173 results on '"le Forestier, Nadine"'
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2. Development of new outcome measures for adult SMA type III and IV: a multimodal longitudinal study
3. The motor unit number index (MUNIX) profile of patients with adult spinal muscular atrophy
4. Phenotype Presentation and Molecular Diagnostic Yield in Non-5q Spinal Muscular Atrophy
5. Les passeurs de mots
6. Extrapyramidal deficits in ALS: a combined biomechanical and neuroimaging study
7. Predictive factors for prognosis after gastrostomy placement in routine non-invasive ventilation users ALS patients
8. Genetic screening of ANXA11 revealed novel mutations linked to amyotrophic lateral sclerosis
9. Radiation Therapy for Hypersalivation: A Prospective Study in 50 Amyotrophic Lateral Sclerosis Patients
10. Detection of ATXN2 Expansions in an Exome Dataset: An Underdiagnosed Cause of Parkinsonism.
11. Traitement de la sialorrhée dans la sclérose latérale amyotrophique et la maladie de Parkinson par radiothérapie des glandes salivaires : analyse de 281 cas
12. Muscle cells of sporadic amyotrophic lateral sclerosis patients secrete neurotoxic vesicles
13. Muscle cells of sporadic ALS patients secrete neurotoxic vesicles
14. Normalities are not the Only Answer for Amyotrophic Lateral Sclerosis Patients
15. Fronto-temporal lobar degeneration: neuropathology in 60 cases
16. Caractérisation des macrophages dans les formes familiales et sporadiques de Sclérose Latérale Amyotrophique (SLA)
17. La maladie d’Alexander à révélation adulte : une clinique variable mais des images IRM stéréotypées
18. L'annonce diagnostique de la sclérose latérale amyotrophique : une éthique de la réalité
19. Phenotype difference between ALS patients with expanded repeats in C9ORF72 and patients with mutations in other ALS-related genes
20. Electrophysiological diagnosis of motor neuron disease and pure motor neuropathy
21. SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype–phenotype correlations
22. Extrapyramidal stiffness in patients with amyotrophic lateral sclerosis
23. Primary lateral sclerosis
24. Lewis-Sumner Syndrome and Tangier Disease
25. Does primary lateral sclerosis exist?: A study of 20 patients and a review of the literature
26. Mutations in UBQLN2 are rare in French amyotrophic lateral sclerosis
27. Outcome of gastrostomy in parkinsonism: A retrospective study
28. Cursive Eye-Writing With Smooth-Pursuit Eye-Movement Is Possible in Subjects With Amyotrophic Lateral Sclerosis
29. The spinal and cerebral profile of adult spinal-muscular atrophy: A multimodal imaging study
30. Emotional feeling in patients suffering from amyotrophic lateral sclerosis
31. Screening of OPTN in French familial amyotrophic lateral sclerosis
32. The French national protocol for Kennedy's disease (SBMA): consensus diagnostic and management recommendations.
33. Traitement de la spasticité des masséters par injections de toxine botulique chez des patients atteints de sclérose latérale amyotrophique
34. D’incertitudes en vérité d’accompagnements au cours des annonces lors de la maladie incurable en neurologie
35. Correction: Cervical Spinal Cord Atrophy Profile in Adult SMN1-Linked SMA
36. Les Passeurs de mots. Une éthique philosophique du soin : à propos d’une enquête nationale au sein des Centres SLA de France
37. Émotions ressenties chez des patients atteints de sclérose latérale amyotrophique.
38. Cervical Spinal Cord Atrophy Profile in Adult SMN1-Linked SMA
39. Plasma Peptide Biomarker Discovery for Amyotrophic Lateral Sclerosis by MALDI –TOF Mass Spectrometry Profiling
40. Validation of robust tools to measure sialorrhea in amyotrophic lateral sclerosis: A study in a large French cohort
41. Predicting Survival of Patients with Amyotrophic Lateral Sclerosis at Presentation: A 15-Year Experience
42. Prise en charge nutritionnelle dans la sclérose latérale amyotrophique : un enjeu médical et éthique
43. Phenotype difference between ALS patients with expanded repeats inC9ORF72and patients with mutations in other ALS-related genes
44. Safety of home parenteral nutrition in patients with amyotrophic lateral sclerosis: A French national survey
45. Impaired glucose tolerance in patients with amyotrophic lateral sclerosis
46. Causes of death in a post‐mortem series of ALS patients
47. Muscle Nogo-a expression is a prognostic marker in lower motor neuron syndromes
48. Affections du motoneurone : la sclérose latérale amyotrophique
49. Neuropsychological changes in patients with primary lateral sclerosis
50. Glutamate levels in cerebrospinal fluid in amyotrophic lateral sclerosis: a reappraisal using a new HPLC method with coulometric detection in a large cohort of patients
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