IRIS
GAMBARDELLA, ANTONIO
 Distribuzione geografica
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Continente #
EU - Europa 977
Totale 977
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Nazione #
IT - Italia 977
Totale 977
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Città #
Genova 519
Rapallo 225
Genoa 220
Bordighera 8
Vado Ligure 5
Totale 977
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Nome #
No evidence of a role for cystatin B gene in juvenile myoclonic epilepsy 130
DEPDC5 mutations are not a frequent cause of familial temporal lobe epilepsy 117
Epilepsy in cerebrovascular diseases: Review of experimental and clinical data with meta-analysis of risk factors 104
Genetics of reflex seizures and epilepsies in humans and animals 86
Mild Lafora disease: Clinical, neurophysiologic, and genetic findings 73
Benign familial infantile convulsions: Mapping of a novel locus on chromosome 2q24 and evidence for genetic heterogeneity 59
Benign Familial Neonatal-Infantile Seizures: Characterization of a New Sodium Channelopathy 41
Homozygous c.649dupC mutation in PRRT2 worsens the BFIS/PKD phenotype with mental retardation, episodic ataxia, and absences 35
Management of biological therapies for chronic plaque psoriasis during COVID-19 emergency in Italy 34
Artificial intelligence for classification of temporal lobe epilepsy with ROI-level MRI data: A worldwide ENIGMA-Epilepsy study 31
Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals 26
Atlas of lesion locations and postsurgical seizure freedom in focal cortical dysplasia: A MELD study 24
Assessing the role of rare genetic variants in drug-resistant, non-lesional focal epilepsy 24
Diagnostic and therapeutic approach to drug-resistant juvenile myoclonic epilepsy 22
Progressive Myoclonus Epilepsies Diagnostic Yield with Next-Generation Sequencing in Previously Unsolved Cases 21
Event-based modeling in temporal lobe epilepsy demonstrates progressive atrophy from cross-sectional data 20
Loss of Neuron Navigator 2 Impairs Brain and Cerebellar Development 20
Interpretable surface-based detection of focal cortical dysplasias: a Multi-centre Epilepsy Lesion Detection study 19
A systems-level analysis highlights microglial activation as a modifying factor in common epilepsies 18
Epilepsy in “Sunflower syndrome”: electroclinical features, therapeutic response, and long-term follow-up 18
GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture 16
Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals 15
Topographic divergence of atypical cortical asymmetry and atrophy patterns in temporal lobe epilepsy 13
Structural network alterations in focal and generalized epilepsy assessed in a worldwide ENIGMA study follow axes of epilepsy risk gene expression 11
Effectiveness of Perampanel as the Only Add-on: Retrospective, Multicenter, Observational Real Life Study on epilepsy patients 10
Electroclinical Features and Long-term Seizure Outcome in Patients With Eyelid Myoclonia With Absences 9
Secukinumab in Patients with Psoriasis and a Personal History of Malignancy: A Multicenter Real-Life Observational Study 7
Networks Underlie Temporal Onset of Dysplasia-Related Epilepsy: A MELD Study 6
Totale 1.009
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Categoria #
all - tutte 5.400
article - articoli 5.400
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 10.800
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020119 5 4 4 8 10 11 22 16 10 17 11 1
2020/2021174 4 1 4 55 25 1 26 27 4 22 3 2
2021/2022147 18 0 3 4 9 11 1 22 7 27 16 29
2022/2023262 22 5 5 20 54 36 2 16 51 3 44 4
2023/2024188 6 24 6 32 17 28 14 11 4 10 8 28
2024/202512 12 0 0 0 0 0 0 0 0 0 0 0
Totale 1.009