IRIS
GAMBARDELLA, ANTONIO
 Distribuzione geografica
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Continente #
NA - Nord America 5.207
EU - Europa 1.466
AS - Asia 135
SA - Sud America 33
OC - Oceania 27
Continente sconosciuto - Info sul continente non disponibili 16
AF - Africa 10
Totale 6.894
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Nazione #
US - Stati Uniti d'America 5.014
SE - Svezia 489
IT - Italia 436
GB - Regno Unito 315
CA - Canada 190
IN - India 62
RO - Romania 54
DE - Germania 33
AU - Australia 22
UA - Ucraina 22
NL - Olanda 21
RU - Federazione Russa 21
FR - Francia 13
IR - Iran 13
CO - Colombia 12
ES - Italia 12
BR - Brasile 11
TR - Turchia 10
EU - Europa 9
JP - Giappone 9
CN - Cina 8
A2 - ???statistics.table.value.countryCode.A2??? 7
FI - Finlandia 7
CH - Svizzera 6
CL - Cile 6
MY - Malesia 6
PL - Polonia 6
ZA - Sudafrica 6
NZ - Nuova Zelanda 5
EG - Egitto 4
GR - Grecia 4
SG - Singapore 4
IE - Irlanda 3
IQ - Iraq 3
LV - Lettonia 3
MD - Moldavia 3
MK - Macedonia 3
MX - Messico 3
PE - Perù 3
TH - Thailandia 3
AE - Emirati Arabi Uniti 2
AT - Austria 2
BE - Belgio 2
BG - Bulgaria 2
CZ - Repubblica Ceca 2
KR - Corea 2
LU - Lussemburgo 2
PT - Portogallo 2
SA - Arabia Saudita 2
AM - Armenia 1
BD - Bangladesh 1
DK - Danimarca 1
HK - Hong Kong 1
ID - Indonesia 1
IL - Israele 1
KH - Cambogia 1
KZ - Kazakistan 1
LK - Sri Lanka 1
NO - Norvegia 1
PK - Pakistan 1
RS - Serbia 1
SY - Repubblica araba siriana 1
TW - Taiwan 1
UY - Uruguay 1
Totale 6.894
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Città #
Chandler 1.256
Princeton 464
Lawrence 461
London 282
Wilmington 273
Chicago 251
Ottawa 160
Des Moines 147
Ashburn 93
Catanzaro 66
Boardman 44
Pune 33
Norwalk 29
Redwood City 29
Horia 27
Redmond 21
Rome 21
Timisoara 18
Falls Church 13
Cetraro 12
Florence 12
Genoa 12
Milan 12
Los Angeles 11
Montréal 11
Ann Arbor 10
Augusta 10
Toronto 10
Naples 9
Aversa 8
Casalnuovo Di Napoli 8
Hanover 7
Mountain View 7
Amsterdam 6
Andover 6
Cagliari 6
Clearwater 6
Helsinki 6
Melbourne 6
Washington 6
West Jordan 6
Bethesda 5
Castiglion Fibocchi 5
Catania 5
Lamezia Terme 5
Misterbianco 5
Paris 5
Turin 5
Arau 4
Berlin 4
Carrara 4
Chennai 4
Cosenza 4
Crosia 4
Duncan 4
Ferrara 4
Konya 4
Leawood 4
Rende 4
San Mateo 4
Secaucus 4
Sydney 4
Tappahannock 4
Tehran 4
Treviso 4
Ardabil 3
Asti 3
Bern 3
Buffalo 3
Cambridge 3
Chisinau 3
Cittanova 3
Crotone 3
Danvers 3
Foggia 3
Guidonia Montecelio 3
Kemerovo 3
Las Rozas 3
Lexington 3
Locri 3
Lowell 3
Malatya 3
Missaglia 3
Montecorice 3
New York 3
Novara 3
Perth 3
Phoenix 3
Potenza 3
Reggio Calabria 3
Riga 3
Rotterdam 3
São Paulo 3
Verona 3
Virginia Beach 3
Willow Grove 3
Amantea 2
Auckland 2
Avella 2
Bari 2
Totale 4.079
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Nome #
Rasmussen's Encephalitis and Related Conditions. The Causes of Epilepsy Common and Uncommon Causes in Adults and Children 60
Genetics of reflex seizures and epilepsies in humans and animals 58
Erratum: Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals (The American Journal of Human Genetics (2021) 108(6) (965–982), (S0002929721001403), (10.1016/j.ajhg.2021.04.009)) 51
A brainstem hypermetabolism in a patient with essential palatal tremor: A simultaneous 18F-FDG-PET/3 T-MRI study 46
Rating Scale for Psychogenic Non-epileptic Seizures: Scale Development and Clinimetric Testing 36
A software pipeline for pre-processing and mining EEG signals: Application in neurology 36
Management of status epilepticus in patients with liver or kidney disease: a narrative review 34
Topographic divergence of atypical cortical asymmetry and atrophy patterns in temporal lobe epilepsy 34
Long-term outcome of mild mesial temporal lobe epilepsy 33
A new SLC20A2 mutation identified in southern Italy family with primary familial brain calcification. 32
Facemask headache: a new nosographic entity among healthcare providers in COVID-19 era 31
Mild non-lesional temporal lobe epilepsy. A common, unrecognized disorder with onset in adulthood 30
Usefulness of a morning routine EEG recording in patients with juvenile myoclonic epilepsy. 29
A puzzling case without solution: isolated late-onset epileptic seizure 29
A novel exon 1 mutation in a patient with atypical lafora progressive myoclonus epilepsy seen as childhood-onset cognitive deficit 29
Non-metabolic causes of triphasic waves: a reappraisal. 28
A hypofibrinolytic state in overweight patients with cerebral venous thrombosis and isolated intracranial hypertension 28
