IRIS
GAMBARDELLA, ANTONIO
 Distribuzione geografica
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Continente #
NA - Nord America 6.107
AS - Asia 2.470
EU - Europa 2.428
SA - Sud America 87
OC - Oceania 28
AF - Africa 17
Continente sconosciuto - Info sul continente non disponibili 16
Totale 11.153
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Nazione #
US - Stati Uniti d'America 5.907
SG - Singapore 1.802
IT - Italia 1.117
SE - Svezia 489
CN - Cina 466
GB - Regno Unito 316
CA - Canada 193
EE - Estonia 108
DE - Germania 79
IN - India 68
NL - Olanda 63
BR - Brasile 60
HK - Hong Kong 56
RO - Romania 56
FI - Finlandia 35
RU - Federazione Russa 35
FR - Francia 25
AU - Australia 23
UA - Ucraina 23
IR - Iran 14
JP - Giappone 13
ES - Italia 12
TR - Turchia 11
AT - Austria 10
CH - Svizzera 10
CO - Colombia 10
CZ - Repubblica Ceca 9
EU - Europa 9
PL - Polonia 9
ZA - Sudafrica 8
A2 - ???statistics.table.value.countryCode.A2??? 7
MX - Messico 7
CL - Cile 6
MY - Malesia 6
IE - Irlanda 5
NZ - Nuova Zelanda 5
BE - Belgio 4
EG - Egitto 4
GR - Grecia 4
IQ - Iraq 4
KR - Corea 4
PE - Perù 4
PK - Pakistan 4
BD - Bangladesh 3
LV - Lettonia 3
MD - Moldavia 3
MK - Macedonia 3
SA - Arabia Saudita 3
VE - Venezuela 3
AR - Argentina 2
BG - Bulgaria 2
ID - Indonesia 2
LU - Lussemburgo 2
NG - Nigeria 2
PT - Portogallo 2
TW - Taiwan 2
UG - Uganda 2
AE - Emirati Arabi Uniti 1
AM - Armenia 1
AZ - Azerbaigian 1
CI - Costa d'Avorio 1
DK - Danimarca 1
EC - Ecuador 1
IL - Israele 1
JO - Giordania 1
KG - Kirghizistan 1
KH - Cambogia 1
KZ - Kazakistan 1
LK - Sri Lanka 1
MT - Malta 1
NO - Norvegia 1
RS - Serbia 1
SY - Repubblica araba siriana 1
TH - Thailandia 1
UY - Uruguay 1
UZ - Uzbekistan 1
Totale 11.153
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Città #
Chandler 1.249
Singapore 563
Santa Clara 558
Milan 465
Princeton 461
Lawrence 458
London 283
Chicago 272
Wilmington 272
Ottawa 160
Des Moines 147
Ashburn 99
Boardman 94
Catanzaro 67
Shanghai 57
Hong Kong 50
Guangzhou 40
Rome 40
Helsinki 34
Pune 33
Norwalk 29
Redwood City 29
Horia 27
Los Angeles 25
Shenzhen 23
Council Bluffs 22
San Nicola Manfredi 22
Redmond 21
Beijing 20
Timisoara 18
Munich 16
Aversa 15
Florence 15
Naples 15
Falls Church 13
Genoa 13
Augusta 12
Cetraro 12
Secaucus 12
Montréal 11
Rui'an 11
Ann Arbor 10
Assago 10
Toronto 10
Wuhan 10
Amsterdam 9
Jiaxing 9
Casalnuovo Di Napoli 8
Wuxi 8
Xuzhou 8
Buffalo 7
Hanover 7
Mountain View 7
Olomouc 7
São Paulo 7
Xi'an 7
Andover 6
Cagliari 6
Clearwater 6
Cosenza 6
Lamezia Terme 6
Melbourne 6
Pasadena 6
Reggio Calabria 6
Washington 6
West Jordan 6
Bethesda 5
Brescia 5
Castiglion Fibocchi 5
Misterbianco 5
Montreal 5
Paris 5
Potenza 5
Rimini 5
Seattle 5
Taranto 5
Turin 5
Wuhu 5
Arau 4
Atlanta 4
Bari 4
Berlin 4
Bologna 4
Carrara 4
Castrolibero 4
Catania 4
Chennai 4
Crosia 4
Dongyang 4
Duncan 4
Elk Grove Village 4
Falerna 4
Ferrara 4
Hangzhou 4
Konya 4
Leawood 4
New York 4
Palermo 4
Perth 4
Rende 4
Totale 6.115
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Nome #
Predictive factors of Status Epilepticus and its recurrence in patients with adult–onset seizures: A multicenter, long follow–up cohort study 113
Genetics of reflex seizures and epilepsies in humans and animals 107
Levetiracetam vs Lamotrigine as First-Line Antiseizure Medication in Female Patients With Idiopathic Generalized Epilepsy 93
Rasmussen's Encephalitis and Related Conditions. The Causes of Epilepsy Common and Uncommon Causes in Adults and Children 68
Rating Scale for Psychogenic Non-epileptic Seizures: Scale Development and Clinimetric Testing 67
Temporal lobe abnormalities on brain MRI in healthy volunteers: a prospective case-control study 65
Neocortical thinning in “benign” mesial temporal lobe epilepsy 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)) 56
A brainstem hypermetabolism in a patient with essential palatal tremor: A simultaneous 18F-FDG-PET/3 T-MRI study 56
Spinal muscular atrophy due to an isolated deletion of exon 8 of the telomeric survival motor neuron gene 52
C19orf12 gene mutations in patients with neurodegeneration with brain iron accumulation 48
A software pipeline for pre-processing and mining EEG signals: Application in neurology 47
Chlorpromazine versus sleep deprivation in activation of EEG in adult-onset partial epilepsy. 46
Long-term outcome of mild mesial temporal lobe epilepsy 43
Incidental evidence of hypointensity in brain grey nuclei on routine MR imaging: when to suspect a neurodegenerative disorder? 42
