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Federico Zara

Showing results (61-70 of 398) with videos related to

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Pediatric Blood & Cancer|June 2, 2022
E2F3 gene expression is a potential negative prognostic marker for localised and MYCN not-amplified neuroblastoma: Results of in silico analysis of 786 samplesMarzia Ognibene, Davide Cangelosi, Stefania Sorrentino, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 6, 2006
Effects in neocortical neurons of mutations of the Na(v)1.2 Na+ channel causing benign familial neonatal-infantile seizuresPaolo Scalmani, Raffaella Rusconi, Elena Armatura, et al.
Epilepsia|September 30, 2005
Late-onset and slow-progressing Lafora disease in four siblings with EPM2B mutationBetul Baykan, Pasquale Striano, Stefania Gianotti, et al.
Epilepsia|July 25, 2007
Life-threatening status epilepticus following gabapentin administration in a patient with benign adult familial myoclonic epilepsyPasquale Striano, Antonietta Coppola, Francesca Madia, et al.
Annals of Neurology|December 15, 2006
Glutamic acid decarboxylase antibodies in idiopathic generalized epilepsy and type 1 diabetesPasquale Striano, Giuseppe Perruolo, Luca Errichiello, et al.
Neuromuscular Disorders : NMD|December 5, 2006
Inherited neuromyotonia: a clinical and genetic study of a familyAntonio Falace, Pasquale Striano, Fiore Manganelli, et al.
Seizure|July 15, 2011
Benign myoclonic epilepsy in infancy followed by childhood absence epilepsySalvatore Mangano, Antonina Fontana, Chiara Spitaleri, et al.
International Journal of Molecular Sciences|November 14, 2023
Neuroblastoma Patients' Outcome and Chromosomal InstabilityMarzia Ognibene, Patrizia De Marco, Loredana Amoroso, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|August 7, 2019
Chiari malformation type I: what information from the genetics?Valeria Capra, Michele Iacomino, Andrea Accogli, et al.
Epilepsia|March 24, 2011
Natural history and long-term evolution in families with autosomal dominant cortical tremor, myoclonus, and epilepsyAntonietta Coppola, Lia Santulli, Luigi Del Gaudio, et al.
Pageof 40

Showing results (61-70 of 398) with videos related to

Sort By:
Pageof 40
Pediatric Blood & Cancer|June 2, 2022
E2F3 gene expression is a potential negative prognostic marker for localised and MYCN not-amplified neuroblastoma: Results of in silico analysis of 786 samplesMarzia Ognibene, Davide Cangelosi, Stefania Sorrentino, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 6, 2006
Effects in neocortical neurons of mutations of the Na(v)1.2 Na+ channel causing benign familial neonatal-infantile seizuresPaolo Scalmani, Raffaella Rusconi, Elena Armatura, et al.
Epilepsia|September 30, 2005
Late-onset and slow-progressing Lafora disease in four siblings with EPM2B mutationBetul Baykan, Pasquale Striano, Stefania Gianotti, et al.
Epilepsia|July 25, 2007
Life-threatening status epilepticus following gabapentin administration in a patient with benign adult familial myoclonic epilepsyPasquale Striano, Antonietta Coppola, Francesca Madia, et al.
Annals of Neurology|December 15, 2006
Glutamic acid decarboxylase antibodies in idiopathic generalized epilepsy and type 1 diabetesPasquale Striano, Giuseppe Perruolo, Luca Errichiello, et al.
Neuromuscular Disorders : NMD|December 5, 2006
Inherited neuromyotonia: a clinical and genetic study of a familyAntonio Falace, Pasquale Striano, Fiore Manganelli, et al.
Seizure|July 15, 2011
Benign myoclonic epilepsy in infancy followed by childhood absence epilepsySalvatore Mangano, Antonina Fontana, Chiara Spitaleri, et al.
International Journal of Molecular Sciences|November 14, 2023
Neuroblastoma Patients' Outcome and Chromosomal InstabilityMarzia Ognibene, Patrizia De Marco, Loredana Amoroso, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|August 7, 2019
Chiari malformation type I: what information from the genetics?Valeria Capra, Michele Iacomino, Andrea Accogli, et al.
Epilepsia|March 24, 2011
Natural history and long-term evolution in families with autosomal dominant cortical tremor, myoclonus, and epilepsyAntonietta Coppola, Lia Santulli, Luigi Del Gaudio, et al.
Pageof 40