Laurent Servais Institut I-Motion Institut de Myologie Biography Publications Institution JoVE Articles Laurent Servais has not added a biography. If you are Laurent Servais and would like to personalize this page please email our Author Liaison for assistance. Publications X-linked Myotubular Myopathy: A Prospective International Natural History Study Neurology. Apr, 2019 | Pubmed ID: 30902907 Nusinersen in Patients Older Than 7 Months with Spinal Muscular Atrophy Type 1: A Cohort Study Neurology. Oct, 2018 | Pubmed ID: 30158155 High Urinary Ferritin Reflects Myoglobin Iron Evacuation in DMD Patients Neuromuscular Disorders : NMD. 07, 2018 | Pubmed ID: 29776718 Downregulation of Myostatin Pathway in Neuromuscular Diseases May Explain Challenges of Anti-myostatin Therapeutic Approaches Nature Communications. 11, 2017 | Pubmed ID: 29192144 DMD and West Syndrome Neuromuscular Disorders : NMD. Oct, 2017 | Pubmed ID: 28802771 Long-term Microdystrophin Gene Therapy is Effective in a Canine Model of Duchenne Muscular Dystrophy Nature Communications. 07, 2017 | Pubmed ID: 28742067 Downregulation of the Glial GLT1 Glutamate Transporter and Purkinje Cell Dysfunction in a Mouse Model of Myotonic Dystrophy Cell Reports. 06, 2017 | Pubmed ID: 28658620 Impaired Presynaptic High-Affinity Choline Transporter Causes a Congenital Myasthenic Syndrome with Episodic Apnea American Journal of Human Genetics. 09, 2016 | Pubmed ID: 27569547 Mild Clinical Presentation in KLHL40-related Nemaline Myopathy (NEM 8) Neuromuscular Disorders : NMD. 10, 2016 | Pubmed ID: 27528495 A Movement Monitor Based on Magneto-Inertial Sensors for Non-Ambulant Patients with Duchenne Muscular Dystrophy: A Pilot Study in Controlled Environment PloS One. 2016 | Pubmed ID: 27271157 Abnormal Glycosylation Profile and High Alpha-Fetoprotein in a Patient with Twinkle Variants JIMD Reports. 2016 | Pubmed ID: 26920903 Non-Ambulant Duchenne Patients Theoretically Treatable by Exon 53 Skipping Have Severe Phenotype Journal of Neuromuscular Diseases. Sep, 2015 | Pubmed ID: 27858743 Serum Proteomic Profiling Reveals Fragments of MYOM3 As Potential Biomarkers for Monitoring the Outcome of Therapeutic Interventions in Muscular Dystrophies Human Molecular Genetics. Sep, 2015 | Pubmed ID: 26060189 Evaluation of the Serum Matrix Metalloproteinase-9 As a Biomarker for Monitoring Disease Progression in Duchenne Muscular Dystrophy Neuromuscular Disorders : NMD. May, 2015 | Pubmed ID: 25791581 Severe Dystonia, Cerebellar Atrophy, and Cardiomyopathy Likely Caused by a Missense Mutation in TOR1AIP1 Orphanet Journal of Rare Diseases. Nov, 2014 | Pubmed ID: 25425325 Safety and Efficacy of Drisapersen for the Treatment of Duchenne Muscular Dystrophy (DEMAND II): an Exploratory, Randomised, Placebo-controlled Phase 2 Study The Lancet. Neurology. Oct, 2014 | Pubmed ID: 25209738 Forelimb Treatment in a Large Cohort of Dystrophic Dogs Supports Delivery of a Recombinant AAV for Exon Skipping in Duchenne Patients Molecular Therapy : the Journal of the American Society of Gene Therapy. Nov, 2014 | Pubmed ID: 25200009 Congenital Muscular Dystrophy Phenotype with Neuromuscular Spindles Excess in a 5-year-old Girl Caused by HRAS Mutation Neuromuscular Disorders : NMD. Nov, 2014 | Pubmed ID: 25070542 Four-year Longitudinal Study of Clinical and Functional Endpoints in Sporadic Inclusion Body Myositis: Implications for Therapeutic Trials Neuromuscular Disorders : NMD. Jul, 2014 | Pubmed ID: 24857365 Proteomics Profiling of Urine Reveals Specific Titin Fragments As Biomarkers of Duchenne Muscular Dystrophy Neuromuscular Disorders : NMD. Jul, 2014 | Pubmed ID: 24813925 Pharmacokinetics and Safety of Single Doses of Drisapersen in Non-ambulant Subjects with Duchenne Muscular Dystrophy: Results of a Double-blind Randomized Clinical Trial Neuromuscular Disorders : NMD. Jan, 2014 | Pubmed ID: 24321374 Distinctive Serum MiRNA Profile in Mouse Models of Striated Muscular Pathologies PloS One. 2013 | Pubmed ID: 23418438 Innovative Methods to Assess Upper Limb Strength and Function in Non-ambulant Duchenne Patients Neuromuscular Disorders : NMD. Feb, 2013 | Pubmed ID: 23219352 Pregnancy in Congenital Myasthenic Syndrome Journal of Neurology. Mar, 2013 | Pubmed ID: 23108489 Hembaserad Monitor för gång-och aktivitetsanalys Charlotte Lilien1, Erwan Gasnier1, Teresa Gidaro1, Andreea Seferian1, Marc Grelet2, David Vissière2, Laurent Servais1,3 1Institut I-Motion, Institut de Myologie, 2Sysnav, 3CHRMN JoVE 59668 Bioengineering
Hembaserad Monitor för gång-och aktivitetsanalys Charlotte Lilien1, Erwan Gasnier1, Teresa Gidaro1, Andreea Seferian1, Marc Grelet2, David Vissière2, Laurent Servais1,3 1Institut I-Motion, Institut de Myologie, 2Sysnav, 3CHRMN JoVE 59668 Bioengineering