受强制性开放获取政策约束的文章 - Roberto Fancellu了解详情
无法在其他位置公开访问的文章：3 篇
Self‐rated health status in spinocerebellar ataxia—Results from a European multicenter study
T Schmitz‐Hübsch, M Coudert, P Giunti, C Globas, L Baliko, R Fancellu, ...
Movement disorders 25 (5), 587-595, 2010
强制性开放获取政策： German Research Foundation, Hungarian Scientific Research Fund
Erythropoietin in Friedreich ataxia: no effect on frataxin in a randomized controlled trial
C Mariotti, R Fancellu, S Caldarazzo, L Nanetti, D Di Bella, M Plumari, ...
Movement Disorders 27 (3), 446-449, 2012
强制性开放获取政策： Government of Spain
Dopaminergic and Serotonergic Degeneration and Cortical [18F]Fluorodeoxyglucose Positron Emission Tomography in De Novo Parkinson's Disease
B Orso, D Arnaldi, N Girtler, A Brugnolo, E Doglione, P Mattioli, E Biassoni, ...
Movement Disorders 36 (10), 2293-2302, 2021
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：5 篇
The natural history of spinocerebellar ataxia type 1, 2, 3, and 6: a 2-year follow-up study
H Jacobi, P Bauer, P Giunti, R Labrum, MG Sweeney, P Charles, A Duerr, ...
Neurology 77 (11), 1035-1041, 2011
强制性开放获取政策： German Research Foundation, Hungarian Scientific Research Fund, Government …
Inventory of Non-Ataxia Signs (INAS): validation of a new clinical assessment instrument
H Jacobi, M Rakowicz, R Rola, R Fancellu, C Mariotti, P Charles, A Dürr, ...
The Cerebellum 12, 418-428, 2013
强制性开放获取政策： German Research Foundation, National Institute of Health and Medical …
Spinocerebellar ataxia types 1, 2, 3 and 6: the clinical spectrum of ataxia and morphometric brainstem and cerebellar findings
H Jacobi, TK Hauser, P Giunti, C Globas, P Bauer, T Schmitz-Hübsch, ...
The Cerebellum 11, 155-166, 2012
强制性开放获取政策： German Research Foundation, Hungarian Scientific Research Fund, Government …
Digenic inheritance of STUB1 variants and TBP polyglutamine expansions explains the incomplete penetrance of SCA17 and SCA48
S Magri, L Nanetti, C Gellera, E Sarto, E Rizzo, A Mongelli, B Ricci, ...
Genetics in Medicine 24 (1), 29-40, 2022
强制性开放获取政策： Government of Italy
Leber's hereditary optic neuropathy: a report on novel mtDNA pathogenic variants
L Peverelli, A Catania, S Marchet, P Ciasca, G Cammarata, L Melzi, ...
Frontiers in Neurology 12, 657317, 2021
强制性开放获取政策： European Commission, Government of Italy
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