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

  • 37 Similar Profiles
Muscles Medicine & Life Sciences
Mutation Medicine & Life Sciences
Muscular Diseases Medicine & Life Sciences
Facioscapulohumeral Muscular Dystrophy Medicine & Life Sciences
Genes Medicine & Life Sciences
Muscular Dystrophies Medicine & Life Sciences
Limb-Girdle Muscular Dystrophies Medicine & Life Sciences
Phenotype Medicine & Life Sciences

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Research Output 2007 2019

  • 1581 Citations
  • 25 h-Index
  • 107 Article
  • 2 Review article
  • 1 Comment/debate

Advances in Quantitative Imaging of Genetic and Acquired Myopathies: Clinical Applications and Perspectives

Paoletti, M., Pichiecchio, A., Cotti Piccinelli, S., Tasca, G., Berardinelli, A. L., Padovani, A. & Filosto, M., 2019, In : Frontiers in Neurology. 10, p. 78

Research output: Contribution to journalReview article

Muscular Diseases
Magnetic Resonance Imaging
Muscles
Post and Core Technique
Software

Impairments in contractility and cytoskeletal organisation cause nuclear defects in nemaline myopathy

Ross, J. A., Levy, Y., Ripolone, M., Kolb, J. S., Turmaine, M., Holt, M., Lindqvist, J., Claeys, K. G., Weis, J., Monforte, M., Tasca, G., Moggio, M., Figeac, N., Zammit, P. S., Jungbluth, H., Fiorillo, C., Vissing, J., Witting, N., Granzier, H., Zanoteli, E. & 3 others, Hardeman, E. C., Wallgren-Pettersson, C. & Ochala, J., Jan 1 2019, In : Acta Neuropathologica. 138, 3, p. 477-495

Research output: Contribution to journalArticle

Nemaline Myopathies
Nuclear Envelope
Cytoskeleton
Mutation
Cytoskeletal Proteins
5 Citations (Scopus)

Diagnostic anoctamin-5 protein defect in patients with ANO5-mutated muscular dystrophy

Vihola, A., Luque, H., Savarese, M., Penttilä, S., Lindfors, M., Leturcq, F., Eymard, B., Tasca, G., Brais, B., Conte, T., Charton, K., Richard, I. & Udd, B., Aug 1 2018, In : Neuropathology and Applied Neurobiology. 44, 5, p. 441-448 8 p.

Research output: Contribution to journalArticle

Muscular Dystrophies
Mutation
Proteins
Antibodies
Skeletal Muscle

Expanding the histopathological spectrum of CFL2-related myopathies

Fattori, F., Fiorillo, C., Rodolico, C., Tasca, G., Verardo, M., Bellacchio, E., Pizzi, S., Ciolfi, A., Fagiolari, G., Lupica, A., Broda, P., Pedemonte, M., Moggio, M., Bruno, C., Tartaglia, M., Bertini, E. & D'Amico, A., 2018, In : Clinical Genetics. 93, 6, p. 1234-1239 6 p.

Research output: Contribution to journalArticle

Cofilin 2
Myotonia Congenita
Muscular Diseases
Muscles
Mutation

Expanding the histopathological spectrum of CFL2-related myopathies

Fattori, F., Fiorillo, C., Rodolico, C., Tasca, G., Verardo, M., Bellacchio, E., Pizzi, S., Ciolfi, A., Fagiolari, G., Lupica, A., Broda, P., Pedemonte, M., Moggio, M., Bruno, C., Tartaglia, M., Bertini, E. & D'Amico, A., Jun 2018, In : Clinical Genetics. 93, 6, p. 1234-1239 6 p.

Research output: Contribution to journalArticle

Cofilin 2
Myotonia Congenita
Muscular Diseases
Muscles
Mutation