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Federico Zara

Showing results (41-50 of 398) with videos related to

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Molecular Genetics & Genomic Medicine|August 4, 2021
A case of Fibrodysplasia Ossificans Progressiva associated with a novel variant of the ACVR1 geneSerena Cappato, Rasa Traberg, Jolita Gintautiene, et al.
Epilepsia|January 6, 2006
Electroclinical and genetic findings in a family with cortical tremor, myoclonus, and epilepsyPasquale Striano, Francesca Madia, Carlo Minetti, et al.
Pharmacological Research|April 16, 2016
Management of genetic epilepsies: From empirical treatment to precision medicinePasquale Striano, Maria Stella Vari, Chiara Mazzocchetti, et al.
Cells|September 14, 2024
V-ATPase Dysfunction in the Brain: Genetic Insights and Therapeutic OpportunitiesAntonio Falace, Greta Volpedo, Marcello Scala, et al.
Italian Journal of Pediatrics|November 10, 2019
NF1 microdeletion syndrome: case report of two new patientsGregorio Serra, Vincenzo Antona, Giovanni Corsello, et al.
Biomolecules|October 28, 2023
ATP12A Proton Pump as an Emerging Therapeutic Target in Cystic Fibrosis and Other Respiratory DiseasesMichał Dębczyński, Giulia Gorrieri, Damian Mojsak, et al.
Frontiers in Cell and Developmental Biology|November 6, 2020
Brain Organoids as Model Systems for Genetic Neurodevelopmental DisordersSimona Baldassari, Ilaria Musante, Michele Iacomino, et al.
BMC Medicine|May 5, 2025
Gut-immune-brain interactions during neurodevelopment: from a brain-centric to a multisystem perspectiveGreta Volpedo, Antonella Riva, Lino Nobili, et al.
International Journal of Molecular Sciences|January 17, 2020
Progress of Induced Pluripotent Stem Cell Technologies to Understand Genetic EpilepsyBruno Sterlini, Floriana Fruscione, Simona Baldassari, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 3, 2009
Sudden death in Unverricht-Lundborg patients: is serotonin the key?Pasquale Striano, Elena D'Amato, Marianna Pezzella, et al.
Pageof 40

Showing results (41-50 of 398) with videos related to

Sort By:
Pageof 40
Molecular Genetics & Genomic Medicine|August 4, 2021
A case of Fibrodysplasia Ossificans Progressiva associated with a novel variant of the ACVR1 geneSerena Cappato, Rasa Traberg, Jolita Gintautiene, et al.
Epilepsia|January 6, 2006
Electroclinical and genetic findings in a family with cortical tremor, myoclonus, and epilepsyPasquale Striano, Francesca Madia, Carlo Minetti, et al.
Pharmacological Research|April 16, 2016
Management of genetic epilepsies: From empirical treatment to precision medicinePasquale Striano, Maria Stella Vari, Chiara Mazzocchetti, et al.
Cells|September 14, 2024
V-ATPase Dysfunction in the Brain: Genetic Insights and Therapeutic OpportunitiesAntonio Falace, Greta Volpedo, Marcello Scala, et al.
Italian Journal of Pediatrics|November 10, 2019
NF1 microdeletion syndrome: case report of two new patientsGregorio Serra, Vincenzo Antona, Giovanni Corsello, et al.
Biomolecules|October 28, 2023
ATP12A Proton Pump as an Emerging Therapeutic Target in Cystic Fibrosis and Other Respiratory DiseasesMichał Dębczyński, Giulia Gorrieri, Damian Mojsak, et al.
Frontiers in Cell and Developmental Biology|November 6, 2020
Brain Organoids as Model Systems for Genetic Neurodevelopmental DisordersSimona Baldassari, Ilaria Musante, Michele Iacomino, et al.
BMC Medicine|May 5, 2025
Gut-immune-brain interactions during neurodevelopment: from a brain-centric to a multisystem perspectiveGreta Volpedo, Antonella Riva, Lino Nobili, et al.
International Journal of Molecular Sciences|January 17, 2020
Progress of Induced Pluripotent Stem Cell Technologies to Understand Genetic EpilepsyBruno Sterlini, Floriana Fruscione, Simona Baldassari, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 3, 2009
Sudden death in Unverricht-Lundborg patients: is serotonin the key?Pasquale Striano, Elena D'Amato, Marianna Pezzella, et al.
Pageof 40