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448 results on '"Meininger, Vincent"'

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

4. Genome-wide Analyses Identify KIF5A as a Novel ALS Gene

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

6. Author Correction: A ferroptosis–based panel of prognostic biomarkers for Amyotrophic Lateral Sclerosis

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

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

10. A ferroptosis–based panel of prognostic biomarkers for Amyotrophic Lateral Sclerosis

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

15. Reduced Expression of the Kinesin-Associated Protein 3 (KIFAP3) Gene Increases Survival in Sporadic Amyotrophic Lateral Sclerosis

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

18. ATXN2 trinucleotide repeat length correlates with risk of ALS

19. Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study

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

23. Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis

27. C9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: A genome-wide meta-analysis

29. A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis

30. No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis

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

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

34. Comparison between PFN1 and SOD1 mutations in amyotrophic lateral sclerosis.

35. Diffusion tensor imaging and voxel based morphometry study in amyotrophic lateral sclerosis: relationships with motor disability

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

39. A Rare Motor Neuron Deleterious Missense Mutation in the DPYSL3 (CRMP4) Gene is Associated with ALS

40. Investigating the contribution of VAPB/ALS8 loss of function in amyotrophic lateral sclerosis

43. Phenotype difference between ALS patients with expanded repeats in C9ORF72 and patients with mutations in other ALS-related genes

47. SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype–phenotype correlations

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