Massarelli M - Search Results

1

A case of restless leg syndrome in a family with LRRK2 gene mutation.

De Rosa A, Guacci A, Peluso S, Del Gaudio L, Massarelli M, Barbato S, Criscuolo C, De Michele G. De Rosa A, et al. Among authors: massarelli m. Int J Neurosci. 2013 Apr;123(4):283-5. doi: 10.3109/00207454.2012.756485. Epub 2013 Feb 4. Int J Neurosci. 2013. PMID: 23227859

2

Closing-in Phenomenon in Huntington's Disease: A Neuropsychological Marker of Frontal/Executive Dysfunction.

De Lucia N, Peluso S, Roca A, Russo CV, Massarelli M, De Michele G, Di Maio L, Salvatore E, De Michele G. De Lucia N, et al. Among authors: massarelli m. Arch Clin Neuropsychol. 2019 Feb 1;34(1):24-30. doi: 10.1093/arclin/acy020. Arch Clin Neuropsychol. 2019. PMID: 29554249

3

Insulin sensitivity and early-phase insulin secretion in normoglycemic Huntington's disease patients.

Russo CV, Salvatore E, Saccà F, Tucci T, Rinaldi C, Sorrentino P, Massarelli M, Rossi F, Savastano S, Di Maio L, Filla A, Colao A, De Michele G. Russo CV, et al. Among authors: massarelli m. J Huntingtons Dis. 2013;2(4):501-7. doi: 10.3233/JHD-130078. J Huntingtons Dis. 2013. PMID: 25062734

4

A longitudinal real-life comparison study of natalizumab and fingolimod.

Lanzillo R, Carotenuto A, Moccia M, Saccà F, Russo CV, Massarelli M, De Rosa A, Brescia Morra V. Lanzillo R, et al. Among authors: massarelli m. Acta Neurol Scand. 2017 Sep;136(3):217-222. doi: 10.1111/ane.12718. Epub 2016 Dec 15. Acta Neurol Scand. 2017. PMID: 27976804

5

Default-mode network changes in Huntington's disease: an integrated MRI study of functional connectivity and morphometry.

Quarantelli M, Salvatore E, Giorgio SM, Filla A, Cervo A, Russo CV, Cocozza S, Massarelli M, Brunetti A, De Michele G. Quarantelli M, et al. Among authors: massarelli m. PLoS One. 2013 Aug 19;8(8):e72159. doi: 10.1371/journal.pone.0072159. eCollection 2013. PLoS One. 2013. PMID: 23977239 Free PMC article.

6

The Framingham cardiovascular risk score in multiple sclerosis.

Moccia M, Lanzillo R, Palladino R, Maniscalco GT, De Rosa A, Russo C, Massarelli M, Carotenuto A, Postiglione E, Caporale O, Triassi M, Brescia Morra V. Moccia M, et al. Among authors: massarelli m. Eur J Neurol. 2015 Aug;22(8):1176-83. doi: 10.1111/ene.12720. Epub 2015 Apr 27. Eur J Neurol. 2015. PMID: 25912468

7

Clinical manifestations of intermediate allele carriers in Huntington disease.

Cubo E, Ramos-Arroyo MA, Martinez-Horta S, Martínez-Descalls A, Calvo S, Gil-Polo C; European HD Network. Cubo E, et al. Neurology. 2016 Aug 9;87(6):571-8. doi: 10.1212/WNL.0000000000002944. Epub 2016 Jul 8. Neurology. 2016. PMID: 27402890

8

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

9

Reduced Cancer Incidence in Huntington's Disease: Analysis in the Registry Study.

McNulty P, Pilcher R, Ramesh R, Necuiniate R, Hughes A, Farewell D, Holmans P, Jones L; REGISTRY Investigators of the European Huntington's Disease Network. McNulty P, et al. J Huntingtons Dis. 2018;7(3):209-222. doi: 10.3233/JHD-170263. J Huntingtons Dis. 2018. PMID: 30103338

10

β-Defensin genomic copy number does not influence the age of onset in Huntington's Disease.

Vittori A, Orth M, Roos RA, Outeiro TF, Giorgini F, Hollox EJ; Registry investigators of the European Huntington's Disease Network. Vittori A, et al. J Huntingtons Dis. 2013;2(1):107-24. doi: 10.3233/JHD-130002. J Huntingtons Dis. 2013. PMID: 25057107

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