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Gellera, Cinzia
292
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Online (292)
Mediatypes
Articles (Online) (130)
Bookchapter (Online) (2)
OpenAccess-fulltext (160)
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1
Six‐minute walk test as outcome measure of fatigability in ..:
Govoni, Alessandra
;
Ricci, Giulia
;
Bonanno, Silvia
...
Muscle & Nerve. , 2024
Link:
https://doi.org/10.1002/..
?
2
Case report: Marked electroclinical improvement by fluoxeti..:
Mosca, Ilaria
;
Freri, Elena
;
Ambrosino, Paolo
...
Frontiers in Cellular Neuroscience. 18 (2024) - p. , 2024
Link:
https://doi.org/10.3389/..
?
3
Progressive myoclonus epilepsies due to SEMA6B mutations. N..:
Castellotti, Barbara
;
Canafoglia, Laura
;
Freri, Elena
...
Epilepsia Open. 8 (2023) 2 - p. 645-650 , 2023
Link:
https://doi.org/10.1002/..
?
4
A novel de novo HCN2 loss‐of‐function variant causing devel..:
DiFrancesco, Jacopo C.
;
Ragona, Francesca
;
Murano, Carmen
...
Epilepsia. 64 (2023) 12 - p. , 2023
Link:
https://doi.org/10.1111/..
?
5
Generation of an iPSC line from a patient with spastic para..:
Santangelo, Serena
;
Bossolasco, Patrizia
;
Magri, Stefania
...
Stem Cell Research. 66 (2023) - p. 103008 , 2023
Link:
https://doi.org/10.1016/..
?
6
Adult-onset leukodystrophy with vanishing white matter: a c..:
Benzoni, Chiara
;
Moscatelli, Marco
;
Farina, Laura
...
Journal of Neurology. 270 (2023) 9 - p. 4219-4234 , 2023
Link:
https://doi.org/10.1007/..
?
7
MiR-146a in ALS: Contribution to Early Peripheral Nerve Deg..:
Giagnorio, Eleonora
;
Malacarne, Claudia
;
Cavalcante, Paola
...
International Journal of Molecular Sciences. 24 (2023) 5 - p. 4610 , 2023
Link:
https://doi.org/10.3390/..
?
8
Complex Ataxia‐Dementia Phenotype in Patients with Digenic ..:
Nanetti, Lorenzo
;
Magri, Stefania
;
Fichera, Mario
...
Movement Disorders. 38 (2023) 4 - p. 665-675 , 2023
Link:
https://doi.org/10.1002/..
?
9
A novel KCNC1 gain‐of‐function variant causing developmenta..:
Ambrosino, Paolo
;
Ragona, Francesca
;
Mosca, Ilaria
...
Epilepsia. 64 (2023) 7 - p. , 2023
Link:
https://doi.org/10.1111/..
?
10
Digenic inheritance of STUB1 variants and TBP polyglutamine..:
Magri, Stefania
;
Nanetti, Lorenzo
;
Gellera, Cinzia
...
Genetics in Medicine. 24 (2022) 1 - p. 29-40 , 2022
Link:
https://doi.org/10.1016/..
?
11
Behavioral and Cognitive Phenotypes of Patients With Amyotr..:
Dalla Bella, Eleonora
;
Bersano, Enrica
;
Bruzzone, Maria Grazia
...
Neurology. 99 (2022) 18 - p. , 2022
Link:
https://doi.org/10.1212/..
?
12
Structural variation analysis of 6,500 whole genome sequenc..:
Al Khleifat, Ahmad
;
Iacoangeli, Alfredo
;
van Vugt, Joke J. F. A.
...
npj Genomic Medicine. 7 (2022) 1 - p. , 2022
Link:
https://doi.org/10.1038/..
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13
Missense mutation in ATXN2 gene (c.2860C > T) in an amyotro..:
Ghezzi, Andrea
;
Martinelli, Ilaria
;
Carra, Serena
...
Neurological Sciences. 43 (2022) 10 - p. 6087-6090 , 2022
Link:
https://doi.org/10.1007/..
?
14
G507D mutation in FUS gene causes familial amyotrophic late..:
Martinelli, Ilaria
;
Zucchi, Elisabetta
;
Pensato, Viviana
...
Neurobiology of Aging. 118 (2022) - p. 124-128 , 2022
Link:
https://doi.org/10.1016/..
?
15
Identification of a cytokine profile in serum and cerebrosp..:
Bonanno, Silvia
;
Cavalcante, Paola
;
Salvi, Erika
...
Frontiers in Cellular Neuroscience. 16 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
1-15