BALESTRINI, SIMONA
 Distribuzione geografica
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Continente #
NA - Nord America 4.453
AS - Asia 4.424
EU - Europa 3.221
SA - Sud America 1.657
AF - Africa 123
OC - Oceania 56
Continente sconosciuto - Info sul continente non disponibili 3
Totale 13.937
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Nazione #
US - Stati Uniti d'America 4.358
RU - Federazione Russa 1.796
BR - Brasile 1.344
CN - Cina 1.154
SG - Singapore 1.083
HK - Hong Kong 680
VN - Vietnam 557
KR - Corea 533
IT - Italia 499
IE - Irlanda 295
SE - Svezia 153
AR - Argentina 135
IN - India 122
FI - Finlandia 94
ID - Indonesia 76
GB - Regno Unito 66
DE - Germania 65
AU - Australia 54
EC - Ecuador 51
NL - Olanda 49
BD - Bangladesh 42
MX - Messico 40
CH - Svizzera 38
ZA - Sudafrica 38
CO - Colombia 35
FR - Francia 35
PY - Paraguay 30
UA - Ucraina 30
PL - Polonia 27
CA - Canada 25
CI - Costa d'Avorio 24
JP - Giappone 24
CL - Cile 20
IQ - Iraq 19
VE - Venezuela 18
MA - Marocco 16
AT - Austria 15
TR - Turchia 15
ES - Italia 14
EG - Egitto 13
JO - Giordania 13
PK - Pakistan 12
UZ - Uzbekistan 12
IL - Israele 11
PE - Perù 11
AE - Emirati Arabi Uniti 9
AZ - Azerbaigian 9
BJ - Benin 7
DO - Repubblica Dominicana 7
IR - Iran 7
JM - Giamaica 7
KZ - Kazakistan 7
LB - Libano 7
SA - Arabia Saudita 7
UY - Uruguay 7
NP - Nepal 6
TN - Tunisia 6
BE - Belgio 5
BO - Bolivia 5
DK - Danimarca 5
HN - Honduras 5
RS - Serbia 5
HU - Ungheria 4
KE - Kenya 4
AL - Albania 3
AO - Angola 3
DZ - Algeria 3
GT - Guatemala 3
LV - Lettonia 3
PT - Portogallo 3
SK - Slovacchia (Repubblica Slovacca) 3
TT - Trinidad e Tobago 3
TW - Taiwan 3
XK - ???statistics.table.value.countryCode.XK??? 3
CZ - Repubblica Ceca 2
EE - Estonia 2
GA - Gabon 2
KW - Kuwait 2
LT - Lituania 2
NO - Norvegia 2
PS - Palestinian Territory 2
RO - Romania 2
SN - Senegal 2
SV - El Salvador 2
AM - Armenia 1
BA - Bosnia-Erzegovina 1
BB - Barbados 1
BG - Bulgaria 1
BH - Bahrain 1
BN - Brunei Darussalam 1
CR - Costa Rica 1
CY - Cipro 1
ET - Etiopia 1
GE - Georgia 1
GY - Guiana 1
KH - Cambogia 1
MK - Macedonia 1
ML - Mali 1
MV - Maldive 1
MW - Malawi 1
Totale 13.926
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Città #
Santa Clara 2.224
Singapore 878
Hong Kong 583
Seoul 521
Hefei 475
Ashburn 322
Dublin 295
Ho Chi Minh City 222
Lawrence 169
Altamura 168
Beijing 159
Moscow 122
São Paulo 105
Boston 99
Princeton 99
Hanoi 96
Fairfield 90
Los Angeles 89
Buffalo 81
Mumbai 71
The Dalles 70
Chandler 69
Helsinki 57
Florence 55
Kent 54
Melbourne 51
Rio de Janeiro 51
Jakarta 40
Bern 37
San Jose 34
San Diego 30
Brasília 29
Belo Horizonte 28
Milan 27
Lappeenranta 26
Munich 26
Curitiba 25
Abidjan 24
Da Nang 24
Guayaquil 23
Houston 23
Haiphong 22
Warsaw 22
Bengaluru 21
Cambridge 21
Dallas 21
Biên Hòa 20
Seattle 20
Shanghai 19
Porto Alegre 18
Rome 18
Woodbridge 18
Campinas 16
Johannesburg 16
Medford 16
Wilmington 16
Buenos Aires 15
Guarulhos 15
Ribeirão Preto 15
Andover 14
Frankfurt am Main 14
Hillsboro 14
Paris 14
Salvador 14
Toronto 14
West Jordan 14
New York 13
Thái Bình 13
Bologna 12
Chicago 12
Nuremberg 12
Quito 12
San Francisco 12
Yubileyny 12
Goiânia 11
Ninh Bình 11
Santo André 11
Turku 11
Baghdad 10
Bogotá 10
Guangzhou 10
Hải Dương 10
Jungnang-gu 10
London 10
Tashkent 10
Tokyo 10
Asunción 9
Caxias do Sul 9
Genoa 9
Lima 9
Manaus 9
Quảng Ngãi 9
Sorocaba 9
Thái Nguyên 9
Can Tho 8
Cascina 8
Contagem 8
Dhaka 8
Elk Grove Village 8
Nanning 8
Totale 8.440
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Nome #
Developmental and epileptic encephalopathies: from genetic heterogeneity to phenotypic continuum 201
The aetiologies of epilepsy 201
Climate change and epilepsy: Insights from clinical and basic science studies 191
Multiorgan manifestations of COL4A1 and COL4A2 variants and proposal for a clinical management protocol 171
A registry for Dravet syndrome: The Italian experience 161
Stretch-activated ion channel TMEM63B associates with developmental and epileptic encephalopathies and progressive neurodegeneration 155
Cardiac phenotype in ATP1A3-related syndromes: A multicenter cohort study 152
Efficacy and Safety of Long-Term Treatment with Stiripentol in Children and Adults with Drug-Resistant Epilepsies: A Retrospective Cohort Study of 196 Patients 148
Dissecting genetics of spectrum of epilepsies with eyelid myoclonia by exome sequencing 143
Ammonia: What adult neurologists need to know 143
Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2 142
Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals 134
Morphometry and network-based atrophy patterns in SCN1A-related Dravet syndrome 130
Clinical outcomes of COVID-19 in long-term care facilities for people with epilepsy 130
Alternating hemiplegia of childhood: An electroclinical study of sleep and hemiplegia 129
Bilateral temporal lobe dysplasia and seizure onset associated with biallelic CNTNAP2 variants 128
Case report: Dravet syndrome, feeding difficulties and gastrostomy 128
A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing 127
Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathies 127
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)) 126
Morphometric network-based abnormalities correlate with psychiatric comorbidities and gene expression in PCDH19-related developmental and epileptic encephalopathy 125
The landscape of epilepsy - related GATOR1 variants 125
Audit of use of stiripentol in adults with Dravet syndrome 125
Focal cortical dysplasia: a practical guide for neurologists 123
Clinical and neurophysiological characterisation of ictal and sleep pattern in alternating hemiplegia of childhood 120
The spectrum of epilepsy with eyelid myoclonia: delineation of disease subtypes from a large multicenter study 119
Applying a perceptions and practicalities approach to understanding nonadherence to antiepileptic drugs 119
Polygenic burden in focal and generalized epilepsies 117
Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17458 subjects 117
AN APPARENT SYMPTOMATIC FOCAL EPILEPSY IN A PATIENT WITH MALIGNANT INSULINOMA ASSOCIATED TO GLUCAGONOMA 115
GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture 114
Real-life survey of pitfalls and successes of precision medicine in genetic epilepsies 112
Transcranial magnetic stimulation as a biomarker of treatment response in children with epilepsy 112
Diagnostic delay and prognosis in primary central nervous system lymphoma compared with glioblastoma multiforme 111
Coasting, embryo development and outcomes of blastocyst transfer: a case-control study 111
Bilateral Perisylvian Polymicrogyria, Intellectual Disability and Nephronophthisis Associated With Compound Heterozygous Pathogenic Variants in the CEP83 Gene 110
Cardiac Phenotype In ATP1A3 Related-Syndromes: A Multicentre Study 110
DNAJC12 deficiency: Mild hyperphenylalaninemia and neurological impairment in two siblings 110
Cortical myoclonus and epilepsy in a family with a new SLC20A2 mutation 109
BURDEN OF UNCONTROLLED EPILEPSY IN PATIENTS REQUIRING AN EMERGENCY ROOM VISIT OR HOSPITALIZATION 108
Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals 107
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)) 106
ANALYSIS OF FACIAL ASYMMETRY AND DYSMORPHISM IN EPILEPSY 105
Cerebellar, limbic, and midbrain volume alterations in sudden unexpected death in epilepsy 105
The role of electroencephalography in epilepsy research-From seizures to interictal activity and comorbidities 104
The impact of Transcranial Magnetic Stimulation (TMS) on seizure course in people with and without epilepsy 101
The ENIGMA-Epilepsy working group: Mapping disease from large data sets 101
Expanding the genetic and phenotypic spectrum of CHD2-related disease: From early neurodevelopmental disorders to adult-onset epilepsy 100
Knocking at the brain's door: a direct measure of brain excitability in alternating hemiplegia of childhood 100
The challenges of treating epilepsy with 25 antiepileptic drugs 99
Pharmacogenomics in epilepsy 99
Use Of A Medium Chain Triglyceride-Based Food For Special Medical Purposes In Children And Adults With Epilepsy: Compliance, Tolerability And Acceptability 99
Perampanel Confirms to Be Effective and Well-Tolerated as an Add-On Treatment in Patients With Brain Tumor-Related Epilepsy (PERADET Study) 99
The impact of Transcranial Magnetic Stimulation (TMS) on EEG and seizure course in people with or without epilepsy 97
Comparative effectiveness of antiepileptic drugs in juvenile myoclonic epilepsy 97
Clinical spectrum of STX1B-related epileptic disorders 97
Increased Common Carotid Artery Wall Thickness Is Associated with Rapid Progression of Asymptomatic Carotid Stenosis 95
Sex-associated differences in the modulation of vascular risk in patients with asymptomatic carotid stenosis 94
Steps to Improve Precision Medicine in Epilepsy. 93