A new SLC20A2 mutation identified in southern Italy family with primary familial brain calcification. 41
A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chomosome 1 40
A functional polymorphism in the SCN1A gene does not influence antiepileptic drug responsiveness in Italian patients with focal epilepsy 39
Topographic divergence of atypical cortical asymmetry and atrophy patterns in temporal lobe epilepsy 39
Perampanel as only add-on epilepsy treatment in elderly: A subgroup analysis of real-world data from retrospective, multicenter, observational study 39
Mild non-lesional temporal lobe epilepsy. A common, unrecognized disorder with onset in adulthood 38
A hypofibrinolytic state in overweight patients with cerebral venous thrombosis and isolated intracranial hypertension 38
Age at onset predicts good seizure outcome in sporadic non-lesional and mesial temporal sclerosis based temporal lobe epilepsy 38
A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chromosome 1 38
A novel exon 1 mutation in a patient with atypical lafora progressive myoclonus epilepsy seen as childhood-onset cognitive deficit 38
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy. 38
Facemask headache: a new nosographic entity among healthcare providers in COVID-19 era 38
Neuropsychological profile of mild temporal lobe epilepsy 37
A puzzling case without solution: isolated late-onset epileptic seizure 37
Advanced morphological neuroimaging study in lateral temporal lobe epilepsy: A multicentric study 37
Structural brain abnormalities in the common epilepsies assessed in 3,876 individuals worldwide 37
A novel ICA-based hardware system for reconfigurable and portable BCI 37
Usefulness of a morning routine EEG recording in patients with juvenile myoclonic epilepsy. 36
Integrity of the corpus callosum in patients with benign temporal lobe epilepsy 36
Partial epilepsy with tonic seizures during sleep: Seizure prognosis in 6 patients 36
A novel NF1 gene mutation in an Italian family with neurofibromatosis type 1. 35
An embedded system for EEG acquisition and processing for brain computer interface applications 35
Brivaracetam: review of its pharmacology and potential use as adjunctive therapy in patients with partial onset seizures 35
Resting-State EEG Classification for PNES Diagnosis 34
Association study between four polymorphisms in the HFE, TF and TFR genes and Parkinson's disease in Southern Italy 34
Non-metabolic causes of triphasic waves: a reappraisal. 34
Polymorphism of the multidrug resistance 1 gene MDR1/ABCB1 C3435T and response to antiepileptic drug treatment in temporal lobe epilepsy 34
Why should we change the term psychogenic nonepileptic seizures (PNES)? 34
3-T magnetic resonance imaging simultaneous automated multimodal approach improves detection of ambiguous visual hippocampal sclerosis. 34
A System for the Analysis of Snore Signals 34
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 34
Diagnostic Biomarkers of Epilepsy 34
Circulating microrna: The potential novel diagnostic biomarkers to predict drug resistance in temporal lobe epilepsy, a pilot study 34
Increased risk for Alzheimer disease with the interaction of MPO and A2M polymorphisms 33
Benign familial infantile convulsions: mapping of a novel locus on chromosome 2q24 and evidence for genetic heterogeneity 33
Randomized trial comparing two different high doses of methylprednisolone in MS: a clinical and MRI study 33
Gerstmann-Straussler-Scheinker disease with PRNP P102L heterozygous mutation presenting as progressive myoclonus epilepsy. 33
Kufs’ disease presenting as late-onset epilepsia partialis continua 33
A Loss-of-Function HCN4 Mutation Associated With Familial Benign Myoclonic Epilepsy in Infancy Causes Increased Neuronal Excitability 33
Accidents at work among people with epilepsy. Results of a European prospective cohort study 33
Deep Learning Representation from Electroencephalography of Early-Stage Creutzfeldt-Jakob Disease and Features for Differentiation from Rapidly Progressive Dementia. 33
A novel de novo HCN1 loss-of-function mutation in genetic generalized epilepsy causing increased neuronal excitability 33
Utilization of antiepileptic drugs during pregnancy: comparative patterns in 38 countries based on data from the EURAP registry 32
Anti-N-methyl-D-aspartate-glutamic-receptor encephalitis presenting as paroxysmal exercise-induced foot weakness 32
Reversible symmetrical external capsule hyperintensity as an early finding of autoimmune encephalitis. 32
