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You searched for: Author/Creator Larsen, Line H. G.

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1. Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutation. Issue 3 (13th February 2016)

2. Impact on Clinical Decision Making of Next-Generation Sequencing in Pediatric Epilepsy in a Tertiary Epilepsy Referral Center. (January 2020)

3. Mesial Temporal Sclerosis in SCN1A-Related Epilepsy: Two Long-Term EEG Case Studies. (July 2019)

4. Mutations in KCNT1 cause a spectrum of focal epilepsies. (30th June 2015)