IRIS
GAMBARDELLA, ANTONIO
 Distribuzione geografica
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Continente #
NA - Nord America 14.545
AS - Asia 7.894
EU - Europa 3.774
SA - Sud America 1.951
Continente sconosciuto - Info sul continente non disponibili 486
AF - Africa 175
OC - Oceania 39
Totale 28.864
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Nazione #
US - Stati Uniti d'America 14.017
SG - Singapore 3.656
CN - Cina 1.757
IT - Italia 1.667
BR - Brasile 1.537
VN - Vietnam 807
IN - India 755
SE - Svezia 510
GB - Regno Unito 430
CA - Canada 351
DE - Germania 308
HK - Hong Kong 252
BD - Bangladesh 209
AR - Argentina 173
FI - Finlandia 124
NL - Olanda 116
EE - Estonia 108
ID - Indonesia 94
MX - Messico 84
RU - Federazione Russa 84
ZA - Sudafrica 73
EC - Ecuador 68
FR - Francia 62
RO - Romania 62
IQ - Iraq 61
PL - Polonia 53
UA - Ucraina 48
JP - Giappone 47
CO - Colombia 45
ES - Italia 37
PK - Pakistan 34
VE - Venezuela 33
TR - Turchia 29
AU - Australia 28
CL - Cile 28
PY - Paraguay 28
AT - Austria 23
MA - Marocco 23
PE - Perù 23
CR - Costa Rica 21
KR - Corea 20
SA - Arabia Saudita 19
CZ - Repubblica Ceca 18
EG - Egitto 18
IE - Irlanda 17
IR - Iran 17
JM - Giamaica 17
UZ - Uzbekistan 15
CH - Svizzera 14
AE - Emirati Arabi Uniti 12
LT - Lituania 12
MY - Malesia 12
UY - Uruguay 12
KE - Kenya 11
GR - Grecia 10
IL - Israele 10
JO - Giordania 10
NP - Nepal 10
HN - Honduras 9
PT - Portogallo 9
TN - Tunisia 9
EU - Europa 8
KZ - Kazakistan 8
NI - Nicaragua 8
PS - Palestinian Territory 8
A2 - ???statistics.table.value.countryCode.A2??? 7
AZ - Azerbaigian 7
DO - Repubblica Dominicana 7
SC - Seychelles 7
TH - Thailandia 7
AL - Albania 6
AO - Angola 6
BE - Belgio 6
CI - Costa d'Avorio 6
DZ - Algeria 6
GT - Guatemala 6
LB - Libano 6
MD - Moldavia 6
NZ - Nuova Zelanda 6
TT - Trinidad e Tobago 6
LV - Lettonia 5
NG - Nigeria 5
RS - Serbia 5
SV - El Salvador 5
BA - Bosnia-Erzegovina 4
BG - Bulgaria 4
DK - Danimarca 4
ET - Etiopia 4
HU - Ungheria 4
MT - Malta 4
OM - Oman 4
PH - Filippine 4
BO - Bolivia 3
HR - Croazia 3
KG - Kirghizistan 3
KW - Kuwait 3
LK - Sri Lanka 3
MK - Macedonia 3
PR - Porto Rico 3
AM - Armenia 2
Totale 28.348
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Città #
San Jose 2.678
Ashburn 1.281
Chandler 1.249
Singapore 1.157
Dallas 1.022
Santa Clara 727
Council Bluffs 608
Bengaluru 565
Hefei 550
Milan 501
Princeton 468
Lawrence 456
Chicago 336
London 310
Ho Chi Minh City 308
Wilmington 278
Beijing 258
Hong Kong 242
Munich 209
Hanoi 180
Ottawa 163
Phoenix 146
Des Moines 145
São Paulo 145
Los Angeles 143
Boardman 128
New York 120
Turku 79
Rome 77
Catanzaro 76
The Dalles 72
Shanghai 63
Chennai 49
San Francisco 47
Naples 46
Rio de Janeiro 46
Guangzhou 44
Montreal 43
Boston 42
Columbus 42
Helsinki 42
Da Nang 41
Warsaw 41
Brooklyn 40
Toronto 40
Orem 37
Buffalo 36
Pune 36
Amsterdam 32
Atlanta 32
Johannesburg 32
Curitiba 31
Haiphong 31
Tokyo 31
Norwalk 29
Redwood City 29
Belo Horizonte 28
Mexico City 28
Denver 27
Horia 27
Shenzhen 27
Seattle 26
Charlotte 25
Florence 25
Porto Alegre 24
Quito 23
Thái Bình 23
Aversa 22
Brasília 22
San Nicola Manfredi 22
Stockholm 22
Redmond 21
Biên Hòa 20
Buenos Aires 20
Bari 19
Genoa 18
Secaucus 18
Timisoara 18
Fortaleza 17
Guayaquil 17
Jakarta 17
Campinas 16
Guarulhos 16
Miami 16
Salvador 16
San José 16
Augusta 15
Catania 15
Palermo 15
Baghdad 14
Dhaka 14
Frankfurt am Main 14
Hải Dương 14
New Delhi 14
Tashkent 14
Can Tho 13
Cape Town 13
Falls Church 13
Las Vegas 13
Lima 13
Totale 16.489
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Nome #
Genetics of reflex seizures and epilepsies in humans and animals 174
Comparative Effectiveness of Brivaracetam, Cenobamate, Lacosamide, and Perampanel in Focal Epilepsy 161
