Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Michele Iacomino

Showing results (1-10 of 71) with videos related to

Pageof 8
Sort By:
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.
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.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|November 9, 2022
Congenital myopathy associated with a novel mutation in <i>MEGF10</i> gene, myofibrillar alteration and progressive courseCarolina Croci, Monica Traverso, Serena Baratto, et al.
Human Gene Therapy|February 23, 2013
Use of a lower dosage liver-detargeted AAV vector to prevent hamster muscular dystrophyIda Luisa Rotundo, Alessio Lancioni, Marco Savarese, et al.
Frontiers in Genetics|January 23, 2023
Case report: <i>LAMC3-</i>associated cortical malformations: Case report of a novel stop-gain variant and literature reviewGiovanni Falcicchio, Antonella Riva, Angela La Neve, et al.
Expert Review of Neurotherapeutics|March 11, 2020
Emerging treatments for progressive myoclonus epilepsiesAntonella Riva, Alberto Guglielmo, Ganna Balagura, et al.
Journal of Pediatric Genetics|September 10, 2021
Complex Neurological Phenotype Associated with a De Novo <i>DHDDS</i> Mutation in a Boy with Intellectual Disability, Refractory Epilepsy, and Movement DisorderGianluca Piccolo, Elisabetta Amadori, Maria Stella Vari, et al.
Brain : a Journal of Neurology|December 20, 2019
Homozygous STXBP1 variant causes encephalopathy and gain-of-function in synaptic transmissionHanna C A Lammertse, Annemiek A van Berkel, Michele Iacomino, et al.
Birth Defects Research|July 17, 2025
Targeted Re-Sequencing of Neural Tube Defects Patients and Families Identifies Rare Variants in Genes Candidate From Animal ModelsFerruccio Romano, Patrizia De Marco, Marzia Ognibene, et al.
Frontiers in Neurology|September 27, 2021
Cortical and Subcortical Network Dysfunction in a Female Patient With <i>NEXMIF</i> EncephalopathyMaria Cristina Cioclu, Antonietta Coppola, Manuela Tondelli, et al.
Pageof 8

Showing results (1-10 of 71) with videos related to

Sort By:
Pageof 8
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.
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.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|November 9, 2022
Congenital myopathy associated with a novel mutation in <i>MEGF10</i> gene, myofibrillar alteration and progressive courseCarolina Croci, Monica Traverso, Serena Baratto, et al.
Human Gene Therapy|February 23, 2013
Use of a lower dosage liver-detargeted AAV vector to prevent hamster muscular dystrophyIda Luisa Rotundo, Alessio Lancioni, Marco Savarese, et al.
Frontiers in Genetics|January 23, 2023
Case report: <i>LAMC3-</i>associated cortical malformations: Case report of a novel stop-gain variant and literature reviewGiovanni Falcicchio, Antonella Riva, Angela La Neve, et al.
Expert Review of Neurotherapeutics|March 11, 2020
Emerging treatments for progressive myoclonus epilepsiesAntonella Riva, Alberto Guglielmo, Ganna Balagura, et al.
Journal of Pediatric Genetics|September 10, 2021
Complex Neurological Phenotype Associated with a De Novo <i>DHDDS</i> Mutation in a Boy with Intellectual Disability, Refractory Epilepsy, and Movement DisorderGianluca Piccolo, Elisabetta Amadori, Maria Stella Vari, et al.
Brain : a Journal of Neurology|December 20, 2019
Homozygous STXBP1 variant causes encephalopathy and gain-of-function in synaptic transmissionHanna C A Lammertse, Annemiek A van Berkel, Michele Iacomino, et al.
Birth Defects Research|July 17, 2025
Targeted Re-Sequencing of Neural Tube Defects Patients and Families Identifies Rare Variants in Genes Candidate From Animal ModelsFerruccio Romano, Patrizia De Marco, Marzia Ognibene, et al.
Frontiers in Neurology|September 27, 2021
Cortical and Subcortical Network Dysfunction in a Female Patient With <i>NEXMIF</i> EncephalopathyMaria Cristina Cioclu, Antonietta Coppola, Manuela Tondelli, et al.
Pageof 8