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Page 1
Familial polyglucosan body myopathy with unusual phenotype.
Fanin M, Nascimbeni AC, Savarese M, Papa V, Cenacchi G, Nigro V, Angelini C. Fanin M, et al. Among authors: cenacchi g. Neuropathol Appl Neurobiol. 2015 Apr;41(3):385-90. doi: 10.1111/nan.12171. Neuropathol Appl Neurobiol. 2015. PMID: 25041762 No abstract available.
MYH7 gene mutation in myosin storage myopathy and scapulo-peroneal myopathy.
Pegoraro E, Gavassini BF, Borsato C, Melacini P, Vianello A, Stramare R, Cenacchi G, Angelini C. Pegoraro E, et al. Among authors: cenacchi g. Neuromuscul Disord. 2007 Apr;17(4):321-9. doi: 10.1016/j.nmd.2007.01.010. Epub 2007 Mar 2. Neuromuscul Disord. 2007. PMID: 17336526
Lipolysis and lipophagy in lipid storage myopathies.
Angelini C, Nascimbeni AC, Cenacchi G, Tasca E. Angelini C, et al. Among authors: cenacchi g. Biochim Biophys Acta. 2016 Jul;1862(7):1367-73. doi: 10.1016/j.bbadis.2016.04.008. Epub 2016 Apr 13. Biochim Biophys Acta. 2016. PMID: 27085974 Free PMC article.
Update on polyglucosan storage diseases.
Cenacchi G, Papa V, Costa R, Pegoraro V, Marozzo R, Fanin M, Angelini C. Cenacchi G, et al. Virchows Arch. 2019 Dec;475(6):671-686. doi: 10.1007/s00428-019-02633-6. Epub 2019 Jul 30. Virchows Arch. 2019. PMID: 31363843 Review.
The role of ultrastructural examination in storage diseases.
Papa V, Tarantino L, Preda P, Badiali De Giorgi L, Fanin M, Pegoraro E, Angelini C, Cenacchi G. Papa V, et al. Among authors: cenacchi g. Ultrastruct Pathol. 2010 Oct;34(5):243-51. doi: 10.3109/01913121003780593. Ultrastruct Pathol. 2010. PMID: 20568989
Ultrastructural changes in LGMD1F.
Cenacchi G, Peterle E, Fanin M, Papa V, Salaroli R, Angelini C. Cenacchi G, et al. Neuropathology. 2013 Jun;33(3):276-80. doi: 10.1111/neup.12003. Epub 2012 Dec 21. Neuropathology. 2013. PMID: 23279333
251 results