Rating Scale for Psychogenic Non-epileptic Seizures: Scale Development and Clinimetric Testing 155
Predictive factors of Status Epilepticus and its recurrence in patients with adult–onset seizures: A multicenter, long follow–up cohort study 154
Levetiracetam vs Lamotrigine as First-Line Antiseizure Medication in Female Patients With Idiopathic Generalized Epilepsy 152
Transcriptomic and electrophysiological alterations underlying phenotypic variability in SCN1A-associated febrile seizures 150
Chlorpromazine versus sleep deprivation in activation of EEG in adult-onset partial epilepsy. 121
Effectiveness of perampanel as only concomitant antiseizure medication for highly active epilepsy: insight from a real-world, multicenter retrospective study 112
A brainstem hypermetabolism in a patient with essential palatal tremor: A simultaneous 18F-FDG-PET/3 T-MRI study 111
PRECLINICAL MARKERS OF NEUROPATHIC DAMAGE IN TYPE 1 DIABETES MELLITUS 110
Glucose transporter-1 deficiency syndrome with extreme phenotypic variability in a five-generation family carrying a novel SLC2A1 variant 107
Rasmussen's Encephalitis and Related Conditions. The Causes of Epilepsy Common and Uncommon Causes in Adults and Children 105
A hypofibrinolytic state in overweight patients with cerebral venous thrombosis and isolated intracranial hypertension 104
A new SLC20A2 mutation identified in southern Italy family with primary familial brain calcification. 102
A functional polymorphism in the SCN1A gene does not influence antiepileptic drug responsiveness in Italian patients with focal epilepsy 102
A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chomosome 1 101
3-T magnetic resonance imaging simultaneous automated multimodal approach improves detection of ambiguous visual hippocampal sclerosis. 101
Temporal lobe abnormalities on brain MRI in healthy volunteers: a prospective case-control study 98
Resting-State EEG Classification for PNES Diagnosis 95
A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chromosome 1 95
C19orf12 gene mutations in patients with neurodegeneration with brain iron accumulation 95
A Functional Genetic Variation of the 5-HTR2A Receptor Affects Age at Onset in Patients with Temporal Lobe Epilepsy 94
A software pipeline for pre-processing and mining EEG signals: Application in neurology 94
Asymmetry of Permutation Entropy in Early Creutzfeldt-Jakob Disease: A Clue to a Specific Pathological Process? 93
A novel exon 1 mutation in a patient with atypical lafora progressive myoclonus epilepsy seen as childhood-onset cognitive deficit 91
A Family With a Complex Phenotype Caused by Two Different Rare Metabolic Disorders: GLUT1 and Very-Long-Chain Fatty Acid Dehydrogenase (VLCAD) Deficiencies 89
Incidental evidence of hypointensity in brain grey nuclei on routine MR imaging: when to suspect a neurodegenerative disorder? 89
A Multilayer Network-Based Method for Brain Connectivity Analysis from EEG Data 88
Neocortical thinning in “benign” mesial temporal lobe epilepsy 88
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)) 87
A. Spinal muscular atrophy due to an isolated deletion of Exon 8 of telomeric survival motor neuron gene 86
Varicella zoster immunity loss in multiple sclerosis patient treated with ocrelizumab 86
Effectiveness and Safety of Adjunctive Cenobamate in People with Focal-Onset Epilepsy: Evidence from the First Interim Analysis of the BLESS Study 85
A real-world comparison among third-generation antiseizure medications: Results from the COMPARE study 85
Perampanel as only add-on epilepsy treatment in elderly: A subgroup analysis of real-world data from retrospective, multicenter, observational study 82
