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Gellera, Cinzia
292  results:
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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