Laurent Servais

Institut I-Motion, Institut de Myologie

Affiliated withInstitut de Myologie CHRMN

Research Area

Biography

Laurent Servais has not added Biography.
If you are Laurent Servais and would like to personalize this page please email our Author Liaison for assistance.

JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 23	2019

Other Publications

Article	Year
Pregnancy in congenital myasthenic syndrome. Journal of neurology\| PubMed ID: 23108489	2013
Innovative methods to assess upper limb strength and function in non-ambulant Duchenne patients. Neuromuscular disorders : NMD\| PubMed ID: 23219352	2013
Distinctive serum miRNA profile in mouse models of striated muscular pathologies. PloS one\| PubMed ID: 23418438	2013
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\| PubMed ID: 24321374	2014
Proteomics profiling of urine reveals specific titin fragments as biomarkers of Duchenne muscular dystrophy. Neuromuscular disorders : NMD\| PubMed ID: 24813925	2014
Four-year longitudinal study of clinical and functional endpoints in sporadic inclusion body myositis: implications for therapeutic trials. Neuromuscular disorders : NMD\| PubMed ID: 24857365	2014
Congenital muscular dystrophy phenotype with neuromuscular spindles excess in a 5-year-old girl caused by HRAS mutation. Neuromuscular disorders : NMD\| PubMed ID: 25070542	2014
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\| PubMed ID: 25200009	2014
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\| PubMed ID: 25209738	2014
Severe dystonia, cerebellar atrophy, and cardiomyopathy likely caused by a missense mutation in TOR1AIP1. Orphanet journal of rare diseases\| PubMed ID: 25425325	2014
Evaluation of the serum matrix metalloproteinase-9 as a biomarker for monitoring disease progression in Duchenne muscular dystrophy. Neuromuscular disorders : NMD\| PubMed ID: 25791581	2015
Serum proteomic profiling reveals fragments of MYOM3 as potential biomarkers for monitoring the outcome of therapeutic interventions in muscular dystrophies. Human molecular genetics\| PubMed ID: 26060189	2015
Abnormal Glycosylation Profile and High Alpha-Fetoprotein in a Patient with Twinkle Variants. JIMD reports\| PubMed ID: 26920903	2016
A Movement Monitor Based on Magneto-Inertial Sensors for Non-Ambulant Patients with Duchenne Muscular Dystrophy: A Pilot Study in Controlled Environment. PloS one\| PubMed ID: 27271157	2016
Mild clinical presentation in KLHL40-related nemaline myopathy (NEM 8). Neuromuscular disorders : NMD\| PubMed ID: 27528495	2016
Impaired Presynaptic High-Affinity Choline Transporter Causes a Congenital Myasthenic Syndrome with Episodic Apnea. American journal of human genetics\| PubMed ID: 27569547	2016
Non-Ambulant Duchenne Patients Theoretically Treatable by Exon 53 Skipping have Severe Phenotype. Journal of neuromuscular diseases\| PubMed ID: 27858743	2015
Downregulation of the Glial GLT1 Glutamate Transporter and Purkinje Cell Dysfunction in a Mouse Model of Myotonic Dystrophy. Cell reports\| PubMed ID: 28658620	2017
Long-term microdystrophin gene therapy is effective in a canine model of Duchenne muscular dystrophy. Nature communications\| PubMed ID: 28742067	2017
DMD and West syndrome. Neuromuscular disorders : NMD\| PubMed ID: 28802771	2017
Downregulation of myostatin pathway in neuromuscular diseases may explain challenges of anti-myostatin therapeutic approaches. Nature communications\| PubMed ID: 29192144	2017
High urinary ferritin reflects myoglobin iron evacuation in DMD patients. Neuromuscular disorders : NMD\| PubMed ID: 29776718	2018
Nusinersen in patients older than 7 months with spinal muscular atrophy type 1: A cohort study. Neurology\| PubMed ID: 30158155	2018
X-linked myotubular myopathy: A prospective international natural history study. Neurology\| PubMed ID: 30902907	2019