SANSONI, VERONICA
SANSONI, VERONICA
Engineering an Environment for the Study of Fibrosis: A 3D Human Muscle Model with Endothelium Specificity and Endomysium
2018 Bersini, S; Gilardi, M; Ugolini, G; Sansoni, V; Talò, G; Perego, S; Zanotti, S; Ostano, P; Mora, M; Soncini, M; Vanoni, M; Lombardi, G; Moretti, M
Identification of two mutations in cis in the SCN1A gene in a family showing genetic epilepsy with febrile seizures plus (GEFS+) and idiopathic generalized epilepsy (IGE)
2017 Binini, N; Sancini, G; Villa, C; DAL MAGRO, R; Sansoni, V; Rusconi, R; Mantegazza, M; Grioni, D; Talpo, F; Toselli, M; Combi, R
Functional Characterization of a CRH Missense Mutation Identified in an ADNFLE Family
2013 Sansoni, V; Forcella, M; Mozzi, A; Fusi, P; Ambrosini, R; Ferini Strambi, L; Combi, R
Nocturnal frontal lobe epilepsy and febrile seizures: genetic and molecular aspects
2013 Sansoni, V
A de novo mutation in an Italian sporadic patient affected by Nocturnal frontal lobe epilepsy
2012 Sansoni, V; Nobili, L; Proserpio, P; Ferini Strambi, L; Combi, R
Familiar Febrile Seizures and Mutations in the Nav1.1 Sodium Channel
2012 Sansoni, V; Grioni, D; Dalpra', L; Combi, R
Nocturnal frontal lobe epilepsy and the acetylcholine receptor.
2012 Ferini Strambi, L; Sansoni, V; Combi, R
Ricerca di mutazioni in una famiglia ADNFLE.
2012 Sansoni, V; Ferini Strambi, L; Combi, R
aCGH analysis of two families showing both autism and epilepsy
2011 Combi, R; Redaelli, S; Sansoni, V; Cornaggia, C; Dalpra', L
Ricerca di mutazioni in pazienti affetti da NFLE
2011 Sansoni, V; Nobili, L; Proserpio, P; Ferini Strambi, L; Combi, R
Role of the SCN1A gene in the pathogenesis of familial febrile seizures and GEFS+
2011 Sansoni, V; Grioni, D; Redaelli, S; Dalpra', L; Combi, R
Study of the genetic basis of autosomal dominant nocturnal frontal lobe epilepsy
2010 Sansoni, V; Bouchardy, I; Picard, F; Combi, R