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Paolo Balestri

Showing results (41-50 of 62) with videos related to

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Human Genetics|July 8, 2005
Loss-of-function mutation of the AF9/MLLT3 gene in a girl with neuromotor development delay, cerebellar ataxia, and epilepsyTiziano Pramparo, Salvatore Grosso, Jole Messa, et al.
American Journal of Medical Genetics. Part A|December 31, 2003
Facial hemangioma and malformation of the cortical development: a broadening of the PHACE spectrum or a new entity?S Grosso, L De Cosmo, E Bonifazi, et al.
Journal of Child Neurology|December 21, 2004
Epilepsy and electroencephalographic findings in pericentric inversion of chromosome 12Salvatore Grosso, Lucia Pucci, MariAngela Farnetani, et al.
Epilepsia|October 9, 2013
Epilepsy and vaccinations: Italian guidelinesDario Pruna, Paolo Balestri, Nelia Zamponi, et al.
The Journal of General Virology|April 15, 2003
Nucleotide variation in Sabin type 2 poliovirus from an immunodeficient patient with poliomyelitisGabriele Buttinelli, Valentina Donati, Stefano Fiore, et al.
Neuromuscular Disorders : NMD|December 3, 2014
A novel homozygous ISPD gene mutation causing phenotype variability in a consanguineous familyGiovanni Baranello, Simona Saredi, Serena Sansanelli, et al.
Journal of Clinical Neurophysiology : Official Publication of the American Electroencephalographic Society|October 29, 2004
Electroencephalographic and epileptic patterns in X chromosome anomaliesSalvatore Grosso, Mariangela A Farnetani, Rosanna Maria Di Bartolo, et al.
Epilepsy Research|December 17, 2008
Zonisamide in children and young adults with refractory epilepsy: an open label, multicenter Italian studyGiangennaro Coppola, Salvatore Grosso, Alberto Verrotti, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 18, 2009
Clinical features of psychogenic non-epileptic seizures in prepubertal and pubertal patients with idiopathic epilepsyAlberto Verrotti, Sergio Agostinelli, Angelika Mohn, et al.
Human Mutation|September 16, 2006
Mutations in the C7orf11 (TTDN1) gene in six nonphotosensitive trichothiodystrophy patients: no obvious genotype-phenotype relationshipsElena Botta, Judith Offman, Tiziana Nardo, et al.
Pageof 7

Showing results (41-50 of 62) with videos related to

Sort By:
Pageof 7
Human Genetics|July 8, 2005
Loss-of-function mutation of the AF9/MLLT3 gene in a girl with neuromotor development delay, cerebellar ataxia, and epilepsyTiziano Pramparo, Salvatore Grosso, Jole Messa, et al.
American Journal of Medical Genetics. Part A|December 31, 2003
Facial hemangioma and malformation of the cortical development: a broadening of the PHACE spectrum or a new entity?S Grosso, L De Cosmo, E Bonifazi, et al.
Journal of Child Neurology|December 21, 2004
Epilepsy and electroencephalographic findings in pericentric inversion of chromosome 12Salvatore Grosso, Lucia Pucci, MariAngela Farnetani, et al.
Epilepsia|October 9, 2013
Epilepsy and vaccinations: Italian guidelinesDario Pruna, Paolo Balestri, Nelia Zamponi, et al.
The Journal of General Virology|April 15, 2003
Nucleotide variation in Sabin type 2 poliovirus from an immunodeficient patient with poliomyelitisGabriele Buttinelli, Valentina Donati, Stefano Fiore, et al.
Neuromuscular Disorders : NMD|December 3, 2014
A novel homozygous ISPD gene mutation causing phenotype variability in a consanguineous familyGiovanni Baranello, Simona Saredi, Serena Sansanelli, et al.
Journal of Clinical Neurophysiology : Official Publication of the American Electroencephalographic Society|October 29, 2004
Electroencephalographic and epileptic patterns in X chromosome anomaliesSalvatore Grosso, Mariangela A Farnetani, Rosanna Maria Di Bartolo, et al.
Epilepsy Research|December 17, 2008
Zonisamide in children and young adults with refractory epilepsy: an open label, multicenter Italian studyGiangennaro Coppola, Salvatore Grosso, Alberto Verrotti, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 18, 2009
Clinical features of psychogenic non-epileptic seizures in prepubertal and pubertal patients with idiopathic epilepsyAlberto Verrotti, Sergio Agostinelli, Angelika Mohn, et al.
Human Mutation|September 16, 2006
Mutations in the C7orf11 (TTDN1) gene in six nonphotosensitive trichothiodystrophy patients: no obvious genotype-phenotype relationshipsElena Botta, Judith Offman, Tiziana Nardo, et al.
Pageof 7