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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

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

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

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

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

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

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

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

43. Theme 02 - GENETICS AND GENOMICS.

44. Genetic counselling in ALS: facts, uncertainties and clinical suggestions

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

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

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

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

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

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

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