IRIS
GAMBARDELLA, ANTONIO
 Distribuzione geografica
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Continente #
NA - Nord America 6.668
AS - Asia 2.857
EU - Europa 2.785
SA - Sud America 257
AF - Africa 34
OC - Oceania 29
Continente sconosciuto - Info sul continente non disponibili 16
Totale 12.646
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Nazione #
US - Stati Uniti d'America 6.429
SG - Singapore 2.106
IT - Italia 1.156
SE - Svezia 501
CN - Cina 466
GB - Regno Unito 355
DE - Germania 220
BR - Brasile 217
CA - Canada 212
FI - Finlandia 109
EE - Estonia 108
IN - India 91
NL - Olanda 69
HK - Hong Kong 58
RO - Romania 56
RU - Federazione Russa 39
FR - Francia 28
UA - Ucraina 28
JP - Giappone 26
MX - Messico 25
PL - Polonia 25
AU - Australia 24
ES - Italia 18
ZA - Sudafrica 18
BD - Bangladesh 17
TR - Turchia 17
CZ - Repubblica Ceca 15
IR - Iran 14
AT - Austria 13
CO - Colombia 11
CH - Svizzera 10
IQ - Iraq 10
EU - Europa 9
SA - Arabia Saudita 8
A2 - ???statistics.table.value.countryCode.A2??? 7
AR - Argentina 7
CL - Cile 7
VE - Venezuela 7
MY - Malesia 6
EG - Egitto 5
IE - Irlanda 5
NZ - Nuova Zelanda 5
PK - Pakistan 5
BE - Belgio 4
GR - Grecia 4
JO - Giordania 4
KR - Corea 4
MA - Marocco 4
PE - Perù 4
VN - Vietnam 4
LV - Lettonia 3
MD - Moldavia 3
MK - Macedonia 3
UZ - Uzbekistan 3
AE - Emirati Arabi Uniti 2
AZ - Azerbaigian 2
BG - Bulgaria 2
EC - Ecuador 2
ID - Indonesia 2
KZ - Kazakistan 2
LT - Lituania 2
LU - Lussemburgo 2
NG - Nigeria 2
PT - Portogallo 2
RS - Serbia 2
TT - Trinidad e Tobago 2
TW - Taiwan 2
UG - Uganda 2
AM - Armenia 1
CI - Costa d'Avorio 1
DK - Danimarca 1
ET - Etiopia 1
IL - Israele 1
KE - Kenya 1
KG - Kirghizistan 1
KH - Cambogia 1
LK - Sri Lanka 1
MT - Malta 1
NO - Norvegia 1
PS - Palestinian Territory 1
PY - Paraguay 1
SY - Repubblica araba siriana 1
TH - Thailandia 1
UY - Uruguay 1
Totale 12.646
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Città #
Chandler 1.249
Singapore 864
Santa Clara 581
Milan 472
Princeton 461
Lawrence 458
London 294
Chicago 285
Wilmington 272
Ottawa 160
Munich 152
Des Moines 147
Ashburn 127
Boardman 95
Turku 72
Catanzaro 67
Los Angeles 61
The Dalles 58
Shanghai 57
Hong Kong 52
Rome 42
Guangzhou 40
Helsinki 34
Pune 33
Norwalk 29
Redwood City 29
San Francisco 28
Horia 27
Brooklyn 26
Shenzhen 23
Council Bluffs 22
San Nicola Manfredi 22
São Paulo 22
Redmond 21
Beijing 20
New York 20
Chennai 18
Timisoara 18
Naples 16
Secaucus 16
Warsaw 16
Aversa 15
Boston 15
Charlotte 15
Florence 15
Stockholm 14
Toronto 14
Amsterdam 13
Augusta 13
Falls Church 13
Genoa 13
Olomouc 13
Tokyo 13
Cetraro 12
Columbus 12
Montréal 11
Rui'an 11
Ann Arbor 10
Assago 10
Dallas 10
Johannesburg 10
Mexico City 10
Seattle 10
Wuhan 10
Atlanta 9
Jiaxing 9
Montreal 9
Taranto 9
Buffalo 8
Casalnuovo Di Napoli 8
Washington 8
Wuxi 8
Xuzhou 8
Hanover 7
Las Vegas 7
Melbourne 7
Mountain View 7
Xi'an 7
Andover 6
Cagliari 6
Clearwater 6
Cosenza 6
Curitiba 6
Lamezia Terme 6
Pasadena 6
Providence 6
Reggio Calabria 6
San Jose 6
West Jordan 6
Belo Horizonte 5
Bethesda 5
Brescia 5
Castiglion Fibocchi 5
Denver 5
Misterbianco 5
Palermo 5
Paris 5
Phoenix 5
Porto Alegre 5
Potenza 5
Totale 7.020
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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 118
Genetics of reflex seizures and epilepsies in humans and animals 116
Levetiracetam vs Lamotrigine as First-Line Antiseizure Medication in Female Patients With Idiopathic Generalized Epilepsy 103
Rating Scale for Psychogenic Non-epileptic Seizures: Scale Development and Clinimetric Testing 75
Rasmussen's Encephalitis and Related Conditions. The Causes of Epilepsy Common and Uncommon Causes in Adults and Children 69
Temporal lobe abnormalities on brain MRI in healthy volunteers: a prospective case-control study 68
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)) 64
Neocortical thinning in “benign” mesial temporal lobe epilepsy 61
A brainstem hypermetabolism in a patient with essential palatal tremor: A simultaneous 18F-FDG-PET/3 T-MRI study 61
C19orf12 gene mutations in patients with neurodegeneration with brain iron accumulation 59
A software pipeline for pre-processing and mining EEG signals: Application in neurology 58
Spinal muscular atrophy due to an isolated deletion of exon 8 of the telomeric survival motor neuron gene 54
A new SLC20A2 mutation identified in southern Italy family with primary familial brain calcification. 53
Chlorpromazine versus sleep deprivation in activation of EEG in adult-onset partial epilepsy. 50