A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chomosome 1 28
A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chromosome 1 28
Polymorphism of the multidrug resistance 1 gene MDR1/ABCB1 C3435T and response to antiepileptic drug treatment in temporal lobe epilepsy 27
Kufs’ disease presenting as late-onset epilepsia partialis continua 27
Age at onset predicts good seizure outcome in sporadic non-lesional and mesial temporal sclerosis based temporal lobe epilepsy 27
A novel NF1 gene mutation in an Italian family with neurofibromatosis type 1. 27
A functional polymorphism in the SCN1A gene does not influence antiepileptic drug responsiveness in Italian patients with focal epilepsy 27
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy. 27
A novel ICA-based hardware system for reconfigurable and portable BCI 27
Incidental evidence of hypointensity in brain grey nuclei on routine MR imaging: when to suspect a neurodegenerative disorder? 27
Utilization of antiepileptic drugs during pregnancy: comparative patterns in 38 countries based on data from the EURAP registry 26
Quality of life outcomes of immediate or delayed treatment of early epilepsy and single seizures 26
Reversible symmetrical external capsule hyperintensity as an early finding of autoimmune encephalitis. 26
Gerstmann-Straussler-Scheinker disease with PRNP P102L heterozygous mutation presenting as progressive myoclonus epilepsy. 26
Temporal lobe abnormalities on brain MRI in healthy volunteers: a prospective case-control study 26
Advanced morphological neuroimaging study in lateral temporal lobe epilepsy: A multicentric study 26
An embedded system for EEG acquisition and processing for brain computer interface applications 26
Deep Learning Representation from Electroencephalography of Early-Stage Creutzfeldt-Jakob Disease and Features for Differentiation from Rapidly Progressive Dementia. 26
Increased risk for Alzheimer disease with the interaction of MPO and A2M polymorphisms 25
Benign familial infantile convulsions: mapping of a novel locus on chromosome 2q24 and evidence for genetic heterogeneity 25
Association study between four polymorphisms in the HFE, TF and TFR genes and Parkinson's disease in Southern Italy 25
Anti-N-methyl-D-aspartate-glutamic-receptor encephalitis presenting as paroxysmal exercise-induced foot weakness 25
Why should we change the term psychogenic nonepileptic seizures (PNES)? 25
Pharmacodynamics of the long-duration response to levodopa in PD 25
Diagnosis and misdiagnosis of adult neuronal ceroid lipofuscinosis (Kufs disease). 25
Determinants of health-related quality of life in pharmacoresistant epilepsy: Results from a large multicenter study of consecutively enrolled patients using validated quantitative assessments 25
A System for the Analysis of Snore Signals 25
Accidents at work among people with epilepsy. Results of a European prospective cohort study 25
Advances in genetic testing and optimization of clinical management in children and adults with epilepsy 25
TSC-associated neuropsychiatric disorders (TAND): findings from the TOSCA natural history study 24
Neuropsychological profile of mild temporal lobe epilepsy 24
Permutation entropy of scalp EEG: A tool to investigate epilepsies: Suggestions from absence epilepsies. 24
Integrity of the corpus callosum in patients with benign temporal lobe epilepsy 24
Functional activity changes in memory and emotional systems of healthy subjects with déjà vu. 24
Chlorpromazine versus sleep deprivation in activation of EEG in adult-onset partial epilepsy. 24
Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2 24
3-T magnetic resonance imaging simultaneous automated multimodal approach improves detection of ambiguous visual hippocampal sclerosis. 24
Alterations in the α2 δ ligand, thrombospondin-1, in a rat model of spontaneous absence epilepsy and in patients with idiopathic/genetic generalized epilepsies. 24
Design of an electronic device for brain computer interface applications 24
A novel mutation in the Notch3 gene in an Italian family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: genetic and magnetic resonance spectroscopic findings 24
Circulating microrna: The potential novel diagnostic biomarkers to predict drug resistance in temporal lobe epilepsy, a pilot study 24
Resting-State EEG Classification for PNES Diagnosis 23
