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Author Details
Full Name
Ganna Balagura
Affiliation
IRCCS Istituto Giannina Gaslini
ORCID
Career Start Year
2018
Papers
27
H Index
11
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
35218524
Loss of Neuron Navigator 2 Impairs Brain and Cerebellar Development.
Cerebellum
2023
33998856
An Open Retrospective Study of a Standardized Cannabidiol Based-Oil in Treatment-Resistant Epilepsy.
Cannabis Cannabinoid Res
2022
35607920
De novo truncating NOVA2 variants affect alternative splicing and lead to heterogeneous neurodevelopmental phenotypes.
Hum Mutat
2022
35573960
A Phenotypic-Driven Approach for the Diagnosis of WOREE Syndrome.
Front Pediatr
2022
35854306
Genotype-phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disorders.
Orphanet J Rare Dis
2022
36142455
Vesicular Glutamate Release from Feeder-FreehiPSC-Derived Neurons.
Int J Mol Sci
2022
36124778
Current and promising therapeutic options for Dravet syndrome.
Expert Opin Pharmacother
2022
35190816
Assessing the landscape of STXBP1-related disorders in 534 individuals.
Brain
2022
35096710
Diagnostic Approach to Macrocephaly in Children.
Front Pediatr
2022
32840150
Intramuscular Midazolam for treatment of Status Epilepticus.
Expert Opin Pharmacother
2021
33851920
Temporal-parietal-occipital epilepsy in GEFS+ associated with SCN1A mutation.
Epileptic Disord
2021
34950099
New Trends and Most Promising Therapeutic Strategies for Epilepsy Treatment.
Front Neurol
2021
35002760
<i>STXBP1</i> Syndrome Is Characterized by Inhibition-Dominated Dynamics of Resting-State EEG.
Front Physiol
2021
34428314
Epilepsy care during the COVID-19 pandemic.
Epilepsia
2021
34033250
The initial impact of the SARS-CoV-2 pandemic on epilepsy research.
Epilepsia Open
2021
33949685
Modeling seizures in the Human Phenotype Ontology according to contemporary ILAE concepts makes big phenotypic data tractable.
Epilepsia
2021
33264411
The Human Phenotype Ontology in 2021.
Nucleic Acids Res
2021
32570172
Targeted re-sequencing in malformations of cortical development: genotype-phenotype correlations.
Seizure
2020
32103957
Adjunctive Rufinamide in Children with Lennox-Gastaut Syndrome: A Literature Review.
Neuropsychiatr Dis Treat
2020
32651081
Clinical spectrum and genotype-phenotype correlations in PRRT2 Italian patients.
Eur J Paediatr Neurol
2020
32875491
Fenfluramine for the Treatment of Dravet Syndrome and Lennox-Gastaut Syndrome.
CNS Drugs
2020
32581702
Loss of Wwox Perturbs Neuronal Migration and Impairs Early Cortical Development.
Front Neurosci
2020
32153206
Emerging treatments for progressive myoclonus epilepsies.
Expert Rev Neurother
2020
30719712
No evidence for a BRD2 promoter hypermethylation in blood leukocytes of Europeans with juvenile myoclonic epilepsy.
Epilepsia
2019
31099271
Moving beyond sodium valproate: choosing the right anti-epileptic drug in children.
Expert Opin Pharmacother
2019
30482063
Emerging drugs for the treatment of Dravet syndrome.
Expert Opin Emerg Drugs
2018
30003498
Pharmacokinetics and Drug Interaction of Antiepileptic Drugs in Children and Adolescents.
Paediatr Drugs
2018
1 - 27 of 27
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