BALESTRINI, SIMONA
 Distribuzione geografica
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Continente #
NA - Nord America 5.885
AS - Asia 5.437
EU - Europa 4.397
SA - Sud America 1.712
AF - Africa 152
OC - Oceania 57
Continente sconosciuto - Info sul continente non disponibili 4
Totale 17.644
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Nazione #
US - Stati Uniti d'America 5.695
RU - Federazione Russa 1.813
CN - Cina 1.427
IT - Italia 1.406
BR - Brasile 1.378
SG - Singapore 1.299
VN - Vietnam 712
HK - Hong Kong 695
KR - Corea 535
IE - Irlanda 296
BD - Bangladesh 280
FR - Francia 189
SE - Svezia 153
AR - Argentina 142
IN - India 137
FI - Finlandia 119
GB - Regno Unito 91
CA - Canada 90
DE - Germania 79
ID - Indonesia 78
JP - Giappone 70
NL - Olanda 58
AU - Australia 55
EC - Ecuador 53
MX - Messico 49
ZA - Sudafrica 42
CH - Svizzera 40
CO - Colombia 37
UA - Ucraina 33
IQ - Iraq 32
PL - Polonia 31
PY - Paraguay 31
CI - Costa d'Avorio 24
CL - Cile 24
TR - Turchia 23
AT - Austria 21
VE - Venezuela 20
ES - Italia 17
MA - Marocco 17
NG - Nigeria 17
JM - Giamaica 15
JO - Giordania 15
PE - Perù 14
UZ - Uzbekistan 14
EG - Egitto 13
IL - Israele 13
PK - Pakistan 13
AE - Emirati Arabi Uniti 11
AZ - Azerbaigian 10
SA - Arabia Saudita 10
TN - Tunisia 9
KZ - Kazakistan 8
BJ - Benin 7
DO - Repubblica Dominicana 7
HN - Honduras 7
IR - Iran 7
LB - Libano 7
NP - Nepal 7
UY - Uruguay 7
BE - Belgio 6
PT - Portogallo 6
BO - Bolivia 5
CR - Costa Rica 5
DK - Danimarca 5
RS - Serbia 5
TH - Thailandia 5
TW - Taiwan 5
HU - Ungheria 4
KE - Kenya 4
PH - Filippine 4
TT - Trinidad e Tobago 4
AL - Albania 3
AO - Angola 3
DZ - Algeria 3
GA - Gabon 3
GT - Guatemala 3
LV - Lettonia 3
OM - Oman 3
SK - Slovacchia (Repubblica Slovacca) 3
SN - Senegal 3
SV - El Salvador 3
XK - ???statistics.table.value.countryCode.XK??? 3
BH - Bahrain 2
CZ - Repubblica Ceca 2
EE - Estonia 2
ET - Etiopia 2
GE - Georgia 2
KW - Kuwait 2
LT - Lituania 2
MY - Malesia 2
NO - Norvegia 2
PR - Porto Rico 2
PS - Palestinian Territory 2
RO - Romania 2
AM - Armenia 1
BA - Bosnia-Erzegovina 1
BB - Barbados 1
BG - Bulgaria 1
BN - Brunei Darussalam 1
BZ - Belize 1
Totale 17.623
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Città #
Santa Clara 2.240
Singapore 1.069
Ashburn 714
Hong Kong 592
Seoul 521
Hefei 475
Milan 332
Dublin 296
Ho Chi Minh City 273
Los Angeles 207
San Jose 176
Lawrence 170
Altamura 168
Beijing 165
Hanoi 136
The Dalles 130
Lauterbourg 129
Rome 129
Moscow 125
São Paulo 106
Council Bluffs 105
Boston 99
Princeton 99
Buffalo 94
Fairfield 90
Helsinki 80
Florence 75
Mumbai 71
Chandler 70
New York 59
Kent 54
Tokyo 54
Rio de Janeiro 52
Melbourne 51
Dallas 41
Jakarta 40
Bern 37
San Diego 34
Belo Horizonte 30
Da Nang 30
Brasília 29
Bologna 28
Haiphong 28
Lappeenranta 27
Naples 27
Shanghai 27
Turin 27
Houston 26
Munich 26
Toronto 26
Curitiba 25
Figino 25
Warsaw 25
Abidjan 24
Frankfurt am Main 24
Guayaquil 24
Biên Hòa 23
Bengaluru 22
Seattle 22
Cambridge 21
Paris 21
Bari 20
Guangzhou 20
Chicago 19
Porto Alegre 19
Johannesburg 18
San Francisco 18
Woodbridge 18
Genoa 17
Buenos Aires 16
Campinas 16
Hillsboro 16
Medford 16
Miano 16
Wilmington 16
Abuja 15
Baghdad 15
Boardman 15
Guarulhos 15
Palermo 15
Ribeirão Preto 15
Salvador 15
Thái Bình 15
Andover 14
Nuremberg 14
Tianjin 14
West Jordan 14
Ninh Bình 13
Thái Nguyên 13
Amsterdam 12
Brooklyn 12
Lima 12
London 12
Quito 12
Tashkent 12
Yubileyny 12
Goiânia 11
Hải Dương 11
Santo André 11
Shenzhen 11
Totale 10.520
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Nome #
The aetiologies of epilepsy 271
Developmental and epileptic encephalopathies: from genetic heterogeneity to phenotypic continuum 227
Climate change and epilepsy: Insights from clinical and basic science studies 214
Multiorgan manifestations of COL4A1 and COL4A2 variants and proposal for a clinical management protocol 204
A registry for Dravet syndrome: The Italian experience 185
Stretch-activated ion channel TMEM63B associates with developmental and epileptic encephalopathies and progressive neurodegeneration 179
Cardiac phenotype in ATP1A3-related syndromes: A multicenter cohort study 173
Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals 172
Ammonia: What adult neurologists need to know 167
Dissecting genetics of spectrum of epilepsies with eyelid myoclonia by exome sequencing 165
Alternating hemiplegia of childhood: An electroclinical study of sleep and hemiplegia 164
Efficacy and Safety of Long-Term Treatment with Stiripentol in Children and Adults with Drug-Resistant Epilepsies: A Retrospective Cohort Study of 196 Patients 158
