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

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

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

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

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

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

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

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

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

10. ALS/FTD phenotype in two Sardinian families carrying both C9ORF72 and TARDBP mutations

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

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

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

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

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

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

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

18. Assessing the Metabolomic Profile of Multiple Sclerosis Patients Treated with Interferon Beta 1a by 1 H-NMR Spectroscopy.

19. Cardiac Abnormalities in Alzheimer Disease: Clinical Relevance Beyond Pathophysiological Rationale and Instrumental Findings?

20. (1)H-NMR analysis provides a metabolomic profile of patients with multiple sclerosis.

21. Vitamin D responsive elements within the HLA-DRB1 promoter region in Sardinian multiple sclerosis associated alleles.

22. Parkin Exon Rearrangements and Sequence Variants in LRRK2 Mutations Carriers: Analysis on a Possible Modifier Effect on LRRK2 Penetrance.

23. Multiple sclerosis in Sardinia is associated and in linkage disequilibrium with HLA-DR3 and -DR4 alleles.

25. Influence of dehydroepiandrosterone on G-6-PD activity and 3H-thymidine uptake of human lymphocytes in vitro.

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