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

2. Production of CSSi013-A (9360) iPSC line from an asymptomatic subject carrying an heterozygous mutation in TDP-43 protein

3. Allele-specific silencing as therapy for familial amyotrophic lateral sclerosis caused by the p.G376D TARDBP mutation

6. ALS-linked FUS mutations confer loss and gain of function in the nucleus by promoting excessive formation of dysfunctional paraspeckles

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

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

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

27. ALS-Related Mutant FUS Protein Is Mislocalized to Cytoplasm and Is Recruited into Stress Granules of Fibroblasts from Asymptomatic FUS P525L Mutation Carriers

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

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

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

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

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

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

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

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

39. Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation

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

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

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

44. Intraspinal stem cell transplantation for amyotrophic lateral sclerosis: Ready for efficacy clinical trials?

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

46. Tauroursodeoxycholic acid in the treatment of patients with amyotrophic lateral sclerosis

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

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

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

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