Clinical outcomes of COVID-19 in long-term care facilities for people with epilepsy 156
Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2 153
Bilateral Perisylvian Polymicrogyria, Intellectual Disability and Nephronophthisis Associated With Compound Heterozygous Pathogenic Variants in the CEP83 Gene 151
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)) 151
Focal cortical dysplasia: a practical guide for neurologists 149
The landscape of epilepsy - related GATOR1 variants 148
Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathies 148
Bilateral temporal lobe dysplasia and seizure onset associated with biallelic CNTNAP2 variants 147
Case report: Dravet syndrome, feeding difficulties and gastrostomy 146
DNAJC12 deficiency: Mild hyperphenylalaninemia and neurological impairment in two siblings 144
Morphometry and network-based atrophy patterns in SCN1A-related Dravet syndrome 143
Morphometric network-based abnormalities correlate with psychiatric comorbidities and gene expression in PCDH19-related developmental and epileptic encephalopathy 143
The role of electroencephalography in epilepsy research-From seizures to interictal activity and comorbidities 143
The ENIGMA-Epilepsy working group: Mapping disease from large data sets 141
Audit of use of stiripentol in adults with Dravet syndrome 140
A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing 139
The spectrum of epilepsy with eyelid myoclonia: delineation of disease subtypes from a large multicenter study 137
Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17458 subjects 136
Applying a perceptions and practicalities approach to understanding nonadherence to antiepileptic drugs 135
Real-life survey of pitfalls and successes of precision medicine in genetic epilepsies 134
Polygenic burden in focal and generalized epilepsies 134
Clinical and neurophysiological characterisation of ictal and sleep pattern in alternating hemiplegia of childhood 134
AN APPARENT SYMPTOMATIC FOCAL EPILEPSY IN A PATIENT WITH MALIGNANT INSULINOMA ASSOCIATED TO GLUCAGONOMA 133
Erratum: Correction: The landscape of epilepsy-related GATOR1 variants (Genetics in medicine : official journal of the American College of Medical Genetics (2019) 21 2 (398-408)) 132
GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture 130
Fibroblast transcriptomics uncovers pathogenic genomic variants in individuals with exome-negative childhood onset epilepsy 130
The impact of Transcranial Magnetic Stimulation (TMS) on seizure course in people with and without epilepsy 128
Coasting, embryo development and outcomes of blastocyst transfer: a case-control study 128
ANALYSIS OF FACIAL ASYMMETRY AND DYSMORPHISM IN EPILEPSY 127
Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals 127
Cortical myoclonus and epilepsy in a family with a new SLC20A2 mutation 127
Diagnostic delay and prognosis in primary central nervous system lymphoma compared with glioblastoma multiforme 125
Cardiac Phenotype In ATP1A3 Related-Syndromes: A Multicentre Study 125
Cerebellar, limbic, and midbrain volume alterations in sudden unexpected death in epilepsy 124
Epilepsy with myoclonic-atonic seizures: an update on genetic causes, nosological limits, and treatment strategies 123
Pharmacogenomics in epilepsy 123
Use Of A Medium Chain Triglyceride-Based Food For Special Medical Purposes In Children And Adults With Epilepsy: Compliance, Tolerability And Acceptability 123
MULTIMODAL RESPONSES INDUCED BY CORTICAL STIMULATION OF THE PARIETAL LOBE: A STEREO-ELECTROENCEPHALOGRAPHY STUDY 121
Expanding the genetic and phenotypic spectrum of CHD2-related disease: From early neurodevelopmental disorders to adult-onset epilepsy 120
Transcranial magnetic stimulation as a biomarker of treatment response in children with epilepsy 120
The challenges of treating epilepsy with 25 antiepileptic drugs 119
Perampanel Confirms to Be Effective and Well-Tolerated as an Add-On Treatment in Patients With Brain Tumor-Related Epilepsy (PERADET Study) 119
Methodology for classification and definition of epilepsy syndromes with list of syndromes: Report of the ILAE Task Force on Nosology and Definitions 117
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes 116
CLINICAL FEATURES OF POST-ICTAL PSYCHOSIS: AN OBSERVATIONAL DESCRIPTIVE STUDY 116
The landscape of epilepsy-related GATOR1 variants (vol 21, pg 398, 2018) 116
BURDEN OF UNCONTROLLED EPILEPSY IN PATIENTS REQUIRING AN EMERGENCY ROOM VISIT OR HOSPITALIZATION 116
Genome-wide association meta-analyses of drug-resistant epilepsy 115
