil, Katrin Watschinger, Martina J Sinnegger-Brauns, Christian Barrère, Emmanuel Bourinet, Joël Nargeot, Jörg Striessnig, Philippe Lory. J Neurosci 2008
58

Two novel alleles of tottering with distinct Ca(v)2.1 calcium channel neuropathologies.
T Miki, T A Zwingman, M Wakamori, C M Lutz, S A Cook, D A Hosford, K Herrup, C F Fletcher, Y Mori, W N Frankel,[...]. Neuroscience 2008
37

Premature stop codons in a facilitating EF-hand splice variant of CaV2.1 cause episodic ataxia type 2.
Tracey D Graves, Paola Imbrici, Esther E Kors, Gisela M Terwindt, Louise H Eunson, Rune R Frants, Joost Haan, Michel D Ferrari, Peter J Goadsby, Michael G Hanna,[...]. Neurobiol Dis 2008
19

Calcium channels, neuromuscular synaptic transmission and neurological diseases.
Francisco J Urbano, Mario R Pagani, Osvaldo D Uchitel. J Neuroimmunol 2008
12

Calcium channel regulation and presynaptic plasticity.
William A Catterall, Alexandra P Few. Neuron 2008
409

Familial hemiplegic migraine.
Curtis F Barrett, Arn M J M van den Maagdenberg, Rune R Frants, Michel D Ferrari. Adv Genet 2008
25

Dominant-negative suppression of Cav2.1 currents by alpha(1)2.1 truncations requires the conserved interaction domain for beta subunits.
Robert S Raike, Holly B Kordasiewicz, Randall M Thompson, Christopher M Gomez. Mol Cell Neurosci 2007
21

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

The cerebellum and migraine.
Maurice Vincent, Nouchine Hadjikhani. Headache 2007
59

Calcium channelopathies: voltage-gated calcium channels.
P J Adams, T P Snutch. Subcell Biochem 2007
30

Dominant-negative effects of human P/Q-type Ca2+ channel mutations associated with episodic ataxia type 2.
Chung-Jiuan Jeng, Yu-Ting Chen, Yi-Wen Chen, Chih-Yung Tang. Am J Physiol Cell Physiol 2006
38

Early onset, non fluctuating spinocerebellar ataxia and a novel missense mutation in CACNA1A gene.
Alessandra Tonelli, Maria Grazia D'Angelo, Roberto Salati, Laura Villa, Chiara Germinasi, Tiziano Frattini, Giovanni Meola, Anna Carla Turconi, Nereo Bresolin, Maria Teresa Bassi. J Neurol Sci 2006
34

CACNA1A mutation in a EA-2 patient responsive to acetazolamide and valproic acid.
Kylie A Scoggan, Joseph H Friedman, Dennis E Bulman. Can J Neurol Sci 2006
21

Long-term improvement of paroxysmal dystonic choreathetosis with acetazolamide.
Veronique Michel, Florence Riant, Elisabeth Tournier-Lasserve, Dominique Guehl, Alain Lagueny, Bernard Bioulac, Pierre Burbaud. J Neurol 2006
3

Channeling studies in yeast: yeast as a model for channelopathies?
Devin M Wolfe, David A Pearce. Neuromolecular Med 2006
12

Calcium channelopathies.
Ricardo Felix. Neuromolecular Med 2006
16


Voltage-gated calcium channels and idiopathic generalized epilepsies.
Houman Khosravani, Gerald W Zamponi. Physiol Rev 2006
126