Nanetti L - Search Results

1

Cortical thickness, stance control, and arithmetic skill: An exploratory study in premanifest Huntington disease.

Nanetti L, Contarino VE, Castaldo A, Sarro L, Bachoud-Levi AC, Giavazzi M, Frittoli S, Ciammola A, Rizzo E, Gellera C, Bruzzone MG, Taroni F, Grisoli M, Mariotti C. Nanetti L, et al. Parkinsonism Relat Disord. 2018 Jun;51:17-23. doi: 10.1016/j.parkreldis.2018.02.033. Epub 2018 Feb 23. Parkinsonism Relat Disord. 2018. PMID: 29496355

2

Rare association of motor neuron disease and spinocerebellar ataxia type 2 (SCA2): a new case and review of the literature.

Nanetti L, Fancellu R, Tomasello C, Gellera C, Pareyson D, Mariotti C. Nanetti L, et al. J Neurol. 2009 Nov;256(11):1926-8. doi: 10.1007/s00415-009-5237-9. Epub 2009 Jul 31. J Neurol. 2009. PMID: 19644730 Review.

3

Co-occurrence of amyotrophic lateral sclerosis and Charcot-Marie-Tooth disease type 2A in a patient with a novel mutation in the mitofusin-2 gene.

Marchesi C, Ciano C, Salsano E, Nanetti L, Milani M, Gellera C, Taroni F, Fabrizi GM, Uncini A, Pareyson D. Marchesi C, et al. Among authors: nanetti l. Neuromuscul Disord. 2011 Feb;21(2):129-31. doi: 10.1016/j.nmd.2010.09.009. Epub 2010 Oct 14. Neuromuscul Disord. 2011. PMID: 20951041

4

Lower limb areflexia without central and peripheral conduction abnormalities is highly suggestive of Gerstmann-Sträussler-Scheinker disease Pro102Leu.

Salsano E, Fancellu R, Di Fede G, Ciano C, Scaioli V, Nanetti L, Politi LS, Tagliavini F, Mariotti C, Pareyson D. Salsano E, et al. Among authors: nanetti l. J Neurol Sci. 2011 Mar 15;302(1-2):85-8. doi: 10.1016/j.jns.2010.11.019. Epub 2010 Dec 16. J Neurol Sci. 2011. PMID: 21167505

5

Choice-option evaluation is preserved in early Huntington and Parkinson's disease.

Minati L, Piacentini S, Ferrè F, Nanetti L, Romito L, Mariotti C, Grisoli M, Medford N, Critchley HD, Albanese A. Minati L, et al. Among authors: nanetti l. Neuroreport. 2011 Oct 26;22(15):753-7. doi: 10.1097/WNR.0b013e32834acb6e. Neuroreport. 2011. PMID: 21876465

6

Erythropoietin in Friedreich ataxia: no effect on frataxin in a randomized controlled trial.

Mariotti C, Fancellu R, Caldarazzo S, Nanetti L, Di Bella D, Plumari M, Lauria G, Cappellini MD, Duca L, Solari A, Taroni F. Mariotti C, et al. Among authors: nanetti l. Mov Disord. 2012 Mar;27(3):446-9. doi: 10.1002/mds.24066. Epub 2012 Jan 4. Mov Disord. 2012. PMID: 22411849 Clinical Trial.

7

ATAXIN2 CAG-repeat length in Italian patients with amyotrophic lateral sclerosis: risk factor or variant phenotype? Implication for genetic testing and counseling.

Gellera C, Ticozzi N, Pensato V, Nanetti L, Castucci A, Castellotti B, Lauria G, Taroni F, Silani V, Mariotti C. Gellera C, et al. Among authors: nanetti l. Neurobiol Aging. 2012 Aug;33(8):1847.e15-21. doi: 10.1016/j.neurobiolaging.2012.02.004. Epub 2012 Mar 16. Neurobiol Aging. 2012. PMID: 22425256

8

Biological and clinical characteristics of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 in the longitudinal RISCA study: analysis of baseline data.

Jacobi H, Reetz K, du Montcel ST, Bauer P, Mariotti C, Nanetti L, Rakowicz M, Sulek A, Durr A, Charles P, Filla A, Antenora A, Schöls L, Schicks J, Infante J, Kang JS, Timmann D, Di Fabio R, Masciullo M, Baliko L, Melegh B, Boesch S, Bürk K, Peltz A, Schulz JB, Dufaure-Garé I, Klockgether T. Jacobi H, et al. Among authors: nanetti l. Lancet Neurol. 2013 Jul;12(7):650-8. doi: 10.1016/S1474-4422(13)70104-2. Epub 2013 May 22. Lancet Neurol. 2013. PMID: 23707147

9

Suicidal ideation in a European Huntington's disease population.

Hubers AA, van Duijn E, Roos RA, Craufurd D, Rickards H, Bernhard Landwehrmeyer G, van der Mast RC, Giltay EJ; REGISTRY investigators of the European Huntington's Disease Network. Hubers AA, et al. J Affect Disord. 2013 Oct;151(1):248-58. doi: 10.1016/j.jad.2013.06.001. Epub 2013 Jul 20. J Affect Disord. 2013. PMID: 23876196 Free article.

10

The V471A polymorphism in autophagy-related gene ATG7 modifies age at onset specifically in Italian Huntington disease patients.

Metzger S, Walter C, Riess O, Roos RA, Nielsen JE, Craufurd D; REGISTRY Investigators of the European Huntington’s Disease Network; Nguyen HP. Metzger S, et al. PLoS One. 2013 Jul 22;8(7):e68951. doi: 10.1371/journal.pone.0068951. Print 2013. PLoS One. 2013. PMID: 23894380 Free PMC article.

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