CINNANTE, CLAUDIA MARIA
CINNANTE, CLAUDIA MARIA
Universita' degli Studi di MILANO
Characterization of patients with Becker muscular dystrophy by histology, magnetic resonance imaging, function, and strength assessments
2022 G.P. Comi, E.H. Niks, C.M. Cinnante, H.E. Kan, K. Vandenborne, R.J. Willcocks, D. Velardo, M. Ripolone, J.J. van Benthem, N.M. van de Velde, S. Nava, L. Ambrosoli, S. Cazzaniga, P.U. Bettica
Sexual Dimorphism in the Brain Correlates of Adult-Onset Depression: A Pilot Structural and Functional 3T MRI Study
2022 M.C. Piani, E. Maggioni, G. Delvecchio, A. Ferro, D. Gritti, S.M. Pozzoli, E. Fontana, P. Enrico, C.M. Cinnante, F.M. Triulzi, J.A. Stanley, E. Battaglioli, P. Brambilla
Family history is key to the interpretation of exome sequencing in the prenatal context: unexpected diagnosis of Basal Cell Nevus Syndrome
2022 B. Rinaldi, C. Cesaretti, S. Boito, R. Villa, S. Guerneri, I. Borzani, T. Rizzuti, D. Marchetti, G. Conte, C. Cinnante, F. Triulzi, N. Persico, M. Iascone, F. Natacci
Case Reports: Novel Missense Variants in the Filamin C Actin Binding Domain Cause Variable Phenotypes
2022 D. Velardo, M.G. D'Angelo, A. Citterio, E. Panzeri, L. Napoli, C. Cinnante, M. Moggio, G.P. Comi, D. Ronchi, M.T. Bassi
Expanding the Phenotypic Spectrum of Vocal Cord and Pharyngeal Weakness With Distal Myopathy due to the p.S85C MATR3 Mutation
2022 A. Manini, D. Velardo, P. Ciscato, C. Cinnante, M. Moggio, G. Comi, S. Corti, D. Ronchi
Amyotrophic lateral sclerosis phenotypes significantly differ in terms of magnetic susceptibility properties of the precentral cortex
2021 G. Conte, V.E. Contarino, S. Casale, C. Morelli, S. Sbaraini, E. Scola, F. Trogu, S. Siggillino, C.M. Cinnante, L. Caschera, F.M. Lo Russo, F.M. Triulzi, V. Silani
Assessment of the membranous labyrinth in infants using a heavily T2-weighted 3D FLAIR sequence without contrast agent administration
2021 G. Conte, S. Casale, L. Caschera, F.M. Lo Russo, C. Paolella, C. Cinnante, F. Di Berardino, D. Zanetti, D. Stocchetti, E. Scola, L. Bassi, F. Triulzi
CACNA1S mutation associated with a case of juvenile-onset congenital myopathy
2021 E. Mauri, D. Piga, S. Pagliarani, F. Magri, A. Manini, M. Sciacco, M. Ripolone, L. Napoli, L. Borellini, C. Cinnante, D. Cassandrini, S. Corti, N. Bresolin, G.P. Comi, A. Govoni
Early Findings in Neonatal Cases of RYR1-Related Congenital Myopathies
2021 E. Mauri, D. Piga, A. Govoni, R. Brusa, S. Pagliarani, M. Ripolone, R. Dilena, C. Cinnante, M. Sciacco, D. Cassandrini, V. Nigro, N. Bresolin, S. Corti, G.P. Comi, F. Magri
Effects of Early Intervention on Visual Function in Preterm Infants : A Randomized Controlled Trial
2020 C. Fontana, A. De Carli, D. Ricci, F. Dessimone, S. Passera, N. Pesenti, M. Bonzini, L. Bassi, L. Squarcina, C. Cinnante, F. Mosca, M. Fumagalli
Prenatal magnetic resonance imaging within the 26th week of gestation may predict the fate of isolated upward rotation of the cerebellar vermis : insights from a multicentre study
2020 G. Conte, L. Caschera, C. Parazzini, C. Cinnante, G. Izzo, G. Talenti, M. Severino, F. Ormitti, G. Palumbo, L. Pinelli, A. Antonelli, L. Manganaro, S. Boito, A. Rossi, F. Triulzi, A. Righini
Pediatric anti-HMGCR necrotizing myopathy: diagnostic challenges and literature review
2020 D. Velardo, I. Faravelli, C. Cinnante, M. Moggio, G.P. Comi
Dystonia-ataxia syndrome with permanent torsional nystagmus caused by ECHS1 deficiency
2020 D. Ronchi, E. Monfrini, S. Bonato, V. Mancinelli, C. Cinnante, S. Salani, A. Bordoni, P. Ciscato, F. Fortunato, M. Villa, A. Di Fonzo, S. Corti, N. Bresolin, G.P. Comi
Hyperacute extensive spinal cord infarction and negative spine magnetic resonance imaging: a case report and review of the literature
2020 G. Costamagna, M. Meneri, E. Abati, R. Brusa, D. Velardo, D. Gagliardi, E. Mauri, C. Cinnante, N. Bresolin, G. Comi, S. Corti, I. Faravelli
Limb girdle muscular dystrophy due to LAMA2 gene mutations: new mutations expand the clinical spectrum of a still challenging diagnosis
2020 F. Magri, R. Brusa, L. Bello, L. Peverelli, R.D. Bo, A. Govoni, C. Cinnante, I. Colombo, F. Fortunato, R. Tironi, S. Corti, N. Grimoldi, M. Sciacco, N. Bresolin, E. Pegoraro, M. Moggio, G.P. Comi
Olfactory Malformations in Mendelian Disorders of the Epigenetic Machinery
2020 S. Aleo, C. Cinnante, S. Avignone, E. Prada, G. Scuvera, P.F. Ajmone, A. Selicorni, M.A. Costantino, F. Triulzi, P. Marchisio, C. Gervasini, D. Milani
Hereditary hemorrhagic telangiectasia associated with cortical development malformation due to a start loss mutation in ENG
2020 D. Villa, C. Cinnante, G. Valcamonica, G. Manenti, S. Lanfranconi, A. Colombi, I. Ghione, M.C. Saetti, M. D'Amico, S. Bonato, N. Bresolin, G.P. Comi, D. Ronchi
Structural brain anomalies in Cri-du-Chat syndrome: MRI findings in 14 patients and possible genotype-phenotype correlations
2020 R. Villa, V.G.C. Fergnani, R. Silipigni, S. Guerneri, C. Cinnante, A. Guala, C. Danesino, E. Scola, G. Conte, M. Fumagalli, S. Gangi, L. Colombo, O. Picciolini, P.F. Ajmone, A. Accogli, F. Madia, E. Tassano, M. Scala, V. Capra, M. Srour, L. Spaccini, A. Righini, D. Greco, L. Castiglia, C. Romano, M.F. Bedeschi
MYH2 myopathy, a new case expands the clinical and pathological spectrum of the recessive form
2020 R. Telese, S. Pagliarani, A. Lerario, P. Ciscato, G. Fagiolari, D. Cassandrini, N. Grimoldi, G. Conte, C. Cinnante, F.M. Santorelli, G.P. Comi, M. Sciacco, L. Peverelli
COVID-19-associated PRES-like encephalopathy with perivascular gadolinium enhancement
2020 G. Conte, S. Avignone, M. Carbonara, M. Meneri, F. Ortolano, C. Cinnante, F. Triulzi