A citation-based method for searching scientific literature

R A Maselli, J Wan, V Dunne, M Graves, R W Baloh, R L Wollmann, J Jen. Neurology 2003
Times Cited: 30



Yu-Qing Cao, Erika S Piedras-RenterĂ­a, Geoffrey B Smith, Gong Chen, Nobutoshi C Harata, Richard W Tsien. Neuron 2004
Times Cited: 126




List of shared articles



Times cited

CaV2.1 channelopathies.
Daniela Pietrobon. Pflugers Arch 2010
140

Neuronal P/Q-type calcium channel dysfunction in inherited disorders of the CNS.
Sanjeev Rajakulendran, Diego Kaski, Michael G Hanna. Nat Rev Neurol 2012
89

Primary episodic ataxias: diagnosis, pathogenesis and treatment.
J C Jen, T D Graves, E J Hess, M G Hanna, R C Griggs, R W Baloh. Brain 2007
206

Characterization of acetylcholine release and the compensatory contribution of non-Ca(v)2.1 channels at motor nerve terminals of leaner Ca(v)2.1-mutant mice.
S Kaja, R C G van de Ven, L A M Broos, R R Frants, M D Ferrari, A M J M van den Maagdenberg, J J Plomp. Neuroscience 2007
18

A mutation in CaV2.1 linked to a severe neurodevelopmental disorder impairs channel gating.
Sidharth Tyagi, Tyler R Bendrick, Dilyana Filipova, Symeon Papadopoulos, Roger A Bannister. J Gen Physiol 2019
4

Severe and progressive neurotransmitter release aberrations in familial hemiplegic migraine type 1 Cacna1a S218L knock-in mice.
Simon Kaja, Rob C G Van de Ven, Ludo A M Broos, Rune R Frants, Michel D Ferrari, Arn M J M Van den Maagdenberg, Jaap J Plomp. J Neurophysiol 2010
18

Gene dosage-dependent transmitter release changes at neuromuscular synapses of CACNA1A R192Q knockin mice are non-progressive and do not lead to morphological changes or muscle weakness.
S Kaja, R C G van de Ven, L A M Broos, H Veldman, J G van Dijk, J J G M Verschuuren, R R Frants, M D Ferrari, A M J M van den Maagdenberg, J J Plomp. Neuroscience 2005
36