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Drugs - Real World Outcomes
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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 Patients
Simona Balestrini, Viola Doccini, Alessandra Boncristiano, et al.
Physiological Reviews
|
August 11, 2022
Developmental and epileptic encephalopathies: from genetic heterogeneity to phenotypic continuum
Renzo 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 polymorphisms
Valerio Conti, Carla Marini, Davide Mei, et al.
European Journal of Human Genetics : EJHG
|
February 16, 2012
Symmetric polymicrogyria and pachygyria associated with TUBB2B gene mutations
Renzo 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 Mutations
Lorenzo 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 intolerance
Anna 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 epilepsy
Claudia 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 Cases
Giacomo 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 ARX
Valerio 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 response
Giuliana Gatti, Anna Rita Ferrari, Renzo Guerrini, et al.
Page
of 61
Search research articles
Search
Showing results (121-130 of 610) with videos related to
Sort By:
Page
of 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 Patients
Simona Balestrini, Viola Doccini, Alessandra Boncristiano, et al.
Physiological Reviews
|
August 11, 2022
Developmental and epileptic encephalopathies: from genetic heterogeneity to phenotypic continuum
Renzo 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 polymorphisms
Valerio Conti, Carla Marini, Davide Mei, et al.
European Journal of Human Genetics : EJHG
|
February 16, 2012
Symmetric polymicrogyria and pachygyria associated with TUBB2B gene mutations
Renzo 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 Mutations
Lorenzo 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 intolerance
Anna 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 epilepsy
Claudia 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 Cases
Giacomo 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 ARX
Valerio 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 response
Giuliana Gatti, Anna Rita Ferrari, Renzo Guerrini, et al.
Page
of 61