IRIS
GAMBARDELLA, ANTONIO
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 8.494
AS - Asia 6.343
EU - Europa 3.175
SA - Sud America 1.824
AF - Africa 135
OC - Oceania 35
Continente sconosciuto - Info sul continente non disponibili 17
Totale 20.023
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 8.159
SG - Singapore 2.946
BR - Brasile 1.461
CN - Cina 1.364
IT - Italia 1.266
VN - Vietnam 776
IN - India 720
SE - Svezia 507
GB - Regno Unito 394
DE - Germania 287
CA - Canada 244
AR - Argentina 154
HK - Hong Kong 137
FI - Finlandia 120
EE - Estonia 108
ID - Indonesia 87
NL - Olanda 85
RU - Federazione Russa 77
MX - Messico 67
ZA - Sudafrica 67
EC - Ecuador 65
BD - Bangladesh 57
RO - Romania 57
PL - Polonia 43
IQ - Iraq 40
UA - Ucraina 40
CO - Colombia 39
FR - Francia 38
JP - Giappone 36
ES - Italia 26
PY - Paraguay 26
AU - Australia 25
TR - Turchia 25
VE - Venezuela 25
PK - Pakistan 24
AT - Austria 23
PE - Perù 21
CL - Cile 20
MA - Marocco 18
CZ - Repubblica Ceca 16
IR - Iran 16
EG - Egitto 14
SA - Arabia Saudita 13
IE - Irlanda 12
KR - Corea 12
UZ - Uzbekistan 11
CH - Svizzera 10
UY - Uruguay 10
EU - Europa 8
KE - Kenya 8
LT - Lituania 8
MY - Malesia 8
NP - Nepal 8
A2 - ???statistics.table.value.countryCode.A2??? 7
AE - Emirati Arabi Uniti 7
GR - Grecia 7
AZ - Azerbaigian 6
IL - Israele 6
JO - Giordania 6
KZ - Kazakistan 6
TN - Tunisia 6
BE - Belgio 5
DO - Repubblica Dominicana 5
LB - Libano 5
MD - Moldavia 5
NZ - Nuova Zelanda 5
PS - Palestinian Territory 5
PT - Portogallo 5
RS - Serbia 5
AL - Albania 4
BG - Bulgaria 4
CI - Costa d'Avorio 4
DK - Danimarca 4
ET - Etiopia 4
TT - Trinidad e Tobago 4
AO - Angola 3
JM - Giamaica 3
KG - Kirghizistan 3
LK - Sri Lanka 3
LV - Lettonia 3
MK - Macedonia 3
NG - Nigeria 3
TH - Thailandia 3
AM - Armenia 2
BA - Bosnia-Erzegovina 2
BO - Bolivia 2
CG - Congo 2
GT - Guatemala 2
HR - Croazia 2
HU - Ungheria 2
KW - Kuwait 2
LU - Lussemburgo 2
NI - Nicaragua 2
PA - Panama 2
TO - Tonga 2
TW - Taiwan 2
UG - Uganda 2
XK - ???statistics.table.value.countryCode.XK??? 2
BB - Barbados 1
BN - Brunei Darussalam 1
Totale 19.999
Salva come PNG Salva come JPEG
Città #
Chandler 1.249
Dallas 988
Singapore 974
Santa Clara 606
Bengaluru 566
Hefei 552
Milan 480
Princeton 460
Lawrence 457
Ashburn 398
London 300
Ho Chi Minh City 296
Chicago 291
Wilmington 273
Munich 209
Hanoi 169
Ottawa 160
Des Moines 146
Beijing 140
São Paulo 136
Hong Kong 130
Boardman 128
Los Angeles 85
Turku 79
Catanzaro 67
The Dalles 63
Shanghai 58
New York 57
Rome 48
Guangzhou 43
Rio de Janeiro 43
Columbus 38
Da Nang 38
Helsinki 38
Pune 37
Brooklyn 36
Council Bluffs 36
San Francisco 35
Warsaw 34
Chennai 33
Curitiba 31
Haiphong 31
Boston 30
Johannesburg 30
Norwalk 29
Redwood City 29
Belo Horizonte 27
Horia 27
Naples 24
Shenzhen 24
Porto Alegre 23
Quito 23
Tokyo 23
Brasília 22
San Nicola Manfredi 22
Thái Bình 22
Redmond 21
Biên Hòa 20
Stockholm 20
Montreal 19
San Jose 19
Charlotte 18
Florence 18
Mexico City 18
Secaucus 18
Timisoara 18
Toronto 18
Amsterdam 17
Buenos Aires 17
Seattle 17
Campinas 16
Fortaleza 16
Guarulhos 16
Jakarta 16
Aversa 15
Genoa 15
Guayaquil 15
Salvador 15
Atlanta 14
Augusta 14
Hải Dương 14
Phoenix 14
Can Tho 13
Cape Town 13
Falls Church 13
Olomouc 13
Boydton 12
Cetraro 12
Dhaka 12
Lima 12
Asunción 11
Montréal 11
New Delhi 11
Rui'an 11
Santo André 11
Ann Arbor 10
Assago 10
Buffalo 10
Bắc Giang 10
Manchester 10
Totale 11.036
Salva come PNG Salva come JPEG
Nome #
Genetics of reflex seizures and epilepsies in humans and animals 143
Predictive factors of Status Epilepticus and its recurrence in patients with adult–onset seizures: A multicenter, long follow–up cohort study 132