GENETIC HETEROGENEITY IN AUTOSOMAL RECESSIVE HEREDITARY MOTOR AND SENSORY NEUROPHATY WITH FOCALLY FOLDED MYELIN SHEATHS (CMT4B) 23
White Matter Abnormalities Differentiate Severe from Benign Temporal Lobe Epilepsy. 23
Brand-to-Generic Levetiracetam Switching: a four-years prospective observational real-life study 23
Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies. 23
Linkage analysis and disease models in benign familial infantile seizures: a study of 16 families 23
A Loss-of-Function HCN4 Mutation Associated With Familial Benign Myoclonic Epilepsy in Infancy Causes Increased Neuronal Excitability 23
A. Spinal muscular atrophy due to an isolated deletion of Exon 8 of telomeric survival motor neuron gene 23
Diagnostic Biomarkers of Epilepsy 23
Brivaracetam: review of its pharmacology and potential use as adjunctive therapy in patients with partial onset seizures 23
A novel de novo HCN1 loss-of-function mutation in genetic generalized epilepsy causing increased neuronal excitability 23
An SNP site in pri-miR-124, a brain expressed miRNA gene, no contribution to mesial temporal lobe epilepsy in an Italian sample. 23
Clinical spectrum of SCN1A mutations 22
Dose-dependent teratogenicity of valproate in mono- and polytherapy: an observational study 22
Cerebral venous thrombosis and isolated intracrania hypertension without papilledema in CDH 22
Loss of long-duration response to levodopa over time in PD: implications for wearing-off 22
Presenilin-2 gene mutation presenting as Lewy Body dementia? 22
Neocortical thinning in “benign” mesial temporal lobe epilepsy 22
Characteristics of a large population of patients with refractory epilepsy attending tertiary referral centers in Italy 22
Prodynorphin gene promoter polymorphism and temporal lobe epilepsy 22
Negative myoclonic status due to a tapering of antiepileptic treatment. A report of three cases. 22
EURAP: An international registry of Antiepileptic drugs and pregnancy 22
Outcome of surgical treatment in patients with localized cortical dysplasia and intractable epilepsy. 22
Blocking out the real diagnosis 22
A novel mutation in the notch3 gene in an Italian family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: genetic and MRI spectroscopic analyses 22
Localization of a gene responsible for autosomal recessive demyelinating neuropathy with focally folded myelin sheaths to chromosome 11q23 by homozygosity mapping and haplotype sharing. 21
Association between the M129V variant allele of PRNP gene and mild temporal lobe epilepsy in women 21
Benign temporal lobe epilepsy 21
Negative myoclonus during valproate-related stupor. Neurophysiological evidence of a cortical non-epileptic origin. 21
Immediate versus deferred antiepileptic drug treatment for early epilepsy and single seizures: a randomised controlled trial 21
Value of clinical features to differentiate refractory epilepsy from mimics: a prospective longitudinal cohort study. 21
Photic-induced epileptic negative myoclonus 21
Clinical and genetic study of a large Charcot-Marie-Tooth type 2A family from southern Italy 21
Familial temporal lobe epilepsy autosomal dominant inheritance in a large pedigree from southern Italy 21
Psychiatric events in epilepsy 21
Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths 21
Validation Study of Italian Version of Inventory for Déjà Vu Experiences Assessment (I-IDEA): A Screening Tool to Detect Déjà Vu Phenomenon in Italian Healthy Individuals 21
Mild Lafora disease: Clinical, neurophysiologic, and genetic findings. 21
Modeling epileptogenic lesions and mapping networks - Imaging genetics for benign mesial temporal lobe epilepsy 21
Analysis of LGI1 promoter sequence, PDYN and GABBR1 polymorphisms in sporadic and familial lateral temporal lobe epilepsy 21
Perampanel as first add-on choice on the treatment of mesial temporal lobe epilepsy: an observational real-life study 21
Guillain-Barré syndrome following BNT162b2 COVID-19 vaccine 21
Totale 2.586
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Categoria #
all - tutte 105.381
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 105.381
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020350 0 0 0 13 19 1 10 19 25 37 77 149
2020/2021425 29 3 5 74 46 13 12 55 126 45 11 6
2021/20221.342 22 5 8 360 147 20 25 305 130 117 193 10
2022/20233.627 934 129 80 383 408 342 12 239 577 217 235 71
2023/20241.492 337 250 160 105 99 391 61 39 13 33 4 0
Totale 7.236