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185 results on '"Salachas, François"'

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151. Environmental risk factors for amyotrophic lateral sclerosis: a case-control study in Canada and France.

152. Clinical trials in pediatric ALS: a TRICALS feasibility study.

153. The Amyotrophic Lateral Sclerosis M114T PFN1 Mutation Deregulates Alternative Autophagy Pathways and Mitochondrial Homeostasis.

154. Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology.

155. Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology.

156. Chitotriosidase as biomarker for early stage amyotrophic lateral sclerosis: a multicenter study.

157. Development of new outcome measures for adult SMA type III and IV: a multimodal longitudinal study.

158. Genetic screening of ANXA11 revealed novel mutations linked to amyotrophic lateral sclerosis.

159. Who and Why? Requests for Presymptomatic Genetic Testing for Amyotrophic Lateral Sclerosis/Frontotemporal Dementia vs Huntington Disease.

160. Predictive factors for prognosis after gastrostomy placement in routine non-invasive ventilation users ALS patients.

161. ATXN1 repeat expansions confer risk for amyotrophic lateral sclerosis and contribute to TDP-43 mislocalization.

162. Ultrasound-Induced Blood-Spinal Cord Barrier Opening in Rabbits.

163. Survival of amyotrophic lateral sclerosis patients after admission to the intensive care unit for acute respiratory failure: an observational cohort study.

164. The motor unit number index (MUNIX) profile of patients with adult spinal muscular atrophy.

165. Extrapyramidal deficits in ALS: a combined biomechanical and neuroimaging study.

166. Phenotypic and genotypic studies of ALS cases in ALS-SMA families.

167. Motor neuron disease of paraneoplastic origin: a rare but treatable condition.

168. Multicenter evaluation of neurofilaments in early symptom onset amyotrophic lateral sclerosis.

169. Novel UBQLN2 mutations linked to amyotrophic lateral sclerosis and atypical hereditary spastic paraplegia phenotype through defective HSP70-mediated proteolysis.

170. Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis.

171. Unusual association of amyotrophic lateral sclerosis and myasthenia gravis: A dysregulation of the adaptive immune system?

172. Endplate denervation correlates with Nogo-A muscle expression in amyotrophic lateral sclerosis patients.

173. Radiation therapy for hypersalivation: a prospective study in 50 amyotrophic lateral sclerosis patients.

174. Muscle histone deacetylase 4 upregulation in amyotrophic lateral sclerosis: potential role in reinnervation ability and disease progression.

175. A rare motor neuron deleterious missense mutation in the DPYSL3 (CRMP4) gene is associated with ALS.

176. Mutations in SQSTM1 encoding p62 in amyotrophic lateral sclerosis: genetics and neuropathology.

177. Improving survival in a large French ALS center cohort.

178. Muscle gene expression is a marker of amyotrophic lateral sclerosis severity.

179. Fronto-temporal lobar degeneration: neuropathology in 60 cases.

180. Questioning on the role of D amino acid oxidase in familial amyotrophic lateral sclerosis.

181. FUS mutations in frontotemporal lobar degeneration with amyotrophic lateral sclerosis.

182. Accumulation of TDP-43 and alpha-actin in an amyotrophic lateral sclerosis patient with the K17I ANG mutation.

183. Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis.

184. Amyotrophic lateral sclerosis with neuronal intranuclear protein inclusions.

185. [SLA: a long way since Charcot].

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