IRIS
GAMBARDELLA, ANTONIO
 Distribuzione geografica
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Continente #
EU - Europa 1.094
Totale 1.094
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Nazione #
IT - Italia 1.094
Totale 1.094
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Città #
Genova 519
Rapallo 218
Genoa 217
Vado Ligure 132
Bordighera 8
Totale 1.094
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Nome #
No evidence of a role for cystatin B gene in juvenile myoclonic epilepsy 135
DEPDC5 mutations are not a frequent cause of familial temporal lobe epilepsy 122
Epilepsy in cerebrovascular diseases: Review of experimental and clinical data with meta-analysis of risk factors 107
Genetics of reflex seizures and epilepsies in humans and animals 95
Mild Lafora disease: Clinical, neurophysiologic, and genetic findings 80
Benign familial infantile convulsions: Mapping of a novel locus on chromosome 2q24 and evidence for genetic heterogeneity 62
Benign Familial Neonatal-Infantile Seizures: Characterization of a New Sodium Channelopathy 47
Homozygous c.649dupC mutation in PRRT2 worsens the BFIS/PKD phenotype with mental retardation, episodic ataxia, and absences 39
Management of biological therapies for chronic plaque psoriasis during COVID-19 emergency in Italy 38
Artificial intelligence for classification of temporal lobe epilepsy with ROI-level MRI data: A worldwide ENIGMA-Epilepsy study 34
Diagnostic and therapeutic approach to drug-resistant juvenile myoclonic epilepsy 30
Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals 28
Assessing the role of rare genetic variants in drug-resistant, non-lesional focal epilepsy 28
Atlas of lesion locations and postsurgical seizure freedom in focal cortical dysplasia: A MELD study 27
Progressive Myoclonus Epilepsies Diagnostic Yield with Next-Generation Sequencing in Previously Unsolved Cases 27
Event-based modeling in temporal lobe epilepsy demonstrates progressive atrophy from cross-sectional data 24
Loss of Neuron Navigator 2 Impairs Brain and Cerebellar Development 24
A systems-level analysis highlights microglial activation as a modifying factor in common epilepsies 23
Interpretable surface-based detection of focal cortical dysplasias: a Multi-centre Epilepsy Lesion Detection study 23
GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture 22
Epilepsy in “Sunflower syndrome”: electroclinical features, therapeutic response, and long-term follow-up 22
Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals 22
Topographic divergence of atypical cortical asymmetry and atrophy patterns in temporal lobe epilepsy 18
Electroclinical Features and Long-term Seizure Outcome in Patients With Eyelid Myoclonia With Absences 14
Secukinumab in Patients with Psoriasis and a Personal History of Malignancy: A Multicenter Real-Life Observational Study 13
Structural network alterations in focal and generalized epilepsy assessed in a worldwide ENIGMA study follow axes of epilepsy risk gene expression 13
Networks Underlie Temporal Onset of Dysplasia-Related Epilepsy: A MELD Study 10
Totale 1.127
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Categoria #
all - tutte 6.465
article - articoli 6.465
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 12.930
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202098 0 0 0 0 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
2022/2023254 22 5 5 19 52 35 2 16 49 3 43 3
2023/2024186 5 24 6 31 17 28 14 11 4 10 8 28
2024/2025140 26 36 6 51 21 0 0 0 0 0 0 0
Totale 1.127