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...

Celý popis

Uložené v:

Podrobná bibliografia
Vydané v:	Cerebellum (London, England) Ročník 24; číslo 6; s. 175
Hlavní autori:	Angerbauer, Raphael, Unterberger, Iris, Nachbauer, Wolfgang, Amprosi, Matthias, Boesch, Sylvia, Cesari, Matteo, Indelicato, Elisabetta
Médium:	Journal Article
Jazyk:	English
Vydavateľské údaje:	New York Springer US 15.11.2025 Springer Nature B.V
Predmet:	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
On-line prístup:	Získať plný text
Tagy:	Pridať tag Žiadne tagy, Buďte prvý, kto otaguje tento záznam!

Buďte prvý, kto okomentuje tento záznam!