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You searched for: Author/Creator Barberis, Marco

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1. A familial amyotrophic lateral sclerosis pedigree discordant for a novel p.Glu46Asp heterozygous OPTN variant and the p.Ala5Val heterozygous SOD1 missense mutation. (May 2020)

2. A novel p.E121G heterozygous missense mutation of SOD1 in an apparently sporadic ALS case with a 14-year course. Issue 1 (March 2015)

3. ALS phenotype is influenced by age, sex, and genetics: A population-based study. (25th February 2020)

4. Amyotrophic lateral sclerosis onset after prolonged treatment with a VEGF receptors inhibitor. Issue 1 (March 2015)

5. Cognitive impairment across ALS clinical stages in a population-based cohort. (3rd September 2019)

6. Common polymorphisms of chemokine (C‐X3‐C motif) receptor 1 gene modify amyotrophic lateral sclerosis outcome: A population‐based study. Issue 2 (25th April 2017)

7. Differential Neuropsychological Profile of Patients With Amyotrophic Lateral Sclerosis With and Without C9orf72 Mutation. (5th January 2021)

8. Exploring the phenotype of Italian patients with ALS with intermediate ATXN2 polyQ repeats. Issue 11 (25th August 2022)

9. GBA variants influence cognitive status in amyotrophic lateral sclerosis. Issue 4 (28th September 2021)

10. Identifying and predicting amyotrophic lateral sclerosis clinical subgroups: a population-based machine-learning study. Issue 5 (May 2022)