B. a Rogvi-Hansen

Novel mutations in EPM2A and NHLRC1 widen the spectrum of Lafora disease

P. Ryvlin, L. Maillard, P. Genton, 2010, Epilepsia.

Double‐blind crossover trial of gabapentin in SPG4‐linked hereditary spastic paraplegia

P. Jennum, K. Fenger, J. Nielsen, 2007, European journal of neurology.

Novel mutations in EPM2A and NHLRC1 widen the spectrum of Lafora disease

P. Ryvlin, L. Maillard, P. Genton, 2010, Epilepsia.