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Auteur Bernasconi P |
Documents disponibles écrits par cet auteur



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The Genetic Landscape of Dystrophin Mutations in Italy: A Nationwide Study
Neri M, Rossi R, Trabanelli C, et al.
Frontiers in Genetics, 2020, 11, p 131
Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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Circulating MyomiRs as Potential Biomarkers to Monitor Response to Nusinersen in Pediatric SMA Patients
Bonanno S, Marcuzzo S, Malacarne C, et al.
Biomedicines, 2020, 8, 2
Revue : Biomedicines, 8, 2 Titre : Circulating MyomiRs as Potential Biomarkers to Monitor Response to Nusinersen in Pediatric SMA Patients Type de document : Article Auteurs : Bonanno S ; Marcuzzo S ; Malacarne C ; Giagnorio E ; Masson R ; Zanin R ; Arnoldi MT ; Andreetta F ; Simoncini O ; Venerando A ; Gellera C ; Pantaleoni C ; Mantegazza R ; Bernasconi P ; Baranello G ; Maggi L Editeur : Switzerland Année de publication : 01/2020 Langues : Anglais (eng) Mots-clés : amyotrophie spinale ; amyotrophie spinale proximale (type II) ; amyotrophie spinale proximale liée à SMN1 ; amyotrophie spinale proximale type 3 ; diagnostic ; étude de cohorte ; étude observationnelle ; évolution de la maladie ; maladie du motoneurone ; maladie neuromusculaire ; marqueur biologique ; microARN ; nusinersen Pubmed / DOI : Pubmed : 31991852 / DOI : 10.3390/biomedicines8020021
N° Profil MNM : 2020013 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/31991852 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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Clinical and Molecular Spectrum of Myotonia and Periodic Paralyses Associated With Mutations in SCN4A in a Large Cohort of Italian Patients
Maggi L, Brugnoni R, Canioni E, et al.
Frontiers in neurology, 2020, 11, p 646
Revue : Frontiers in neurology, 11 Titre : Clinical and Molecular Spectrum of Myotonia and Periodic Paralyses Associated With Mutations in SCN4A in a Large Cohort of Italian Patients Type de document : Article Auteurs : Maggi L ; Brugnoni R ; Canioni E ; Tonin P ; Saletti V ; Sola P ; Piccinelli SC ; Colleoni L ; Ferrigno P ; Pini A ; Masson R ; Manganelli F ; Lietti D ; Vercelli L ; Ricci G ; Bruno C ; Tasca G ; Pizzuti A ; Padovani A ; Fusco C ; Pegoraro E ; Ruggiero L ; Ravaglia S ; Siciliano G ; Morandi L ; Dubbioso R ; Mongini T ; Filosto M ; Tramacere I ; Mantegazza R ; Bernasconi P Année de publication : 2020 Pages : p 646 Langues : Anglais (eng) Pubmed / DOI : Pubmed : 32849172 / DOI : 10.3389/fneur.2020.00646
N° Profil MNM : 2020091 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/32849172 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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MicroRNA signature associated with treatment response in myasthenia gravis: A further step towards precision medicine
Cavalcante P, Mizrachi T, Barzago C, et al.
Pharmacological Research, 2019, 148
Revue : Pharmacological Research, 148 Titre : MicroRNA signature associated with treatment response in myasthenia gravis: A further step towards precision medicine Type de document : Article Auteurs : Cavalcante P, Auteur ; Mizrachi T ; Barzago C ; Scandiffio L ; Bortone F ; Bonanno S ; Frangiamore R ; Mantegazza R ; Bernasconi P ; Brenner T ; Vaknin-Dembinsky A ; Antozzi C Editeur : Netherlands Année de publication : 08/2019 Langues : Anglais (eng) Pubmed / DOI : Pubmed : 31401213 / DOI : 10.1016/j.phrs.2019.104388
N° Profil MNM : 2019082 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/31401213 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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Italian recommendations for diagnosis and management of congenital myasthenic syndromes
Maggi L, Bernasconi P, D'Amico A, et al.
Neurological sciences, 2019, 40, 3, p 457
Revue : Neurological sciences, 40, 3 Titre : Italian recommendations for diagnosis and management of congenital myasthenic syndromes Type de document : Article Auteurs : Maggi L, Auteur ; Bernasconi P ; D'Amico A ; Brugnoni R ; Fiorillo C ; Garibaldi M ; Astrea G ; Bruno C ; Santorelli FM ; Liguori R ; Antonini G ; Evoli A ; Bertini E ; Rodolico C ; Mantegazza R Année de publication : 03/2019 Pages : p 457 Langues : Anglais (eng) Pubmed / DOI : DOI : 10.1007/s10072-018-3682-x / Pubmed : 30554356
N° Profil MNM : 2018122 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/30554356 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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Myasthenia gravis: from autoantibodies to therapy
Mantegazza R, Bernasconi P, Cavalcante P
Current opinion in neurology, 2018, 31, 5, p 517
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Exosomes and exosomal miRNAs from muscle-derived fibroblasts promote skeletal muscle fibrosis
Zanotti S, Zanotti S, Gibertini S, et al.
