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Page 1
An exploration of anger phenomenology in multiple sclerosis.
Nocentini U, Tedeschi G, Migliaccio R, Dinacci D, Lavorgna L, Bonavita S, Bresciamorra V, Comanducci G, Coniglio G, Livrea P, Mannu R, Orefice G, Paciello M, Patti F, Quattrone A, Salemi G, Savettieri G, Simone IL, Valentino P, Zappia M, Bonavita V, Musicco M, Caltagirone C. Nocentini U, et al. Among authors: comanducci g. Eur J Neurol. 2009 Dec;16(12):1312-7. doi: 10.1111/j.1468-1331.2009.02727.x. Epub 2009 Jun 29. Eur J Neurol. 2009. PMID: 19566900
Novel SACS mutations in autosomal recessive spastic ataxia of Charlevoix-Saguenay type.
Grieco GS, Malandrini A, Comanducci G, Leuzzi V, Valoppi M, Tessa A, Palmeri S, Benedetti L, Pierallini A, Gambelli S, Federico A, Pierelli F, Bertini E, Casali C, Santorelli FM. Grieco GS, et al. Among authors: comanducci g. Neurology. 2004 Jan 13;62(1):103-6. doi: 10.1212/01.wnl.0000104491.66816.77. Neurology. 2004. PMID: 14718707
Six novel mutations of the RUNX2 gene in Italian patients with cleidocranial dysplasia.
Tessa A, Salvi S, Casali C, Garavelli L, Digilio MC, Dotti MT, Di Giandomenico S, Valoppi M, Grieco GS, Comanducci G, Bianchini G, Fortini D, Federico A, Giannotti A, Santorelli FM. Tessa A, et al. Among authors: comanducci g. Hum Mutat. 2003 Jul;22(1):104. doi: 10.1002/humu.9155. Hum Mutat. 2003. PMID: 12815605
Cerebellar atrophy in congenital fibrosis of the extraocular muscles type 1.
Di Fabio R, Comanducci G, Piccolo F, Santorelli FM, De Berardinis T, Tessa A, Sabatini U, Pierelli F, Casali C. Di Fabio R, et al. Among authors: comanducci g. Cerebellum. 2013 Feb;12(1):140-3. doi: 10.1007/s12311-012-0396-0. Cerebellum. 2013. PMID: 22699964 No abstract available.