• 2994 Citations
  • 31 h-Index
1992 …2020
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Fingerprint Dive into the research topics where Angela Lucia Berardinelli is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 14 Similar Profiles
Duchenne Muscular Dystrophy Medicine & Life Sciences
Muscular Dystrophies Medicine & Life Sciences
Facioscapulohumeral Muscular Dystrophy Medicine & Life Sciences
Mutation Medicine & Life Sciences
Muscles Medicine & Life Sciences
Muscular Diseases Medicine & Life Sciences
Italy Medicine & Life Sciences
Phenotype Medicine & Life Sciences

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

Research Output 1992 2020

  • 2994 Citations
  • 31 h-Index
  • 131 Article
  • 1 Review article

Antibodies to neurofascin, contactin-1, and contactin-associated protein 1 in CIDP: Clinical relevance of IgG isotype

Cortese, A., Lombardi, R., Briani, C., Callegari, I., Benedetti, L., Manganelli, F., Luigetti, M., Ferrari, S., Clerici, A. M., Marfia, G. A., Rigamonti, A., Carpo, M., Fazio, R., Corbo, M., Mazzeo, A., Giannini, F., Cosentino, G., Zardini, E., Currò, R., Gastaldi, M. & 27 others, Vegezzi, E., Alfonsi, E., Berardinelli, A., Kouton, L., Manso, C., Giannotta, C., Doneddu, P., Dacci, P., Piccolo, L., Ruiz, M., Salvalaggio, A., De Michelis, C., Spina, E., Topa, A., Bisogni, G., Romano, A., Mariotto, S., Mataluni, G., Cerri, F., Stancanelli, C., Sabatelli, M., Schenone, A., Marchioni, E., Lauria, G., Nobile-Orazio, E., Devaux, J. & Franciotta, D., Jan 2020, In : Neurology: Neuroimmunology and NeuroInflammation. 7, 1

Research output: Contribution to journalArticle

Contactin 1
Contactins
Chronic Inflammatory Demyelinating Polyradiculoneuropathy
Immunoglobulin Isotypes
Immunoglobulin G

Antibodies to neurofascin, contactin-1, and contactin-associated protein 1 in CIDP: Clinical relevance of IgG isotype: Neurology - Neuroimmunology Neuroinflammation

Cortese, A., Lombardi, R., Briani, C., Callegari, I., Benedetti, L., Manganelli, F., Luigetti, M., Ferrari, S., Clerici, A. M., Marfia, G. A., Rigamonti, A., Carpo, M., Fazio, R., Corbo, M., Mazzeo, A., Giannini, F., Cosentino, G., Zardini, E., Currò, R., Gastaldi, M. & 27 others, Vegezzi, E., Alfonsi, E., Berardinelli, A., Kouton, L., Manso, C., Giannotta, C., Doneddu, P., Dacci, P., Piccolo, L., Ruiz, M., Salvalaggio, A., De Michelis, C., Spina, E., Topa, A., Bisogni, G., Romano, A., Mariotto, S., Mataluni, G., Cerri, F., Stancanelli, C., Sabatelli, M., Schenone, A., Marchioni, E., Lauria, G., Nobile-Orazio, E., Devaux, J. & Franciotta, D., 2020, In : Neurology: Neuroimmunology and NeuroInflammation. 7, 1, p. e639

Research output: Contribution to journalArticle

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

Correction: Long-term natural history data in Duchenne muscular dystrophy ambulant patients with mutations amenable to skip exons 44, 45, 51 and 53

on behalf on the International DMD group, Aug 1 2019, In : PLoS One. 14, 7, p. e0220714

Research output: Contribution to journalArticle

muscular dystrophy
Duchenne Muscular Dystrophy
Natural History
natural history
exons

Longitudinal natural history in young boys with Duchenne muscular dystrophy

Coratti, G., Brogna, C., Norcia, G., Ricotti, V., Abbott, L., D'Amico, A., Berardinelli, A., Vita, G. L., Lucibello, S., Messina, S., Sansone, V., Albamonte, E., Colia, G., Salmin, F., Gardani, A., Manzur, A., Main, M., Baranello, G., Arnoldi, M. T., Parsons, J. & 6 others, Carry, T., Connolly, A. M., Bertini, E., Muntoni, F., Pane, M. & Mercuri, E., 2019, In : Neuromuscular Disorders. 29, (11), p. 857-862 6 p.

Research output: Contribution to journalArticle

Duchenne Muscular Dystrophy
Natural History
Adrenal Cortex Hormones
Mutation
Disease Progression