RANIERI, MICHELA
RANIERI, MICHELA
Universita' degli Studi di MILANO
Hypocalcaemic cardiomyopathy presenting as heart failure exacerbation due to untreated primary hypoparathyroidism
2024 M. Mapelli, A.A. Nepitella, S. Ferdico, A. Formenti, A. Baggiano, J. Campodonico, M. Ranieri, G. Vettor, M. Ianniruberto, S. Rizzo, C. Basso, G. Pontone, P. Agostoni
Antisense Oligonucleotide Therapy for the Treatment of C9ORF72 ALS/FTD Diseases
2014 G. Riboldi, C. Zanetta, M. Ranieri, M. Nizzardo, C. Simone, F. Magri, N. Bresolin, G.P. Comi, S. Corti
Mutations in DNA2 link progressive myopathy to mitochondrial DNA instability
2013 D. Ronchi, A. Di Fonzo, W. Lin, A. Bordoni, C. Liu, E. Fassone, S. Pagliarani, M. Rizzuti, L. Zheng, M. Filosto, M.T. Ferrò, M. Ranieri, F. Magri, L. Peverelli, H. Li, Y. Yuan, S. Corti, M. Sciacco, M. Moggio, N. Bresolin, B. Shen, G.P. Comi
Screening of the PFN1 gene in sporadic amyotrophic lateral sclerosis and in frontotemporal dementia
2013 T. Cinzia, N. Ticozzi, V. Pensato, L. Corrado, R. Del Bo, C. Bertolin, C. Fenoglio, S. Gagliardi, D. Calini, G. Lauria, B. Castellotti, A. Bagarotti, S. Corti, D. Galimberti, A. Cagnin, C. Gabelli, M. Ranieri, M. Ceroni, G. Siciliano, L. Mazzini, C. Cereda, E. Scarpini, G. Sorarù, G.P. Comi, S. D'Alfonso, C. Gellera, A. Ratti, J.E. Landers, V. Silani
Next-generation sequeencing discloses DGUOK mutations in adult patients with mtDNA multiple deletions
2013 D. Ronchi, C. Garone, A. Bordoni, P.G. Rios, S.E. Calvo, M. Ripolone, M. Ranieri, M. Rizzuti, R. Xhani, M. Servida, F. Magri, S. Corti, N. Bresolin, V.K. Mootha, M. Moggio, S. Di Mauro, G.P. Comi, M. Sciacco
Mitochondrial fusion proteins and human diseases
2013 M. Ranieri, S. Brajkovic, G. Riboldi, D. Ronchi, F. Rizzo, N. Bresolin, S. Corti, 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
C9ORF72 repeat expansion in a large Italian ALS cohort : evidence of a founder effect
2012 A. Ratti, L. Corrado, B. Castellotti, R. Del Bo, I. Fogh, C. Cereda, C. Tiloca, C. D'Ascenzo, A. Bagarotti, V. Pensato, M. Ranieri, S. Gagliardi, D. Calini, L. Mazzini, F. Taroni, S.P. Corti, M. Ceroni, G.D. Oggioni, K. Lin, J.F. Powell, G. Sorarù, N. Ticozzi, G.P. Comi, S. D'Alfonso, C. Gellera, V. Silani
C9ORF72 hexanucleotide repeat expansion in a Cohort of Italian patients affected by Amyotrophic Lateral Sclerosis with and without frontotemporal dementia
2012 R. Del Bo, S. Corti, G. Riboldi, M. Ranieri, C. Fenoglio, D. Galimberti, E. Scarpini, N. Bresolin, G. Comi
Next-generation sequencing reveals DGUOK mutations in adult patients with mitochondrial DNA multiple deletions
2012 D. Ronchi, C. Garone, A. Bordoni, P. Gutierrez Rios, S.E. Calvo, M. Ripolone, M. Ranieri, M. Rizzuti, L. Villa, F. Magri, S. Corti, N. Bresolin, V.K. Mootha, M. Moggio, S. Dimauro, G.P. Comi, M. Sciacco
Considerations on a mutation in the NOTCH3 gene sparing a cysteine residue: a rare polymorphism rather than a CADASIL variant
2012 A. Bersano, M. Ranieri, A. Ciammola, C. Cinnante, S. Lanfranconi, M.T. Dotti, L. Candelise, C. Baschirotto, I. Ghione, E. Ballabio, N. Bresolin, M.T. Bassi
Clinical and genetical heterogeneity in a cohort of pediatric patients affected with mitochondrial disorders
2011 M. Ranieri, D. Ronchi, S. Orcesi, V. Spartà, A. Cosi, A. Bordoni, V. Lucchini, F. Fortunato, E. Fassone, D. Tonduti, G. Rulfi, M. Rizzuti, M. Ripolone, M. Sciacco, M. Moggio, S. Corti, S. Savasta, A. Berardinelli, P. Veggiotti, G.P. Comi
Tyr78Phe Transthyretin Mutation with Predominant Motor Neuropathy as the Initial Presentation
2011 G. Riboldi, R. Del Bo, M. Ranieri, F. Magri, M. Sciacco, M. Moggio, N. Bresolin, S. Corti, G.P. Comi
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
No major progranulin genetic variability contribution to disease etiopathogenesis in an ALS Italian cohort
2011 S. Corti, D. Santoro, I. Ghione, C. Fenoglio, S. Ghezzi, M. Ranieri, D. Galimberti, M. Mancuso, G. Siciliano, C. Briani, L. Murri, E. Scarpini, J. Schymick, B. Traynor, N. Bresolin, G. Comi
Guillain-Barre syndrome after rtPA therapy for acute stroke
2010 A. Bersano, D. Santoro, A. Prelle, S. Lanfranconi, M. Ranieri, C. Tadeo, N. Bresolin, P. Baron
Contribution of FUS gene to FTLD-ALS spectrum: a genetic study in an Italian color of 484 patients
2010 R. Del Bo, S. Corti, S. Archetti, A. Papetti, G. Riboldi, S. Ghezzi, M. Ranieri, D. Santoro, A. Padovani, N. Bresolin, G.P. Comi, B. Borroni
A splicing site OPA1 mutation associated with autosomal dominant optic atrophy in an Italian family
2010 M. Ranieri, R. Del Bo, S. Corti, A. Bordoni, G. Mancarella, N. Bresolin, G.P. Comi