IRIS
GAMBARDELLA, ANTONIO
 Distribuzione geografica
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Continente #
NA - Nord America 12.762
AS - Asia 7.815
EU - Europa 3.678
SA - Sud America 1.945
Continente sconosciuto - Info sul continente non disponibili 481
AF - Africa 171
OC - Oceania 39
Totale 26.891
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Nazione #
US - Stati Uniti d'America 12.315
SG - Singapore 3.623
CN - Cina 1.742
IT - Italia 1.596
BR - Brasile 1.533
VN - Vietnam 807
IN - India 752
SE - Svezia 510
GB - Regno Unito 423
DE - Germania 304
CA - Canada 302
HK - Hong Kong 243
BD - Bangladesh 209
AR - Argentina 172
FI - Finlandia 124
NL - Olanda 113
EE - Estonia 108
ID - Indonesia 93
MX - Messico 83
RU - Federazione Russa 82
ZA - Sudafrica 73
EC - Ecuador 67
FR - Francia 62
RO - Romania 62
IQ - Iraq 61
PL - Polonia 50
UA - Ucraina 48
CO - Colombia 45
JP - Giappone 42
ES - Italia 36
PK - Pakistan 33
VE - Venezuela 33
TR - Turchia 29
AU - Australia 28
CL - Cile 28
PY - Paraguay 28
AT - Austria 23
MA - Marocco 23
PE - Perù 23
SA - Arabia Saudita 19
CZ - Repubblica Ceca 18
EG - Egitto 18
IR - Iran 17
UZ - Uzbekistan 15
IE - Irlanda 14
CH - Svizzera 13
JM - Giamaica 13
KR - Corea 13
AE - Emirati Arabi Uniti 12
UY - Uruguay 12
LT - Lituania 11
MY - Malesia 11
GR - Grecia 10
JO - Giordania 10
KE - Kenya 10
NP - Nepal 10
PT - Portogallo 9
EU - Europa 8
IL - Israele 8
KZ - Kazakistan 8
PS - Palestinian Territory 8
TN - Tunisia 8
A2 - ???statistics.table.value.countryCode.A2??? 7
AZ - Azerbaigian 7
DO - Repubblica Dominicana 7
TH - Thailandia 7
AL - Albania 6
AO - Angola 6
BE - Belgio 6
CI - Costa d'Avorio 6
DZ - Algeria 6
HN - Honduras 6
LB - Libano 6
MD - Moldavia 6
NI - Nicaragua 6
NZ - Nuova Zelanda 6
SC - Seychelles 6
TT - Trinidad e Tobago 6
CR - Costa Rica 5
LV - Lettonia 5
RS - Serbia 5
BA - Bosnia-Erzegovina 4
BG - Bulgaria 4
DK - Danimarca 4
ET - Etiopia 4
GT - Guatemala 4
HU - Ungheria 4
MT - Malta 4
NG - Nigeria 4
OM - Oman 4
PH - Filippine 4
SV - El Salvador 4
BO - Bolivia 3
HR - Croazia 3
KG - Kirghizistan 3
KW - Kuwait 3
LK - Sri Lanka 3
MK - Macedonia 3
AM - Armenia 2
CG - Congo 2
Totale 26.384
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Città #
San Jose 2.294
Chandler 1.249
Singapore 1.144
Ashburn 1.072
Dallas 1.002
Santa Clara 678
Bengaluru 565
Hefei 550
Milan 495
Council Bluffs 487
Princeton 459
Lawrence 456
Chicago 314
London 310
Ho Chi Minh City 308
Wilmington 277
Beijing 246
Hong Kong 233
Munich 209
Hanoi 180
Ottawa 162
Des Moines 145
São Paulo 141
Boardman 128
Los Angeles 118
New York 88
Turku 79
Catanzaro 76
Rome 74
The Dalles 72
Shanghai 63
Chennai 49
Rio de Janeiro 46
Guangzhou 44
Helsinki 42
Naples 42
Columbus 41
Da Nang 41
San Francisco 40
Brooklyn 39
Warsaw 39
Pune 36
Boston 35
Orem 35
Amsterdam 32
Johannesburg 32
Curitiba 31
Haiphong 31
Buffalo 30
Toronto 30
Norwalk 29
Redwood City 29
Belo Horizonte 28
Mexico City 28
Horia 27
Montreal 27
Shenzhen 27
Tokyo 27
Phoenix 26
Charlotte 24
Porto Alegre 24
Quito 23
Thái Bình 23
Aversa 22
Brasília 22
San Nicola Manfredi 22
Stockholm 22
Atlanta 21
Florence 21
Redmond 21
Biên Hòa 20
Buenos Aires 19
Seattle 19
Bari 18
Secaucus 18
Timisoara 18
Fortaleza 17
Guayaquil 17
Jakarta 17
Campinas 16
Genoa 16
Guarulhos 16
Salvador 16
Augusta 15
Catania 15
Baghdad 14
Dhaka 14
Hải Dương 14
New Delhi 14
Tashkent 14
Can Tho 13
Cape Town 13
Falls Church 13
Lima 13
Olomouc 13
Palermo 13
Boydton 12
Cetraro 12
Frankfurt am Main 12
Manchester 12
Totale 15.335
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Nome #
Genetics of reflex seizures and epilepsies in humans and animals 165