Levetiracetam vs Lamotrigine as First-Line Antiseizure Medication in Female Patients With Idiopathic Generalized Epilepsy 125
Rating Scale for Psychogenic Non-epileptic Seizures: Scale Development and Clinimetric Testing 98
Temporal lobe abnormalities on brain MRI in healthy volunteers: a prospective case-control study 88
A brainstem hypermetabolism in a patient with essential palatal tremor: A simultaneous 18F-FDG-PET/3 T-MRI study 87
PRECLINICAL MARKERS OF NEUROPATHIC DAMAGE IN TYPE 1 DIABETES MELLITUS 86
A new SLC20A2 mutation identified in southern Italy family with primary familial brain calcification. 85
A functional polymorphism in the SCN1A gene does not influence antiepileptic drug responsiveness in Italian patients with focal epilepsy 84
A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chomosome 1 81
3-T magnetic resonance imaging simultaneous automated multimodal approach improves detection of ambiguous visual hippocampal sclerosis. 81
A novel exon 1 mutation in a patient with atypical lafora progressive myoclonus epilepsy seen as childhood-onset cognitive deficit 79
A Functional Genetic Variation of the 5-HTR2A Receptor Affects Age at Onset in Patients with Temporal Lobe Epilepsy 77
Rasmussen's Encephalitis and Related Conditions. The Causes of Epilepsy Common and Uncommon Causes in Adults and Children 77
C19orf12 gene mutations in patients with neurodegeneration with brain iron accumulation 75
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)) 74
Neocortical thinning in “benign” mesial temporal lobe epilepsy 72
A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chromosome 1 72
A software pipeline for pre-processing and mining EEG signals: Application in neurology 72
A hypofibrinolytic state in overweight patients with cerebral venous thrombosis and isolated intracranial hypertension 71
A Family With a Complex Phenotype Caused by Two Different Rare Metabolic Disorders: GLUT1 and Very-Long-Chain Fatty Acid Dehydrogenase (VLCAD) Deficiencies 69
A. Spinal muscular atrophy due to an isolated deletion of Exon 8 of telomeric survival motor neuron gene 68
Varicella zoster immunity loss in multiple sclerosis patient treated with ocrelizumab 68
A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine. 67
Effectiveness of perampanel as only concomitant antiseizure medication for highly active epilepsy: insight from a real-world, multicenter retrospective study 66
Glucose transporter-1 deficiency syndrome with extreme phenotypic variability in a five-generation family carrying a novel SLC2A1 variant 65
Chlorpromazine versus sleep deprivation in activation of EEG in adult-onset partial epilepsy. 65
Incidental evidence of hypointensity in brain grey nuclei on routine MR imaging: when to suspect a neurodegenerative disorder? 64
A Multilayer Network-Based Method for Brain Connectivity Analysis from EEG Data 63
Asymmetry of Permutation Entropy in Early Creutzfeldt-Jakob Disease: A Clue to a Specific Pathological Process? 63
Network-based atrophy modeling in the common epilepsies: A worldwide ENIGMA study 62
Mild non-lesional temporal lobe epilepsy. A common, unrecognized disorder with onset in adulthood 61
Spinal muscular atrophy due to an isolated deletion of exon 8 of the telomeric survival motor neuron gene 61
Accidents at work among people with epilepsy. Results of a European prospective cohort study 61
A new Italian instrument for the assessment of irritability in patients with epilepsy. 60
