Sfoglia per Autore
The synergistic relationship between Alzheimer's disease and sleep disorders: An update
2015 Villa, C; Ferini Strambi, L; Combi, R
DEPDC5 mutations in families presenting as autosomal dominant nocturnal frontal lobe epilepsy
2014 Picard, F; Makrythanasis, P; Navarro, V; Ishida, S; de Bellescize, J; Ville, D; Weckhuysen, S; Fosselle, E; Suls, A; De Jonghe, P; Vasselon Raina, M; Lesca, G; Depienne, C; An Gourfinkel, I; Vlaicu, M; Baulac, M; Mundwiller, E; Couarch, P; Combi, R; Ferini Strambi, L; Gambardella, A; Antonarakis, S; Leguern, E; Steinlein, O; Baulac, S
Identification and functional characterisation of a new KCNJ2 mutation
2014 Rivolta, I; Sala, L; Rocchetti, M; Giovannoni, R; Cornaggia, C; Combi, R
Nocturnal Frontal Lobe Epilepsy
2014 Nobili, L; Proserpio, P; Combi, R; Provini, F; Plazzi, G; Bisulli, F; Tassi, L; Tinuper, P
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
Familiar Febrile Seizures and Mutations in the Nav1.1 Sodium Channel
2012 Sansoni, V; Grioni, D; Dalpra', L; Combi, R
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
Ricerca di mutazioni in una famiglia ADNFLE.
2012 Sansoni, V; Ferini Strambi, L; Combi, R
Nocturnal frontal lobe epilepsy and the acetylcholine receptor.
2012 Ferini Strambi, L; Sansoni, V; Combi, R
aCGH analysis of two families showing both autism and epilepsy
2011 Combi, R; Redaelli, S; Sansoni, V; Cornaggia, C; Dalpra', L
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
Ricerca di mutazioni in pazienti affetti da NFLE
2011 Sansoni, V; Nobili, L; Proserpio, P; Ferini Strambi, L; Combi, R
Mutations of the orexin system, a regulator of sleep arousal, are not a common cause of ADNFLE.
2011 Bouchardy, I; Steinlein, O; Combi, R; Ferini Strambi, L; Gambardella, A; Rudolf, G; Morris, M; Picard, F
Study of the genetic basis of autosomal dominant nocturnal frontal lobe epilepsy
2010 Sansoni, V; Bouchardy, I; Picard, F; Combi, R
Clinical and genetic evaluation of a family showing both autism and epilepsy
2010 Combi, R; Redaelli, S; Beghi, M; Clerici, M; Cornaggia, C; Dalpra', L
Clinical and genetic familial study of a large cohort of Italian children with idiopathic epilepsy
2009 Combi, R; Grioni, D; Contri, M; Redaelli, S; Redaelli, F; Bassi, M; Barisani, D; Lavitrano, M; Tredici, G; Tenchini, M; Bertolini, M; Dalpra', L
Distinct pools of cancer stem-like cells coexist within human glioblastomas and display different tumorigenicity and independent genomic evolution
2009 Piccirillo, S; Combi, R; Cajola, L; Patrizi, A; Redaelli, S; Bentivegna, A; Baronchelli, S; Maira, G; Pollo, B; Mangiola, A; Dimeco, F; Dalpra', L; Vescovi, A
CHRNA2 mutations are rare in the NFLE population: Evaluation of a large cohort of Italian patients
2009 Combi, R; Ferini Strambi, L; Tenchini, M
Maternal polymorphisms for methyltetrahydrofolate reductase and methionine synthetase reductase and risk of children with Down syndrome
2009 Pozzi, E; Vergani, P; Dalpra', L; Combi, R; Silvestri, D; Crosti, F; Dell’Orto, M; Valsecchi, M
A rescuable folding defective Nav1.1 (SCN1A) Na+channel mutant causes GEFS+: common mechanism in Nav1.1 related epilepsies?
2009 Rusconi, R; Combi, R; Cestèle, S; Grioni, D; Franceschetti, S; Dalpra', L; Mantegazza, M
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