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Balagura, Ganna
100
results:
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Format
Online (100)
Mediatypes
Articles (Online) (27)
OpenAccess-fulltext (73)
Sorted by: Relevance
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1
Early Developmental Intervention and Enriched Environment i..:
Perinelli, Martina Giorgia
;
Naboni, Cecilia
;
Balagura, Ganna
...
Neurology Clinical Practice. 14 (2024) 3 - p. , 2024
Link:
https://doi.org/10.1212/..
?
2
High-throughput assay for regulated secretion of neuropepti..:
Baginska, Urszula
;
Balagura, Ganna
;
Toonen, Ruud F.
.
Journal of Biological Chemistry. 300 (2024) 6 - p. 107321 , 2024
Link:
https://doi.org/10.1016/..
?
3
Allelic heterogeneity and abnormal vesicle recycling in PLA..:
Iacomino, Michele
;
Houerbi, Nadia
;
Fortuna, Sara
...
Frontiers in Molecular Neuroscience. 17 (2024) - p. , 2024
Link:
https://doi.org/10.3389/..
?
4
GWAS meta-analysis of over 29,000 people with epilepsy iden..:
International League Against Epilepsy Consortium on Complex Epilepsies
;
Stevelink, Remi
;
Campbell, Ciarán
...
Nature Genetics. 55 (2023) 9 - p. 1471-1482 , 2023
Link:
https://doi.org/10.1038/..
?
5
Identification of Central Nervous System Oncologic Disease ..:
Kajana, Xhuliana
;
Spinelli, Sonia
;
Garbarino, Andrea
...
Biomolecules. 13 (2023) 12 - p. 1730 , 2023
Link:
https://doi.org/10.3390/..
?
6
Vesicular Glutamate Release from Feeder-FreehiPSC-Derived N..:
Baldassari, Simona
;
Cervetto, Chiara
;
Amato, Sarah
...
International Journal of Molecular Sciences. 23 (2022) 18 - p. 10545 , 2022
Link:
https://doi.org/10.3390/..
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7
Loss of Neuron Navigator 2 Impairs Brain and Cerebellar Dev..:
Accogli, Andrea
;
Lu, Shenzhao
;
Musante, Ilaria
...
The Cerebellum. 22 (2022) 2 - p. 206-222 , 2022
Link:
https://doi.org/10.1007/..
?
8
A Phenotypic-Driven Approach for the Diagnosis of WOREE Syn..:
Riva, Antonella
;
Nobile, Giulia
;
Giacomini, Thea
...
Frontiers in Pediatrics. 10 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
?
9
De novo truncatingNOVA2variants affect alternative splicing..:
Scala, Marcello
;
Drouot, Nathalie
;
MacLennan, Suzanna C.
...
Human Mutation. 43 (2022) 9 - p. 1299-1313 , 2022
Link:
https://doi.org/10.1002/..
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10
Genotype–phenotype correlations and disease mechanisms in P..:
Borgia, Paola
;
Baldassari, Simona
;
Pedemonte, Nicoletta
...
Orphanet Journal of Rare Diseases. 17 (2022) 1 - p. , 2022
Link:
https://doi.org/10.1186/..
?
11
Natural History Study of STXBP1-Developmental and Epileptic..:
Stamberger, Hannah
;
Crosiers, David
;
Balagura, Ganna
...
Neurology. 99 (2022) 3 - p. , 2022
Link:
https://doi.org/10.1212/..
?
12
Diagnostic Approach to Macrocephaly in Children:
Accogli, Andrea
;
Geraldo, Ana Filipa
;
Piccolo, Gianluca
...
Frontiers in Pediatrics. 9 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
?
13
Epilepsy care during the COVID‐19 pandemic:
Cross, J Helen
;
Kwon, Churl‐Su
;
Asadi‐Pooya, Ali Akbar
...
Epilepsia. 62 (2021) 10 - p. 2322-2332 , 2021
Link:
https://doi.org/10.1111/..
?
14
STXBP1 Syndrome Is Characterized by Inhibition-Dominated Dy..:
Houtman, Simon J.
;
Lammertse, Hanna C. A.
;
van Berkel, Annemiek A.
...
Frontiers in Physiology. 12 (2021) - p. , 2021
Link:
https://doi.org/10.3389/..
?
15
Assessing the landscape of STXBP1-related disorders in 534 ..:
Xian, Julie
;
Parthasarathy, Shridhar
;
Ruggiero, Sarah M
...
Brain. 145 (2021) 5 - p. 1668-1683 , 2021
Link:
https://doi.org/10.1093/..
1-15