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Charlotte Lilien

Showing results (1-10 of 15) with videos related to

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Trends in Molecular Medicine|January 10, 2025
Pushing the boundaries: future directions in the management of spinal muscular atrophyFiona Moultrie, Laura Chiverton, Isabel Hatami, et al.
Neuromuscular Disorders : NMD|June 1, 2025
A systematic review on motor outcome measures in congenital myopathyMatthew Woods, Gemma Fisher, Sarah Johnson, et al.
Medecine Sciences : M/S|December 21, 2019
[French adaptation of motor function scales for patients with spinal muscular atrophy]Christelle Pons, Aurélie Barrière, Guillaume Bertrand, et al.
Journal of Visualized Experiments : Jove|August 27, 2019
Home-Based Monitor for Gait and Activity AnalysisCharlotte Lilien, Erwan Gasnier, Teresa Gidaro, et al.
Journal of Neuromuscular Diseases|August 25, 2025
Rehabilitation research in spinal muscular atrophy: a call to actionCharlotte Lilien, Leslie Nelson, Lisa Edel, et al.
Journal of Neuromuscular Diseases|October 31, 2022
Clinical Trial Readiness for Spinal Muscular Atrophy: Experience of an International Educational-Training InitiativeEduardo F Tizzano, Vanessa Christie-Brown, Giovanni Baranello, et al.
Orphanet Journal of Rare Diseases|January 7, 2021
Hierarchical Bayesian modelling of disease progression to inform clinical trial design in centronuclear myopathyEve Fouarge, Arnaud Monseur, Bruno Boulanger, et al.
Journal of Clinical Medicine|June 27, 2024
Patients' Perceptions of Nusinersen Effects According to Their Responder StatusCharlotte Lilien, Eva Vrscaj, Gita Thapaliya, et al.
Annals of Clinical and Translational Neurology|August 28, 2021
Upper limb disease evolution in exon 53 skipping eligible patients with Duchenne muscular dystrophyCharlotte Lilien, Harmen Reyngoudt, Andreea Mihaela Seferian, et al.
Respiratory Research|September 16, 2024
An algorithm for discontinuing mechanical ventilation in boys with x-linked myotubular myopathy after positive response to gene therapy: the ASPIRO experienceRobert J Graham, Reshma Amin, Nadir Demirel, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Trends in Molecular Medicine|January 10, 2025
Pushing the boundaries: future directions in the management of spinal muscular atrophyFiona Moultrie, Laura Chiverton, Isabel Hatami, et al.
Neuromuscular Disorders : NMD|June 1, 2025
A systematic review on motor outcome measures in congenital myopathyMatthew Woods, Gemma Fisher, Sarah Johnson, et al.
Medecine Sciences : M/S|December 21, 2019
[French adaptation of motor function scales for patients with spinal muscular atrophy]Christelle Pons, Aurélie Barrière, Guillaume Bertrand, et al.
Journal of Visualized Experiments : Jove|August 27, 2019
Home-Based Monitor for Gait and Activity AnalysisCharlotte Lilien, Erwan Gasnier, Teresa Gidaro, et al.
Journal of Neuromuscular Diseases|August 25, 2025
Rehabilitation research in spinal muscular atrophy: a call to actionCharlotte Lilien, Leslie Nelson, Lisa Edel, et al.
Journal of Neuromuscular Diseases|October 31, 2022
Clinical Trial Readiness for Spinal Muscular Atrophy: Experience of an International Educational-Training InitiativeEduardo F Tizzano, Vanessa Christie-Brown, Giovanni Baranello, et al.
Orphanet Journal of Rare Diseases|January 7, 2021
Hierarchical Bayesian modelling of disease progression to inform clinical trial design in centronuclear myopathyEve Fouarge, Arnaud Monseur, Bruno Boulanger, et al.
Journal of Clinical Medicine|June 27, 2024
Patients' Perceptions of Nusinersen Effects According to Their Responder StatusCharlotte Lilien, Eva Vrscaj, Gita Thapaliya, et al.
Annals of Clinical and Translational Neurology|August 28, 2021
Upper limb disease evolution in exon 53 skipping eligible patients with Duchenne muscular dystrophyCharlotte Lilien, Harmen Reyngoudt, Andreea Mihaela Seferian, et al.
Respiratory Research|September 16, 2024
An algorithm for discontinuing mechanical ventilation in boys with x-linked myotubular myopathy after positive response to gene therapy: the ASPIRO experienceRobert J Graham, Reshma Amin, Nadir Demirel, et al.
Pageof 2