Perampanel as first add-on choice on the treatment of mesial temporal lobe epilepsy: an observational real-life study 60
White matter abnormalities across different epilepsy syndromes in adults: an ENIGMA-Epilepsy study 60
Perampanel as only add-on epilepsy treatment in elderly: A subgroup analysis of real-world data from retrospective, multicenter, observational study 60
A puzzling case without solution: isolated late-onset epileptic seizure 59
Advanced morphological neuroimaging study in lateral temporal lobe epilepsy: A multicentric study 59
A novel ICA-based hardware system for reconfigurable and portable BCI 59
Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72 59
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 58
Effectiveness and Safety of Adjunctive Cenobamate in People with Focal-Onset Epilepsy: Evidence from the First Interim Analysis of the BLESS Study 57
Age at onset predicts good seizure outcome in sporadic non-lesional and mesial temporal sclerosis based temporal lobe epilepsy 57
A Loss-of-Function HCN4 Mutation Associated With Familial Benign Myoclonic Epilepsy in Infancy Causes Increased Neuronal Excitability 57
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy. 57
Long-term outcome of mild mesial temporal lobe epilepsy 57
A novel de novo HCN1 loss-of-function mutation in genetic generalized epilepsy causing increased neuronal excitability 57
A real-world comparison among third-generation antiseizure medications: Results from the COMPARE study 56
Resting-State EEG Classification for PNES Diagnosis 55
Blocking out the real diagnosis 55
Kufs disease due to mutation of CLN6: clinical, pathological and molecular genetic features. 55
Facemask headache: a new nosographic entity among healthcare providers in COVID-19 era 55
Phenotypic Variability in Novel Doublecortin Gene Variants Associated with Subcortical Band Heterotopia 54
Circulating microrna: The potential novel diagnostic biomarkers to predict drug resistance in temporal lobe epilepsy, a pilot study 54
Hypertension, seizures, and epilepsy: a review on pathophysiology and management 53
A clinical spectrum of the myoclonic manifestations associated with typical absences in childhood absence epilepsy. A video-polygraphic study 53
Antiepileptic Drug Teratogenicity and De Novo Genetic Variation Load 53
The ENIGMA-Epilepsy working group: Mapping disease from large data sets 53
Association study between four polymorphisms in the HFE, TF and TFR genes and Parkinson's disease in Southern Italy 52
Autosomal dominant lateral temporal epilepsy: absence of mutations in ADAM22 and Kv1 channel genes encoding LGI1-associated proteins. 52
Structural brain abnormalities in the common epilepsies assessed in a worldwide ENIGMA study 52
Automatic detection of obstructive sleep apnea syndrome based on snore signals 52
Brivaracetam: review of its pharmacology and potential use as adjunctive therapy in patients with partial onset seizures 52
Guillain-Barré syndrome following BNT162b2 COVID-19 vaccine 52
Topographic divergence of atypical cortical asymmetry and atrophy patterns in temporal lobe epilepsy 52
Idiopathic generalized epilepsy in a family with SCN4A-related myotonia 52
Climate change and hyponatremia-related hospital admissions in people with focal epilepsy exposed to carbamazepine or its derivatives 51
Identification of an Nav1.1 sodium channel (SCN1A) loss-of-function mutation associated with familial simple febrile seizures 51
Accidents in patients with epilepsy: Types, circumstances, and complications: A European cohort study 51
