S. Chiari

Lissencephaly: Expanded imaging and clinical classification

Renzo Guerrini, William B Dobyns, A James Barkovich, 2017, American journal of medical genetics. Part A.

Analysis of 17 genes detects mutations in 81% of 811 patients with lissencephaly

G. Carvill, D. Ledbetter, M. Ross, 2018, Genetics in Medicine.

Clinical and genetic factors predicting Dravet syndrome in infants with SCN1A mutations

G. Avanzini, L. Grisotto, V. Cetica, 2017, Neurology.

Clinical and genetic factors predicting Dravet syndrome in infants with SCN 1 A mutations

G. Avanzini, L. Grisotto, V. Cetica, 2022 .

Analysis of 17 genes detects mutations in 81% of 811 patients with lissencephaly

G. Carvill, D. Ledbetter, M. Ross, 2018, Genetics in Medicine.

Diagnostic implications of genetic copy number variation in epilepsy plus

H. Mefford, P. Stankiewicz, L. Lagae, 2019, Epilepsia.