Familial ALS-superoxide dismutases associate with mitochondria and shift their redox potentials, Ferri, A., Cozzolino M., Crosio C., Nencini M., Casciati Arianna, Gralla E.B., Rotilio G., Valentine J.S., and Carrì M.T. , Proceedings of the National Academy of Sciences of the United States of America, Volume 103, Number 37, p.13860-13865, (2006)

Cell death in amyotrophic lateral sclerosis: Interplay between neuronal and glial cells, Ferri, A., Nencini M., Casciati Arianna, Cozzolino M., Angelini D.F., Longone P., Spalloni A., Rotilio G., and Carrì M.T. , FASEB Journal, Volume 18, Number 11, p.1261-1263, (2004)

Overexpression of superoxide dismutase 1 protects against β-amyloid peptide toxicity: Effect of estrogen and copper chelators, Celsi, F., Ferri A., Casciati Arianna, D'Ambrosi N., Rotilio G., Costa A., Volonté C., and Carrì M.T. , Neurochemistry International, Volume 44, Number 1, p.25-33, (2004)

Mitochondrial dysfunction due to mutant copper/zinc superoxide dismutase associated with amyotrophic lateral sclerosis is reversed by N-acetylcysteine, Beretta, S., Sala G., Mattavelli L., Ceresa C., Casciati Arianna, Ferri A., Carrì M.T., and Ferrarese C. , Neurobiology of Disease, Volume 13, Number 3, p.213-221, (2003)

Oxidative modulation of nuclear factor-κB in human cells expressing mutant fALS-typical superoxide dismutases, Casciati, Arianna, Ferri A., Cozzolino M., Celsi F., Nencini M., Rotilio G., and Carrì M.T. , Journal of Neurochemistry, Volume 83, Number 5, p.1019-1029, (2002)

Copper-dependent oxidative stress, alteration of signal transduction and neurodegeneration in amyotrophic lateral sclerosis, Carrì, M.T., Ferri A., Casciati Arianna, Celsi F., Ciriolo M.R., and Rotilio G. , Functional Neurology, Volume 16, Number 4 SUPPL., p.181-188, (2001)

Neurochemistry of SOD1 and familial amyotrophic lateral sclerosis, Currì, M.T., Ceroni M., Ferri A., Gabbianelli R., Casciati Arianna, and Costa A. , Functional Neurology, Volume 16, Number 1, p.73-82, (2001)

Oxidative inactivation of calcineurin by Cu,Zn superoxide dismutase G93A, a mutant typical of familial amyotrophic lateral sclerosis, Ferri, A., Gabbianelli R., Casciati Arianna, Celsi F., Rotilio G., and Carrì M.T. , Journal of Neurochemistry, Volume 79, Number 3, p.531-538, (2001)

Calcineurin activity is regulated both by redox compounds and by mutant familial amyotrophic lateral sclerosis-superoxide dismutase, Ferri, A., Gabbianelli R., Casciati Arianna, Paolucci E., Rotilio G., and Carrì M.T. , Journal of Neurochemistry, Volume 75, Number 2, p.606-613, (2000)