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Granata, Tiziana
243
results:
Search for persons
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Online (243)
Mediatypes
Articles (Online) (137)
Bookchapter (Online) (3)
OpenAccess-fulltext (103)
Sorted by: Relevance
Sorted by: Year
?
1
Novel lissencephaly-associated NDEL1 variant reveals distin..:
Tsai, Meng-Han
;
Ke, Hao-Chen
;
Lin, Wan-Cian
...
Acta Neuropathologica. 147 (2024) 1 - p. , 2024
Link:
https://doi.org/10.1007/..
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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/..
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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
Retrospective study on neonatal seizures in a tertiary cent..:
Dilena, Robertino
;
Molisso, Maria T.
;
De Carli, Agnese
...
Epilepsy & Behavior. 159 (2024) - p. 109971 , 2024
Link:
https://doi.org/10.1016/..
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6
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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7
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/..
?
8
GLUT1-DS Italian registry: past, present, and future: a use..:
Varesio, Costanza
;
De Giorgis, Valentina
;
Veggiotti, Pierangelo
...
Orphanet Journal of Rare Diseases. 18 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1186/..
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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/..
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10
A registry for Dravet syndrome: The Italian experience:
Balestrini, Simona
;
Doccini, Viola
;
Giometto, Sabrina
...
Epilepsia Open. 8 (2023) 2 - p. 517-534 , 2023
Link:
https://doi.org/10.1002/..
?
11
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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12
Clinical and Neurophysiologic Phenotypes in Neonates WithBR..:
Carapancea, Evelina
;
Cornet, Marie-Coralie
;
Milh, Mathieu
...
Neurology. 100 (2023) 12 - p. , 2023
Link:
https://doi.org/10.1212/..
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13
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/..
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14
GNAO1-related movement disorder: An update on phenomenology..:
Novelli, Maria
;
Galosi, Serena
;
Zorzi, Giovanna
...
Parkinsonism & Related Disorders. 111 (2023) - p. 105405 , 2023
Link:
https://doi.org/10.1016/..
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15
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/..
1-15