Predictive factors of Status Epilepticus and its recurrence in patients with adult–onset seizures: A multicenter, long follow–up cohort study 150
Rating Scale for Psychogenic Non-epileptic Seizures: Scale Development and Clinimetric Testing 148
Levetiracetam vs Lamotrigine as First-Line Antiseizure Medication in Female Patients With Idiopathic Generalized Epilepsy 146
Transcriptomic and electrophysiological alterations underlying phenotypic variability in SCN1A-associated febrile seizures 145
Comparative Effectiveness of Brivaracetam, Cenobamate, Lacosamide, and Perampanel in Focal Epilepsy 120
Chlorpromazine versus sleep deprivation in activation of EEG in adult-onset partial epilepsy. 117
A brainstem hypermetabolism in a patient with essential palatal tremor: A simultaneous 18F-FDG-PET/3 T-MRI study 106
PRECLINICAL MARKERS OF NEUROPATHIC DAMAGE IN TYPE 1 DIABETES MELLITUS 104
Effectiveness of perampanel as only concomitant antiseizure medication for highly active epilepsy: insight from a real-world, multicenter retrospective study 101
A hypofibrinolytic state in overweight patients with cerebral venous thrombosis and isolated intracranial hypertension 99
A functional polymorphism in the SCN1A gene does not influence antiepileptic drug responsiveness in Italian patients with focal epilepsy 99
A new SLC20A2 mutation identified in southern Italy family with primary familial brain calcification. 97
Temporal lobe abnormalities on brain MRI in healthy volunteers: a prospective case-control study 97
A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chomosome 1 96
3-T magnetic resonance imaging simultaneous automated multimodal approach improves detection of ambiguous visual hippocampal sclerosis. 96
Glucose transporter-1 deficiency syndrome with extreme phenotypic variability in a five-generation family carrying a novel SLC2A1 variant 95
A software pipeline for pre-processing and mining EEG signals: Application in neurology 91
C19orf12 gene mutations in patients with neurodegeneration with brain iron accumulation 91
A Functional Genetic Variation of the 5-HTR2A Receptor Affects Age at Onset in Patients with Temporal Lobe Epilepsy 90
Rasmussen's Encephalitis and Related Conditions. The Causes of Epilepsy Common and Uncommon Causes in Adults and Children 87
A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chromosome 1 87
A novel exon 1 mutation in a patient with atypical lafora progressive myoclonus epilepsy seen as childhood-onset cognitive deficit 87
Asymmetry of Permutation Entropy in Early Creutzfeldt-Jakob Disease: A Clue to a Specific Pathological Process? 85
Neocortical thinning in “benign” mesial temporal lobe epilepsy 84
A Family With a Complex Phenotype Caused by Two Different Rare Metabolic Disorders: GLUT1 and Very-Long-Chain Fatty Acid Dehydrogenase (VLCAD) Deficiencies 84
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)) 84
Effectiveness and Safety of Adjunctive Cenobamate in People with Focal-Onset Epilepsy: Evidence from the First Interim Analysis of the BLESS Study 82
Resting-State EEG Classification for PNES Diagnosis 82
A. Spinal muscular atrophy due to an isolated deletion of Exon 8 of telomeric survival motor neuron gene 81
Varicella zoster immunity loss in multiple sclerosis patient treated with ocrelizumab 81
A Multilayer Network-Based Method for Brain Connectivity Analysis from EEG Data 79
Perampanel as only add-on epilepsy treatment in elderly: A subgroup analysis of real-world data from retrospective, multicenter, observational study 79
A real-world comparison among third-generation antiseizure medications: Results from the COMPARE study 78
