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Bianca Buchignani

Showing results (11-20 of 24) with videos related to

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Developmental Medicine and Child Neurology|September 5, 2025
Expressive language and social communication abilities in children with spinal muscular atrophy type 1Chiara Brusa, Bianca Buchignani, Chiara Cutri, et al.
Journal of Neuromuscular Diseases|January 8, 2024
Characterization of Phenotypic Variability in Becker Muscular Dystrophy for Clinical Practice and Towards Trial Readiness: A Two-Years Follow up StudyGiulia Ricci, Alessandra Govoni, Francesca Torri, et al.
NMR in Biomedicine|February 23, 2024
Magnetic resonance fingerprinting-based myelin water fraction mapping for the assessment of white matter maturation and integrity in typical development and leukodystrophiesMarta Lancione, Matteo Cencini, Elena Scaffei, et al.
International Journal of Environmental Research and Public Health|August 7, 2021
Parental Distress in the Time of COVID-19: A Cross-Sectional Study on Pediatric Patients with Neuropsychiatric Conditions during LockdownGianluca Sesso, Eleonora Bonaventura, Bianca Buchignani, et al.
Scientific Reports|July 24, 2025
Neurodevelopmental and mental disorders in children with type I and presymptomatic spinal muscular atrophyBianca Buchignani, Giorgia Coratti, Chiara Cutrì, et al.
Neuromuscular Disorders : NMD|September 14, 2023
Profile of cognitive abilities in spinal muscular atrophy type II and III: what is the role of motor impairment?Bianca Buchignani, Gianpaolo Cicala, Federica Moriconi, et al.
Journal of Clinical Medicine|January 21, 2023
A Longitudinal Follow-Up Study of Intellectual Function in Duchenne Muscular Dystrophy over Age: Is It Really Stable?Daniela P R Chieffo, Federica Moriconi, Marika Pane, et al.
Cell Death & Disease|December 10, 2025
A novel mutation in FDX2 provides insights into the pathogenesis of MEOAL mitochondrial neuromuscular diseaseDavide Doni, Deborah Grifagni, Federica Cavion, et al.
Archives of Disease in Childhood|January 30, 2024
Communicative development inventory in type 1 and presymptomatic infants with spinal muscular atrophy: a cohort studyBianca Buchignani, Gianpaolo Cicala, Francesca Cumbo, et al.
Brain Sciences|December 2, 2020
Behavioural and Emotional Changes during COVID-19 Lockdown in an Italian Paediatric Population with Neurologic and Psychiatric DisordersEugenia Conti, Giuseppina Sgandurra, Giacomo De Nicola, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Developmental Medicine and Child Neurology|September 5, 2025
Expressive language and social communication abilities in children with spinal muscular atrophy type 1Chiara Brusa, Bianca Buchignani, Chiara Cutri, et al.
Journal of Neuromuscular Diseases|January 8, 2024
Characterization of Phenotypic Variability in Becker Muscular Dystrophy for Clinical Practice and Towards Trial Readiness: A Two-Years Follow up StudyGiulia Ricci, Alessandra Govoni, Francesca Torri, et al.
NMR in Biomedicine|February 23, 2024
Magnetic resonance fingerprinting-based myelin water fraction mapping for the assessment of white matter maturation and integrity in typical development and leukodystrophiesMarta Lancione, Matteo Cencini, Elena Scaffei, et al.
International Journal of Environmental Research and Public Health|August 7, 2021
Parental Distress in the Time of COVID-19: A Cross-Sectional Study on Pediatric Patients with Neuropsychiatric Conditions during LockdownGianluca Sesso, Eleonora Bonaventura, Bianca Buchignani, et al.
Scientific Reports|July 24, 2025
Neurodevelopmental and mental disorders in children with type I and presymptomatic spinal muscular atrophyBianca Buchignani, Giorgia Coratti, Chiara Cutrì, et al.
Neuromuscular Disorders : NMD|September 14, 2023
Profile of cognitive abilities in spinal muscular atrophy type II and III: what is the role of motor impairment?Bianca Buchignani, Gianpaolo Cicala, Federica Moriconi, et al.
Journal of Clinical Medicine|January 21, 2023
A Longitudinal Follow-Up Study of Intellectual Function in Duchenne Muscular Dystrophy over Age: Is It Really Stable?Daniela P R Chieffo, Federica Moriconi, Marika Pane, et al.
Cell Death & Disease|December 10, 2025
A novel mutation in FDX2 provides insights into the pathogenesis of MEOAL mitochondrial neuromuscular diseaseDavide Doni, Deborah Grifagni, Federica Cavion, et al.
Archives of Disease in Childhood|January 30, 2024
Communicative development inventory in type 1 and presymptomatic infants with spinal muscular atrophy: a cohort studyBianca Buchignani, Gianpaolo Cicala, Francesca Cumbo, et al.
Brain Sciences|December 2, 2020
Behavioural and Emotional Changes during COVID-19 Lockdown in an Italian Paediatric Population with Neurologic and Psychiatric DisordersEugenia Conti, Giuseppina Sgandurra, Giacomo De Nicola, et al.
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