SERVIDA, MAURA
SERVIDA, MAURA
Universita' degli Studi di MILANO
Survival gain in glioblastoma patients treated with dendritic cell immunotherapy is associated with increased NK but not CD8+ T cell activation in the presence of adjuvant temozolomide
2018 S. Pellegatta, M. Eoli, V. Cuccarini, E. Anghileri, B. Pollo, S. Pessina, S. Frigerio, M. Servida, L. Cuppini, C. Antozzi, S. Cuzzubbo, C. Corbetta, R. Paterra, F. Acerbi, P. Ferroli, F. Dimeco, L. Fariselli, E.A. Parati, M.G. Bruzzone, G. Finocchiaro
Clinical evaluation and cellular electrophysiology of a recessive CLCN1 patient
2013 S. Lucchiari, G. Ulzi, F. Magri, M. Bucchia, F. Corbetta, M. Servida, M. Moggio, G.P. Comi, M. Lecchi
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
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
Congenital myopathy with ptosis, ophthalmoplegia and muscle dystrophic changes: a possible sporadic case of myosin heavy chain type IIa myopathy.
2009 V. Lucchini, L. Napoli, V. Crugnola, M. Servida, P. Ciscato, A. Bordoni, D. Ronchi, A. Lerario, A. Oldfors, A. Prelle, N. Bresolin, G.P. Comi, M. Moggio, Y. Torrente, M. Sciacco
Decline of ALS-FRS and Norris scale scores in a group of patients affected by ALS and treated with lithium
2009 D. Santoro, I. Ghione, S. Corti, M. Servida, A. Prelle, N. Bresolin, G.P. Comi
Mitochondrial, Ehlers-Danlos and CADASIL features in the same family: a genetic puzzle or a new disease entità?
2009 I. Colombo, M. Servida, A. Bordoni, P. Ciscato, A. Prelle, G.P. Comi, M.T. Bassi, A. Bassotti, M. Valli, N. Bresolin, M. Moggio, M. Sciacco
Studio retrospettivo di biopsie muscolari di pazienti con possibile diagnosi di miopatia miofibrillare
2009 M. Servida, I. Colombo, M.E. Fruguglietti, P. Ciscato, L. Napoli, M. Sciacco, C. Lamperti, M. Serafini, N. Grimoldi, G.P. Comi, N. Bresolin, M. Moggio, A. Prelle
Mitocondriapatia, Ehlers-Danlos, e CADASIL: coesistenza di caratteristiche delle tre patologie nella stessa famiglia.
2009 I. Colombo, M. Servida, A. Bordoni, P. Ciscato, A. Prelle, G.P. Comi, M.T. Bassi, R. Guerrini, E. Parrini, N. Bresolin, M. Moggio, M. Sciacco
Morphological pattern of muscle biopsy in a large cohort of FSHD patients
2008 V. Crugnola, V. Ghiaroni, P. Ciscato, M. Servida, A. Prelle, M. Sciacco, F. Tiberio, S. Borsa, R. Tupler, N. Bresolin, M. Moggio, C. Lamperti
Cephalalgia, myopathy and familial dementia with CADASIL-like MRI and multiple mtDNA deletions
2008 M. Servida, L. Napoli, D. Ronchi, P. Ciscato, A. Bordoni, A. Prelle, G. Comi, M. Moggio, N. Bresolin, M. Sciacco
mtDNA depletion in a case of fatal infant cytochrome c oxidase deficiency presenting with clinical feature of type 1 spinal muscular atrophy
2008 V. Lucchini, M. Berardinelli, M. Carpanelli, M. Sciacco, A. Bordoni, D. Ronchi, E. Fassone, M. Servida, M. Pluderi, G.P. Comi, M. Moggio, N. Bresolin, C. Lamperti
Cephalalgia, myopathy and familial dementia with CADASIL-like MRI and multiple mtDNA deletions
2008 M. Servida, L. Napoli, D. Ronchi, P. Ciscato, A. Bordoni, A. Prelle, G.P. Comi, M. Moggio, N. Bresolin, M. Sciacco
A Late Role of ANT-1 Overexpression in the Pathogenesis of FSHD
2008 C. Lamperti, V. Crugnola, M. Servida, G. Fagiolari, M. Serafini, A. Prelle, M. Sciacco, F. Fortunato, L. Napoli, A. Di Fonzo, G.P. Comi, R.G. Tupler, N. Bresolin, M. Moggio
Colocalization of ribonuclear inclusions with muscle blind like-proteins in a family with myotonic dystrophy type 2 associated with a short CCTG expansion
2008 S. Lucchiari, S. Pagliarani, S.P. Corti, E. Mancinelli, M. Servida, M.E. Fruguglietti, V. Sansone, M. Moggio, N. Bresolin, G.P. Comi, G. Meola
Clinical features of an adult-onset Leigh syndrome caused by the T9176C mutation in the mitochondrial DNA ATPase 6 gene
2008 D. Ronchi, A. Bordoni, R. Virgilio, E. Fassone, A. DiFonzo, M. Servida, M. Ronconi, V. Lucchini, M. Matteoli, N. Bresolin, G.P. Comi
Myotonic dystrophy type 2: clinical, neurophysiological mnd muscular features of a family with short CCTG expansion.
2007 S. Lucchiari, S. Corti, S. Pagliarani, M. Servida, E. Fruguglietti, M. Moggio, N. Bresolin, G.P. Comi