Efficacy of levetiracetam in patients with episodic ataxia type 2 caused by CACNA1A mutation: three case reports
Author:
Publisher
Springer Science and Business Media LLC
Subject
Psychiatry and Mental health,Neurology (clinical),Dermatology,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s10072-021-05368-y.pdf
Reference14 articles.
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3. Van Bogaert P, Szliwowski H (1996) EEG findings in acetazolamide-responsive hereditary paroxysmal ataxia. Neurophysiol Clin 26(5):335–340
4. Rajakulendran S, Graves TD, Labrum RW, Kotzadimitriou D, Eunson L, Davis MB, Davies R, Wood NW, Kullmann DM, Hanna MG, Schorge S (2010) Genetic and functional characterisation of the P/Q calcium channel in episodic ataxia with epilepsy. J Physiol 588(Pt 11):1905–1913. https://doi.org/10.1113/jphysiol.2009.186437
5. Mantuano E, Romano S, Veneziano L, Gellera C, Castellotti B, Caimi S, Testa D, Estienne M, Zorzi G, Bugiani M, Rajabally YA, Barcina MJ, Servidei S, Panico A, Frontali M, Mariotti C (2010) Identification of novel and recurrent CACNA1A gene mutations in fifteen patients with episodic ataxia type 2. J Neurol Sci 291(1–2):30–36. https://doi.org/10.1016/j.jns.2010.01.010
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