BALAGURA, GANNA
 Distribuzione geografica
Continente #
EU - Europa 1.216
Totale 1.216
Nazione #
IT - Italia 1.216
Totale 1.216
Città #
Genova 492
Genoa 343
Rapallo 312
Vado Ligure 64
Bordighera 5
Totale 1.216
Nome #
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders 112
The bedside and the bench of STXBP1-DEE in the wake of precision medicine 101
No evidence for a BRD2 promoter hypermethylation in blood leukocytes of Europeans with juvenile myoclonic epilepsy 94
Clinical spectrum and genotype-phenotype correlations in PRRT2 Italian patients 81
Emerging treatments for progressive myoclonus epilepsies 61
Loss of Wwox Perturbs Neuronal Migration and Impairs Early Cortical Development 60
Targeted re-sequencing in malformations of cortical development: genotype-phenotype correlations 57
Fenfluramine for the Treatment of Dravet Syndrome and Lennox–Gastaut Syndrome 53
Genotype-phenotype correlations in patients with de novo KCNQ2 pathogenic variants 53
Adjunctive rufinamide in children with lennox-gastaut syndrome: A literature review 50
Moving beyond sodium valproate: choosing the right anti-epileptic drug in children 48
Emerging drugs for the treatment of Dravet syndrome 46
Pharmacokinetics and drug interaction of antiepileptic drugs in children and adolescents 43
Intramuscular Midazolam for treatment of Status Epilepticus 39
Epilepsy Course and Developmental Trajectories in STXBP1-DEE 38
Diagnostic Approach to Macrocephaly in Children 35
A Phenotypic-Driven Approach for the Diagnosis of WOREE Syndrome 31
Genotype-phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disorders 31
Vesicular glutamate release from feeder-free hiPSC-derived neurons 29
New Trends and Most Promising Therapeutic Strategies for Epilepsy Treatment 27
De novo truncating NOVA2 variants affect alternative splicing and lead to heterogeneous neurodevelopmental phenotypes 25
Assessing the landscape of STXBP1-related disorders in 534 individuals 24
STXBP1 Syndrome Is Characterized by Inhibition-Dominated Dynamics of Resting-State EEG 22
Loss of Neuron Navigator 2 Impairs Brain and Cerebellar Development 21
Natural History Study of STXBP1-Developmental and Epileptic Encephalopathy Into Adulthood 20
GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture 19
Current and promising therapeutic options for Dravet syndrome 17
An Open Retrospective Study of a Standardized Cannabidiol Based-Oil in Treatment-Resistant Epilepsy 16
Temporal-parietal-occipital epilepsy in GEFS+ associated with SCN1A mutation 7
Identification of Central Nervous System Oncologic Disease Biomarkers in EVs from Cerebrospinal Fluid (CSF) of Pediatric Patients: A Pilot Neuro-Proteomic Study 2
Totale 1.262
Categoria #
all - tutte 6.623
article - articoli 6.388
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 13.011


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202081 0 0 2 5 8 8 14 9 11 12 6 6
2020/2021234 3 2 10 71 7 4 4 28 10 33 40 22
2021/2022192 8 4 5 8 10 15 11 35 11 44 5 36
2022/2023369 24 40 11 48 46 47 2 28 58 5 41 19
2023/2024275 11 30 8 29 28 57 11 18 11 9 32 31
2024/202594 37 48 9 0 0 0 0 0 0 0 0 0
Totale 1.262