Matrix biology : journal of the International Society for Matrix Biology, 2018
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Elevated TGF Beta2 serum levels in Emery-Dreifuss Muscular Dystrophy: Implications for myocyte and tenocyte differentiation and fibrogenic processes
Bernasconi P, Carboni N, Ricci G, et al.
Nucleus (Austin, Tex.), 2018, 9, 1, p 292
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Transcriptional and epigenetic analyses of the DMD locus reveal novel cis?acting DNA elements that govern muscle dystrophin expression
Gherardi S, Bovolenta M, Passarelli C, et al.
Biochimica et biophysica acta, 2017, 1860, 11, p 1138
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Skeletal Muscle Laminopathies: A Review of Clinical and Molecular Features
Maggi L, Carboni N, Bernasconi P
Cells, 2016, 5, 3
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Increased expression of Toll-like receptors 7 and 9 in myasthenia gravis thymus characterized by active Epstein-Barr virus infection
Cavalcante P, Galbardi B, Franzi S, et al.
Immunobiology, 2016, 221, 4, p 516
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Fibrosis and inflammation are greater in muscles of beta-sarcoglycan-null mouse than mdx mouse.
Gibertini S, Zanotti S, Savadori P, et al.
Cell and tissue research, 2014, 356, 2, p. 427-43
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VAV1 and BAFF, via NFkappaB pathway, are genetic risk factors for myasthenia gravis
Avidan N, Le Panse R, Harbo HF, et al.
Annals of clinical and translational neurology, 2014, 1, 5, p 329
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LMNA-associated myopathies : The Italian experience in a large cohort of patients
Maggi L, D'Amico A, Pini A, et al.
Neurology, 2014, 83, 18, p 1634
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Etiology of myasthenia gravis : innate immunity signature in pathological thymus
Cavalcante P, Cufi P, Mantegazza R, et al.
Autoimmunity reviews, 2013, 12, 9, p. 863-874
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Etiology of myasthenia gravis: innate immunity signature in pathological thymus
Cavalcante P, Cufi P, Mantegazza R, et al.
Autoimmunity reviews, 2013, 12, 9, p 863
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Autoimmune mechanisms in myasthenia gravis
Cavalcante P, Bernasconi P, Mantegazza R
Current opinion in neurology, 2012, 25, 5, p. 621-629
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Inflammation and Epstein-Barr virus infection are common features of myasthenia gravis thymus : possible roles in pathogenesis
Cavalcante P, Maggi L, Colleoni L, et al.
Autoimmune diseases, 2011, 2011, p. 213092
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The thymus in myasthenia gravis : site of "innate autoimmunity"?
Cavalcante P, Le Panse R, Berrih-Aknin S, et al.
Muscle & Nerve, 2011, 44, 4, p. 467-484
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Epstein-Barr virus persistence and reactivation in myasthenia gravis thymus
Cavalcante P, Serafini B, Rosicarelli B, et al.
Annals of neurology, 2010, 67, 6, p. 726-738
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Detection of poliovirus-infected macrophages in thymus of patients with myasthenia gravis
Cavalcante P, Barberis M, Cannone M, et al.
Neurology, 2010, 74, 14, p. 1118-1126
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Risk of arrhythmia in type I myotonic dystrophy : the role of clinical and genetic variables
Cudia P, Bernasconi P, Chiodelli R, et al.
Journal of neurology, neurosurgery and psychiatry, 2009, 80, 7, p. 790-793
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Identification of a point mutation in the skeletal muscle ryanodine receptor gene associated in the homozygous state to central core disease (Poster)
Collectif, Melli G, Colleoni L, et al.
Neuromuscular disorders : NMD, 2008, 18, 9-10, p. 809-810
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In vitro dissection of the pathogenic mechanisms of muscle fibrosis in Duchenne muscular dystrophy (Poster)
Collectif, Zanotti S, Saredi S, et al.
Neuromuscular disorders : NMD, 2008, 18, 9-10, p. 778
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Risk of arrhythmia in type 1 myotonic dystrophy: The role of clinical and genetic variables in a large cohort of patients (Poster)
Collectif, Cudia P, Bernasconi P, et al.
Neuromuscular disorders : NMD, 2008, 18, 9-10, p. 745
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