Incidental evidence of hypointensity in brain grey nuclei on routine MR imaging: when to suspect a neurodegenerative disorder? 78
Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72 77
A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine. 76
Age at onset predicts good seizure outcome in sporadic non-lesional and mesial temporal sclerosis based temporal lobe epilepsy 75
Spinal muscular atrophy due to an isolated deletion of exon 8 of the telomeric survival motor neuron gene 75
White matter abnormalities across different epilepsy syndromes in adults: an ENIGMA-Epilepsy study 75
A puzzling case without solution: isolated late-onset epileptic seizure 74
Network-based atrophy modeling in the common epilepsies: A worldwide ENIGMA study 74
Advanced morphological neuroimaging study in lateral temporal lobe epilepsy: A multicentric study 73
A new Italian instrument for the assessment of irritability in patients with epilepsy. 72
A Loss-of-Function HCN4 Mutation Associated With Familial Benign Myoclonic Epilepsy in Infancy Causes Increased Neuronal Excitability 72
Accidents at work among people with epilepsy. Results of a European prospective cohort study 72
A novel de novo HCN1 loss-of-function mutation in genetic generalized epilepsy causing increased neuronal excitability 72
Phenotypic Variability in Novel Doublecortin Gene Variants Associated with Subcortical Band Heterotopia 71
Long-term outcome of mild mesial temporal lobe epilepsy 71
Perampanel as first add-on choice on the treatment of mesial temporal lobe epilepsy: an observational real-life study 70
Facemask headache: a new nosographic entity among healthcare providers in COVID-19 era 70
Distinguishing seizures in autoimmune limbic encephalitis from mesial temporal lobe epilepsy with hippocampal sclerosis: Clues of a temporal plus network 69
Hypertension, seizures, and epilepsy: a review on pathophysiology and management 69
Humoral and T-cell response to SARS-CoV-2 mRNA vaccine in multiple sclerosis patients: Correlations with DMTs and clinical variables 68
Mild non-lesional temporal lobe epilepsy. A common, unrecognized disorder with onset in adulthood 68
A novel ICA-based hardware system for reconfigurable and portable BCI 68
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 68
Brivaracetam: review of its pharmacology and potential use as adjunctive therapy in patients with partial onset seizures 68
Idiopathic generalized epilepsy in a family with SCN4A-related myotonia 68
Effectiveness of perampanel as the only add‐on: Retrospective, multicenter, observational real‐life study on epilepsy patients 67
Association study between four polymorphisms in the HFE, TF and TFR genes and Parkinson's disease in Southern Italy 67
Circulating microrna: The potential novel diagnostic biomarkers to predict drug resistance in temporal lobe epilepsy, a pilot study 67
A systems-level analysis highlights microglial activation as a modifying factor in common epilepsies 66
Epilepsy in “Sunflower syndrome”: electroclinical features, therapeutic response, and long-term follow-up 66
Fatigue in natalizumab-treated Multiple Sclerosis patients: How much is wearing-off to blame? 65
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes 65
A possible case of natalizumab-dependent suicide attempt: A brief review about drugs and suicide. 65
Kufs disease due to mutation of CLN6: clinical, pathological and molecular genetic features. 65
Perampanel in post-stroke epilepsy: Clinical practice data from the PERampanel as Only Concomitant antiseizure medication (PEROC) study 64
