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EPILEPSY RESEARCH
Rivista
Codice:
E059098
ISSN:
0920-1211
Dati Generali
Dati Generali
Pubblicazioni (25)
Pulisci
Ordina Pubblicazioni:
ascendente
decrescente
Association of intronic variants of the KCNAB1 gene with lateral temporal epilepsy
Articolo
Autosomal dominant lateral temporal epilepsy (ADLTE): Absence of chromosomal rearrangements in LGI1 gene
Articolo
Autosomal dominant lateral temporal epilepsy (ADLTE): Novel structural and single-nucleotide LGI1 mutations in families with predominant visual auras
Articolo
Autosomal dominant lateral temporal epilepsy (ADLTE): absence of chromosomal rearrangements in LGI1 gene.
Articolo
Autosomal dominant lateral temporal epilepsy: absence of mutations in ADAM22 and Kv1 channel genes encoding LGI1-associated proteins
Articolo
Autosomal dominant lateral temporal epilepsy: absence of mutations in ADAM22 and Kv1 channel genes encoding LGI1-associated proteins.
Articolo
CNTNAP2 mutations and autosomal dominant epilepsy with auditory features
Articolo
Chemokines as new inflammatory players in the pathogenesis of epilepsy
Articolo
Correlation between GABA(A) receptor density and vagus nerve stimulation in individuals with drug-resistant partial epilepsy.
Articolo
Distribution of epileptiform discharges during nREM sleep in the CSWSS syndrome: relationship with sigma and delta activities.
Articolo
Epileptic seizures are preceded by a decrease in synchronization
Articolo
Failure to confirm association of a polymorphism in KCNMB4 gene with mesial temporal lobe epilepsy.
Articolo
Familial epilepsy and developmental dysphasia: description of an Italian pedigree with autosomal dominant inheritance and screening of candidate loci.
Articolo
Family history and frontal lobe seizures predict long-term remission in newly diagnosed cryptogenic focal epilepsy.
Articolo
Family history and frontal lobe seizures predict long-term remission in newly diagnosed cryptogenic focal epilepsy.
Articolo
Further evidence of genetic heterogeneity in families with autosomal dominant nocturnal frontal lobe epilepsy.
Articolo
Genetic analysis of the LGI/Epitempin gene family in sporadic and familial lateral temporal lobe epilepsy.
Articolo
Ictal impending danger--"sixth sense seizures"--in patients with benign focal epileptic seizures of adolescence.
Articolo
Improved spatial characterization of the epileptic brain by focusing on nonlinearity
Articolo
Mutations in PRRT2 result in familial infantile seizures with heterogeneous phenotypes including febrile convulsions and probable SUDEP.
Articolo
Mutations in PRRT2 result in familial infantile seizures with heterogeneous phenotypes including febrile convulsions and probable SUDEP.
Articolo
Neonatal onset of hot water reflex seizures in monozygotic twins subsequently manifesting episodes of alternating hemiplegia.
Articolo
Open label, long-term, pragmatic study on levetiracetam in the treatment of juvenile myoclonic epilepsy.
Articolo
Suggestive linkage of familial mesial temporal lobe epilepsy to chromosome 3q26
Articolo
Usefulness of a morning routine EEG recording in patients with juvenile myoclonic epilepsy.
Articolo
No Results Found
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