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

2. 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)

3. 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)

4. Genetic epidemiology of ALS in Italy: OS2211

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

7. NEK1 variants confer susceptibility to amyotrophic lateral sclerosis

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

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

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

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

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

13. Apoptosis induced by proteasome inhibition in human myoblast cultures

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

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

17. Genetic epidemiology of ALS in Italy

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

41. Elevated Global DNA Methylation Is Not Exclusive to Amyotrophic Lateral Sclerosis and Is Also Observed in Spinocerebellar Ataxia Types 1 and 2.

42. The role of de novo mutations in the development of amyotrophic lateral sclerosis.

43. Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis.

44. Genetic analysis of the SOD1 and C9ORF72 genes in Hungarian patients with amyotrophic lateral sclerosis.

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

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

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

48. Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis.

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

50. C9orf72 repeat expansions are restricted to the ALS-FTD spectrum.

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