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A Novel CAPN1 Mutation Causes a Pure Hereditary Spastic Paraplegia in an Italian Family.
Cotti Piccinelli S, Bassi MT, Citterio A, Manganelli F, Tozza S, Santorelli FM, Gallo Cassarino S, Caria F, Baldelli E, Galvagni A, Santoro L, Padovani A, Filosto M. Cotti Piccinelli S, et al. Among authors: caria f. Front Neurol. 2019 Jun 5;10:580. doi: 10.3389/fneur.2019.00580. eCollection 2019. Front Neurol. 2019. PMID: 31231303 Free PMC article.
A Comprehensive Update on Late-Onset Pompe Disease.
Labella B, Cotti Piccinelli S, Risi B, Caria F, Damioli S, Bertella E, Poli L, Padovani A, Filosto M. Labella B, et al. Among authors: caria f. Biomolecules. 2023 Aug 22;13(9):1279. doi: 10.3390/biom13091279. Biomolecules. 2023. PMID: 37759679 Free PMC article. Review.
Leprosy Neuropathy in a Non-Endemic Area: A Clinical and Pathological Study.
Cotti Piccinelli S, Tagliapietra M, Cavallaro T, Labella B, Risi B, Caria F, Damioli S, Poli L, Padovani A, Ferrari S, Filosto M. Cotti Piccinelli S, et al. Among authors: caria f. Biomedicines. 2023 Sep 6;11(9):2468. doi: 10.3390/biomedicines11092468. Biomedicines. 2023. PMID: 37760909 Free PMC article.
Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE-MTDPS1).
Filosto M, Cotti Piccinelli S, Caria F, Gallo Cassarino S, Baldelli E, Galvagni A, Volonghi I, Scarpelli M, Padovani A. Filosto M, et al. Among authors: caria f. J Clin Med. 2018 Oct 26;7(11):389. doi: 10.3390/jcm7110389. J Clin Med. 2018. PMID: 30373120 Free PMC article. Review.
Unclassified clinical presentations of chronic inflammatory demyelinating polyradiculoneuropathy.
Doneddu PE, Akyil H, Manganelli F, Briani C, Cocito D, Benedetti L, Mazzeo A, Fazio R, Filosto M, Cosentino G, Di Stefano V, Antonini G, Marfia GA, Inghilleri M, Siciliano G, Clerici AM, Carpo M, Schenone A, Luigetti M, Lauria G, Matà S, Rosso T, Minicuci GM, Lucchetta M, Cavaletti G, Liberatore G, Spina E, Campagnolo M, Peci E, Germano F, Gentile L, Strano C, Cotti Piccinelli S, Vegezzi E, Leonardi L, Mataluni G, Ceccanti M, Schirinzi E, Romozzi M, Nobile-Orazio E; Italian CIDP Database study group. Doneddu PE, et al. J Neurol Neurosurg Psychiatry. 2023 Aug;94(8):614-621. doi: 10.1136/jnnp-2022-331011. Epub 2023 Apr 4. J Neurol Neurosurg Psychiatry. 2023. PMID: 37015771
Autosomal recessive Bethlem myopathy: A clinical, genetic and functional study.
Caria F, Cescon M, Gualandi F, Pichiecchio A, Rossi R, Rimessi P, Cotti Piccinelli S, Gallo Cassarino S, Gregorio I, Galvagni A, Ferlini A, Padovani A, Bonaldo P, Filosto M. Caria F, et al. Neuromuscul Disord. 2019 Sep;29(9):657-663. doi: 10.1016/j.nmd.2019.07.007. Epub 2019 Jul 30. Neuromuscul Disord. 2019. PMID: 31471117
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