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Francesco Fortunato

Showing results (21-30 of 120) with videos related to

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Stem Cell Research|March 7, 2026
Generation of hiPSCs lines from PRICKLE2-mutant individuals with epilepsyClara Zannino, Antonella Esposito, Mariagrazia Talarico, et al.
International Journal of Molecular Sciences|May 25, 2024
Phenotypic Variability in Novel Doublecortin Gene Variants Associated with Subcortical Band HeterotopiaRadha Procopio, Francesco Fortunato, Monica Gagliardi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 27, 2021
Facemask headache: a new nosographic entity among healthcare providers in COVID-19 eraLaura Rapisarda, Michele Trimboli, Francesco Fortunato, et al.
Human Genetics|May 1, 2004
An intragenic deletion/inversion event in the DMD gene determines a novel exon creation and results in a BMD phenotypeRachele Cagliani, Manuela Sironi, Emma Ciafaloni, et al.
Muscle & Nerve|August 20, 2004
Developmental and tissue-specific regulation of a novel dysferlin isoformSabrina Salani, Sabrina Lucchiari, Francesco Fortunato, et al.
Epilepsia|May 5, 2025
Focal epilepsy with sensory seizures associated with arginine:glycine amidinotransferase deficiency: A clinical and advanced magnetic resonance imaging studyFrancesco Fortunato, Roberta De Fiores, Ilaria Sammarra, et al.
Critical Care (London, England)|March 12, 2015
Platelet mitochondrial dysfunction in critically ill patients: comparison between sepsis and cardiogenic shockAlessandro Protti, Francesco Fortunato, Andrea Artoni, et al.
International Journal of Molecular Sciences|January 11, 2025
Novel <i>KCNQ2</i> Variants Related to a Variable Phenotypic Spectrum Ranging from Epilepsy with Auditory Features to Severe Developmental and Epileptic EncephalopathiesMariagrazia Talarico, Radha Procopio, Monica Gagliardi, et al.
Genes|November 27, 2024
Two Novel Variants in the <i>CHRNA2</i> and <i>SCN2A</i> Genes in Italian Patients with Febrile SeizuresRadha Procopio, Monica Gagliardi, Mariagrazia Talarico, et al.
Neurology. Genetics|December 31, 2025
Characterization of Sleep in Alternating Hemiplegia of Childhood: An International SurveyFrancesco Fortunato, Umesh Vivekananda, Katherine Elizabeth Behl, et al.
Pageof 12

Showing results (21-30 of 120) with videos related to

Sort By:
Pageof 12
Stem Cell Research|March 7, 2026
Generation of hiPSCs lines from PRICKLE2-mutant individuals with epilepsyClara Zannino, Antonella Esposito, Mariagrazia Talarico, et al.
International Journal of Molecular Sciences|May 25, 2024
Phenotypic Variability in Novel Doublecortin Gene Variants Associated with Subcortical Band HeterotopiaRadha Procopio, Francesco Fortunato, Monica Gagliardi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 27, 2021
Facemask headache: a new nosographic entity among healthcare providers in COVID-19 eraLaura Rapisarda, Michele Trimboli, Francesco Fortunato, et al.
Human Genetics|May 1, 2004
An intragenic deletion/inversion event in the DMD gene determines a novel exon creation and results in a BMD phenotypeRachele Cagliani, Manuela Sironi, Emma Ciafaloni, et al.
Muscle & Nerve|August 20, 2004
Developmental and tissue-specific regulation of a novel dysferlin isoformSabrina Salani, Sabrina Lucchiari, Francesco Fortunato, et al.
Epilepsia|May 5, 2025
Focal epilepsy with sensory seizures associated with arginine:glycine amidinotransferase deficiency: A clinical and advanced magnetic resonance imaging studyFrancesco Fortunato, Roberta De Fiores, Ilaria Sammarra, et al.
Critical Care (London, England)|March 12, 2015
Platelet mitochondrial dysfunction in critically ill patients: comparison between sepsis and cardiogenic shockAlessandro Protti, Francesco Fortunato, Andrea Artoni, et al.
International Journal of Molecular Sciences|January 11, 2025
Novel <i>KCNQ2</i> Variants Related to a Variable Phenotypic Spectrum Ranging from Epilepsy with Auditory Features to Severe Developmental and Epileptic EncephalopathiesMariagrazia Talarico, Radha Procopio, Monica Gagliardi, et al.
Genes|November 27, 2024
Two Novel Variants in the <i>CHRNA2</i> and <i>SCN2A</i> Genes in Italian Patients with Febrile SeizuresRadha Procopio, Monica Gagliardi, Mariagrazia Talarico, et al.
Neurology. Genetics|December 31, 2025
Characterization of Sleep in Alternating Hemiplegia of Childhood: An International SurveyFrancesco Fortunato, Umesh Vivekananda, Katherine Elizabeth Behl, et al.
Pageof 12