Age at onset predicts good seizure outcome in sporadic non-lesional and mesial temporal sclerosis based temporal lobe epilepsy 80
A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine. 80
Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72 79
Advanced morphological neuroimaging study in lateral temporal lobe epilepsy: A multicentric study 78
A puzzling case without solution: isolated late-onset epileptic seizure 77
A Loss-of-Function HCN4 Mutation Associated With Familial Benign Myoclonic Epilepsy in Infancy Causes Increased Neuronal Excitability 77
A novel de novo HCN1 loss-of-function mutation in genetic generalized epilepsy causing increased neuronal excitability 77
Perampanel in post-stroke epilepsy: Clinical practice data from the PERampanel as Only Concomitant antiseizure medication (PEROC) study 76
Spinal muscular atrophy due to an isolated deletion of exon 8 of the telomeric survival motor neuron gene 76
A new Italian instrument for the assessment of irritability in patients with epilepsy. 76
White matter abnormalities across different epilepsy syndromes in adults: an ENIGMA-Epilepsy study 76
Humoral and T-cell response to SARS-CoV-2 mRNA vaccine in multiple sclerosis patients: Correlations with DMTs and clinical variables 75
Hypertension, seizures, and epilepsy: a review on pathophysiology and management 75
Network-based atrophy modeling in the common epilepsies: A worldwide ENIGMA study 75
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes 74
Facemask headache: a new nosographic entity among healthcare providers in COVID-19 era 74
Distinguishing seizures in autoimmune limbic encephalitis from mesial temporal lobe epilepsy with hippocampal sclerosis: Clues of a temporal plus network 73
Phenotypic Variability in Novel Doublecortin Gene Variants Associated with Subcortical Band Heterotopia 73
Accidents at work among people with epilepsy. Results of a European prospective cohort study 73
A novel ICA-based hardware system for reconfigurable and portable BCI 73
Perampanel as first add-on choice on the treatment of mesial temporal lobe epilepsy: an observational real-life study 73
Brivaracetam: review of its pharmacology and potential use as adjunctive therapy in patients with partial onset seizures 73
Idiopathic generalized epilepsy in a family with SCN4A-related myotonia 73
A systems-level analysis highlights microglial activation as a modifying factor in common epilepsies 72
Effectiveness of perampanel as the only add‐on: Retrospective, multicenter, observational real‐life study on epilepsy patients 72
Fatigue in natalizumab-treated Multiple Sclerosis patients: How much is wearing-off to blame? 72
Long-term outcome of mild mesial temporal lobe epilepsy 72
Circulating microrna: The potential novel diagnostic biomarkers to predict drug resistance in temporal lobe epilepsy, a pilot study 72
Two cases of unilateral wasting and weakness of distal upper limb: Similar onset and different diagnosis in young patients 71
Climate change and hyponatremia-related hospital admissions in people with focal epilepsy exposed to carbamazepine or its derivatives 71
A possible case of natalizumab-dependent suicide attempt: A brief review about drugs and suicide. 71
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 71
Mild non-lesional temporal lobe epilepsy. A common, unrecognized disorder with onset in adulthood 70
Association study between four polymorphisms in the HFE, TF and TFR genes and Parkinson's disease in Southern Italy 70
Epilepsy in “Sunflower syndrome”: electroclinical features, therapeutic response, and long-term follow-up 69
Predictors of Seizure Recurrence in Women With Idiopathic Generalized Epilepsy Who Switch From Valproate to Another Medication 68
