Nanetti L - Search Results

1

Comorbidities in Friedreich ataxia: incidence and manifestations from early to advanced disease stages.

Fichera M, Castaldo A, Mongelli A, Marchini G, Gellera C, Nanetti L, Mariotti C. Fichera M, et al. Among authors: nanetti l. Neurol Sci. 2022 Dec;43(12):6831-6838. doi: 10.1007/s10072-022-06360-w. Epub 2022 Sep 2. Neurol Sci. 2022. PMID: 36053339

2

Different patterns of movement-related cortical oscillations in patients with myoclonus and in patients with spinocerebellar ataxia.

Visani E, Mariotti C, Nanetti L, Mongelli A, Castaldo A, Panzica F, Franceschetti S, Canafoglia L. Visani E, et al. Among authors: nanetti l. Clin Neurophysiol. 2019 May;130(5):714-721. doi: 10.1016/j.clinph.2019.01.021. Epub 2019 Feb 16. Clin Neurophysiol. 2019. PMID: 30889419

3

Missing the pathological expansion in Huntington disease: de novo c.51C>G variant on the expanded allele causing intrafamilial allele dropout.

Magri S, Nanetti L, Mongelli A, Rizzo E, Taroni F, Mariotti C, Gellera C. Magri S, et al. Among authors: nanetti l. Am J Med Genet A. 2021 Feb;185(2):397-400. doi: 10.1002/ajmg.a.61973. Epub 2020 Nov 27. Am J Med Genet A. 2021. PMID: 33247537

4

Novel and recurrent spastin mutations in a large series of SPG4 Italian families.

Nanetti L, Baratta S, Panzeri M, Tomasello C, Lovati C, Azzollini J, Gellera C, Di Bella D, Taroni F, Mariotti C. Nanetti L, et al. Neurosci Lett. 2012 Oct 18;528(1):42-5. doi: 10.1016/j.neulet.2012.08.036. Epub 2012 Aug 25. Neurosci Lett. 2012. PMID: 22960362

5

Predictive genetic tests in neurodegenerative disorders: a methodological approach integrating psychological counseling for at-risk individuals and referring clinicians.

Mariotti C, Ferruta A, Gellera C, Nespolo C, Fancellu R, Genitrini S, Di Bella D, Panzeri M, Nanetti L, Tomasello C, Taroni F, Foresti G, Astori S. Mariotti C, et al. Among authors: nanetti l. Eur Neurol. 2010;64(1):33-41. doi: 10.1159/000315033. Epub 2010 Jun 30. Eur Neurol. 2010. PMID: 20588047

6

Whole body cholesterol metabolism is impaired in Huntington's disease.

Leoni V, Mariotti C, Nanetti L, Salvatore E, Squitieri F, Bentivoglio AR, Bandettini di Poggio M, Piacentini S, Monza D, Valenza M, Cattaneo E, Di Donato S. Leoni V, et al. Among authors: nanetti l. Neurosci Lett. 2011 May 2;494(3):245-9. doi: 10.1016/j.neulet.2011.03.025. Epub 2011 Mar 22. Neurosci Lett. 2011. PMID: 21406216

7

Pendular nystagmus in progressive ataxia and palatal tremor.

Bassani R, Mariotti C, Nanetti L, Grisoli M, Savoiardo M, Pareyson D, Salsano E. Bassani R, et al. Among authors: nanetti l. J Neurol. 2011 Oct;258(10):1877-9. doi: 10.1007/s00415-011-6007-z. Epub 2011 Mar 25. J Neurol. 2011. PMID: 21437662 No abstract available.

8

Homozygous variant in OTX2 and possible genetic modifiers identified in a patient with combined pituitary hormone deficiency, ocular involvement, myopathy, ataxia, and mitochondrial impairment.

Catania A, Legati A, Peverelli L, Nanetti L, Marchet S, Zanetti N, Lamperti C, Ghezzi D. Catania A, et al. Among authors: nanetti l. Am J Med Genet A. 2019 May;179(5):827-831. doi: 10.1002/ajmg.a.61092. Epub 2019 Feb 17. Am J Med Genet A. 2019. PMID: 30773800

9

PMP22 messenger RNA levels in skin biopsies: testing the effectiveness of a Charcot-Marie-Tooth 1A biomarker.

Nobbio L, Visigalli D, Radice D, Fiorina E, Solari A, Lauria G, Reilly MM, Santoro L, Schenone A, Pareyson D; CMT-TRIAAL Group. Nobbio L, et al. Brain. 2014 Jun;137(Pt 6):1614-20. doi: 10.1093/brain/awu071. Epub 2014 May 8. Brain. 2014. PMID: 24812204

10

Responsiveness of clinical outcome measures in Charcot-Marie-Tooth disease.

Piscosquito G, Reilly MM, Schenone A, Fabrizi GM, Cavallaro T, Santoro L, Manganelli F, Vita G, Quattrone A, Padua L, Gemignani F, Visioli F, Laurà M, Calabrese D, Hughes RA, Radice D, Solari A, Pareyson D; CMT-TRIAAL Group; CMT-TRAUK Group. Piscosquito G, et al. Eur J Neurol. 2015 Dec;22(12):1556-63. doi: 10.1111/ene.12783. Epub 2015 Jul 31. Eur J Neurol. 2015. PMID: 26227902

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