Author

Raunak Singh

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Case report Open access Sep 2026

Drug-resistant epilepsy in an autosomal recessive copper metabolism disorder from SLC33A1 mutation

SLC33A1 mutation (Huppke-Brendel Syndrome) is a rare, autosomal recessive disorder associated with copper metabolism and characterized by global developmental delay, sensorineural hearing loss, congenital cataract and generalized hypotonia. We report two siblings under 6 years with novel SLC33A1 gene mutation, born fro...

Raunak Singh, Cheng-Yen Kuo, Shelja Sharma et al. · Epilepsy & Behavior Reports · 0 citations

Open access Sep 2026

Invasive network neuromodulation for insular epilepsy: A three-center retrospective study.

This study expands the limited literature on insular neuromodulation by demonstrating effectiveness of RNS and CSS, suggesting potential benefit from combined thalamocortical targeting, and defining parasagittal trajectories as a surgical approach for optimal lead proximity.

Raunak Singh, N. Gregg, K. Starnes et al. · Epilepsia · 0 citations