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Rippling muscle disease and facioscapulohumeral dystrophy-like phenotype in a patient carrying a heterozygous CAV3 T78M mutation and a D4Z4 partial deletion: Further evidence for "double trouble" overlapping syndromes.
Ricci G, Scionti I, Alì G, Volpi L, Zampa V, Fanin M, Angelini C, Politano L, Tupler R, Siciliano G. Ricci G, et al. Among authors: ali g. Neuromuscul Disord. 2012 Jun;22(6):534-40. doi: 10.1016/j.nmd.2011.12.001. Epub 2012 Jan 14. Neuromuscul Disord. 2012. PMID: 22245016 Free PMC article.
Advances in molecular diagnostics for mitochondrial diseases.
Mancuso M, Orsucci D, Ali G, Lo Gerfo A, Fontanini G, Siciliano G. Mancuso M, et al. Among authors: ali g. Expert Opin Med Diagn. 2009 Sep;3(5):557-69. doi: 10.1517/17530050902967610. Epub 2009 Jul 16. Expert Opin Med Diagn. 2009. PMID: 23495985
An "inflammatory" mitochondrial myopathy. A case report.
Mancuso M, Orsucci D, Ienco EC, Ricci G, Ali G, Servadio A, Fontanini G, Filosto M, Vielmi V, Rocchi A, Petrozzi L, Logerfo A, Siciliano G. Mancuso M, et al. Among authors: ali g. Neuromuscul Disord. 2013 Nov;23(11):907-10. doi: 10.1016/j.nmd.2013.07.011. Epub 2013 Aug 8. Neuromuscul Disord. 2013. PMID: 24011700
Proximal Myopathy due to m.5835G>A Mutation in Mitochondrial MT-TY Gene.
Simoncini C, Montano V, Alì G, Costa R, Siciliano G, Mancuso M. Simoncini C, et al. Among authors: ali g. Case Rep Neurol Med. 2018 Dec 10;2018:8406712. doi: 10.1155/2018/8406712. eCollection 2018. Case Rep Neurol Med. 2018. PMID: 30643656 Free PMC article.
853 results