Di Donato S - Search Results

1

Frontal cortex BOLD signal changes in premanifest Huntington disease: a possible fMRI biomarker.

Ferraro S, Nanetti L, Piacentini S, Mandelli ML, Bertolino N, Ghielmetti F, Epifani F, Nigri A, Taroni F, Bruzzone MG, Di Donato S, Savoiardo M, Mariotti C, Grisoli M. Ferraro S, et al. Among authors: di donato s. Neurology. 2014 Jul 1;83(1):65-72. doi: 10.1212/WNL.0000000000000538. Epub 2014 Jun 4. Neurology. 2014. PMID: 24898924 Free PMC article.

2

Plasma 24S-hydroxycholesterol and caudate MRI in pre-manifest and early Huntington's disease.

Leoni V, Mariotti C, Tabrizi SJ, Valenza M, Wild EJ, Henley SM, Hobbs NZ, Mandelli ML, Grisoli M, Björkhem I, Cattaneo E, Di Donato S. Leoni V, et al. Among authors: di donato s. Brain. 2008 Nov;131(Pt 11):2851-9. doi: 10.1093/brain/awn212. Epub 2008 Sep 4. Brain. 2008. PMID: 18772220

3

Spinocerebellar ataxia type 17 (SCA17): oculomotor phenotype and clinical characterization of 15 Italian patients.

Mariotti C, Alpini D, Fancellu R, Soliveri P, Grisoli M, Ravaglia S, Lovati C, Fetoni V, Giaccone G, Castucci A, Taroni F, Gellera C, Di Donato S. Mariotti C, et al. Among authors: di donato s. J Neurol. 2007 Nov;254(11):1538-46. doi: 10.1007/s00415-007-0579-7. Epub 2007 Oct 15. J Neurol. 2007. PMID: 17934876

4

Spinocerebellar ataxia type 28.

Mariotti C, Bella DD, Di Donato S, Taroni F. Mariotti C, et al. Among authors: di donato s. Handb Clin Neurol. 2012;103:575-9. doi: 10.1016/B978-0-444-51892-7.00039-5. Handb Clin Neurol. 2012. PMID: 21827917

5

An overview of the patient with ataxia.

Mariotti C, Fancellu R, Di Donato S. Mariotti C, et al. Among authors: di donato s. J Neurol. 2005 May;252(5):511-8. doi: 10.1007/s00415-005-0814-z. J Neurol. 2005. PMID: 15895274 Review.

6

Pathogenic effect of an intermediate-size SCA-6 allele (CAG)(19) in a homozygous patient.

Mariotti C, Gellera C, Grisoli M, Mineri R, Castucci A, Di Donato S. Mariotti C, et al. Among authors: di donato s. Neurology. 2001 Oct 23;57(8):1502-4. doi: 10.1212/wnl.57.8.1502. Neurology. 2001. PMID: 11673601

7

Decreased diffusivity in the caudate nucleus of presymptomatic huntington disease gene carriers: which explanation?

Mandelli ML, Savoiardo M, Minati L, Mariotti C, Aquino D, Erbetta A, Genitrini S, Di Donato S, Bruzzone MG, Grisoli M. Mandelli ML, et al. Among authors: di donato s. AJNR Am J Neuroradiol. 2010 Apr;31(4):706-10. doi: 10.3174/ajnr.A1891. Epub 2009 Nov 26. AJNR Am J Neuroradiol. 2010. PMID: 19942704 Free PMC article.

8

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: di donato s. 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

9

Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study.

Moss DJH, Pardiñas AF, Langbehn D, Lo K, Leavitt BR, Roos R, Durr A, Mead S; TRACK-HD investigators; REGISTRY investigators; Holmans P, Jones L, Tabrizi SJ. Moss DJH, et al. Lancet Neurol. 2017 Sep;16(9):701-711. doi: 10.1016/S1474-4422(17)30161-8. Epub 2017 Jun 20. Lancet Neurol. 2017. PMID: 28642124

10

Pathways to motor incoordination: the inherited ataxias.

Taroni F, DiDonato S. Taroni F, et al. Nat Rev Neurosci. 2004 Aug;5(8):641-55. doi: 10.1038/nrn1474. Nat Rev Neurosci. 2004. PMID: 15263894 Review. No abstract available.

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