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

  • 3 Similar Profiles
Facioscapulohumeral Muscular Dystrophy Medicine & Life Sciences
Muscles Medicine & Life Sciences
Sarcoglycanopathies Medicine & Life Sciences
Oculopharyngeal Muscular Dystrophy Medicine & Life Sciences
Muscular Diseases Medicine & Life Sciences
Nemaline Myopathies Medicine & Life Sciences
Magnetic Resonance Imaging Medicine & Life Sciences
Hereditary Spastic Paraplegia Medicine & Life Sciences

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Research Output 2018 2020

European muscle MRI study in limb girdle muscular dystrophy type R1/2A (LGMDR1/LGMD2A)

Barp, A., Laforet, P., Bello, L., Tasca, G., Vissing, J., Monforte, M., Ricci, E., Choumert, A., Stojkovic, T., Malfatti, E., Pegoraro, E., Semplicini, C., Stramare, R., Scheidegger, O., Haberlova, J., Straub, V., Marini-Bettolo, C., Løkken, N., Diaz-Manera, J., Urtizberea, J. A. & 4 others, Mercuri, E., Kynčl, M., Walter, M. C. & Carlier, R. Y., Jan 2020, In : Journal of Neurology. 267, 1, p. 45-56 12 p.

Research output: Contribution to journalArticle

Magnetic Resonance Imaging
Muscles
Calpain
Disease Progression
Lower Extremity

Muscle hypertrophy in amyloid myopathy

Tasca, G., Modoni, A., Nicoletti, T., Monforte, M., Cuccaro, A. & Ricci, E., Feb 2019, In : Neuromuscular Disorders. 29, 2, p. 150-151 2 p.

Research output: Contribution to journalArticle

MYO-MRI diagnostic protocols in genetic myopathies

MYO-MRI Working Group, Sep 16 2019, In : Neuromuscular Disorders.

Research output: Contribution to journalReview article

Muscular Diseases
Muscles
Muscular Dystrophies
Disease Progression
Publications

The variability of SMCHD1 gene in FSHD patients: evidence of new mutations

Strafella, C., Caputo, V., Galota, R. M., Campoli, G., Bax, C., Colantoni, L., Minozzi, G., Orsini, C., Politano, L., Tasca, G., Novelli, G., Ricci, E., Giardina, E. & Cascella, R., Dec 1 2019, In : Human Molecular Genetics. 28, 23, p. 3912-3920 9 p.

Research output: Contribution to journalArticle

Facioscapulohumeral Muscular Dystrophy
Mutation
3' Untranslated Regions
Genes
Genetic Association Studies

Tracking muscle wasting and disease activity in facioscapulohumeral muscular dystrophy by qualitative longitudinal imaging

Monforte, M., Laschena, F., Ottaviani, P., Bagnato, M. R., Pichiecchio, A., Tasca, G. & Ricci, E., Oct 30 2019, In : Journal of Cachexia, Sarcopenia and Muscle.

Research output: Contribution to journalArticle

Facioscapulohumeral Muscular Dystrophy
Wasting Syndrome
Muscles
Natural History
Disease Progression