Mariateresa Pizzo

Lack of Mid1, the Mouse Ortholog of the Opitz Syndrome Gene, Causes Abnormal Development of the Anterior Cerebellar Vermis

G. Meroni, M. Pizzo, B. Fontanella, 2010, The Journal of Neuroscience.

Clinical and Genetic Evaluation of a Cohort of Pediatric Patients with Severe Inherited Retinal Dystrophies

S. Banfi, M. Pizzo, M. Mutarelli, 2017, Genes.

miR‐181a/b downregulation exerts a protective action on mitochondrial disease models

M. Zeviani, R. Flavell, Roberta Tammaro, 2019, EMBO molecular medicine.

4-12-2019 miR-181 a / b downregulation exerts a protective action on mitochondrial disease models

Roberta, M. Zeviani, R. Flavell, 2019 .

miR‐181a/b downregulation: a mutation‐independent therapeutic approach for inherited retinal diseases

D. Piccolo, E. Surace, B. Franco, 2022, EMBO molecular medicine.

Genetic epidemiology of inherited retinal diseases in a large patient cohort followed at a single center in Italy

P. Melillo, F. Cremers, S. Banfi, 2022, Scientific Reports.