Jen JC, Graves TD, Hess EJ, et al. Primary episodic ataxias: Diagnosis, pathogenesis and treatment. Brain. 2007 ; 130: 2484-2493
Jung J, Testard H, Tournier-Lasserve E, et al. Phenotypic variability of episodic ataxia type 2 mutations: A family study. Eur J Neurol. 2010 ; 64: 114-116
Denier C, Ducros A, Vahedi K, et al. High prevalence of CACNA1A truncations and broader clinical spectrum in episodic ataxia type 2. Neurology. 1999 ; 52: 1816-1821
Headache Classification Subcommittee of the International Headache Society. The International Classification of Headache Disorders: 2nd edition. Cephalalgia 2004; (24 Suppl 1): 9-160.
Wan J, Mamsa H, Johnston JL, et al. Large genomic deletions in CACNA1A cause episodic ataxia type 2. Front Neurol. 2011 ; 2: 51-51
Noseda R, Burstein R. Advances in understanding the mechanisms of migraine-type photophobia. Curr Opin Neurol. 2011 ; 24: 197-202
Pietrobon D. Insights into migraine mechanisms and CaV2.1 calcium channel function from mouse models of familial hemiplegic migraine. J Physiol. 2010 ; 588: 1871-1878
Schorge S and Rajakulendran S. The P/Q channel in human disease: Untangling the genetics and physiology. WIREs Membr Transp Signal. Epub ahead of print 23 January 2012. DOI: 101002/wmts22.
Helmich RC, Siebner HR, Giffin N, et al. The dynamic regulation of cortical excitability is altered in episodic ataxia type 2. Brain. 2010 ; 133: 3519-3529
Coppola G, Ambrosini A, Di Clemente L, et al. Interictal abnormalities of gamma band activity in visual evoked responses in migraine: An indication of thalamocortical dysrhythmia?. Cephalalgia. 2007 ; 27: 1360-1367
