Resting-State EEG Analysis Characterizes the Signature of CACNA1A-and GAA-FGF14-Related Channelopathies

Cerebellar ataxia frequently results from ion channel dysfunction, with CACNA1A- and GAA- FGF14 -related diseases representing two of the most prevalent genetic etiologies. While both disorders may share overlapping clinical features, their pathophysiology remain distinct and incompletely understood...

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Vydáno v:	Cerebellum (London, England) Ročník 24; číslo 6; s. 175
Hlavní autoři:	Angerbauer, Raphael, Unterberger, Iris, Nachbauer, Wolfgang, Amprosi, Matthias, Boesch, Sylvia, Cesari, Matteo, Indelicato, Elisabetta
Médium:	Journal Article
Jazyk:	angličtina
Vydáno:	New York Springer US 15.11.2025 Springer Nature B.V
Témata:	Adolescent Adult Ataxia Bayesian analysis Biomedical and Life Sciences Biomedicine Brain Brain - physiopathology Calcium Channels - genetics Cerebellar ataxia Cerebellar Ataxia - genetics Cerebellar Ataxia - physiopathology Cerebellum Channelopathies - genetics Channelopathies - physiopathology Child EEG Electrodes Electroencephalography Electroencephalography - methods Epilepsy Female Fibroblast Growth Factors - genetics Humans Male Mental disorders Middle Aged Migraine Neural networks Neurobiology Neurology Neurosciences Normal distribution Patients Retrospective Studies Theta rhythms Variables Young Adult Resting-state EEG Spinocerebellar ataxia type 27B CACNA1A FGF14 Connectivity analysis
ISSN:	1473-4230, 1473-4222, 1473-4230
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