Raffaele Lopreiato

Mutations in PMCA2 and hereditary deafness: a molecular analysis of the pump defect.

Ernesto Carafoli, M. Giacomello, M. Brini, 2011, Cell calcium.

Mitochondrial fission and cristae disruption increase the response of cell models of Huntington's disease to apoptotic stimuli

Ernesto Carafoli, Luca Scorrano, L. Scorrano, 2010, EMBO molecular medicine.

A novel PMCA3 mutation in an ataxic patient with hypomorphic phosphomannomutase 2 (PMM2) heterozygote mutations: Biochemical characterization of the pump defect.

Giuseppe Zanotti, Ernesto Carafoli, Enza Maria Valente, 2017, Biochimica et biophysica acta. Molecular basis of disease.

Functional homology between yeast piD261/Bud32 and human PRPK: both phosphorylate p53 and PRPK partially complements piD261/Bud32 deficiency

G. Carignani, M. Montenarh, C. Götz, 2003, FEBS letters.