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Child: Care, Health and Development|December 29, 2021
Perceived impact of lockdown on daily life in children with physical disabilities and their families during the COVID-19 pandemicRoxane Varengue, Sylvain Brochard, Sandra Bouvier, et al.
Pediatric Pulmonology|March 21, 2022
Respiratory management of spinal muscular atrophy type 1 patients treated with NusinersenJoris Menard, Andreea M Seferian, Emmanuelle Fleurence, et al.
Pediatric Critical Care Medicine : a Journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies|June 27, 2017
Thigh Ultrasound Monitoring Identifies Decreases in Quadriceps Femoris Thickness as a Frequent Observation in Critically Ill ChildrenFrederic V Valla, David K Young, Muriel Rabilloud, et al.
Annals of Physical and Rehabilitation Medicine|August 21, 2020
Emerging health challenges for children with physical disabilities and their parents during the COVID-19 pandemic: The ECHO French surveyMarine Cacioppo, Sandra Bouvier, Rodolphe Bailly, et al.
Archives of Physical Medicine and Rehabilitation|June 29, 2014
Rasch analysis of the motor function measure in patients with congenital muscle dystrophy and congenital myopathyCarole Vuillerot, Pascal Rippert, Virginie Kinet, et al.
PLOS Digital Health|January 13, 2025
Use of assistive technology to assess distal motor function in subjects with neuromuscular diseaseDominique Vincent-Genod, Sylvain Roche, Aurélie Barrière, et al.
Brain : a Journal of Neurology|May 2, 2026
Combining SMN2 splicing modifiers with HDAC6 inhibition improves spinal muscular atrophy outcomesAlexis Osseni, Rasha Slika, Laurent Coudert, et al.
Pediatric Physical Therapy : the Official Publication of the Section on Pediatrics of the American Physical Therapy Association|October 26, 2022
Scoring People With Spinal Muscular Atrophy on the Motor Function Measure Using the Microsoft KinectDominique Vincent-Genod, Pascal Rippert, Justine Coton, et al.
Archives of Physical Medicine and Rehabilitation|May 28, 2014
English cross-cultural translation and validation of the neuromuscular score: a system for motor function classification in patients with neuromuscular diseasesCarole Vuillerot, Katherine G Meilleur, Minal Jain, et al.
Neuromuscular Disorders : NMD|November 28, 2020
Long-term follow-up of patients with type 2 and non-ambulant type 3 spinal muscular atrophy (SMA) treated with olesoxime in the OLEOS trialFrancesco Muntoni, Enrico Bertini, Giacomo Comi, et al.
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