CINNANTE, CLAUDIA MARIA
CINNANTE, CLAUDIA MARIA
Universita' degli Studi di MILANO
Diffusion tensor imaging reveals subclinical alterations in muscles of patients with Becker muscular dystrophy
2024 S. Nava, G. Conte, F.M. Triulzi, G.P. Comi, F. Magri, D. Velardo, C.M. Cinnante
Duropathy as a rare motor neuron disease mimic: from bibrachial amyotrophy to infratentorial superficial siderosis
2024 V. Iakovleva, F. Verde, C. Cinnante, A. Sillani, G. Conte, E. Corsini, E. Ciusani, A. Erbetta, V. Silani, N. Ticozzi
Case report: A novel patient presenting TRIM32-related limb-girdle muscular dystrophy
2023 M. Rimoldi, G. Romagnoli, F. Magri, S. Antognozzi, C. Cinnante, E. Saccani, P. Ciscato, S. Zanotti, D. Velardo, S. Corti, G.P. Comi, D. Ronchi
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
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
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
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
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
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
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
Multicentric Retrospective Evaluation of Five Classic Infantile Pompe Disease Subjects Under Enzyme Replacement Therapy With Early Infratentorial Involvement
2020 M. Paoletti, A. Pichiecchio, G.S. Colafati, G. Conte, F. Deodato, S. Gasperini, F. Menni, F. Furlan, L. Rubert, F.M. Triulzi, C. Cinnante
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
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
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
Brain Morphology of Cannabis Users With or Without Psychosis: A Pilot MRI Study
2020 G. Delvecchio, L. Oldani, G.M. Mandolini, A. Pigoni, V. Ciappolino, G. Schiena, M. Lazzaretti, E. Caletti, V. Barbieri, C. Cinnante, F. Triulzi, P. Brambilla
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