20182019

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2019

A novel S379A TARDBP mutation associated to late-onset sporadic ALS

Sprovieri, T., Ungaro, C., Perrone, B., Naimo, G. D., Spataro, R., Cavallaro, S., La Bella, V. & Conforti, F. L., Oct 1 2019, In : Neurological Sciences. 40, 10, p. 2111-2118 8 p.

Research output: Contribution to journalArticle

Early and rapidly progressing respiratory failure in a patient with amyotrophic lateral sclerosis: when FVC% is misleading

Crescimanno, G., Romano, M., Spataro, R., La Bella, V. & Marrone, O., Feb 2019, In : Neurological Sciences. 40, 2, p. 421-422 2 p.

Research output: Contribution to journalArticle

Mutations in ATP13A2 (PARK9) are associated with an amyotrophic lateral sclerosis-like phenotype, implicating this locus in further phenotypic expansion

Spataro, R., Kousi, M., Farhan, S. M. K., Willer, J. R., Ross, J. P., Dion, P. A., Rouleau, G. A., Daly, M. J., Neale, B. M., La Bella, V. & Katsanis, N., Apr 16 2019, In : Human Genomics. 13, 1, 1 p.

Research output: Contribution to journalArticle

Open Access

Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis

The ITALSGEN Consortium & The International ALS Genomics Consortium, Jan 1 2019, In : Annals of Neurology.

Research output: Contribution to journalArticle

2018

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

Rossi, D., Volanti, P., Brambilla, L., Colletti, T., Spataro, R. & La Bella, V., Mar 2018, In : Journal of Neurology. 265, 3, p. 510-521 12 p.

Research output: Contribution to journalArticle