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Renzo Guerrini

Showing results (121-130 of 610) with videos related to

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Drugs - Real World Outcomes|June 10, 2022
Efficacy and Safety of Long-Term Treatment with Stiripentol in Children and Adults with Drug-Resistant Epilepsies: A Retrospective Cohort Study of 196 PatientsSimona Balestrini, Viola Doccini, Alessandra Boncristiano, et al.
Physiological Reviews|August 11, 2022
Developmental and epileptic encephalopathies: from genetic heterogeneity to phenotypic continuumRenzo Guerrini, Valerio Conti, Massimo Mantegazza, et al.
American Journal of Medical Genetics. Part A|January 5, 2011
Contractions in the second polyA tract of ARX are rare, non-pathogenic polymorphismsValerio Conti, Carla Marini, Davide Mei, et al.
European Journal of Human Genetics : EJHG|February 16, 2012
Symmetric polymicrogyria and pachygyria associated with TUBB2B gene mutationsRenzo Guerrini, Davide Mei, Duccio Maria Cordelli, et al.
Molecular Therapy. Nucleic Acids|October 26, 2016
Double-target Antisense U1snRNAs Correct Mis-splicing Due to c.639+861C>T and c.639+919G>A GLA Deep Intronic MutationsLorenzo Ferri, Giuseppina Covello, Anna Caciotti, et al.
European Journal of Gastroenterology & Hepatology|January 12, 2008
Different genotypes in a large Italian family with recurrent hereditary fructose intoleranceAnna Caciotti, Maria Alice Donati, Andrea Adami, et al.
Epilepsia Open|January 30, 2026
Neuropsychological profile and social cognition in children and adolescents with temporal lobe epilepsyClaudia Accolla, Martina Preti, Pietro Cappelletto, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|October 28, 2020
Atypical Ocular Coloboma in Tuberous Sclerosis-2: Report of Two Novel CasesGiacomo M Bacci, Silvio Polizzi, Francesco Mari, et al.
American Journal of Medical Genetics. Part A|March 19, 2011
Corpus callosum agenesis, severe mental retardation, epilepsy, and dyskinetic quadriparesis due to a novel mutation in the homeodomain of ARXValerio Conti, Carla Marini, Simone Gana, et al.
Therapeutic Drug Monitoring|January 28, 2003
Plasma gabapentin concentrations in children with epilepsy: influence of age, relationship with dosage, and preliminary observations on correlation with clinical responseGiuliana Gatti, Anna Rita Ferrari, Renzo Guerrini, et al.
Pageof 61

Showing results (121-130 of 610) with videos related to

Sort By:
Pageof 61
Drugs - Real World Outcomes|June 10, 2022
Efficacy and Safety of Long-Term Treatment with Stiripentol in Children and Adults with Drug-Resistant Epilepsies: A Retrospective Cohort Study of 196 PatientsSimona Balestrini, Viola Doccini, Alessandra Boncristiano, et al.
Physiological Reviews|August 11, 2022
Developmental and epileptic encephalopathies: from genetic heterogeneity to phenotypic continuumRenzo Guerrini, Valerio Conti, Massimo Mantegazza, et al.
American Journal of Medical Genetics. Part A|January 5, 2011
Contractions in the second polyA tract of ARX are rare, non-pathogenic polymorphismsValerio Conti, Carla Marini, Davide Mei, et al.
European Journal of Human Genetics : EJHG|February 16, 2012
Symmetric polymicrogyria and pachygyria associated with TUBB2B gene mutationsRenzo Guerrini, Davide Mei, Duccio Maria Cordelli, et al.
Molecular Therapy. Nucleic Acids|October 26, 2016
Double-target Antisense U1snRNAs Correct Mis-splicing Due to c.639+861C>T and c.639+919G>A GLA Deep Intronic MutationsLorenzo Ferri, Giuseppina Covello, Anna Caciotti, et al.
European Journal of Gastroenterology & Hepatology|January 12, 2008
Different genotypes in a large Italian family with recurrent hereditary fructose intoleranceAnna Caciotti, Maria Alice Donati, Andrea Adami, et al.
Epilepsia Open|January 30, 2026
Neuropsychological profile and social cognition in children and adolescents with temporal lobe epilepsyClaudia Accolla, Martina Preti, Pietro Cappelletto, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|October 28, 2020
Atypical Ocular Coloboma in Tuberous Sclerosis-2: Report of Two Novel CasesGiacomo M Bacci, Silvio Polizzi, Francesco Mari, et al.
American Journal of Medical Genetics. Part A|March 19, 2011
Corpus callosum agenesis, severe mental retardation, epilepsy, and dyskinetic quadriparesis due to a novel mutation in the homeodomain of ARXValerio Conti, Carla Marini, Simone Gana, et al.
Therapeutic Drug Monitoring|January 28, 2003
Plasma gabapentin concentrations in children with epilepsy: influence of age, relationship with dosage, and preliminary observations on correlation with clinical responseGiuliana Gatti, Anna Rita Ferrari, Renzo Guerrini, et al.
Pageof 61