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Mignarri, Andrea
95
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Online (95)
Mediatypes
Articles (Online) (54)
OpenAccess-fulltext (41)
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Sorted by: Year
?
1
Spinocerebellar ataxia 27B: a frequent and slowly progressi..:
Satolli, Sara
;
Rossi, Salvatore
;
Vegezzi, Elisa
...
Journal of Neurology. , 2024
Link:
https://doi.org/10.1007/..
?
2
Oculomotor features in SCA27B patients:
Lopergolo, Diego
;
Bargagli, Alessia
;
Satolli, Sara
...
Clinical Neurophysiology. 158 (2024) - p. 56-58 , 2024
Link:
https://doi.org/10.1016/..
?
3
Correction to: Monoallelic KIF1A-related disorders: a multi..:
Della Vecchia, Stefania
;
Tessa, Alessandra
;
Dosi, Claudia
...
Journal of Neurology. 270 (2023) 4 - p. 2345-2346 , 2023
Link:
https://doi.org/10.1007/..
?
4
Using Cluster Analysis to Overcome the Limits of Traditiona..:
Dosi, Claudia
;
Rubegni, Anna
;
Baldacci, Jacopo
...
Genes. 14 (2023) 2 - p. 298 , 2023
Link:
https://doi.org/10.3390/..
?
5
24S-Hydroxycholesterol and Cerebellar Degeneration: Insight..:
Locci, Sara
;
Nidiaci, Valentina
;
De Stefano, Nicola
..
The Cerebellum. 22 (2022) 5 - p. 1020-1022 , 2022
Link:
https://doi.org/10.1007/..
?
6
Clinical Features and Outcome of the Guillain–Barre Syndrom..:
Ginanneschi, Federica
;
Giannini, Fabio
;
Sicurelli, Francesco
...
Frontiers in Neurology. 13 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
?
7
Primary familial brain calcification with mild phenotype du..:
Locci, Sara
;
Bianchi, Silvia
;
De Stefano, Nicola
.
Neurological Sciences. 43 (2022) 10 - p. 6091-6093 , 2022
Link:
https://doi.org/10.1007/..
?
8
Correction to: Monoallelic KIF1A-related disorders: a multi..:
Della Vecchia, Stefania
;
Tessa, Alessandra
;
Dosi, Claudia
...
Journal of Neurology. 269 (2021) 1 - p. 451-451 , 2021
Link:
https://doi.org/10.1007/..
?
9
Monoallelic KIF1A-related disorders: a multicenter cross se..:
Vecchia, Stefania Della
;
Tessa, Alessandra
;
Dosi, Claudia
...
Journal of Neurology. 269 (2021) 1 - p. 437-450 , 2021
Link:
https://doi.org/10.1007/..
?
10
Co-occurrence of DMPK expansion and CLCN1 mutation in a pat..:
Locci, Sara
;
Cardani, Rosanna
;
Brunori, Paola
...
Neurological Sciences. 42 (2021) 12 - p. 5365-5368 , 2021
Link:
https://doi.org/10.1007/..
?
11
Gordon Holmes syndrome caused by two novel mutations in the..:
Locci, Sara
;
Bianchi, Silvia
;
Tessa, Alessandra
..
Clinical Neurology and Neurosurgery. 207 (2021) - p. 106763 , 2021
Link:
https://doi.org/10.1016/..
?
12
Expert opinion on diagnosing, treating and managing patient..:
Stelten, Bianca M. L.
;
Dotti, Maria Teresa
;
Verrips, Aad
...
Orphanet Journal of Rare Diseases. 16 (2021) 1 - p. , 2021
Link:
https://doi.org/10.1186/..
?
13
NGS in Hereditary Ataxia: When Rare Becomes Frequent:
Galatolo, Daniele
;
De Michele, Giovanna
;
Silvestri, Gabriella
...
International Journal of Molecular Sciences. 22 (2021) 16 - p. 8490 , 2021
Link:
https://doi.org/10.3390/..
?
14
Episodic ataxia and severe infantile phenotype in spinocere..:
De Michele, Giovanna
;
Galatolo, Daniele
;
Galosi, Serena
...
Journal of Neurology. 269 (2021) 3 - p. 1476-1484 , 2021
Link:
https://doi.org/10.1007/..
?
15
Clinical and genetic features of a large cohort of Italian ..:
Rossi, Salvatore
;
Santorelli, Filippo Maria
;
Silvestri, Gabriella
...
Journal of the Neurological Sciences. 429 (2021) - p. 118251 , 2021
Link:
https://doi.org/10.1016/..
1-15