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235 results on '"Moglia C"'

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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. The HFE p.H63D (p.His63Asp) Polymorphism Is a Modifier of ALS Outcome in Italian and French Patients with SOD1 Mutations

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

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

8. Markers of blood-brain barrier disruption increase early and persistently in COVID-19 patients with neurological manifestations

9. Effect modification of the association between total cigarette smoking and ALS risk by intensity, duration and time-since-quitting: Euro-MOTOR

10. Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALS

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

12. The diagnostic value of the Italian version of the Edinburgh Cognitive and Behavioral ALS Screen (ECAS)

14. 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)

15. 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)

16. Effect modification of the association between total cigarette smoking and ALS risk by intensity, duration and time-since-quitting: Euro-MOTOR

17. Theme 10 - Disease Stratification and Phenotyping of Patients.

18. Theme 02 - Genetics and Genomics.

20. Brain Metabolic Correlates of Apathy in Amyotrophic Lateral Sclerosis: a 18F-FDG-PET study

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

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

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

24. Multicentre, cross-cultural, population-based, case-control study of physical activity as risk factor for amyotrophic lateral sclerosis

25. Metabolic changes across different levels of cognitive impairment in ALS: a 18F-FDG-PET study

26. Decline of cognitive and behavioral functions in amyotrophic lateral sclerosis: a longitudinal study

27. Association between alcohol exposure and the risk of amyotrophic lateral sclerosis in the Euro-MOTOR study

30. Early weight loss in amyotrophic lateral sclerosis: Outcome relevance and clinical correlates in a population-based cohort

31. Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis

32. Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis

33. Theme 02 - GENETICS AND GENOMICS.

34. ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion

35. Rapamycin treatment for amyotrophic lateral sclerosis protocol for a phase II randomized, double-blind, placebo-controlled, multicenter, clinical trial (RAP-ALS trial)

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

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

38. Cardiovascular diseases may play a negative role in the prognosis of amyotrophic lateral sclerosis

39. HFE p.H63D polymorphism does not influence ALS phenotype and survival

40. A case-control study of hormonal exposures as etiologic factors for ALS in women

41. A Multicentric Prospective Incidence Study of Guillain-Barré Syndrome in Italy. The ITANG Study

43. Cardiovascular diseases may play a negative role in the prognosis of amyotrophic lateral sclerosis

45. Factors predicting survival in ALS: a multicenter Italian study

46. CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients

47. Correlation between Apolipoprotein E genotype and brain metabolism in amyotrophic lateral sclerosis.

48. ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion

49. Monocytes of patients with amyotrophic lateral sclerosis linked to gene mutations display altered TDP-43 subcellular distribution

50. ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry

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