Results 221 to 230 of about 236,683 (245)
Abstract The 15q11.2 microdeletion is a chromosomal condition associated with a broad epileptic phenotype. It is differentiated from Angelman syndrome, which is typically a larger maternal deletion in an overlapping area. We describe a patient with a 15q11.2 microdeletion that has clinical and EEG biomarker features similar to those seen in Angelman ...
Hok Leong Chin +2 more
wiley +1 more source
Aphasic status epilepticus due to Epstein–Barr virus meningoencephalitis – A clinical vignette
Epileptic Disorders, EarlyView.
Gemma Bassani +6 more
wiley +1 more source
EEG findings in SERAC1‐related MEGD(H)EL syndrome
Epileptic Disorders, EarlyView.
Apurva Patel, Dalila Lewis, Thomas Koch
wiley +1 more source
Asymmetric sleep spindles after thalamic stroke
Epileptic Disorders, EarlyView.
Côme‐Alexandre Meyruey +1 more
wiley +1 more source
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