Battaglia, Domenica Immacolata
 Distribuzione geografica
Continente #
NA - Nord America 6.888
AS - Asia 4.420
EU - Europa 4.131
SA - Sud America 886
Continente sconosciuto - Info sul continente non disponibili 236
AF - Africa 122
OC - Oceania 17
Totale 16.700
Nazione #
US - Stati Uniti d'America 6.674
SG - Singapore 2.112
DE - Germania 1.208
CN - Cina 969
BR - Brasile 715
IT - Italia 554
SE - Svezia 506
FR - Francia 442
VN - Vietnam 374
UA - Ucraina 296
GB - Regno Unito 228
IE - Irlanda 199
PL - Polonia 185
FI - Finlandia 145
ID - Indonesia 136
IN - India 133
JP - Giappone 130
BD - Bangladesh 112
CA - Canada 110
RU - Federazione Russa 109
HK - Hong Kong 100
AR - Argentina 60
MX - Messico 57
TR - Turchia 57
IQ - Iraq 54
BE - Belgio 36
EC - Ecuador 33
PK - Pakistan 33
ES - Italia 31
NL - Olanda 30
AT - Austria 29
KR - Corea 28
ZA - Sudafrica 28
IR - Iran 25
CZ - Repubblica Ceca 23
SA - Arabia Saudita 23
RO - Romania 21
UZ - Uzbekistan 20
CL - Cile 19
KE - Kenya 18
LT - Lituania 18
VE - Venezuela 17
MA - Marocco 15
AU - Australia 13
EG - Egitto 13
JM - Giamaica 13
CH - Svizzera 12
CI - Costa d'Avorio 12
IL - Israele 12
JO - Giordania 12
CO - Colombia 11
TN - Tunisia 11
KZ - Kazakistan 10
TW - Taiwan 10
HN - Honduras 9
PE - Perù 9
PH - Filippine 9
UY - Uruguay 9
MY - Malesia 8
PT - Portogallo 8
AE - Emirati Arabi Uniti 7
AZ - Azerbaigian 7
PY - Paraguay 7
DZ - Algeria 6
GR - Grecia 6
OM - Oman 6
BO - Bolivia 5
DK - Danimarca 5
HU - Ungheria 5
BA - Bosnia-Erzegovina 4
BG - Bulgaria 4
ET - Etiopia 4
GT - Guatemala 4
LB - Libano 4
LV - Lettonia 4
NP - Nepal 4
SN - Senegal 4
A2 - ???statistics.table.value.countryCode.A2??? 3
AL - Albania 3
AM - Armenia 3
BB - Barbados 3
CR - Costa Rica 3
CY - Cipro 3
KG - Kirghizistan 3
LK - Sri Lanka 3
MK - Macedonia 3
NO - Norvegia 3
NZ - Nuova Zelanda 3
TT - Trinidad e Tobago 3
AO - Angola 2
BH - Bahrain 2
BN - Brunei Darussalam 2
BY - Bielorussia 2
DO - Repubblica Dominicana 2
HR - Croazia 2
MD - Moldavia 2
MN - Mongolia 2
NG - Nigeria 2
PA - Panama 2
RS - Serbia 2
Totale 16.437
Città #
Singapore 1.150
Ashburn 708
San Jose 681
Chandler 660
New York 243
Jacksonville 202
Beijing 201
Dublin 186
Los Angeles 181
Warsaw 170
San Mateo 155
Ho Chi Minh City 129
Jakarta 126
Tokyo 125
Lauterbourg 122
Hefei 106
Dallas 102
Ann Arbor 98
Hong Kong 95
Milan 94
Rome 93
Hanoi 89
Munich 86
Frankfurt am Main 85
Marseille 85
Houston 83
Nanjing 81
The Dalles 80
Wilmington 80
Moscow 73
Nürnberg 70
Buffalo 68
St Louis 67
Woodbridge 66
Council Bluffs 62
Santa Clara 62
São Paulo 62
Fairfield 61
Dearborn 60
Lawrence 57
Boston 54
Helsinki 54
Seattle 50
Cattolica 49
Redwood City 47
Norwalk 41
Bremen 40
Nanchang 37
Princeton 37
Atlanta 35
London 32
Brussels 31
Nuremberg 31
Brooklyn 30
Chicago 30
Toronto 30
Boardman 28
Kent 28
Redmond 28
Denver 27
Lancaster 26
Seoul 26
Orem 25
Phoenix 25
Mountain View 24
Stockholm 24
Detroit 23
San Francisco 23
Guangzhou 22
Montreal 22
University Park 22
Belo Horizonte 21
Da Nang 21
Turku 21
Mexico City 20
Zhengzhou 20
Vienna 19
Baghdad 18
Brasília 18
Izmir 18
Tianjin 18
Cambridge 17
Kunming 17
Nairobi 17
Tashkent 17
Manchester 16
Paris 16
Prague 16
Chennai 15
Hangzhou 15
Hebei 15
Johannesburg 15
Shenyang 15
Augusta 14
Charlotte 14
Düsseldorf 14
Elkhart 14
Kish 14
Poplar 14
Rio de Janeiro 14
Totale 8.488
Nome #
Chromosome 9p deletion syndrome and sex reversal: novel findings and redefinition of the critically deleted regions 456
Visual Function in Children with GNAO1-Related Encephalopathy 288
