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Association in the same patient of autosomal dominant progressive external ophthalmoplegia with multiple mtDNA deletions and X-linked ichthyosis: clinical, biochemical, histological, submicroscopic and molecular genetic study.
Federico A, Dotti MT, Cardaioli E, Grieco G, Malandrini A, Manneschi L, Plewnia K, Rufa A, Renieri A, Bruttini M, Perticoni GF. Federico A, et al. Among authors: perticoni gf. J Submicrosc Cytol Pathol. 1998 Oct;30(4):521-6. J Submicrosc Cytol Pathol. 1998. PMID: 9851061
Inheritance of a novel RYR1 mutation in a family with myotonic dystrophy type 1.
Gambelli S, Malandrini A, Berti G, Gaudiano C, Zicari E, Brunori P, Perticoni G, Orrico A, Galli L, Sorrentino V, Lunardi J, Federico A, Dotti MT. Gambelli S, et al. Clin Genet. 2007 Jan;71(1):93-4. doi: 10.1111/j.1399-0004.2006.00725.x. Clin Genet. 2007. PMID: 17204054 No abstract available.
Levetiracetam versus carbamazepine in patients with late poststroke seizures: a multicenter prospective randomized open-label study (EpIC Project).
Consoli D, Bosco D, Postorino P, Galati F, Plastino M, Perticoni GF, Ottonello GA, Passarella B, Ricci S, Neri G, Toni D; EPIC Study. Consoli D, et al. Among authors: perticoni gf. Cerebrovasc Dis. 2012;34(4):282-9. doi: 10.1159/000342669. Epub 2012 Nov 1. Cerebrovasc Dis. 2012. PMID: 23128439 Free article. Clinical Trial.
Shoe-makers' polyneuropathy in Italy: the aetiological problem.
Abbritti G, Siracusa A, Cianchetti C, Coli A, Curradi F, Perticoni GF, De Rosa F. Abbritti G, et al. Among authors: perticoni gf. Br J Ind Med. 1976 May;33(2):92-9. doi: 10.1136/oem.33.2.92. Br J Ind Med. 1976. PMID: 1276096 Free PMC article.