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The electrophysiological footprint of CACNA1A disorders.

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第一作者： Elisabetta,Indelicato

第一单位： Center for Rare Movement Disorders Innsbruck, Department of Neurology, Medical University of Innsbruck, Anichstrasse 35, 6020, Innsbruck, Austria.

作者： Elisabetta,Indelicato ^[1] ; Iris,Unterberger ^[2] ; Wolfgang,Nachbauer ^[1] ; Andreas,Eigentler ^[1] ; Matthias,Amprosi ^[1] ; Fiona,Zeiner ^[3] ; Edda,Haberlandt ^[4] ; Manuela,Kaml ^[2] ; Elke,Gizewski ^[5] ; Sylvia,Boesch ^[6]

作者单位： Center for Rare Movement Disorders Innsbruck, Department of Neurology, Medical University of Innsbruck, Anichstrasse 35, 6020, Innsbruck, Austria. ^[1] Epileptology Division, Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria. ^[2] Department of Pediatrics I, Medical University of Innsbruck, Innsbruck, Austria. ^[3] Department of Pediatrics I, Medical University of Innsbruck, Innsbruck, Austria.;Department of Pediatrics, City Hospital, Dornbirn, Austria. ^[4] Department of Neuroradiology, Medical University of Innsbruck, Innsbruck, Austria. ^[5] Center for Rare Movement Disorders Innsbruck, Department of Neurology, Medical University of Innsbruck, Anichstrasse 35, 6020, Innsbruck, Austria. sylvia.boesch@i-med.ac.at. ^[6]

关键词 Epilepsy Episodic ataxia type 2 Familial hemiplegic migraine type 1 Intermittent epileptic discharges Spinocerebellar ataxia type 6 Voltage-gated calcium channels

医学主题词钙通道(Calcium Channels);癫痫(Epilepsy);人类(Humans);先兆偏头痛(Migraine with Aura);表型(Phenotype);脊髓小脑共济失调(Spinocerebellar Ataxias)

DOI 10.1007/s00415-021-10415-x

PMID 33544220

发布时间 2021-07-30

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