Shams Ribault
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View article: Striking the Balance: Embracing Technology While Upholding Humanistic Principles in Neurorehabilitation
Striking the Balance: Embracing Technology While Upholding Humanistic Principles in Neurorehabilitation Open
Background The rapid advancement of technology-focused strategies in neurorehabilitation has brought optimism to individuals with neurological disorders, caregivers, and physicians while reshaping medical practice and training. Objectives …
View article: To other new educational ways for interdisciplinary cooperation and innovation: about a student-driven hackathon
To other new educational ways for interdisciplinary cooperation and innovation: about a student-driven hackathon Open
Background Teaching and learning interdisciplinarity are key features in medical education, to prepare students to their future practice. Hackathons are an innovative approach to promote team working and demonstrated an interest in higher …
View article: A protocol for a systematic review on motivation assessments in ABI patients: a survey of available tools
A protocol for a systematic review on motivation assessments in ABI patients: a survey of available tools Open
Acquired Brain Injury (ABI) is a term that covers several aetiologies, including stroke and traumatic brain injury. Patients with ABI can experience a range of symptoms, both physical and cognitive, that can limit their quality of life and…
View article: Psychometric Characteristics of the Motor Function Measure in Neuromuscular Diseases: A Systematic Review1
Psychometric Characteristics of the Motor Function Measure in Neuromuscular Diseases: A Systematic Review1 Open
Background: Recent pharmaceutical breakthroughs in neuromuscular diseases may considerably change the prognosis and natural history these diseases. The ability to measure clinically relevant outcomes such as motor function is critical for …
View article: Homozygous <i>COQ7</i> mutation: a new cause of potentially treatable distal hereditary motor neuropathy
Homozygous <i>COQ7</i> mutation: a new cause of potentially treatable distal hereditary motor neuropathy Open
Distal hereditary motor neuropathy represents a group of motor inherited neuropathies leading to distal weakness. We report a family of two brothers and a sister affected by distal hereditary motor neuropathy in whom a homozygous variant c…
View article: Correction to: Use of MFM-20 to monitor SMA types 1 and 2 patients treated with nusinersen
Correction to: Use of MFM-20 to monitor SMA types 1 and 2 patients treated with nusinersen Open
View article: Severe congenital myasthenic syndromes caused by agrin mutations affecting secretion by motoneurons
Severe congenital myasthenic syndromes caused by agrin mutations affecting secretion by motoneurons Open
Congenital myasthenic syndromes (CMS) are predominantly characterized by muscle weakness and fatigability and can be caused by a variety of mutations in genes required for neuromuscular junction formation and maintenance. Among them, AGRN …
View article: Expanding the phenotypic variability of <i>MORC2</i> gene mutations: From Charcot‐Marie‐Tooth disease to late‐onset pure motor neuropathy
Expanding the phenotypic variability of <i>MORC2</i> gene mutations: From Charcot‐Marie‐Tooth disease to late‐onset pure motor neuropathy Open
MORC2 gene encodes a ubiquitously expressed nuclear protein involved in chromatin remodeling, DNA repair, and transcriptional regulation. Heterozygous mutations in MORC2 gene have been associated with a spectrum of disorders affecting the …
View article: To other new educational ways for interdisciplinary cooperation and innovation: about a student-driven hackathon
To other new educational ways for interdisciplinary cooperation and innovation: about a student-driven hackathon Open
Background: Innovation in healthcare cannot be conceived without an interdisciplinary approach. Hackathons are an innovative approach to promote team working and demonstrated an interest in higher education through inquiry-based learning. …
View article: New MORC2 gene mutations are associated with distinctive features: from axonal neuropathy to late adult-onset spinal muscular atrophy like phenotype
New MORC2 gene mutations are associated with distinctive features: from axonal neuropathy to late adult-onset spinal muscular atrophy like phenotype Open
MORC2 gene encodes a ubiquitously expressed nuclear protein involved in chromatin remodeling, DNA repair, and transcriptional regulation. Heterozygous mutations in MORC2 gene have been associated with a spectrum of disorders affecting the …
View article: Medical student engagement in a massive COVID‐19‐screening programme
Medical student engagement in a massive COVID‐19‐screening programme Open
International audience
View article: Limited evidence of physical therapy on balance after stroke: A systematic review and meta-analysis
Limited evidence of physical therapy on balance after stroke: A systematic review and meta-analysis Open
Functional task-training associated with musculoskeletal intervention and/or cardiopulmonary intervention and sensory interventions seem to be immediately effective in improving balance and postural stability, respectively. The heterogenei…
GLUcose COntrol Safety & Efficacy in type 2 DIabetes, a systematic review and NETwork meta-analysis Open