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7. Artificial intelligence and statistical methods for stratification and prediction of progression in amyotrophic lateral sclerosis: A systematic review

8. Predicting assisted ventilation in Amyotrophic Lateral Sclerosis using a mixture of experts and conformal predictors

11. Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosis

14. European Academy of Neurology (EAN) guideline on the management of amyotrophic lateral sclerosis in collaboration with European Reference Network for Neuromuscular Diseases (ERNEURO‐NMD)

17. Mutations in the tail and rod domains of the neurofilament heavy-chain gene increase the risk of ALS

18. European academy of neurology (EAN) guideline on the management of amyotrophic lateral sclerosis in collaboration with European reference network for neuromuscular diseases (ERN EURO-NMD)

20. Creatine Kinase and Respiratory Decline in Amyotrophic Lateral Sclerosis.

21. Profiling tofersen as a treatment of superoxide dismutase 1 amyotrophic lateral sclerosis.

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

25. Impact of diabetes mellitus on the respiratory function of amyotrophic lateral sclerosis patients.

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

28. Skeletal muscle in amyotrophic lateral sclerosis

31. Current challenges in primary lateral sclerosis diagnosis.

32. Genetic variability in sporadic amyotrophic lateral sclerosis

33. Large-scale analyses of CAV1 and CAV2 suggest their expression is higher in post-mortem ALS brain tissue and affects survival

34. Whole genome sequencing analysis reveals post-zygotic mutation variability in monozygotic twins discordant for amyotrophic lateral sclerosis

35. Genetic variability in sporadic amyotrophic lateral sclerosis

36. Large-scale analyses of CAV1 and CAV2 suggest their expression is higher in post-mortem ALS brain tissue and affects survival

37. Respiratory phenotypes in amyotrophic lateral sclerosis as determined by respiratory questions on the Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised and their relation to respiratory tests

38. Genetic variability in sporadic amyotrophic lateral sclerosis

39. Courage-als: a randomized, double-blind phase 3 study designed to improve participant experience and increase the probability of success

40. Large-scale analyses of CAV1 and CAV2 suggest their expression is higher in post-mortem ALS brain tissue and affects survival

41. Whole genome sequencing analysis reveals post-zygotic mutation variability in monozygotic twins discordant for amyotrophic lateral sclerosis

42. Large-scale analyses of CAV1 and CAV2 suggest their expression is higher in post-mortem ALS brain tissue and affects survival

49. Telomere length analysis in amyotrophic lateral sclerosis using large-scale whole genome sequence data

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