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Diffusion-weighted brain imaging study of patients with clinical diagnosis of corticobasal degeneration, progressive supranuclear palsy and Parkinson's disease.
Rizzo G, Martinelli P, Manners D, Scaglione C, Tonon C, Cortelli P, Malucelli E, Capellari S, Testa C, Parchi P, Montagna P, Barbiroli B, Lodi R. Rizzo G, et al. Among authors: capellari s. Brain. 2008 Oct;131(Pt 10):2690-700. doi: 10.1093/brain/awn195. Epub 2008 Sep 26. Brain. 2008. PMID: 18819991
Pathologic correlates of diffusion MRI changes in Creutzfeldt-Jakob disease.
Manners DN, Parchi P, Tonon C, Capellari S, Strammiello R, Testa C, Tani G, Malucelli E, Spagnolo C, Cortelli P, Montagna P, Lodi R, Barbiroli B. Manners DN, et al. Among authors: capellari s. Neurology. 2009 Apr 21;72(16):1425-31. doi: 10.1212/WNL.0b013e3181a18846. Neurology. 2009. PMID: 19380702
Magnetic resonance diagnostic markers in clinically sporadic prion disease: a combined brain magnetic resonance imaging and spectroscopy study.
Lodi R, Parchi P, Tonon C, Manners D, Capellari S, Strammiello R, Rinaldi R, Testa C, Malucelli E, Mostacci B, Rizzo G, Pierangeli G, Cortelli P, Montagna P, Barbiroli B. Lodi R, et al. Among authors: capellari s. Brain. 2009 Oct;132(Pt 10):2669-79. doi: 10.1093/brain/awp210. Epub 2009 Sep 15. Brain. 2009. PMID: 19755520 Free PMC article.
Loss of temporal retinal nerve fibers in Parkinson disease: a mitochondrial pattern?
La Morgia C, Barboni P, Rizzo G, Carbonelli M, Savini G, Scaglione C, Capellari S, Bonazza S, Giannoccaro MP, Calandra-Buonaura G, Liguori R, Cortelli P, Martinelli P, Baruzzi A, Carelli V. La Morgia C, et al. Among authors: capellari s. Eur J Neurol. 2013 Jan;20(1):198-201. doi: 10.1111/j.1468-1331.2012.03701.x. Epub 2012 Mar 21. Eur J Neurol. 2013. PMID: 22436028
Nuclear lamins: functions and clinical implications.
Cortelli P, Terlizzi R, Capellari S, Benarroch E. Cortelli P, et al. Among authors: capellari s. Neurology. 2012 Oct 16;79(16):1726-31. doi: 10.1212/WNL.0b013e31826ea887. Neurology. 2012. PMID: 23071165 Review. No abstract available.
Analysis of LMNB1 duplications in autosomal dominant leukodystrophy provides insights into duplication mechanisms and allele-specific expression.
Giorgio E, Rolyan H, Kropp L, Chakka AB, Yatsenko S, Di Gregorio E, Lacerenza D, Vaula G, Talarico F, Mandich P, Toro C, Pierre EE, Labauge P, Capellari S, Cortelli P, Vairo FP, Miguel D, Stubbolo D, Marques LC, Gahl W, Boespflug-Tanguy O, Melberg A, Hassin-Baer S, Cohen OS, Pjontek R, Grau A, Klopstock T, Fogel B, Meijer I, Rouleau G, Bouchard JP, Ganapathiraju M, Vanderver A, Dahl N, Hobson G, Brusco A, Brussino A, Padiath QS. Giorgio E, et al. Among authors: capellari s. Hum Mutat. 2013 Aug;34(8):1160-71. doi: 10.1002/humu.22348. Epub 2013 May 28. Hum Mutat. 2013. PMID: 23649844 Free PMC article.
Gait disorders in fatal familial insomnia.
Cortelli P, Fabbri M, Calandra-Buonaura G, Capellari S, Tinuper P, Parchi P, Lugaresi E. Cortelli P, et al. Among authors: capellari s. Mov Disord. 2014 Mar;29(3):420-4. doi: 10.1002/mds.25786. Epub 2013 Dec 27. Mov Disord. 2014. PMID: 24375448
223 results