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Mignarri, Andrea
95  results:
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1

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/..
 
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2

Spinocerebellar ataxia 27B: a frequent and slowly progressi..:

Satolli, Sara ; Rossi, Salvatore ; Vegezzi, Elisa...
Journal of Neurology.  , 2024
Link: https://doi.org/10.1007/..
 
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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/..
 
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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/..
 
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5

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/..
 
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6

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/..
 
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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/..
 
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8

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/..
 
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9

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/..
 
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10

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/..
 
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11

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/..
 
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12

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/..
 
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13

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/..
 
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14

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/..
 
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15

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/..
 
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