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41 results on '"Mora, Gabriele"'

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

6. Safety and efficacy of oral levosimendan in people with amyotrophic lateral sclerosis (the REFALS study): a randomised, double-blind, placebo-controlled phase 3 trial

8. The unfolded protein response in amyotrophic later sclerosis: Results of a phase 2 trial

10. Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

13. Safety and efficacy of nabiximols on spasticity symptoms in patients with motor neuron disease (CANALS): a multicentre, double-blind, randomised, placebo-controlled, phase 2 trial

14. Mutations in the Sphingolipid Pathway Gene SPTLC1 are a Cause of Amyotrophic Lateral Sclerosis

15. Mitochondrial dysfunction in fibroblasts of Multiple System Atrophy

16. A novel p.Ser108LeufsTer15 SOD1 mutation leading to the formation of a premature stop codon in an apparently sporadic ALS patient: insights into the underlying pathomechanisms

17. Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS

18. Genome-Wide Analyses Identify KIF5A as a Novel ALS Gene

20. Mutational analysis of COQ2 in patients with MSA in Italy

21. TBK1 is associated with ALS and ALS-FTD in Sardinian patients

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

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

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

25. Analysis of amyotrophic lateral sclerosis as a multistep process: a population-based modelling study

26. Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study

28. UNC13A influences survival in Italian amyotrophic lateral sclerosis patients: a population-based study

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

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

32. The chromosome 9 ALS and FTD locus is probably derived from a single founder

34. FUS mutations in sporadic amyotrophic lateral sclerosis

35. Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS

36. Consistent bone marrow-derived cell mobilization following repeated short courses of granulocyte–colony-stimulating factor in patients with amyotrophic lateral sclerosis: results from a multicenter prospective trial

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

40. Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data

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