C. Preziuso

Defective PITRM 1 mitochondrial peptidase is associated with A b amyloidotic neurodegeneration

Amati, M. Zeviani, S. Johansson, 2015 .

Short peptides from leucyl-tRNA synthetase rescue disease-causing mitochondrial tRNA point mutations

Robert W. Taylor, A. Fiorillo, V. Morea, 2015, Human molecular genetics.

Impaired mitochondrial biogenesis is a common feature to myocardial hypertrophy and end-stage ischemic heart failure

Robert W. Taylor, C. Nediani, V. Petrozza, 2016, Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology.

Cardiac mesenchymal stromal cells are a source of adipocytes in arrhythmogenic cardiomyopathy

G. Pontone, A. Dello Russo, M. Capogrossi, 2015, European heart journal.

Defective PITRM 1 mitochondrial peptidase is associated with A amyloidotic neurodegeneration

M. Zeviani, S. Johansson, A. Reyes, 2015 .

Targeting estrogen receptor β as preventive therapeutic strategy for Leber's hereditary optic neuropathy.

M. Montopoli, A. Ghelli, V. Carelli, 2015, Human molecular genetics.

Homozygous NOTCH3 null mutation and impaired NOTCH3 signaling in recessive early-onset arteriopathy and cavitating leukoencephalopathy

R. Lodi, T. Pippucci, C. Tonon, 2015, EMBO molecular medicine.

Defective PITRM1 mitochondrial peptidase is associated with Aβ amyloidotic neurodegeneration

M. Zeviani, S. Johansson, A. Reyes, 2015, EMBO molecular medicine.