Mariotti C - Search Results

1

Impaired temporal processing of tactile and proprioceptive stimuli in cerebellar degeneration.

Tinazzi M, Morgante F, Peretti A, Mariotti C, Panzeri M, Fiorio M, Fasano A. Tinazzi M, et al. Among authors: mariotti c. PLoS One. 2013 Nov 11;8(11):e78628. doi: 10.1371/journal.pone.0078628. eCollection 2013. PLoS One. 2013. PMID: 24244328 Free PMC article. Clinical Trial.

2

Supratentorial and pontine MRI abnormalities characterize recessive spastic ataxia of Charlevoix-Saguenay. A comprehensive study of an Italian series.

Prodi E, Grisoli M, Panzeri M, Minati L, Fattori F, Erbetta A, Uziel G, D'Arrigo S, Tessa A, Ciano C, Santorelli FM, Savoiardo M, Mariotti C. Prodi E, et al. Among authors: mariotti c. Eur J Neurol. 2013 Jan;20(1):138-46. doi: 10.1111/j.1468-1331.2012.03815.x. Epub 2012 Jul 21. Eur J Neurol. 2013. PMID: 22816526

3

Erythropoietin in Friedreich ataxia.

Mariotti C, Nachbauer W, Panzeri M, Poewe W, Taroni F, Boesch S. Mariotti C, et al. J Neurochem. 2013 Aug;126 Suppl 1:80-7. doi: 10.1111/jnc.12301. J Neurochem. 2013. PMID: 23859343 Free article. Review.

4

SETX mutations are a frequent genetic cause of juvenile and adult onset cerebellar ataxia with neuropathy and elevated serum alpha-fetoprotein.

Nanetti L, Cavalieri S, Pensato V, Erbetta A, Pareyson D, Panzeri M, Zorzi G, Antozzi C, Moroni I, Gellera C, Brusco A, Mariotti C. Nanetti L, et al. Among authors: mariotti c. Orphanet J Rare Dis. 2013 Aug 14;8:123. doi: 10.1186/1750-1172-8-123. Orphanet J Rare Dis. 2013. PMID: 23941260 Free PMC article.

5

The role of the cerebellum in dynamic changes of the sense of body ownership: a study in patients with cerebellar degeneration.

Fiorio M, Mariotti C, Panzeri M, Antonello E, Classen J, Tinazzi M. Fiorio M, et al. Among authors: mariotti c. J Cogn Neurosci. 2014 Apr;26(4):712-21. doi: 10.1162/jocn_a_00522. Epub 2013 Nov 18. J Cogn Neurosci. 2014. PMID: 24236765

6

The cerebellum and visual perceptual learning: evidence from a motion extrapolation task.

Deluca C, Golzar A, Santandrea E, Lo Gerfo E, Eštočinová J, Moretto G, Fiaschi A, Panzeri M, Mariotti C, Tinazzi M, Chelazzi L. Deluca C, et al. Among authors: mariotti c. Cortex. 2014 Sep;58:52-71. doi: 10.1016/j.cortex.2014.04.017. Epub 2014 Jun 2. Cortex. 2014. PMID: 24959702

7

Biological and clinical characteristics of the European Friedreich's Ataxia Consortium for Translational Studies (EFACTS) cohort: a cross-sectional analysis of baseline data.

Reetz K, Dogan I, Costa AS, Dafotakis M, Fedosov K, Giunti P, Parkinson MH, Sweeney MG, Mariotti C, Panzeri M, Nanetti L, Arpa J, Sanz-Gallego I, Durr A, Charles P, Boesch S, Nachbauer W, Klopstock T, Karin I, Depondt C, vom Hagen JM, Schöls L, Giordano IA, Klockgether T, Bürk K, Pandolfo M, Schulz JB. Reetz K, et al. Among authors: mariotti c. Lancet Neurol. 2015 Feb;14(2):174-82. doi: 10.1016/S1474-4422(14)70321-7. Epub 2015 Jan 5. Lancet Neurol. 2015. PMID: 25566998 Clinical Trial.

8

Quantifiable evaluation of cerebellar signs in children.

Filipovic Pierucci A, Mariotti C, Panzeri M, Giunti P, Boesch S, Schulz JB, Pandolfo M, Durr A, Tezenas du Montcel S; EFACTS Study Group. Filipovic Pierucci A, et al. Among authors: mariotti c. Neurology. 2015 Mar 24;84(12):1225-32. doi: 10.1212/WNL.0000000000001403. Epub 2015 Feb 25. Neurology. 2015. PMID: 25716360

9

Long-term disease progression in spinocerebellar ataxia types 1, 2, 3, and 6: a longitudinal cohort study.

Jacobi H, du Montcel ST, Bauer P, Giunti P, Cook A, Labrum R, Parkinson MH, Durr A, Brice A, Charles P, Marelli C, Mariotti C, Nanetti L, Panzeri M, Rakowicz M, Sulek A, Sobanska A, Schmitz-Hübsch T, Schöls L, Hengel H, Baliko L, Melegh B, Filla A, Antenora A, Infante J, Berciano J, van de Warrenburg BP, Timmann D, Szymanski S, Boesch S, Kang JS, Pandolfo M, Schulz JB, Molho S, Diallo A, Klockgether T. Jacobi H, et al. Among authors: mariotti c. Lancet Neurol. 2015 Nov;14(11):1101-8. doi: 10.1016/S1474-4422(15)00202-1. Epub 2015 Sep 13. Lancet Neurol. 2015. PMID: 26377379

10

MRI Evidence of Cerebellar and Extraocular Muscle Atrophy Differently Contributing to Eye Movement Abnormalities in SCA2 and SCA28 Diseases.

Politi LS, Bianchi Marzoli S, Godi C, Panzeri M, Ciasca P, Brugnara G, Castaldo A, Di Bella D, Taroni F, Nanetti L, Mariotti C. Politi LS, et al. Among authors: mariotti c. Invest Ophthalmol Vis Sci. 2016 May 1;57(6):2714-20. doi: 10.1167/iovs.15-18732. Invest Ophthalmol Vis Sci. 2016. PMID: 27196319

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