Functional hemispherectomy in children with epilepsy and CSWS due to unilateral early brain injury including thalamus: sudden recovery of CSWS 279
Does Anticonvulsant Treatment Influence Pain Perception in Epileptic Children? 279
Unusual 4p16.3 deletions suggest an additional chromosome region for the Wolf-Hirschhorn syndrome-associated seizures disorder 243
Sleep-potentiated epileptiform activity in early thalamic injuries: Study in a large series (60 cases) 210
Posterior resection for childhood lesional epilepsy: neuropsychological evolution 203
Novel de novo heterozygous loss-of-function variants in MED13L and further delineation of the MED13L haploinsufficiency syndrome 201
Chromosome 9p deletion syndrome and sex reversal: novel findings and redefinition of the critically deleted regions. 195
Sleep disturbances in preschool age children with cerebral palsy: a questionnaire study 186
Early onset myoclonic epilepsy and 15q26 microdeletion: Observation of the first case. 185
Increased sleep spindle activity in patients with Costello syndrome (HRAS gene mutation) 184
Unusual 4p16.3 deletions suggest an additional chromosome region for the Wolf-Hirschhorn syndrome-associated seizures disorder 183
Surgery of children with frontal lobe lesional epilepsy: neuropsychological study 180
Electrical and autonomic cardiac function in patients with Dravet syndrome 178
Epilepsy surgery of posterior quadrant dysplasia in the first year of life: experience of a single centre with long term follow-up 176
Neurosurgery for pediatric epilepsy: Evidence from a systematic review on neuropsychological, cognitive, and behavioral outcomes 173
Neuropsychological development in children with Dravet syndrome. 173
Beyond seizure control: Functional and caregiver-reported outcomes of long-term fenfluramine treatment in Dravet syndrome 172
Early neurovisual development in Dravet syndrome 171
Wolf-Hirschhorn syndrome-associated chromosome changes are not mediated by olfactory receptor gene clusters nor by inversion polymorphism on 4p16 170
Sleep disturbances in preschool age children with cerebral palsy: a questionnaire study 170
Proposal of a clinical score for the molecular test for Pitt-Hopkins syndrome 169
Intragenic KANSL1 mutations and chromosome 17q21.31 deletions: broadening the clinical spectrum and genotype-phenotype correlations in a large cohort of patients 169
Early neurodevelopmental characterization in children with cobalamin C/defect 169
Electrical and autonomic cardiac function in patients with Dravet syndrome 166
Pretreatment neuropsychological deficits in children with brain tumors 163
Epilepsy and BRAF mutations: Phenotypes, natural history and genotype-phenotype correlations 161
Fighting autoinflammation in FIRES: The role of interleukins and early immunomodulation 156
The Pitt-Hopkins syndrome: report of 16 new patients and clinical diagnostic criteria 155
Newborn with Ohtahara Syndrome and absence of respiratory trigger: ethical issues in the NICU|Neonata con Sindrome di Ohtahara e assenza di trigger respiratorio: questioni etiche in Terapia Intensiva Neonatale 152
Early onset myoclonic epilepsy and 15q26 microdeletion: observation of the first case 152
Pretreatment neuropsychological deficits in children with brain tumors 150
Efficacy of ketamine in refractory convulsive status epilepticus in children: A protocol for a sequential design, multicentre, randomised, controlled, open-label, non-profit trial (KETASER01) 150
Cortical Visual Impairment in CDKL5 Deficiency Disorder 150
Disorders of early language development in Dravet syndrome 149
