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Journal of Neurology|October 14, 2015
Autosomal dominant epilepsy with auditory features: a new LGI1 family including a phenocopy with cortical dysplasiaKarl Martin Klein, Manuela Pendziwiat, Rony Cohen, et al.
Neurology|September 23, 2025
Quantitative EEG Biomarkers in the Genetic Epilepsies and Associations With Neurologic OutcomesPeter D Galer, Jillian L McKee, Sarah M Ruggiero, et al.
Ebiomedicine|August 27, 2022
Modulating effects of FGF12 variants on Na<sub>V</sub>1.2 and Na<sub>V</sub>1.6 being associated with developmental and epileptic encephalopathy and Autism spectrum disorder: A case seriesSimone Seiffert, Manuela Pendziwiat, Tatjana Bierhals, et al.
Medrxiv : the Preprint Server for Health Sciences|October 17, 2024
Quantitative EEG Spectral Features Differentiate Genetic Epilepsies and Predict Neurologic OutcomesPeter D Galer, Jillian L McKee, Sarah M Ruggiero, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|July 13, 2022
Current practice in diagnostic genetic testing of the epilepsiesIlona Krey, Konrad Platzer, Alina Esterhuizen, et al.
Nature Communications|October 9, 2015
Detyrosinated microtubules modulate mechanotransduction in heart and skeletal muscleJaclyn P Kerr, Patrick Robison, Guoli Shi, et al.
Epilepsia|June 18, 2022
Precision medicine for genetic epilepsy on the horizon: Recent advances, present challenges, and suggestions for continued progressJuliet K Knowles, Ingo Helbig, Cameron S Metcalf, et al.
Epilepsy Research|June 23, 2018
PCDH19-related epilepsy in a male with Klinefelter syndrome: Additional evidence supporting PCDH19 cellular interference disease mechanismEdward J Romasko, Elizabeth T DeChene, Jorune Balciuniene, et al.
Medrxiv : the Preprint Server for Health Sciences|October 3, 2025
Quantification of neuromotor control in <i>STXBP1</i> -Related Disorders with wearable sensorsJulie M Orlando, Bintou Bane, Torrey Chisari, et al.
Epilepsy Research|January 12, 2013
The role of SLC2A1 in early onset and childhood absence epilepsiesHiltrud Muhle, Ingo Helbig, Tobias Guldberg Frøslev, et al.
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