Kufs disease due to mutation of CLN6: clinical, pathological and molecular genetic features. 67
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy. 67
Automatic detection of obstructive sleep apnea syndrome based on snore signals 67
A familial t(4;8) translocation segregates with epilepsy and migraine with aura 67
An Italian multicentre study of perampanel in progressive myoclonus epilepsies 67
Deep learning representation from electroencephalography of early-stage creutzfeldt-jakob disease and features for differentiation from rapidly progressive dementia 67
Human iPSC Modeling of Genetic Febrile Seizure Reveals Aberrant Molecular and Physiological Features Underlying an Impaired Neuronal Activity 66
The mystery of unexplained traumatic sudden falls. A clinical case that adds a new feasible cause 66
Epilepsy in cerebrovascular diseases: Review of experimental and clinical data with meta-analysis of risk factors 66
Deep Learning Representation from Electroencephalography of Early-Stage Creutzfeldt-Jakob Disease and Features for Differentiation from Rapidly Progressive Dementia. 66
Topographic divergence of atypical cortical asymmetry and atrophy patterns in temporal lobe epilepsy 66
May anti‐seizure medications alter brain structure in temporal lobe epilepsy? A prospective study 65
Functional seizures and binge eating disorder: A cross-sectional study 65
The one-and-a-half syndrome: a distinctive clinical finding in a patient with multiple sclerosis 65
A clinical spectrum of the myoclonic manifestations associated with typical absences in childhood absence epilepsy. A video-polygraphic study 65
A large family with pure autosomal dominant hereditary spastic paraplegia from southern Italy mapping to chromosome 14q11.2-q24.3 65
Determinants of health-related quality of life in pharmacoresistant epilepsy: Results from a large multicenter study of consecutively enrolled patients using validated quantitative assessments 65
Analysis of LGI1 promoter sequence, PDYN and GABBR1 polymorphisms in sporadic and familial lateral temporal lobe epilepsy 65
Novel KCNQ2 Variants Related to a Variable Phenotypic Spectrum Ranging from Epilepsy with Auditory Features to Severe Developmental and Epileptic Encephalopathies 65
National survey on the prevalence of single-gene aetiologies for genetic developmental and epileptic encephalopathies in Italy 64
Integrity of the corpus callosum in patients with benign temporal lobe epilepsy 64
Listeria infection after treatment with alemtuzumab: A case report and literature review. would antibiotic prophylaxis be considered? 64
Antiepileptic Drug Teratogenicity and De Novo Genetic Variation Load 64
Guillain-Barré syndrome following BNT162b2 COVID-19 vaccine 64
Blocking out the real diagnosis 63
No evidence of a role for cystatin B gene in juvenile myoclonic epilepsy. 63
Autosomal dominant lateral temporal epilepsy: absence of mutations in ADAM22 and Kv1 channel genes encoding LGI1-associated proteins. 63
Advances in genetic testing and optimization of clinical management in children and adults with epilepsy 63
Operative Strategies for Patients with Cortical Dysplastic Lesions and Intractable Epilepsy 63
Totale 8.286
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Categoria #
all - tutte 272.866
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 272.866
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.298 0 0 0 359 147 20 25 303 129 117 191 7
2022/20233.587 923 127 79 382 405 337 10 238 569 215 232 70
2023/20241.623 335 248 155 103 98 386 58 38 13 32 46 111
2024/20255.680 749 395 268 222 330 717 177 215 733 389 495 990
2025/202612.978 617 1.370 1.619 2.254 1.196 451 1.580 750 1.582 834 525 200
2026/20272.892 214 811 1.355 512 0 0 0 0 0 0 0 0
Totale 28.864