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Investigation of quantitative magnetisation transfer parameters of lesions and normal appearing white matter in multiple sclerosis.
NMR Biomed. 2009 Jul;22(6):646-53. doi: 10.1002/nbm.1379.
NMR Biomed. 2009.
PMID: 19322806
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
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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
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Intrafamilial variability in hereditary spastic paraplegia associated with an SPG4 gene mutation.
Santorelli FM, Patrono C, Fortini D, Tessa A, Comanducci G, Bertini E, Pierallini A, Amabile GA, Casali C.
Santorelli FM, et al. Among authors: comanducci g.
Neurology. 2000 Sep 12;55(5):702-5. doi: 10.1212/wnl.55.5.702.
Neurology. 2000.
PMID: 10980739
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Current insights into familial spastic paraparesis: new advances in an old disease.
Fortini D, Cricchi F, Di Fabio R, Damiano M, Comanducci G, Benedetti L, Valoppi M, Grieco GS, D'Eugenio O, Celato A, Santorelli F, Casali C, Amabile GA, Pierelli F.
Fortini D, et al. Among authors: comanducci g.
Funct Neurol. 2003 Jan-Mar;18(1):43-9.
Funct Neurol. 2003.
PMID: 12760414
Review.
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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
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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.
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Apathetic syndrome from carotid dissection: a dangerous condition.
Gerace C, Corsi FM, Comanducci G.
Gerace C, et al. Among authors: comanducci g.
BMJ Case Rep. 2013 Sep 2;2013:bcr2013009686. doi: 10.1136/bcr-2013-009686.
BMJ Case Rep. 2013.
PMID: 24000207
Free PMC article.
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