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Marika Pane

Showing results (41-50 of 221) with videos related to

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Muscle & Nerve|January 20, 2025
Pregnancy in the Era of Disease-Modifying Therapies for Spinal Muscular Atrophy: Considerations From a Case ReportGabriele Vadi, Sara Loprieno, Francesca Torri, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|December 13, 2023
Cognitive function in DMD carriers: personal case series and literature reviewLaura Carraro, Arianna Iosca, Maria Irene Dainesi, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|June 2, 2005
Prognostic value of EEG performed at term age in preterm infantsTeresa Randò, Daniela Ricci, Rita Luciano, et al.
Molecular Neurobiology|November 26, 2024
High Expression of SMN circ4-2b-3 in SMA I Children Treated with Nusinersen is Associated with Improved Motor OutcomesMarika Guerra, Alberto Marini, Vittoria Pagliarini, et al.
Neuromuscular Disorders : NMD|March 29, 2005
Muscle MRI in Ullrich congenital muscular dystrophy and Bethlem myopathyEugenio Mercuri, Anne Lampe, Joanna Allsop, et al.
Neuromuscular Disorders : NMD|November 15, 2017
Expanded access program with Nusinersen in SMA type I in Italy: Strengths and pitfalls of a successful experienceSonia Messina, Marika Pane, Valeria Sansone, et al.
Archives of Neurology|September 14, 2011
Muscle magnetic resonance imaging in congenital myopathies due to ryanodine receptor type 1 gene mutationsAndrea Klein, Heinz Jungbluth, Emma Clement, et al.
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.
Developmental Medicine and Child Neurology|September 4, 2024
Parental diagnostic delay and developmental outcomes in congenital and childhood-onset myotonic dystrophy type 1Federica Trucco, Emilio Albamonte, Marika Pane, et al.
Neuromuscular Disorders : NMD|February 8, 2005
Muscle MRI findings in patients with limb girdle muscular dystrophy with calpain 3 deficiency (LGMD2A) and early contracturesEugenio Mercuri, Kate Bushby, Enzo Ricci, et al.
Pageof 23

Showing results (41-50 of 221) with videos related to

Sort By:
Pageof 23
Muscle & Nerve|January 20, 2025
Pregnancy in the Era of Disease-Modifying Therapies for Spinal Muscular Atrophy: Considerations From a Case ReportGabriele Vadi, Sara Loprieno, Francesca Torri, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|December 13, 2023
Cognitive function in DMD carriers: personal case series and literature reviewLaura Carraro, Arianna Iosca, Maria Irene Dainesi, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|June 2, 2005
Prognostic value of EEG performed at term age in preterm infantsTeresa Randò, Daniela Ricci, Rita Luciano, et al.
Molecular Neurobiology|November 26, 2024
High Expression of SMN circ4-2b-3 in SMA I Children Treated with Nusinersen is Associated with Improved Motor OutcomesMarika Guerra, Alberto Marini, Vittoria Pagliarini, et al.
Neuromuscular Disorders : NMD|March 29, 2005
Muscle MRI in Ullrich congenital muscular dystrophy and Bethlem myopathyEugenio Mercuri, Anne Lampe, Joanna Allsop, et al.
Neuromuscular Disorders : NMD|November 15, 2017
Expanded access program with Nusinersen in SMA type I in Italy: Strengths and pitfalls of a successful experienceSonia Messina, Marika Pane, Valeria Sansone, et al.
Archives of Neurology|September 14, 2011
Muscle magnetic resonance imaging in congenital myopathies due to ryanodine receptor type 1 gene mutationsAndrea Klein, Heinz Jungbluth, Emma Clement, et al.
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.
Developmental Medicine and Child Neurology|September 4, 2024
Parental diagnostic delay and developmental outcomes in congenital and childhood-onset myotonic dystrophy type 1Federica Trucco, Emilio Albamonte, Marika Pane, et al.
Neuromuscular Disorders : NMD|February 8, 2005
Muscle MRI findings in patients with limb girdle muscular dystrophy with calpain 3 deficiency (LGMD2A) and early contracturesEugenio Mercuri, Kate Bushby, Enzo Ricci, et al.
Pageof 23