1994 …2020

Research output per year

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Fingerprint Dive into the research topics where Stefano Previtali is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

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Research Output

Genetic modifiers of respiratory function in Duchenne muscular dystrophy

Bello, L., D’Angelo, G., Villa, M., Fusto, A., Vianello, S., Merlo, B., Sabbatini, D., Barp, A., Gandossini, S., Magri, F., Comi, G. P., Pedemonte, M., Tacchetti, P., Lanzillotta, V., Trucco, F., D’Amico, A., Bertini, E., Astrea, G., Politano, L., Masson, R. & 21 others, Baranello, G., Albamonte, E., De Mattia, E., Rao, F., Sansone, V. A., Previtali, S., Messina, S., Vita, G. L., Berardinelli, A., Mongini, T., Pini, A., Pane, M., Mercuri, E., Vianello, A., Bruno, C., Hoffman, E. P., Morgenroth, L., Gordish-Dressman, H., McDonald, C. M., Pegoraro, E. & Investigators, CINRG-DNHS., 2020, In : Annals of Clinical and Translational Neurology. 7, 5, p. 786-798 13 p.

Research output: Contribution to journalArticle

  • Genetic modifiers of respiratory function in Duchenne muscular dystrophy

    CINRG-DNHS Investigators, Bello, L., D’Angelo, G., Villa, M., Fusto, A., Vianello, S., Merlo, B., Sabbatini, D., Barp, A., Gandossini, S., Magri, F., Comi, G. P., Pedemonte, M., Tacchetti, P., Lanzillotta, V., Trucco, F., D’Amico, A., Bertini, E., Astrea, G., Politano, L. & 21 others, Masson, R., Baranello, G., Albamonte, E., De Mattia, E., Rao, F., Sansone, V. A., Previtali, S., Messina, S., Vita, G. L., Berardinelli, A., Mongini, T., Pini, A., Pane, M., Mercuri, E., Vianello, A., Bruno, C., Hoffman, E. P., Morgenroth, L., Gordish-Dressman, H., McDonald, C. M. & Pegoraro, E., 2020, In : Annals of Clinical and Translational Neurology. 7, 5, p. 786-798

    Research output: Contribution to journalArticle

    Open Access
  • Genetic modifiers of respiratory function in Duchenne muscular dystrophy

    CINRG-DNHS Investigators, Apr 28 2020, In : Annals of Clinical and Translational Neurology.

    Research output: Contribution to journalArticle

  • Phenotypic Variability Among Patients With D4Z4 Reduced Allele Facioscapulohumeral Muscular Dystrophy

    Ruggiero, L., Mele, F., Manganelli, F., Bruzzese, D., Ricci, G., Vercelli, L., Govi, M., Vallarola, A., Tripodi, S., Villa, L., Di Muzio, A., Scarlato, M., Bucci, E., Antonini, G., Maggi, L., Rodolico, C., Tomelleri, G., Filosto, M., Previtali, S., Angelini, C. & 7 others, Berardinelli, A., Pegoraro, E., Moggio, M., Mongini, T., Siciliano, G., Santoro, L. & Tupler, R., May 1 2020, In : JAMA network open. 3, 5, p. e204040

    Research output: Contribution to journalArticle

  • Sodium Channel Myotonia Due to Novel Mutations in Domain I of Nav1.4

    Pagliarani, S., Lucchiari, S., Scarlato, M., Redaelli, E., Modoni, A., Magri, F., Fossati, B., Previtali, S. C., Sansone, V. A., Lecchi, M., Lo Monaco, M., Meola, G. & Comi, G. P., Apr 29 2020, In : Frontiers in Neurology. 11, 255.

    Research output: Contribution to journalArticle

    Open Access