Neurologic phenotypes associated with COL4A1/2 mutations Expanding the spectrum of disease 115
Late diagnoses of Dravet syndrome: How many individuals are we missing? 115
The impact of Transcranial Magnetic Stimulation (TMS) on EEG and seizure course in people with or without epilepsy 114
Systolic and diastolic heart failure and renal dysfunction in hospitalized elderly patients 114
Fenfluramine treatment for Dravet syndrome: Long term real-world analysis demonstrates safety and reduced health care burden 113
Electroclinical Features and Long-term Seizure Outcome in Patients With Eyelid Myoclonia With Absences 113
Comparative effectiveness of antiepileptic drugs in juvenile myoclonic epilepsy 113
Genome-wide Polygenic Burden of Rare Deleterious Variants in Sudden Unexpected Death in Epilepsy 113
TBC1D24 genotype-phenotype correlation: Epilepsies and other neurologic features 113
Clinical spectrum of STX1B-related epileptic disorders 113
Drug-resistant epilepsy, early-onset hypertension and white matter lesions: A hidden paraganglioma 113
The expanding field of genetic developmental and epileptic encephalopathies: current understanding and future perspectives 112
An interconnected data infrastructure to support large-scale rare disease research 112
Cenobamate as add-on treatment for SCN8A developmental and epileptic encephalopathy 112
Knocking at the brain's door: a direct measure of brain excitability in alternating hemiplegia of childhood 111
Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnoses 110
Multimodal responses induced by cortical stimulation of the parietal lobe: a stereo-electroencephalography study 109
ATP1A3 Variants, Variably Penetrant Short QT Intervals, and Lethal Ventricular Arrhythmias 109
Transcranial magnetic stimulation as a tool to understand genetic conditions associated with epilepsy 109
Muscle and brain sodium channelopathies: genetic causes, clinical phenotypes, and management approaches 108
Genetics of the Epilepsies 107
Genome-wide association study: Exploring the genetic basis for responsiveness to ketogenic dietary therapies for drug-resistant epilepsy 106
One-Year Progression of Moderate Asymptomatic Carotid Stenosis Predicts the Risk of Vascular Events 106
Sex-associated differences in the modulation of vascular risk in patients with asymptomatic carotid stenosis 106
Increased Common Carotid Artery Wall Thickness Is Associated with Rapid Progression of Asymptomatic Carotid Stenosis 106
Severe carotid stenosis and impaired cerebral hemodynamics can influence cognitive deterioration 106
K.Vita: a feasibility study of a blend of medium chain triglycerides to manage drug-resistant epilepsy 106
De novo mutations of KIAA2022 in females cause intellectual disability and intractable epilepsy 105
Sex-based electroclinical differences and prognostic factors in epilepsy with eyelid myoclonia 104
Steps to Improve Precision Medicine in Epilepsy. 104
Two-center experience of cannabidiol use in adults with Dravet syndrome 104
Postictal Psychosis in Epilepsy: A Clinicogenetic Study 104
Treatment of Epileptic Encephalopathies 103
Methodology of a Natural History Study of a Rare Neurodevelopmental Disorder: Alternating Hemiplegia of Childhood as a Prototype Disease 101
Risk-conferring HLA variants in an epilepsy cohort: benefits of multifaceted use of whole genome sequencing in clinical practice 101
The impact of COVID-19 in Dravet syndrome: A UK survey 101
Rare dysfunctional SCN2A variants are associated with malformation of cortical development 100
Rare and Complex Epilepsies from Childhood to Adulthood: Requirements for Separate Management or Scope for a Lifespan Holistic Approach? 100
Percutaneous transluminal angioplasty for chronic cerebrospinal venous insufficiency in multiple sclerosis: dichotomy between subjective and objective outcome scores 100
Erratum: Ammonia: What adult neurologists need to know (Pract Neurol (2021) 21 (36-42) DOI: 10.1136/practneurol-2020-002654) 100
Totale 12.942
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Categoria #
all - tutte 55.288
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 55.288
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022419 0 0 0 1 0 1 0 15 195 11 77 119
2022/20231.138 177 403 34 23 8 198 124 31 45 31 21 43
2023/2024732 11 39 139 50 38 49 49 210 16 81 23 27
2024/20255.900 215 687 294 763 1.701 870 161 136 258 171 301 343
2025/20269.319 821 1.210 1.235 1.669 539 280 658 443 467 361 430 1.206
2026/2027253 253 0 0 0 0 0 0 0 0 0 0 0
Totale 17.843