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Your search keyword '"Volanti P"' showing total 45 results

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45 results on '"Volanti P"'

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

2. Identifying clinical complexity in patients affected by severe acquired brain injury in neurorehabilitation: a cross sectional survey

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

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

5. The HFE H63D (p.His63Asp) polymorphism is a modifier of ALS outcome in Italian and French patients with SOD1 mutations

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

7. The MITOS system predicts long-term survival in amyotrophic lateral sclerosis

8. Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72

10. Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

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

13. Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

14. Large proportion of amyotrophic lateral sclerosis cases in Sardinia due to a single founder mutation of the TARDBP gene

15. A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD

16. Lithium carbonate in amyotrophic lateral sclerosis: lack of efficacy in a dose-finding trial

18. Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis

24. C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population

25. Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72

27. Erythropoietin in amyotrophic lateral sclerosis: a multicentre, randomized, double blind, placebo controlled, phase III study

28. The HFE p.HIS63ASP polymorphism modifies ALS outcome in patients with SOD1 mutations

29. Efficacy of erythropoietin in amyotrophic lateral sclerosis: a multicentre, randomised, double blind, placebo controlled, phase III study (IPOS TRIAL)

30. C9ORF72 in a Large Series of Italian and Sardinian Familial and Sporadic ALS Patients

31. The Italian validation of the Communicative Effectiveness Index Questionnaire: a multicentric study

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

33. Validation of the DYALS (dysphagia in amyotrophic lateral sclerosis) questionnaire for the evaluation of dysphagia in ALS patients

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

35. Clinical features and outcomes of the flail arm and flail leg and pure lower motor neuron MND variants: A multicentre Italian study

36. CSF neurofilament proteins as diagnostic and prognostic biomarkers for amyotrophic lateral sclerosis

37. Comparative Analysis of C9orf72 and Sporadic Disease in a Large Multicenter ALS Population: The Effect of Male Sex on Survival of C9orf72 Positive Patients

38. Plasma cortisol level in amyotrophic lateral sclerosis

39. MARITAL STATUS IS A PROGNOSTIC FACTOR IN AMYOTROPHIC LATERAL SCLEROSIS

40. Predictors of non-invasive ventilation tolerance in amyotrophic lateral sclerosis

41. Response to the letter to the Editor: Comments on marital status is a prognostic factor in amyotrophic lateral sclerosis. Safiri S et al

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

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

44. C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population

45. Carcinoma of the tongue and bulbar-onset amyotrophic lateral sclerosis: unusual differential diagnosis

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