A citation-based method for searching scientific literature

Y Mori, T Friedrich, M S Kim, A Mikami, J Nakai, P Ruth, E Bosse, F Hofmann, V Flockerzi, T Furuichi. Nature 1991
Times Cited: 766



J C Jen, T D Graves, E J Hess, M G Hanna, R C Griggs, R W Baloh. Brain 2007
Times Cited: 206




List of shared articles



Times cited

Calcium Channel Splice Variants and Their Effects in Brain and Cardiovascular Function.
Sean Qing Zhang Yeow, Kelvin Wei Zhern Loh, Tuck Wah Soong. Adv Exp Med Biol 2021
0

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
8

Cognitive impairment in children with CACNA1A mutations.
Veronique Humbertclaude, Florence Riant, Benjamin Krams, Valerie Zimmermann, Nicolas Nagot, Daniel Annequin, Bernard Echenne, Elisabeth Tournier-Lasserve, Agathe Roubertie. Dev Med Child Neurol 2020
17

Paroxysmal movement disorders - practical update on diagnosis and management.
Claudio M De Gusmao, Laura Silveira-Moriyama. Expert Rev Neurother 2019
9

Episodic ataxias.
Joanna C Jen, Jijun Wan. Handb Clin Neurol 2018
4

Episodic ataxias.
Joanna C Jen, Jijun Wan. Handb Clin Neurol 2018
23

Silver nanoparticle exposure induces rat motor dysfunction through decrease in expression of calcium channel protein in cerebellum.
Nuoya Yin, Yang Zhang, Zhaojun Yun, Qian Liu, Guangbo Qu, Qunfang Zhou, Ligang Hu, Guibin Jiang. Toxicol Lett 2015
25

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
37


Episodic ataxias 1 and 2.
Robert W Baloh. Handb Clin Neurol 2012
23

Identification of CACNA1A large deletions in four patients with episodic ataxia.
Florence Riant, Christelle Lescoat, Katayoun Vahedi, Elsa Kaphan, Annick Toutain, Thierry Soisson, Sylvette R Wiener-Vacher, Elisabeth Tournier-Lasserve. Neurogenetics 2010
27

KCa channels as therapeutic targets in episodic ataxia type-2.
Karina Alviña, Kamran Khodakhah. J Neurosci 2010
78

The therapeutic mode of action of 4-aminopyridine in cerebellar ataxia.
Karina Alviña, Kamran Khodakhah. J Neurosci 2010
116

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
36


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
39

Large CACNA1A deletion in a family with episodic ataxia type 2.
Florence Riant, Reda Mourtada, Pascale Saugier-Veber, Elisabeth Tournier-Lasserve. Arch Neurol 2008
31