Pharmacodynamics of the long-duration response to levodopa in PD 32
C19orf12 gene mutations in patients with neurodegeneration with brain iron accumulation. 32
Alterations in the α2 δ ligand, thrombospondin-1, in a rat model of spontaneous absence epilepsy and in patients with idiopathic/genetic generalized epilepsies. 32
Determinants of health-related quality of life in pharmacoresistant epilepsy: Results from a large multicenter study of consecutively enrolled patients using validated quantitative assessments 32
TARDBP gene mutations in south Italian patients with amyotrophic lateral sclerosis. 32
Psychopathological constellation in Psychogenic Non-Epileptic Seizures 32
Asymmetry of Permutation Entropy in Early Creutzfeldt-Jakob Disease: A Clue to a Specific Pathological Process? 32
TSC-associated neuropsychiatric disorders (TAND): findings from the TOSCA natural history study 31
Loss of long-duration response to levodopa over time in PD: implications for wearing-off 31
Presenilin-2 gene mutation presenting as Lewy Body dementia? 31
Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2 31
Linkage analysis and disease models in benign familial infantile seizures: a study of 16 families 31
Characteristics of a large population of patients with refractory epilepsy attending tertiary referral centers in Italy 31
Psychiatric events in epilepsy 31
Diagnosis and misdiagnosis of adult neuronal ceroid lipofuscinosis (Kufs disease). 31
A new Italian instrument for the assessment of irritability in patients with epilepsy. 31
Mild Lafora disease: Clinical, neurophysiologic, and genetic findings. 31
Modeling epileptogenic lesions and mapping networks - Imaging genetics for benign mesial temporal lobe epilepsy 31
Design of an electronic device for brain computer interface applications 31
Kufs disease due to mutation of CLN6: clinical, pathological and molecular genetic features. 31
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 31
Guillain-Barré syndrome following BNT162b2 COVID-19 vaccine 31
Association between the M129V variant allele of PRNP gene and mild temporal lobe epilepsy in women 30
Quality of life outcomes of immediate or delayed treatment of early epilepsy and single seizures 30
A clinical spectrum of the myoclonic manifestations associated with typical absences in childhood absence epilepsy. A video-polygraphic study 30
White Matter Abnormalities Differentiate Severe from Benign Temporal Lobe Epilepsy. 30
Non-paraneoplastic limbic encephalitis characterized by mesio-temporal seizures and extratemporal lesions: a case report 30
Familial temporal lobe epilepsy autosomal dominant inheritance in a large pedigree from southern Italy 30
Prodynorphin gene promoter polymorphism and temporal lobe epilepsy 30
A Functional Genetic Variation of the 5-HTR2A Receptor Affects Age at Onset in Patients with Temporal Lobe Epilepsy 30
A. Spinal muscular atrophy due to an isolated deletion of Exon 8 of telomeric survival motor neuron gene 30
Automatic detection of obstructive sleep apnea syndrome based on snore signals 30
Advances in genetic testing and optimization of clinical management in children and adults with epilepsy 30
REM-Sleep Behavior Disorder in Patients With Essential Tremor: What Is Its Clinical Significance? 30
Perampanel as first add-on choice on the treatment of mesial temporal lobe epilepsy: an observational real-life study 30
Humoral and T-cell response to SARS-CoV-2 mRNA vaccine in multiple sclerosis patients: Correlations with DMTs and clinical variables 29
Clinical spectrum of SCN1A mutations 29
Dose-dependent teratogenicity of valproate in mono- and polytherapy: an observational study 29
Cerebral venous thrombosis and isolated intracrania hypertension without papilledema in CDH 29
GENETIC HETEROGENEITY IN AUTOSOMAL RECESSIVE HEREDITARY MOTOR AND SENSORY NEUROPHATY WITH FOCALLY FOLDED MYELIN SHEATHS (CMT4B) 29
Totale 3.780
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Categoria #
all - tutte 168.183
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 168.183
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020226 0 0 0 0 0 0 0 0 0 0 77 149
2020/2021424 29 3 5 73 46 13 12 55 126 45 11 6
2021/20221.336 22 5 8 360 147 20 25 303 129 117 193 7
2022/20233.591 927 127 79 382 405 337 10 238 569 215 232 70
2023/20241.634 335 250 157 103 98 389 60 39 13 32 47 111
2024/20254.229 751 400 269 222 330 719 185 216 737 389 11 0
Totale 11.564