A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers.

Simultaneous Treatment of Epilepsy and Secondary Dystonia After Anterior Temporal Lobectomy and Amygdalohippocampectomy.

Treatment of medically refractory seizures with responsive neurostimulation: 2 pediatric cases.

Common terms for rare epilepsies: Synonyms, associated terms, and links to structured vocabularies.

Unaffected mosaic C9orf72 case: RNA foci, dipeptide proteins, but upregulated C9orf72 expression.

Epilepsy surgery in patients with autism.

C9orf72 isoforms in Amyotrophic Lateral Sclerosis and Frontotemporal Lobar Degeneration.

A microRNA-328 binding site in PAX6 is associated with centrotemporal spikes of rolandic epilepsy.

Deficiency of the zinc finger protein ZFP106 causes motor and sensory neurodegeneration.

Risk factors for reading disability in families with rolandic epilepsy.

Isoform-specific antibodies reveal distinct subcellular localizations of C9orf72 in amyotrophic lateral sclerosis.

Jump from pre-mutation to pathologic expansion in C9orf72.

The C9orf72 repeat expansion itself is methylated in ALS and FTLD patients.

A novel SOD1-ALS mutation separates central and peripheral effects of mutant SOD1 toxicity.

Seizure patterns in childhood.