COSI, ALESSANDRA
COSI, ALESSANDRA
Universita' degli Studi di MILANO
Le mycophénolate mofétil en traitement d’induction et traitement d’entretien à long terme dans la prise en charge de la vascularite primitive du système nerveux central chez l’enfant
2018 A. Rosati, A. Cosi, M. Basile, A. Brambilla, R. Guerrini, R. Cimaz, G. Simonini
Mycophenolate mofetil as induction and long-term maintaining treatment in childhood : primary angiitis of the central nervous system
2017 A. Rosati, A. Cosi, M. Basile, A. Brambilla, R. Guerrini, R. Cimaz, G. Simonini
Long-Term Efficacy and Safety of Mycophenolate Mofetil in Childhood Primary Central Nervous System Vasculitis
2015 A. Brambilla, A. Cosi, A. Rosati, R. Guerrini, R. Cimaz, G. Simonini
The novel mitochondrial tRNAAsn gene mutation m.5709T>C produces ophthalmoparesis and respiratory impairment
2012 D. Ronchi, M. Sciacco, A. Bordoni, M. Raimondi, M. Ripolone, E. Fassone, A. Di Fonzo, M. Rizzuti, P. Ciscato, A. Cosi, M. Servida, M. Moggio, S. Corti, N. Bresolin, G. P. Comi
Optic atrophy plus phenotype due to mutations in the OPA1 gene: two more Italian families
2012 M. Ranieri, R. Del Bo, A. Bordoni, D. Ronchi, I. Colombo, G. Riboldi, A. Cosi, M. Servida, F. Magri, M. Moggio, N. Bresolin, G.P. Comi, S. Corti
CNS involvement in a cohort of pediatric patients affected with mitochondrial disorders caused by heterogeneous biochemical and genetic defects
2011 D. Ronchi, S. Orcesi, V. Spartà, A. Cosi, A. Bordoni, V. Lucchini, F. Fortunato, E. Fassone, D. Tonduti, G. Rulfi, M. Ranieri, M. Rizzuti, M. Ripolone, M. Sciacco, M. Moggio, S. Corti, S. Savata, A. Berardinelli, P. Veggiotti, G.P. Comi
Clinical and molecular features of an infant patient affected by Leigh Disease associated to m.14459G > A mitochondrial DNA mutation :aA case report
2011 D. Ronchi, A. Cosi, D. Tonduti, S. Orcesi, A. Bordoni, F. Fortunato, M. Rizzuti, M. Sciacco, M. Collotta, S. Cagdas, G. Capovilla, M. Moggio, A. Berardinelli, P. Veggiotti, G.P. Comi
Two novel mutations in PEO1 (twinkle) gene associated with chronic external ophthalmoplegia
2011 D. Ronchi, E. Fassone, A. Bordoni, M. Sciacco, V. Lucchini, A. Di Fonzo, M. Rizzuti, I. Colombo, L. Napoli, P. Ciscato, M. Moggio, A. Cosi, M. Collotta, S. Corti, N. Bresolin, G.P. Comi
Unusual adult-onset Leigh syndrome presentation due to the mitochondrial m.9176T > C mutation
2011 D. Ronchi, A. Bordoni, A. Cosi, M. Rizzuti, E. Fassone, A. Di Fonzo, M. Servida, M. Sciacco, M. Collotta, M. Ronzoni, V. Lucchini, M. Mattioli, M. Moggio, N. Bresolin, S. Corti, G. Comi