I agree that this site is using cookies. You can find further informations here.
X
Freri, Elena
155  results:
Online X
?
1

De novo monoallelic Reelin missense variants cause dominant..:

Riva, Martina ; Ferreira, Sofia ; Hayashi, Kotaro...
Journal of Clinical Investigation.  134 (2024)  16 - p. , 2024
Link: https://doi.org/10.1172/..
 
?
2

Early occurrence of photic-reflex myoclonus in CDKL5-defici..:

Caputo, Davide ; Franceschetti, Silvana ; Canafoglia, Laura...
Clinical Neurophysiology.  163 (2024)  - p. 37-38 , 2024
Link: https://doi.org/10.1016/..
 
?
3

Cortical Myoclonus and Complex Paroxysmal Dyskinesias in a ..:

Freri, Elena ; Canafoglia, Laura ; Ciaccio, Claudia...
Movement Disorders.  39 (2024)  7 - p. 1238-1240 , 2024
Link: https://doi.org/10.1002/..
 
?
4

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/..
 
?
5

The effect of executive function on health related quality ..:

Zanaboni, Martina Paola ; Pasca, Ludovica ; Bergamoni, Stefania...
Epilepsy & Behavior.  152 (2024)  - p. 109607 , 2024
Link: https://doi.org/10.1016/..
 
?
6

Long‐term effectiveness of add‐on perampanel in patients wi..:

Matricardi, Sara ; Cesaroni, Elisabetta ; Bonanni, Paolo...
Epilepsia.  64 (2023)  6 - p. , 2023
Link: https://doi.org/10.1111/..
 
?
7

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/..
 
?
8

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/..
 
?
9

Repetitive Sleep Starts in Allan-Herndon-Dudley Syndrome:

Solazzi, Roberta ; Nanni, Giuliana ; Esposito, Silvia...
Pediatric Neurology.  147 (2023)  - p. 24-27 , 2023
Link: https://doi.org/10.1016/..
 
?
10

CDKL5 deficiency disorder: progressive brain atrophy may be..:

Specchio, Nicola ; Trivisano, Marina ; Lenge, Matteo...
Cerebral Cortex.  33 (2023)  17 - p. 9709-9717 , 2023
Link: https://doi.org/10.1093/..
 
?
11

Case report: SLC6A1 mutations presenting with isolated abse..:

Caputo, Davide ; Franceschetti, Silvana ; Castellotti, Barbara...
Frontiers in Neuroscience.  17 (2023)  - p. , 2023
Link: https://doi.org/10.3389/..
 
?
12

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/..
 
?
13

Monoallelic and biallelic mutations in RELN underlie a grad..:

Di Donato, Nataliya ; Guerrini, Renzo ; Billington Jr, Charles J...
Brain.  145 (2022)  9 - p. 3274-3287 , 2022
Link: https://doi.org/10.1093/..
 
?
14

Ocular phenotype and electroretinogram abnormalities in Laf..:

Orsini, Alessandro ; Ferrari, Daniele ; Riva, Antonella...
Journal of Neurology.  269 (2022)  7 - p. 3597-3604 , 2022
Link: https://doi.org/10.1007/..
 
?
15

Functional Characterization of Two Variants at the Intron 6..:

Mosca, Ilaria ; Rivolta, Ilaria ; Labalme, Audrey...
Frontiers in Pharmacology.  13 (2022)  - p. , 2022
Link: https://doi.org/10.3389/..
 
1-15