Detalhe da pesquisa
1.
Ataxia and Hypogonadism: a Review of the Associated Genes and Syndromes.
Cerebellum
; 23(2): 688-701, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-36997834
2.
Introversion and Neuroticism in Akinetic-Rigid Parkinson's Disease: Association With Frontal-Executive Dysfunction.
J Neuropsychiatry Clin Neurosci
; 35(3): 228-235, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36999250
3.
Screening for Fabry disease in a series of Parkinson's disease patients and literature review.
Neurol Sci
; 44(4): 1235-1241, 2023 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-36547780
4.
Autonomic disorders and myocardial 123I-metaiodobenzylguanidine scintigraphy in Huntington's disease.
J Nucl Cardiol
; 29(2): 642-648, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32803674
5.
Constructional Impairments and Their Neural Correlates in Nondemented Adults With Cerebral Autosomal-dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy.
Cogn Behav Neurol
; 35(4): 247-254, 2022 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36149396
6.
Cutaneous sensory and autonomic denervation in progressive supranuclear palsy.
Neuropathol Appl Neurobiol
; 47(5): 653-663, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33421177
7.
Optical coherence tomography angiography findings in Huntington's disease.
Neurol Sci
; 42(3): 995-1001, 2021 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-32700226
8.
Othello syndrome in Parkinson's disease: a systematic review and report of a case series.
Neurol Sci
; 42(7): 2721-2729, 2021 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-33978871
9.
Coverage of the requirements of first and second level stroke unit in Italy.
Neurol Sci
; 42(3): 1073-1079, 2021 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-32737805
10.
Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber's hereditary optic neuropathy.
PLoS Genet
; 14(2): e1007210, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29444077
11.
NGS in Hereditary Ataxia: When Rare Becomes Frequent.
Int J Mol Sci
; 22(16)2021 Aug 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-34445196
12.
DNA damage signatures in peripheral blood cells as biomarkers in prodromal huntington disease.
Ann Neurol
; 85(2): 296-301, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30549309
13.
Application of the p9NORM correction method to timed neuropsychological tests in Parkinson's disease and multiple system atrophy.
Neurol Sci
; 41(12): 3633-3641, 2020 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-32462388
14.
Spinocerebellar ataxia type 48: last but not least.
Neurol Sci
; 41(9): 2423-2432, 2020 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-32342324
15.
Primary familial brain calcification caused by a novel homozygous MYORG mutation in a consanguineous Italian family.
Neurogenetics
; 20(2): 99-102, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30895394
16.
Degenerative and acquired sporadic adult onset ataxia.
Neurol Sci
; 40(7): 1335-1342, 2019 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-30927137
17.
The flavor test is a sensitive tool in identifying the flavor sensorineural dysfunction in Parkinson's disease.
Neurol Sci
; 40(7): 1351-1356, 2019 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-30895397
18.
Longitudinal study of a cohort of MSA-C patients in South Italy: survival and clinical features.
Neurol Sci
; 40(10): 2105-2109, 2019 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-31152261
19.
Mutations in the SPAST gene causing hereditary spastic paraplegia are related to global topological alterations in brain functional networks.
Neurol Sci
; 40(5): 979-984, 2019 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-30737580
20.
The Italian version of the quick mild cognitive impairment (Qmci-I) screen: normative study on 307 healthy subjects.
Aging Clin Exp Res
; 31(3): 353-360, 2019 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-29949025