Incidental evidence of hypointensity in brain grey nuclei on routine MR imaging: when to suspect a neurodegenerative disorder? 48
A hypofibrinolytic state in overweight patients with cerebral venous thrombosis and isolated intracranial hypertension 47
A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chomosome 1 47
A functional polymorphism in the SCN1A gene does not influence antiepileptic drug responsiveness in Italian patients with focal epilepsy 47
Perampanel as only add-on epilepsy treatment in elderly: A subgroup analysis of real-world data from retrospective, multicenter, observational study 46
Mild non-lesional temporal lobe epilepsy. A common, unrecognized disorder with onset in adulthood 45
A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chromosome 1 44
A novel exon 1 mutation in a patient with atypical lafora progressive myoclonus epilepsy seen as childhood-onset cognitive deficit 44
Long-term outcome of mild mesial temporal lobe epilepsy 44
Facemask headache: a new nosographic entity among healthcare providers in COVID-19 era 44
3-T magnetic resonance imaging simultaneous automated multimodal approach improves detection of ambiguous visual hippocampal sclerosis. 43
Advanced morphological neuroimaging study in lateral temporal lobe epilepsy: A multicentric study 42
A. Spinal muscular atrophy due to an isolated deletion of Exon 8 of telomeric survival motor neuron gene 42
Resting-State EEG Classification for PNES Diagnosis 41
A Functional Genetic Variation of the 5-HTR2A Receptor Affects Age at Onset in Patients with Temporal Lobe Epilepsy 41
Topographic divergence of atypical cortical asymmetry and atrophy patterns in temporal lobe epilepsy 41
A puzzling case without solution: isolated late-onset epileptic seizure 40
Age at onset predicts good seizure outcome in sporadic non-lesional and mesial temporal sclerosis based temporal lobe epilepsy 40
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy. 40
A novel ICA-based hardware system for reconfigurable and portable BCI 40
Phenotypic Variability in Novel Doublecortin Gene Variants Associated with Subcortical Band Heterotopia 39
Neuropsychological profile of mild temporal lobe epilepsy 39
Integrity of the corpus callosum in patients with benign temporal lobe epilepsy 39
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 39
Brivaracetam: review of its pharmacology and potential use as adjunctive therapy in patients with partial onset seizures 39
Determinants of health-related quality of life in pharmacoresistant epilepsy: Results from a large multicenter study of consecutively enrolled patients using validated quantitative assessments 38
Structural brain abnormalities in the common epilepsies assessed in 3,876 individuals worldwide 38
Partial epilepsy with tonic seizures during sleep: Seizure prognosis in 6 patients 38
Asymmetry of Permutation Entropy in Early Creutzfeldt-Jakob Disease: A Clue to a Specific Pathological Process? 38
A novel de novo HCN1 loss-of-function mutation in genetic generalized epilepsy causing increased neuronal excitability 38
Idiopathic generalized epilepsy in a family with SCN4A-related myotonia 38
Usefulness of a morning routine EEG recording in patients with juvenile myoclonic epilepsy. 37
Association study between four polymorphisms in the HFE, TF and TFR genes and Parkinson's disease in Southern Italy 37
Randomized trial comparing two different high doses of methylprednisolone in MS: a clinical and MRI study 37
Gerstmann-Straussler-Scheinker disease with PRNP P102L heterozygous mutation presenting as progressive myoclonus epilepsy. 37
Why should we change the term psychogenic nonepileptic seizures (PNES)? 37
A Loss-of-Function HCN4 Mutation Associated With Familial Benign Myoclonic Epilepsy in Infancy Causes Increased Neuronal Excitability 37
A System for the Analysis of Snore Signals 37
Accidents at work among people with epilepsy. Results of a European prospective cohort study 37
Deep Learning Representation from Electroencephalography of Early-Stage Creutzfeldt-Jakob Disease and Features for Differentiation from Rapidly Progressive Dementia. 37
Diagnostic Biomarkers of Epilepsy 37
Perampanel as first add-on choice on the treatment of mesial temporal lobe epilepsy: an observational real-life study 37
Psychopathological constellation in Psychogenic Non-Epileptic Seizures 37
Circulating microrna: The potential novel diagnostic biomarkers to predict drug resistance in temporal lobe epilepsy, a pilot study 37
