Marianna Castelli

Mutations in CYP2U1, DDHD2 and GBA2 genes are rare causes of complicated forms of hereditary spastic paraparesis

N. Bresolin, A. Martinuzzi, M. Filosto, 2014, Journal of Neurology.

ZFYVE26/SPASTIZIN and SPG11/SPATACSIN mutations in hereditary spastic paraplegia types AR-SPG15 and AR-SPG11 have different effects on autophagy and endocytosis

E. Clementi, F. Santorelli, C. Vantaggiato, 2018, Autophagy.

Novel SETX variants in a patient with ataxia, neuropathy, and oculomotor apraxia are associated with normal sensitivity to oxidative DNA damaging agents

N. Bresolin, R. Borgatti, C. Vantaggiato, 2014, Brain and Development.

The Fine Tuning of Drp1-Dependent Mitochondrial Remodeling and Autophagy Controls Neuronal Differentiation

E. Clementi, C. Vantaggiato, M. Bassi, 2019, Front. Cell. Neurosci..

A novel heterozygous SETX mutation in a patient presenting with chorea and motor neuron disease

I. Appollonio, C. Ferrarese, M. Bassi, 2014, Amyotrophic lateral sclerosis & frontotemporal degeneration.