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6. Neurofilament Light Chain Levels Interact with Neurodegenerative Patterns and Motor Neuron Dysfunction in Amyotrophic Lateral Sclerosis

8. Long-term safety and efficacy of patisiran for hereditary transthyretin-mediated amyloidosis with polyneuropathy: 12-month results of an open-label extension study

9. Motor unit number index as an individual biomarker: Reference limits of intra-individual variability over time in healthy subjects

10. Antibodies against the node of Ranvier: a real-life evaluation of incidence, clinical features and response to treatment based on a prospective analysis of 1500 sera

15. SORD‐related peripheral neuropathy in a French and Swiss cohort: clinical features, genetic analysis and sorbitol dosage.

18. SORD‐related peripheral neuropathy in a French and Swiss cohort: Clinical features, genetic analyses, and sorbitol dosages.

20. Reply: High prevalence of CHCHD10 mutations in patients with frontotemporal dementia from China

22. Reply: Is CHCHD10 Pro34Ser pathogenic for frontotemporal dementia and amyotrophic lateral sclerosis?

23. Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation

24. Reply: CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosis

27. Reply: Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis?

28. Reply: Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis

29. Reply: Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease

31. Impact of a frequent nearsplice SOD1 variant in amyotrophic lateral sclerosis: optimising SOD1 genetic screening for gene therapy opportunities

33. A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement

35. A phase II−III trial of olesoxime in subjects with amyotrophic lateral sclerosis

36. Mutations of the FHL1 gene cause Emery-Dreifuss muscular dystrophy

37. Effect of familial clustering in the genetic screening of 235 French ALS families

38. Long-term safety and efficacy of patisiran for hereditary transthyretin-mediated amyloidosis with polyneuropathy: 12-month results of an open-label extension study

39. Structural Connectivity Alterations in Amyotrophic Lateral Sclerosis: A Graph Theory Based Imaging Study

40. Reply: MFN2, a new gene responsible for mitochondrial DNA depletion

45. Quantitative muscle MRI study of patients with sporadic inclusion body myositis

47. Assessing the upper motor neuron in amyotrophic lateral sclerosis using the triple stimulation technique: A multicenter prospective study.

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