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S Buoni

Showing results (11-20 of 25) with videos related to

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Clinical Genetics|September 2, 2008
Novel PTEN mutations in neurodevelopmental disorders and macrocephalyA Orrico, L Galli, S Buoni, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|May 1, 1994
Vigabatrin treatment in childrenA Fois, S Buoni, R M Di Bartolo, et al.
Clinical Genetics|June 13, 2009
Mutational analysis of the SCN1A, SCN1B and GABRG2 genes in 150 Italian patients with idiopathic childhood epilepsiesA Orrico, L Galli, S Grosso, et al.
Annals of Human Genetics|December 16, 2004
The FBN1 (R2726W) mutation is not fully penetrantS Buoni, R Zannolli, F Macucci, et al.
Neurology|October 27, 2004
Delayed response of seizures with vagus nerve stimulation in Lennox-Gastaut syndromeS Buoni, R Zannolli, F Macucci, et al.
Neurology|March 1, 2006
SCN1A (2528delG) novel truncating mutation with benign outcome of severe myoclonic epilepsy of infancyS Buoni, A Orrico, L Galli, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|June 28, 2005
Occipital intermittent rhythmic delta activity only following eye closure in atypical CNS SalmonellosisS Buoni, R Zannolli, R M Di Bartolo, et al.
Journal of Child Neurology|March 25, 1998
Segregation analysis in typical absence epilepsyS Buoni, S Grosso, G Di Cosmo, et al.
Journal of Child Neurology|September 29, 2001
Homocystinuria with transverse sinus thrombosisS Buoni, M Molinelli, A Mariottini, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|June 23, 2009
Neurological outcome following isolated 10-12 mm fetal ventriculomegalyK Melchiorre, M Liberati, C Celentano, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
Clinical Genetics|September 2, 2008
Novel PTEN mutations in neurodevelopmental disorders and macrocephalyA Orrico, L Galli, S Buoni, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|May 1, 1994
Vigabatrin treatment in childrenA Fois, S Buoni, R M Di Bartolo, et al.
Clinical Genetics|June 13, 2009
Mutational analysis of the SCN1A, SCN1B and GABRG2 genes in 150 Italian patients with idiopathic childhood epilepsiesA Orrico, L Galli, S Grosso, et al.
Annals of Human Genetics|December 16, 2004
The FBN1 (R2726W) mutation is not fully penetrantS Buoni, R Zannolli, F Macucci, et al.
Neurology|October 27, 2004
Delayed response of seizures with vagus nerve stimulation in Lennox-Gastaut syndromeS Buoni, R Zannolli, F Macucci, et al.
Neurology|March 1, 2006
SCN1A (2528delG) novel truncating mutation with benign outcome of severe myoclonic epilepsy of infancyS Buoni, A Orrico, L Galli, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|June 28, 2005
Occipital intermittent rhythmic delta activity only following eye closure in atypical CNS SalmonellosisS Buoni, R Zannolli, R M Di Bartolo, et al.
Journal of Child Neurology|March 25, 1998
Segregation analysis in typical absence epilepsyS Buoni, S Grosso, G Di Cosmo, et al.
Journal of Child Neurology|September 29, 2001
Homocystinuria with transverse sinus thrombosisS Buoni, M Molinelli, A Mariottini, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|June 23, 2009
Neurological outcome following isolated 10-12 mm fetal ventriculomegalyK Melchiorre, M Liberati, C Celentano, et al.
Pageof 3