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1. Prevalence and motor-functional correlates of frontotemporal-spectrum disorders in a large cohort of non-demented ALS patients

6. Genome-wide structural variant analysis identifies risk loci for non-Alzheimer’s dementias

8. Predictors for progression in amyotrophic lateral sclerosis associated to SOD1 mutation: insight from two population-based registries

10. Safety and efficacy of arimoclomol in patients with early amyotrophic lateral sclerosis (ORARIALS-01): a randomised, double-blind, placebo-controlled, multicentre, phase 3 trial

11. Impact of Universal Use of the McGrath Videolaryngoscope as a Device for All Intubations in the Cardiac Operating Room. A Prospective Before-After VIDEOLAR-CAR Study

12. Construction and Evaluation of a Realistic Low-Cost Model for Training in Chest-Tube Insertion

13. Genetic evaluation of dementia with Lewy bodies implicates distinct disease subgroups.

14. Randomized, double-blind, placebo-controlled trial of rapamycin in amyotrophic lateral sclerosis

15. Control of a hippocampal recurrent excitatory circuit by cannabinoid receptor-interacting protein Gap43

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

20. Factors predicting disease progression in C9ORF72 ALS patients

21. Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture

23. Genome-wide structural variant analysis identifies risk loci for non-Alzheimer’s dementias

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

27. Disentangling the relationship between social cognition, executive functions and behaviour changes in amyotrophic lateral sclerosis

28. Use of the combination of spirometry, arterial blood gas analysis and overnight oximetry to predict the outcomes of patients affected by motor neuron disease: The Milan‐Torin respiratory score (Mi‐To‐RS)

29. High Frequency of Cognitive and Behavioural Impairment in ALS Patients with SOD1 Pathogenic Variants (P5-11.004)

30. Sex-related Differences in ALS Survival and Progression: Insights from a Population-based Study (P6-11.004)

31. Association of Intermediate HTT CAG Repeats with Increased Risk and Disease Severity in Amyotrophic Lateral Sclerosis (P5-11.003)

32. Disentangling the Relationship Between Social Cognition, Executive Functions, and Behaviour Changes in Amyotrophic Lateral Sclerosis (S18.009)

33. High Frequency of Cognitive and Behavioral Impairment in Amyotrophic Lateral Sclerosis Patients with SOD1 Pathogenic Variants

34. Sex Differences in Amyotrophic Lateral Sclerosis Survival and Progression: A Multidimensional Analysis

36. Identifying and predicting amyotrophic lateral sclerosis clinical subgroups: a population-based machine-learning study

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

43. Hereditary motor sensory neuropathy with proximal involvement (HMSN‐P) associated with TFG p.Pro285Leu variant in an Italian family with a motor neuron disease‐like clinical picture

44. Distinct neural signatures of pulvinar in C9orf72 amyotrophic lateral sclerosis mutation carriers and noncarriers

45. Cognitive and Behavioral Features of Patients With Amyotrophic Lateral Sclerosis Who Are Carriers of the TARDBP Pathogenic Variant

46. Calculated Maximal Volume Ventilation (cMVV) as a Marker of Early Respiratory Failure in Amyotrophic Lateral Sclerosis (ALS)

47. Resting‐state fMRI functional connectome of C9orf72 mutation status

49. Clinical and Metabolic Signature of UNC13A rs12608932 Variant in Amyotrophic Lateral Sclerosis

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