SANSONE, VALERIA ADA MARIA
SANSONE, VALERIA ADA MARIA
Dipartimento di Scienze Biomediche per la Salute
12-Month Progression of Motor and Functional Outcomes in Congenital Myotonic Dystrophy
2021 K. Quigg, K. Berggren, M. Mcintyre, K. Bates, F. Salmin, J. Casiraghi, A. D’Amico, G. Astrea, F. Ricci, M. Mckay, J. Baldwin, J. Burns, C. Campbell, V. Sansone, N. Johnson
1st Italian SMA Family Association Consensus Meeting: Management and recommendations for respiratory involvement in spinal muscular atrophy (SMA) types I–III, Rome, Italy, 30–31 January 2015
2015 V.A. Sansone, F. Racca, G. Ottonello, A. Vianello, A. Berardinelli, G. Crescimanno, J.L. Casiraghi
207th ENMC Workshop on chronic respiratory insufficiency in myotonic dystrophies : management and implications for research, 27-29 June 2014, Naarden, The Netherlands
2015 V.A. Sansone, C. Gagnon
252nd ENMC international workshop: Developing best practice guidelines for management of mouthpiece ventilation in neuromuscular disorders. March 6th to 8th 2020, Amsterdam, the Netherlands
2020 M. Chatwin, M. Gonçalves, J. Gonzalez-Bermejo, M. Toussaint, J. O Benditt, D. Mckim, B. Hov, V.A.M. Sansone, H. là Ne Prigent, A. Carlucci, P. Wijkstra, T. Andersen, B. Garabelli, J. Escarrabill, T. Pinto, N. Audag, L. Verweij-van den Oudenrijn, A. Onga, W. Hughes, C. Devaux, J. Chaulet, J. Sancho
3D facial features in Andersen-Tawil syndrome: a family report
2015 C. Dolci, V. Pucciarelli, V.F. Ferrario, V. Sansone
[Expression of a defect in the respiratory chain in cultured human cells]
1991 G. Meola, G. Rotondo, M. Velicogna, R. Toppi, V. Sansone, N. Bresolin, G. Comi, A. Bordoni, P. Amati, C. Ausenda
A 10-year follow-up of a patient affected by myotonic dystrophy type 1 with implantable cardioverter-defibrillator implanted for secondary prevention
2019 G. De Ambroggi, H. Ali, R. Cappato, V. Sansone, L. De Ambroggi
A 5-center experience with intrathecal administration of nusinersen in SMA1 in Italy
2018 V. Sansone, M. Pane, S. Messina, C. Bruno, A. D'Amico, E. Albamonte, M. Catteruccia, M. Sframeli, M. Pedemonte, G. Vita, E. Bertini, E. Mercuri
A family with an unusual myotonic and myopathic phenotype and no CTG expansion (proximal myotonic myopathy syndrome): a challenge for future molecular studies
1996 G. Meola, V. Sansone, S. Radice, S. Skradski, L. Ptacek
A multidisciplinary approach improves quality of life perception in patients with amyotrophic lateral sclerosis
2009 C. Lunetta, V. Sansone, M.C. Panzeri, F. Pagnini, G. Meola, M. Corbo
A newly-described myotonic disorder (proximal myotonic myopathy--PROMM): personal experience and review of the literature
1996 G. Meola, V. Sansone
Adapted physical activity and therapeutic exercise in late-onset Pompe disease (LOPD): a two-step rehabilitative approach
2019 G. Iolascon, M. Vitacca, E. Carraro, C. Chisari, P. Fiore, S. Messina, T. Mongini, A. Moretti, V. Sansone, A. Toscano, G. Siciliano
Adattamento in Italiano e validazione del Dysphagia Handicap Index (I-DHI)
2021 D. Ginocchio, A. Ninfa, N. Pizzorni, C. Lunetta, V. Sansone, A. Schindler
Age and baseline values predict 12 and 24-month functional changes in type 2 SMA
2020 G. Coratti, M. Pera, S. Lucibello, J. Montes, A. Pasternak, A. Mayhew, A. Glanzman, S. Young, M. Pane, M. Scoto, S. Messina, N. Goemans, A. Osorio, M. Pedemonte, V. Sansone, E. Bertini, D. De Vivo, R. Finkel, F. Muntoni, E. Mercuri, C. ISMAC group and
Age related treatment effect in type II Spinal Muscular Atrophy pediatric patients treated with nusinersen.
2021 G. Coratti, M. Pane, S. Lucibello, M. Pera, A. Pasternak, J. Montes, V. Sansone, T. Duong, S. Young, S. Messina, A. D’Amico, M. Civitello, A. Glanzman, C. Bruno, F. Salmin, P. Tacchetti, S. Carnicella, M. Sframeli, L. Antonaci, A. Frongia, D. De Vivo, B. Darras, J. Day, E. Bertini, F. Muntoni, R. Finkel, E. Mercuri
Age, corticosteroid treatment and site of mutations affect motor functional changes in young boys with Duchenne Muscular Dystrophy
2022 G. Coratti, J. Lenkowicz, G. Norcia, S. Lucibello, E. Ferraroli, A. D'Amico, L. Bello, E. Pegoraro, S. Messina, F. Ricci, T. Mongini, A. Berardinelli, R. Masson, S.C. Previtali, G. D'Angelo, F. Magri, G.P. Comi, L. Politano, L. Passamano, G. Vita, V.A. Sansone, E. Albamonte, C. Panicucci, C. Bruno, A. Pini, E. Bertini, S. Patarnello, M. Pane, E. Mercuri, L. Fanelli, N. Forcina, G. Stanca, S. Carnicella, R. De Sanctis, C. Brogna, C. Cutrona, A.L. Frongia, M.C. Pera, L. Antonaci, G. Ferrantini, B. Berti, D. Leone, C. Palermo, M. Giannotta, G. Colia, A. Carlesi, G. De Luca, I. Mizzoni, A. Bonetti, M. Catteruccia, V. Di Bella, M. Sframeli, M. Russo, E. Rolle, A. Gardani, S. Parravicini, R. Zanin, M.T. Arnoldi, C. Dosi, I. Pedrinelli, G. Baranello, E. Albamonte, F. Salmin, S. Morando
ALS Cognitive Behavioral Screen (ALS-CBS): normative values for the Italian population and clinical usability
2019 L. Tremolizzo, A. Lizio, G. Santangelo, S. Diamanti, C. Lunetta, F. Gerardi, S. Messina, S. La Foresta, N. Riva, Y. Falzone, M. Filippi, S. Woolley, V. Sansone, M. Siciliano, C. Ferrarese, I. Appollonio
Alterazioni proteine tau liquorali e quoziente intellettivo (QI) nelle Distrofie Miotonichew di tipo 1 (DM1) e di tipo 2 (DM2).
2008 V. Sansone, S. Gandossini, M. Cotelli, M. Calabria, D. Galimberti, C. Fenoglio, E. Scarpini, G. Meola
Amyotrophic lateral sclerosis in pregnancy is associated with a vascular endothelial growth factor promoter genotype
2014 C. Lunetta, V.A. Sansone, S. Penco, L. Mosca, C. Tarlarini, F. Avemaria, E. Maestri, M.G. Melazzini, G. Meola, M. Corbo
Amyotrophic lateral sclerosis presenting during pregnancy : report of clinical and genetic features of three cases
2009 C. Lunetta, V. Sansone, S. Penco, M.C. Panzeri, E. Maestri, G. Meola, M. Corbo