Heart rate variability alterations in Dravet Syndrome: The role of status epilepticus and a possible association with mortality risk 148
Clinical-genetic features and peculiar muscle histopathology in infantile DNM1L-related mitochondrial epileptic encephalopathy 147
Linear Diagnostic Procedure Elicited by Clinical Genetics and Validated by mRNA Analysis in Neuronal Ceroid Lipofuscinosis 7 Associated with a Novel Non-Canonical Splice Site Variant in MFSD8 143
Brain structural changes in patients with cardio-facio-cutaneous syndrome: effects of BRAF gene mutation and epilepsy on brain development. A case–control study by quantitative magnetic resonance imaging 142
HYPOVENTILATION IN REM SLEEP IN A CASE OF 17p11.2 DELETION (SMITH-MAGENIS SYNDROME) 138
Calcified cephalohematoma as an unusual cause of EEG anomalies: Case report 137
A registry for Dravet syndrome: The Italian experience 136
Cognitive development in Dravet syndrome: a retrospective, multicenter study of 26 patients 136
"CHARGE-like presentation, craniosynostosis and mild Mowat-Wilson Syndrome diagnosed by recognition of the distinctive facial gestalt in a cohort of 28 new cases" American Journal of Medical Genetics Part A. 164:2557-2566, 2014 136
Chiari 1 Malformation and Epilepsy in Children: A Missing Relationship 135
Neuropsychological development in children with Dravet syndrome 134
-Electroclinical patterns and evolution of epilepsy in the 4p- syndrome 133
Role of high-density EEG (hdEEG) in pre-surgical epilepsy evaluation in children: case report and review of the literature 133
Survey of rehabilitation approaches and plans for individuals with dravet syndrome (RAPIDS) in Italy: Current practices and strategies to progress 132
Interactions between antiepileptic and chemoterapeutic drugs in children with brain tumors: is it time to change treatment? 132
Phenomenology and clinical course of movement disorder in GNAO1 variants: Results from an analytical review 131
Disorders of early language development in Dravet syndrome 131
Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotype 130
CHARGE-like presentation, craniosynostosis and mild Mowat-Wilson Syndrome diagnosed by recognition of the distinctive facial gestalt in a cohort of 28 new cases 130
Visual and visuoperceptual function in children with Panayiotopoulos syndrome 129
Defining the electroclinical phenotype and outcome of PCDH19-related epilepsy: A multicenter study 129
Hereditary Hyperekplexia: A New Family and a Systematic Review of GLRA1 Gene-Related Phenotypes 129
Cognitive-behavioral profiles in teenagers with Dravet syndrome 128
Postoperative Epileptic Seizures in Children: Is the Brain Incision a Risk Factor? 128
Acneiform eruption induced by ethosuximide 127
Protocadherin 19 mutations in girls with infantile-onset epilepsy 126
Temporal lobe epilepsy surgery in children and adults: A multicenter study 126
Symptomatic and presumed symptomatic focal epilepsies in childhood: An observational, prospective multicentre study 125
Efficacy and safety of Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: A real-world study 125
Postoperative Epileptic Seizures in Children 121
Sleep-potentiated epileptiform activity in early thalamic injuries: Study in a large series (60 cases) 121
The impact of valproic acid treatment on weight gain in pediatric patients with epilepsy 120
A novel homozygous variant in JAM3 gene causing hemorrhagic destruction of the brain, subependymal calcification, and congenital cataracts (HDBSCC) with neonatal onset 119
