• 6738 Citations
  • 41 h-Index
1977 …2019
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Fingerprint Dive into the research topics where Marina Mora is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 56 Similar Profiles
Muscles Medicine & Life Sciences
Mutation Medicine & Life Sciences
Muscular Dystrophies Medicine & Life Sciences
Muscular Diseases Medicine & Life Sciences
Duchenne Muscular Dystrophy Medicine & Life Sciences
Dystrophin Medicine & Life Sciences
Genes Medicine & Life Sciences
Congenital Structural Myopathies Medicine & Life Sciences

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Research Output 1977 2019

  • 6738 Citations
  • 41 h-Index
  • 185 Article
  • 3 Chapter
  • 1 Letter
  • 1 Review article

Expanding the central nervous system disease spectrum associated with FLNC mutation

Previtali, S. C., Scarlato, M., Vezzulli, P., Ruggieri, A., Velardo, D., Benedetti, S., Torini, G., Colombo, B., Maggi, L., Di Bella, D., Gellera, C., D'Angelo, G. & Mora, M., Jan 1 2019, In : Muscle and Nerve.

Research output: Contribution to journalArticle

1 Citation (Scopus)

Botulinum toxin type A affects the transcriptome of cell cultures derived from muscle biopsies of controls and spastic patients

Zanotti, S., Kapetis, D., Gibertini, S., Salerno, F., Ciusani, E., Colombo, C., Gronchi, A., Morandi, L., Mantegazza, R., Molteni, F. & Mora, M., Aug 1 2018, In : Toxicology in Vitro. 50, p. 124-136 13 p.

Research output: Contribution to journalArticle

Type A Botulinum Toxins
Muscle Spasticity
Botulinum Toxins
Biopsy
Transcriptome
Genetic Association Studies
Cross-Sectional Studies
Dystroglycans
Mutation
Congenital Myasthenic Syndromes

Copy number variants account for a tiny fraction of undiagnosed myopathic patients

Giugliano, T., Savarese, M., Garofalo, A., Picillo, E., Fiorillo, C., D’amico, A., Maggi, L., Ruggiero, L., Vercelli, L., Magri, F., Fattori, F., Torella, A., Ergoli, M., Rubegni, A., Fanin, M., Musumeci, O., De Bleecker, J., Peverelli, L., Moggio, M., Mercuri, E. & 13 others, Toscano, A., Mora, M., Santoro, L., Mongini, T., Bertini, E., Bruno, C., Minetti, C., Comi, G. P., Santorelli, F. M., Angelini, C., Politano, L., Piluso, G. & Nigro, V., 2018, In : Genes. 9, 11

Research output: Contribution to journalArticle

Copy number variants account for a tiny fraction of undiagnosed myopathic patients

Giugliano, T., Savarese, M., Garofalo, A., Picillo, E., Fiorillo, C., D’amico, A., Maggi, L., Ruggiero, L., Vercelli, L., Magri, F., Fattori, F., Torella, A., Ergoli, M., Rubegni, A., Fanin, M., Musumeci, O., De Bleecker, J., Peverelli, L., Moggio, M., Mercuri, E. & 13 others, Toscano, A., Mora, M., Santoro, L., Mongini, T., Bertini, E., Bruno, C., Minetti, C., Comi, G. P., Santorelli, F. M., Angelini, C., Politano, L., Piluso, G. & Nigro, V., Nov 1 2018, In : Genes. 9, 11, 524.

Research output: Contribution to journalArticle

Genes
Muscles
Dystrophin
Comparative Genomic Hybridization
Muscular Diseases