Benign familial infantile convulsions: mapping of a novel locus on chromosome 2q24 and evidence for genetic heterogeneity 36
Quality of life outcomes of immediate or delayed treatment of early epilepsy and single seizures 36
Non-metabolic causes of triphasic waves: a reappraisal. 36
A novel NF1 gene mutation in an Italian family with neurofibromatosis type 1. 36
C19orf12 gene mutations in patients with neurodegeneration with brain iron accumulation. 36
A new Italian instrument for the assessment of irritability in patients with epilepsy. 36
An embedded system for EEG acquisition and processing for brain computer interface applications 36
Advances in genetic testing and optimization of clinical management in children and adults with epilepsy 36
Polymorphism of the multidrug resistance 1 gene MDR1/ABCB1 C3435T and response to antiepileptic drug treatment in temporal lobe epilepsy 35
Kufs’ disease presenting as late-onset epilepsia partialis continua 35
Hippocampal and thalamic atrophy in mild temporal lobe epilepsy: a VBM study 35
Automatic detection of obstructive sleep apnea syndrome based on snore signals 35
Glucose transporter-1 deficiency syndrome with extreme phenotypic variability in a five-generation family carrying a novel SLC2A1 variant 34
Humoral and T-cell response to SARS-CoV-2 mRNA vaccine in multiple sclerosis patients: Correlations with DMTs and clinical variables 34
Increased risk for Alzheimer disease with the interaction of MPO and A2M polymorphisms 34
Presenilin-2 gene mutation presenting as Lewy Body dementia? 34
Anti-N-methyl-D-aspartate-glutamic-receptor encephalitis presenting as paroxysmal exercise-induced foot weakness 34
Reversible symmetrical external capsule hyperintensity as an early finding of autoimmune encephalitis. 34
White Matter Abnormalities Differentiate Severe from Benign Temporal Lobe Epilepsy. 34
Pharmacodynamics of the long-duration response to levodopa in PD 34
Alterations in the α2 δ ligand, thrombospondin-1, in a rat model of spontaneous absence epilepsy and in patients with idiopathic/genetic generalized epilepsies. 34
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 34
Action palatal tremor in a patient with primary intestinal lymphoma 34
Varicella zoster immunity loss in multiple sclerosis patient treated with ocrelizumab 34
Utilization of antiepileptic drugs during pregnancy: comparative patterns in 38 countries based on data from the EURAP registry 33
A clinical spectrum of the myoclonic manifestations associated with typical absences in childhood absence epilepsy. A video-polygraphic study 33
Linkage analysis and disease models in benign familial infantile seizures: a study of 16 families 33
Familial temporal lobe epilepsy autosomal dominant inheritance in a large pedigree from southern Italy 33
Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths 33
Diagnosis and misdiagnosis of adult neuronal ceroid lipofuscinosis (Kufs disease). 33
Mild Lafora disease: Clinical, neurophysiologic, and genetic findings. 33
A Family With a Complex Phenotype Caused by Two Different Rare Metabolic Disorders: GLUT1 and Very-Long-Chain Fatty Acid Dehydrogenase (VLCAD) Deficiencies 33
REM-Sleep Behavior Disorder in Patients With Essential Tremor: What Is Its Clinical Significance? 33
Guillain-Barré syndrome following BNT162b2 COVID-19 vaccine 33
TSC-associated neuropsychiatric disorders (TAND): findings from the TOSCA natural history study 32
Association between the M129V variant allele of PRNP gene and mild temporal lobe epilepsy in women 32
Loss of long-duration response to levodopa over time in PD: implications for wearing-off 32
The mystery of unexplained traumatic sudden falls. A clinical case that adds a new feasible cause 32
Brand-to-Generic Levetiracetam Switching: a four-years prospective observational real-life study 32
Functional activity changes in memory and emotional systems of healthy subjects with déjà vu. 32
Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies. 32
Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2 32
Totale 4.201
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Categoria #
all - tutte 194.055
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 194.055
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
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
2024/20255.705 751 400 269 222 330 719 185 216 737 389 495 992
2025/202630 30 0 0 0 0 0 0 0 0 0 0 0
Totale 13.070