Multicenter prospective longitudinal study in 34 patients with Dravet syndrome: Neuropsychological development in the first six years of life 119
Cortical malformations and COL4A1 mutation: Three new cases 118
Outlining a core neuropsychological phenotype for Dravet syndrome 118
Congenital immunodeficiency in an individual with Wiedemann–Steiner syndrome due to a novel missense mutation in KMT2A 115
Pyridoxine supplementation in PACS2-related encephalopathy: A case report of possible precision therapy 113
Clinical features and genetic analysis of two siblings with startle disease in an Italian family: a case report. 113
Phosphatase and tensin homolog (PTEN) variants and epilepsy: A multicenter case series 111
Cognitive-behavioral profiles in teenagers with Dravet syndrome 110
Trends in pediatric epilepsy surgery in Europe between 2008 and 2015: Country-, center-, and age-specific variation 109
Sleep disorders in children with cerebral palsy: neurodevelopmental and behavioral correlates 108
Dravet syndrome: Early electroclinical findings and long-term outcome in adolescents and adults 108
Multimodal assessment of motor pathways and intracortical connections in functional hemispherectomy 106
Sturge-Weber syndrome: an update on the relevant issues for neurosurgeons 105
Glyburide ameliorates motor coordination and glucose homeostasis in a child with diabetes associated with the KCNJ11/S225T, del226-232 mutation 102
PRRT2 mutations in familial infantile seizures, paroxysmal dyskinesia, and hemiplegic migraine 99
Short- vs long-term assessment of heart rate variability: Clinical significance in Dravet Syndrome 98
Clinical and genetic factors predicting Dravet syndrome in infants with SCN1A mutations 96
Corrigendum to “Increasing volume and complexity of pediatric epilepsy surgery with stable seizure outcome between 2008 and 2014: A nationwide multicenter study” [Epilepsy Behav. Oct 2017; 75C:151-157](S1525505017304961)(10.1016/j.yebeh.2017.08.010) 95
Chiari 1 Malformation and Epilepsy in Children: A Missing Relationship 94
Outlining a core neuropsychological phenotype for Dravet syndrome 93
Increasing volume and complexity of pediatric epilepsy surgery with stable seizure outcome between 2008 and 2014: A nationwide multicenter study 92
Non-Stationary Outcome of Alternating Hemiplegia of Childhood into Adulthood 92
Disorders of early language development in Dravet syndrome 91
Molecular Genetics and Interferon Signature in the Italian Aicardi Goutières Syndrome Cohort: Report of 12 New Cases and Literature Review 91
KETASER01 protocol: What went right and what went wrong 90
Early development in Dravet syndrome; visual function impairment precedes cognitive decline 90
Epileptic children with hemispheres’ asymmetry. Quantitative brain magnetic resonance-based analysis of apparently unaffected hemisphere. Case-control study 90
Cognitive decline in Dravet syndrome: is there a cerebellar role? 89
Fatal status epilepticus in dravet syndrome 89
GABRA1-Related Disorders: From Genetic to Functional Pathways 88
Does anticonvulsant treatment influence pain perception in epileptic children? 88
Totale 14.323
Categoria #
all - tutte 70.316
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 70.316


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022696 0 64 16 33 38 60 18 147 52 41 92 135
2022/20231.916 224 249 135 297 78 232 110 187 218 20 87 79
2023/20241.171 35 274 35 143 61 226 61 36 19 29 111 141
2024/20252.427 36 62 162 122 228 96 99 116 383 192 482 449
2025/20266.276 935 174 386 704 1.022 303 1.063 247 452 447 222 321
2026/20271.034 257 777 0 0 0 0 0 0 0 0 0 0
Totale 16.700