受强制性开放获取政策约束的文章 - Anna Castaldo了解详情
无法在其他位置公开访问的文章：7 篇
Spinocerebellar ataxia type 1: one-year longitudinal study to identify clinical and MRI measures of disease progression in patients and presymptomatic carriers
A Nigri, L Sarro, A Mongelli, A Castaldo, L Porcu, C Pinardi, M Grisoli, ...
The Cerebellum 21 (1), 133-144, 2022
强制性开放获取政策： Government of Italy
ANO10 mutational screening in recessive ataxia: genetic findings and refinement of the clinical phenotype
L Nanetti, E Sarto, A Castaldo, S Magri, A Mongelli, D Rossi Sebastiano, ...
Journal of Neurology 266, 378-385, 2019
强制性开放获取政策： Government of Italy
Stance instability in preclinical SCA1 mutation carriers: a 4-year prospective posturography study
L Nanetti, D Alpini, V Mattei, A Castaldo, A Mongelli, G Brenna, C Gellera, ...
Gait & posture 57, 11-14, 2017
强制性开放获取政策： Government of Italy
Monitoring disease progression in spinocerebellar ataxias: implications for treatment and clinical research
L Sarro, L Nanetti, A Castaldo, C Mariotti
Expert review of neurotherapeutics 17 (9), 919-931, 2017
强制性开放获取政策： Government of Italy
Comorbidities in Friedreich ataxia: incidence and manifestations from early to advanced disease stages
M Fichera, A Castaldo, A Mongelli, G Marchini, C Gellera, L Nanetti, ...
Neurological Sciences 43 (12), 6831-6838, 2022
强制性开放获取政策： Government of Italy
Cortical network dysfunction revealed by magnetoencephalography in carriers of spinocerebellar ataxia 1 or 2 mutation
E Visani, C Mariotti, L Nanetti, A Mongelli, A Castaldo, F Panzica, ...
Clinical Neurophysiology 131 (7), 1548-1555, 2020
强制性开放获取政策： Government of Italy
Different patterns of movement-related cortical oscillations in patients with myoclonus and in patients with spinocerebellar ataxia
E Visani, C Mariotti, L Nanetti, A Mongelli, A Castaldo, F Panzica, ...
Clinical Neurophysiology 130 (5), 714-721, 2019
强制性开放获取政策： Government of Italy
可在其他位置公开访问的文章：15 篇
Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study
DJH Moss, AF Pardiñas, D Langbehn, K Lo, BR Leavitt, R Roos, A Durr, ...
The Lancet Neurology 16 (9), 701-711, 2017
强制性开放获取政策： UK Medical Research Council, National Institute for Health Research, UK …
Progression characteristics of the European Friedreich’s Ataxia Consortium for Translational Studies (EFACTS): a 2 year cohort study
K Reetz, I Dogan, RD Hilgers, P Giunti, C Mariotti, A Durr, S Boesch, ...
The Lancet Neurology 15 (13), 1346-1354, 2016
强制性开放获取政策： Federal Ministry of Education and Research, Germany
Progression characteristics of the European Friedreich's Ataxia Consortium for Translational Studies (EFACTS): a 4-year cohort study
K Reetz, I Dogan, RD Hilgers, P Giunti, MH Parkinson, C Mariotti, ...
The Lancet Neurology 20 (5), 362-372, 2021
强制性开放获取政策： US National Institutes of Health, Austrian Science Fund
Clinical and genetic characteristics of late-onset Huntington's disease
M Oosterloo, EK Bijlsma, SM Van Kuijk, F Minkels, CEM de Die-Smulders
Parkinsonism & related disorders 61, 101-105, 2019
强制性开放获取政策： UK Medical Research Council, Wellcome Trust
Progression of cerebellar atrophy in spinocerebellar ataxia type 2 gene carriers: a longitudinal MRI study in preclinical and early disease stages
A Nigri, L Sarro, A Mongelli, C Pinardi, L Porcu, A Castaldo, S Ferraro, ...
Frontiers in Neurology 11, 616419, 2020
强制性开放获取政策： Government of Italy
Prediction of survival with long‐term disease progression in Most common spinocerebellar ataxia
A Diallo, H Jacobi, A Cook, P Giunti, MH Parkinson, R Labrum, A Durr, ...
Movement Disorders 34 (8), 1220-1227, 2019
强制性开放获取政策： German Research Foundation, National Institute for Health Research, UK …
Fiberoptic endoscopic evaluation of swallowing in early-to-advanced stage Huntington’s disease
A Schindler, N Pizzorni, J Sassone, L Nanetti, A Castaldo, B Poletti, ...
Scientific Reports 10 (1), 15242, 2020
强制性开放获取政策： Fondazione Telethon, Italy, Government of Italy
MRI evidence of cerebellar and extraocular muscle atrophy differently contributing to eye movement abnormalities in SCA2 and SCA28 diseases
LS Politi, SB Marzoli, C Godi, M Panzeri, P Ciasca, G Brugnara, ...
Investigative Ophthalmology & Visual Science 57 (6), 2714-2720, 2016
强制性开放获取政策： Government of Italy
Cognitive reserve in early manifest Huntington disease patients: leisure time is associated with lower cognitive and functional impairment
S Migliore, G D’Aurizio, E Scaricamazza, S Maffi, C Ceccarelli, G Ristori, ...
Journal of personalized medicine 12 (1), 36, 2022
强制性开放获取政策： Government of Italy
Utility of the Parkinson’s disease-Cognitive Rating Scale for the screening of global cognitive status in Huntington’s disease
S Martinez-Horta, A Horta-Barba, J Perez-Perez, F Sampedro, N de Lucia, ...
Journal of Neurology 267, 1527-1535, 2020
强制性开放获取政策： UK Medical Research Council, Government of Spain
Complex Ataxia‐Dementia Phenotype in Patients with Digenic TBP/STUB1 Spinocerebellar Ataxia
L Nanetti, S Magri, M Fichera, A Castaldo, A Nigri, C Pinardi, A Mongelli, ...
Movement Disorders 38 (4), 665-675, 2023
强制性开放获取政策： Fondazione Cariplo, Government of Italy
Multifaceted and Age-Dependent Phenotypes Associated With Biallelic PNPLA6 Gene Variants: Eight Novel Cases and Review of the Literature
L Nanetti, D Di Bella, S Magri, M Fichera, E Sarto, A Castaldo, A Mongelli, ...
Frontiers in Neurology 12, 793547, 2022
强制性开放获取政策： Government of Italy
JNK signaling provides a novel therapeutic target for Rett syndrome
CA Musi, AM Castaldo, AE Valsecchi, S Cimini, N Morello, R Pizzo, ...
BMC biology 19, 1-20, 2021
强制性开放获取政策： European Commission, Government of Italy
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