Genome-wide association meta-analyses of drug-resistant epilepsy 93
CLINICAL FEATURES OF POST-ICTAL PSYCHOSIS: AN OBSERVATIONAL DESCRIPTIVE STUDY 93
TBC1D24 genotype-phenotype correlation: Epilepsies and other neurologic features 92
Two-center experience of cannabidiol use in adults with Dravet syndrome 92
Sex-based electroclinical differences and prognostic factors in epilepsy with eyelid myoclonia 91
Genome-wide association study: Exploring the genetic basis for responsiveness to ketogenic dietary therapies for drug-resistant epilepsy 89
One-Year Progression of Moderate Asymptomatic Carotid Stenosis Predicts the Risk of Vascular Events 89
Electroclinical Features and Long-term Seizure Outcome in Patients With Eyelid Myoclonia With Absences 88
Risk-conferring HLA variants in an epilepsy cohort: benefits of multifaceted use of whole genome sequencing in clinical practice 88
Severe carotid stenosis and impaired cerebral hemodynamics can influence cognitive deterioration 88
Methodology for classification and definition of epilepsy syndromes with list of syndromes: Report of the ILAE Task Force on Nosology and Definitions 87
Methodology of a Natural History Study of a Rare Neurodevelopmental Disorder: Alternating Hemiplegia of Childhood as a Prototype Disease 87
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes 87
Genetics of the Epilepsies 87
Genome-wide Polygenic Burden of Rare Deleterious Variants in Sudden Unexpected Death in Epilepsy 87
Treatment of Epileptic Encephalopathies 87
Late diagnoses of Dravet syndrome: How many individuals are we missing? 87
The expanding field of genetic developmental and epileptic encephalopathies: current understanding and future perspectives 86
MULTIMODAL RESPONSES INDUCED BY CORTICAL STIMULATION OF THE PARIETAL LOBE: A STEREO-ELECTROENCEPHALOGRAPHY STUDY 86
Systolic and diastolic heart failure and renal dysfunction in hospitalized elderly patients 86
Neurologic phenotypes associated with COL4A1/2 mutations Expanding the spectrum of disease 85
Systolic and diastolic heart failure and renal dysfunction in hospitalized elderly patients 85
Widespread genomic influences on phenotype in Dravet syndrome, a 'monogenic' condition 84
Cenobamate as add-on treatment for SCN8A developmental and epileptic encephalopathy 84
From Cannabis to Cannabidiol to Treat Epilepsy, Where Are We? 84
Transcranial magnetic stimulation as a tool to understand genetic conditions associated with epilepsy 84
Sex-associated differences in the modulation of vascular risk in patients with asymptomatica carotid stenosis 84
Rare and Complex Epilepsies from Childhood to Adulthood: Requirements for Separate Management or Scope for a Lifespan Holistic Approach? 83
K.Vita: a feasibility study of a blend of medium chain triglycerides to manage drug-resistant epilepsy 83
Erratum: Ammonia: What adult neurologists need to know (Pract Neurol (2021) 21 (36-42) DOI: 10.1136/practneurol-2020-002654) 83
Drug-resistant epilepsy, early-onset hypertension and white matter lesions: A hidden paraganglioma 83
Monogenic Epilepsies: Disease Mechanisms, Clinical Phenotypes, and Targeted Therapies 83
Markers for the Risk of Progression from Mild Cognitive Impairment to Alzheimer's Disease 82
RETINAL NERVE FIBRE LAYER ASYMMETRY ASSOCIATED WITH DIAGNOSIS OF FOCAL EPILEPSY IN A DRUG-RESISTANT POPULATION 81
The impact of COVID-19 in Dravet syndrome: A UK survey 81
Retinal nerve fibre layer thinning is associated with drug resistance in epilepsy 80
De novo mutations of KIAA2022 in females cause intellectual disability and intractable epilepsy 80
An interconnected data infrastructure to support large-scale rare disease research 79
Fibroblast transcriptomics uncovers pathogenic genomic variants in individuals with exome-negative childhood onset epilepsy 79
Personalized treatment in the epilepsies: challenges and opportunities 79
Percutaneous transluminal angioplasty for chronic cerebrospinal venous insufficiency in multiple sclerosis: dichotomy between subjective and objective outcome scores 79
Totale 10.672
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Categoria #
all - tutte 45.350
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 45.350
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202125 0 0 0 0 0 0 2 9 4 6 2 2
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
2025/20265.844 821 1.210 1.235 1.669 539 280 90 0 0 0 0 0
Totale 14.115