Analysis of LGI1 promoter sequence, PDYN and GABBR1 polymorphisms in sporadic and familial lateral temporal lobe epilepsy 51
Genetics heterogeneity in patients with pantothenate kinase-associated neurodegeneration and classic magnetic resonance imaging eye-of-the-tiger pattern 51
A systems-level analysis highlights microglial activation as a modifying factor in common epilepsies 50
A System for the Analysis of Snore Signals 50
The parkin gene is not involved in late-onset Parkinson’s disease 50
TARDBP gene mutations in south Italian patients with amyotrophic lateral sclerosis. 50
Epilepsy in cerebrovascular diseases: Review of experimental and clinical data with meta-analysis of risk factors 50
Advances in genetic testing and optimization of clinical management in children and adults with epilepsy 50
Epilepsy in “Sunflower syndrome”: electroclinical features, therapeutic response, and long-term follow-up 50
Effectiveness of perampanel as the only add‐on: Retrospective, multicenter, observational real‐life study on epilepsy patients 49
Humoral and T-cell response to SARS-CoV-2 mRNA vaccine in multiple sclerosis patients: Correlations with DMTs and clinical variables 49
Fatigue in natalizumab-treated Multiple Sclerosis patients: How much is wearing-off to blame? 49
A possible case of natalizumab-dependent suicide attempt: A brief review about drugs and suicide. 49
An Italian multicentre study of perampanel in progressive myoclonus epilepsies 49
Coverage of the requirements of first and second level stroke unit in Italy 49
Distinguishing seizures in autoimmune limbic encephalitis from mesial temporal lobe epilepsy with hippocampal sclerosis: Clues of a temporal plus network 48
Integrity of the corpus callosum in patients with benign temporal lobe epilepsy 48
Why should we change the term psychogenic nonepileptic seizures (PNES)? 48
Deep Learning Representation from Electroencephalography of Early-Stage Creutzfeldt-Jakob Disease and Features for Differentiation from Rapidly Progressive Dementia. 48
Natural clusters of tuberous sclerosis complex (TSC)-associated neuropsychiatric disorders (TAND): New findings from the TOSCA TAND research project 48
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes 47
National survey on the prevalence of single-gene aetiologies for genetic developmental and epileptic encephalopathies in Italy 47
Levetiracetam in patients with generalised epilepsy and myoclonic seizures: a open label study 47
Partial epilepsy with tonic seizures during sleep: Seizure prognosis in 6 patients 47
Operative Strategies for Patients with Cortical Dysplastic Lesions and Intractable Epilepsy 47
The impact of one-year COVID-19 containment measures in patients with mesial temporal lobe epilepsy: A longitudinal survey-based study 47
The mystery of unexplained traumatic sudden falls. A clinical case that adds a new feasible cause 46
Clinical and neurophysiologic features of progressive myoclonus epilepsy without renal failure caused by SCARB2 mutations. 46
Palatal tremor in a patient with primary intestinal lymphoma 46
Totale 6.109
Salva come PNG Salva come JPEG
Categoria #
all - tutte 225.232
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 225.232
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021268 0 0 0 0 0 13 12 55 126 45 11 6
2021/20221.334 22 5 8 359 147 20 25 303 129 117 192 7
2022/20233.589 925 127 79 382 405 337 10 238 569 215 232 70
2023/20241.631 335 249 157 103 98 388 60 39 13 32 46 111
2024/20255.699 750 397 269 222 330 718 185 216 736 389 495 992
2025/20267.446 618 1.377 1.627 2.268 1.201 355 0 0 0 0 0 0
Totale 20.470