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An intronic mutation causes severe LGMD2A in a large inbred family belonging to a genetic isolate in the Alps.
Clin Genet. 2012 Dec;82(6):601-2. doi: 10.1111/j.1399-0004.2012.01873.x. Epub 2012 Apr 9.
Clin Genet. 2012.
PMID: 22486197
No abstract available.
Incomplete penetrance in limb-girdle muscular dystrophy type 1F.
Fanin M, Peterle E, Fritegotto C, Nascimbeni AC, Tasca E, Torella A, Nigro V, Angelini C.
Fanin M, et al. Among authors: fritegotto c.
Muscle Nerve. 2015 Aug;52(2):305-6. doi: 10.1002/mus.24539. Epub 2015 Jun 7.
Muscle Nerve. 2015.
PMID: 25487718
No abstract available.
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Micro-RNA expression in muscle and fiber morphometry in myotonic dystrophy type 1.
Fritegotto C, Ferrati C, Pegoraro V, Angelini C.
Fritegotto C, et al.
Neurol Sci. 2017 Apr;38(4):619-625. doi: 10.1007/s10072-017-2811-2. Epub 2017 Jan 11.
Neurol Sci. 2017.
PMID: 28078570
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Periostin and Epithelial-Mesenchymal Transition Score as Novel Prognostic Markers for Leiomyosarcoma, Myxofibrosarcoma, and Undifferentiated Pleomorphic Sarcoma.
Piano MA, Brunello A, Cappellesso R, Del Bianco P, Mattiolo A, Fritegotto C, Montini B, Zamuner C, Del Fiore P, Rastrelli M, Sommariva A, De Salvo GL, Montesco MC, Rossi CR, Zagonel V, Calabrò ML.
Piano MA, et al. Among authors: fritegotto c.
Clin Cancer Res. 2020 Jun 15;26(12):2921-2931. doi: 10.1158/1078-0432.CCR-19-2297. Epub 2020 Mar 3.
Clin Cancer Res. 2020.
PMID: 32127392
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