A. Misk

Multiplex families with epilepsy

G. Carvill, I. Scheffer, H. Mefford, 2016, Neurology.

Founder Effect with Variable Age at Onset in Arab Families with Lafora Disease and EPM2A Mutation

S. Berkovic, D. Lev, J. Serratosa, 2007, Epilepsia.

KIF1A missense mutations in SPG30, an autosomal recessive spastic paraplegia: distinct phenotypes according to the nature of the mutations

G. Gyapay, S. Klebe, A. Durr, 2012, European Journal of Human Genetics.

Fe/S protein assembly gene IBA57 mutation causes hereditary spastic paraplegia

A. Brice, G. Stevanin, J. Gomori, 2015, Neurology.

Blood–brain barrier disruption in post-traumatic epilepsy

I. Shelef, A. Friedman, D. Zumsteg, 2007, Journal of Neurology, Neurosurgery, and Psychiatry.

Mutation of the nuclear lamin gene LMNB2 in progressive myoclonus epilepsy with early ataxia.

I. Scheffer, S. Berkovic, A. Korczyn, 2015, Human molecular genetics.

Epilepsy with Early Ataxia

S. Berkovic, A. Korczyn, M. Bahlo, 2015 .