Costanza Lamperti

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 5

Top Topics

Ejection Fraction

Top Venues

Orphanet journal of rare diseases

Neurology. Genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Daniele Sala, Silvia Marchet, Lorenzo Nanetti, Andrea Legati, Caterina Mariotti, Eleonora Lamantea, Daniele Ghezzi, Alessia Catania, Costanza Lamperti
A novel MT-ATP6 variant associated with complicated ataxia in two unrelated Italian patients: case report and functional studies. Orphanet journal of rare diseases 19 (1) (2024)
Daniele Sala, Silvia Marchet, Lorenzo Nanetti, Andrea Legati, Caterina Mariotti, Eleonora Lamantea, Daniele Ghezzi, Alessia Catania, Costanza Lamperti
A novel MT-ATP6 variant associated with complicated ataxia in two unrelated Italian patients: case report and functional studies. Orphanet journal of rare diseases 19 (1) (2024)
Daniele Sala, Silvia Marchet, Lorenzo Nanetti, Andrea Legati, Caterina Mariotti, Eleonora Lamantea, Daniele Ghezzi, Alessia Catania, Costanza Lamperti
A novel MT-ATP6 variant associated with complicated ataxia in two unrelated Italian patients: case report and functional studies. Orphanet journal of rare diseases 19 (1) (2024)
Daniele Sala, Silvia Marchet, Lorenzo Nanetti, Andrea Legati, Caterina Mariotti, Eleonora Lamantea, Daniele Ghezzi, Alessia Catania, Costanza Lamperti
A novel MT-ATP6 variant associated with complicated ataxia in two unrelated Italian patients: case report and functional studies. Orphanet journal of rare diseases 19 (1) (2024)
Vincenzo Montano, Francesco Gruosso, Valerio Carelli, Giacomo Pietro Comi, Massimiliano Mirabella, Costanza Lamperti, Tiziana Mongini, Olimpia Musumeci, Serenella Servidei, Paola Tonin, Antonio Toscano, Angela Modenese, Guido Primiano, Maria Lucia Valentino, Sara Bortolani, Silvia Marchet, Megi Meneri, Graziana Tavilla, Gabriele Siciliano, Michelangelo Mancuso
Primary mitochondrial myopathy: Clinical features and outcome measures in 118 cases from Italy. Neurology. Genetics 6 (6) (2020)