Search

Your search keyword '"Tiloca C"' showing total 81 results

Search Constraints

Start Over You searched for: Author "Tiloca C" Remove constraint Author: "Tiloca C"
81 results on '"Tiloca C"'

Search Results

1. Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (Nature Genetics, (2021), 53, 12, (1636-1648), 10.1038/s41588-021-00973-1)

2. Cerebrospinal fluid phosphorylated neurofilament heavy chain and chitotriosidase in primary lateral sclerosis

3. Association of Variants in the SPTLC1 Gene with Juvenile Amyotrophic Lateral Sclerosis

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

5. Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (vol 53, pg 1636, 2021)

6. Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (Nature Genetics, (2021), 53, 12, (1636-1648), 10.1038/s41588-021-00973-1)

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

8. Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

9. Genetic epidemiology of ALS in Italy: OS2211

10. CSF angiogenin levels in amyotrophic lateral Sclerosis-Frontotemporal dementia spectrum

12. CSF angiogenin levels in amyotrophic lateral Sclerosis-Frontotemporal dementia spectrum

13. NEK1 variants confer susceptibility to amyotrophic lateral sclerosis

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

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

16. Italian debates, studies and experiences concerning reuse projects of dismissed religious heritage

17. CSF angiogenin levels in amyotrophic lateral Sclerosis-Frontotemporal dementia spectrum.

18. Poly(GP) proteins are a useful pharmacodynamic marker for C9ORF72-associated amyotrophic lateral sclerosis

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

20. Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS

21. TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis: identification of novel mutations

22. The validation of the Italian Edinburgh Cognitive and Behavioural ALS Screen (ECAS)

23. Apoptosis induced by proteasome inhibition in human myoblast cultures

24. Screening of the PFN1 gene in sporadic amyotrophic lateral sclerosis and in frontotemporal dementia

26. Novel optineurin mutations in patients with familial and sporadic amyotrophic lateral sclerosis.

28. Genetic epidemiology of ALS in Italy

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

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

33. Cerebrospinal fluid phosphorylated neurofilament heavy chain and chitotriosidase in primary lateral sclerosis

34. CSF angiogenin levels in amyotrophic lateral Sclerosis-Frontotemporal dementia spectrum

35. The validation of the Italian Edinburgh Cognitive and Behavioural ALS Screen (ECAS)

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

37. Mechanism-free repurposing of drugs for C9orf72-related ALS/FTD using large-scale genomic data.

38. Exploring epigenetic drift and rare epivariations in amyotrophic lateral sclerosis by epigenome-wide association study.

40. Motor, cognitive and behavioural profiles of C9orf72 expansion-related amyotrophic lateral sclerosis.

41. Coexistence of Amyotrophic Lateral Sclerosis and Alzheimer's Disease: Case Report and Review of the Literature.

42. TARDBP mutations in a cohort of Italian patients with Parkinson's disease and atypical parkinsonisms.

43. Cerebrospinal fluid phosphorylated neurofilament heavy chain and chitotriosidase in primary lateral sclerosis.

44. PON1 is a disease modifier gene in amyotrophic lateral sclerosis: association of the Q192R polymorphism with bulbar onset and reduced survival.

46. ALS-associated missense and nonsense TBK1 mutations can both cause loss of kinase function.

47. No C9orf72 repeat expansion in patients with primary progressive multiple sclerosis.

48. Characterization of the c9orf72 GC-rich low complexity sequence in two cohorts of Italian and Turkish ALS cases.

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

50. The LRRK2 Variant E193K Prevents Mitochondrial Fission Upon MPP+ Treatment by Altering LRRK2 Binding to DRP1.

Catalog

Books, media, physical & digital resources