Climate change and hyponatremia-related hospital admissions in people with focal epilepsy exposed to carbamazepine or its derivatives 64
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy. 64
Epilepsy in cerebrovascular diseases: Review of experimental and clinical data with meta-analysis of risk factors 64
Deep learning representation from electroencephalography of early-stage creutzfeldt-jakob disease and features for differentiation from rapidly progressive dementia 64
Two cases of unilateral wasting and weakness of distal upper limb: Similar onset and different diagnosis in young patients 63
Deep Learning Representation from Electroencephalography of Early-Stage Creutzfeldt-Jakob Disease and Features for Differentiation from Rapidly Progressive Dementia. 63
Automatic detection of obstructive sleep apnea syndrome based on snore signals 63
Antiepileptic Drug Teratogenicity and De Novo Genetic Variation Load 63
Topographic divergence of atypical cortical asymmetry and atrophy patterns in temporal lobe epilepsy 63
Functional seizures and binge eating disorder: A cross-sectional study 62
National survey on the prevalence of single-gene aetiologies for genetic developmental and epileptic encephalopathies in Italy 62
A clinical spectrum of the myoclonic manifestations associated with typical absences in childhood absence epilepsy. A video-polygraphic study 62
The mystery of unexplained traumatic sudden falls. A clinical case that adds a new feasible cause 62
Blocking out the real diagnosis 62
Autosomal dominant lateral temporal epilepsy: absence of mutations in ADAM22 and Kv1 channel genes encoding LGI1-associated proteins. 62
Analysis of LGI1 promoter sequence, PDYN and GABBR1 polymorphisms in sporadic and familial lateral temporal lobe epilepsy 62
Operative Strategies for Patients with Cortical Dysplastic Lesions and Intractable Epilepsy 62
An Italian multicentre study of perampanel in progressive myoclonus epilepsies 62
Integrity of the corpus callosum in patients with benign temporal lobe epilepsy 61
A large family with pure autosomal dominant hereditary spastic paraplegia from southern Italy mapping to chromosome 14q11.2-q24.3 61
A familial t(4;8) translocation segregates with epilepsy and migraine with aura 61
Guillain-Barré syndrome following BNT162b2 COVID-19 vaccine 61
Human iPSC Modeling of Genetic Febrile Seizure Reveals Aberrant Molecular and Physiological Features Underlying an Impaired Neuronal Activity 60
The parkin gene is not involved in late-onset Parkinson’s disease 60
Listeria infection after treatment with alemtuzumab: A case report and literature review. would antibiotic prophylaxis be considered? 60
Advances in genetic testing and optimization of clinical management in children and adults with epilepsy 60
Genetics heterogeneity in patients with pantothenate kinase-associated neurodegeneration and classic magnetic resonance imaging eye-of-the-tiger pattern 60
A Reappraisal on cortical myoclonus and brief Remarks on myoclonus of different Origins 59
Functional integrity of benzodiazepine receptors of the geniculo-striate visual pathways in Creutzfeldt-Jakob disease. A pharmacological evoked potential study 59
PCDH19 mutations in female patients from Southern Italy. 59
Brand-to-Generic Levetiracetam Switching: a four-years prospective observational real-life study 59
Totale 7.772
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Categoria #
all - tutte 258.376
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 258.376
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.311 0 5 8 359 147 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
2026/2027919 214 705 0 0 0 0 0 0 0 0 0 0
Totale 26.891