IRIS UniCatt

Battaglia, Domenica Immacolata
 Distribuzione geografica
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Continente #
NA - Nord America 4.447
EU - Europa 3.725
AS - Asia 3.426
SA - Sud America 791
AF - Africa 94
OC - Oceania 17
Continente sconosciuto - Info sul continente non disponibili 4
Totale 12.504
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Nazione #
US - Stati Uniti d'America 4.307
SG - Singapore 1.742
DE - Germania 1.183
CN - Cina 865
BR - Brasile 662
SE - Svezia 503
IT - Italia 408
FR - Francia 310
UA - Ucraina 294
GB - Regno Unito 204
IE - Irlanda 197
PL - Polonia 179
VN - Vietnam 155
ID - Indonesia 131
FI - Finlandia 130
IN - India 112
RU - Federazione Russa 104
CA - Canada 70
HK - Hong Kong 57
TR - Turchia 53
AR - Argentina 47
BD - Bangladesh 47
MX - Messico 45
IQ - Iraq 37
JP - Giappone 37
BE - Belgio 34
AT - Austria 27
KR - Corea 27
EC - Ecuador 26
IR - Iran 24
NL - Olanda 23
ZA - Sudafrica 22
RO - Romania 21
CZ - Repubblica Ceca 20
ES - Italia 20
PK - Pakistan 19
SA - Arabia Saudita 18
KE - Kenya 16
LT - Lituania 16
VE - Venezuela 15
AU - Australia 13
MA - Marocco 13
UZ - Uzbekistan 13
CL - Cile 11
JO - Giordania 11
CI - Costa d'Avorio 10
CO - Colombia 10
EG - Egitto 10
KZ - Kazakistan 10
CH - Svizzera 9
IL - Israele 9
TW - Taiwan 9
AE - Emirati Arabi Uniti 6
JM - Giamaica 6
TN - Tunisia 6
UY - Uruguay 6
AZ - Azerbaigian 5
HN - Honduras 5
MY - Malesia 5
PE - Perù 5
PY - Paraguay 5
DZ - Algeria 4
GR - Grecia 4
HU - Ungheria 4
LV - Lettonia 4
OM - Oman 4
PH - Filippine 4
PT - Portogallo 4
A2 - ???statistics.table.value.countryCode.A2??? 3
AL - Albania 3
BA - Bosnia-Erzegovina 3
BG - Bulgaria 3
BO - Bolivia 3
CY - Cipro 3
ET - Etiopia 3
KG - Kirghizistan 3
LB - Libano 3
LK - Sri Lanka 3
NO - Norvegia 3
NZ - Nuova Zelanda 3
SN - Senegal 3
AM - Armenia 2
BB - Barbados 2
BN - Brunei Darussalam 2
BY - Bielorussia 2
DK - Danimarca 2
DO - Repubblica Dominicana 2
HR - Croazia 2
NP - Nepal 2
PA - Panama 2
RS - Serbia 2
TH - Thailandia 2
TT - Trinidad e Tobago 2
AO - Angola 1
BH - Bahrain 1
BZ - Belize 1
CW - ???statistics.table.value.countryCode.CW??? 1
EE - Estonia 1
GA - Gabon 1
GD - Grenada 1
Totale 12.482
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Città #
Singapore 800
Chandler 660
Ashburn 487
Jacksonville 201
Dublin 186
New York 183
Beijing 178
Warsaw 168
San Mateo 155
Los Angeles 138
Jakarta 124
Hefei 106
Ann Arbor 98
Munich 86
Marseille 84
Milan 82
Nanjing 81
Houston 80
Wilmington 78
Rome 73
Dallas 71
Moscow 71
Nürnberg 70
Woodbridge 66
Frankfurt am Main 63
Fairfield 61
Dearborn 60
Ho Chi Minh City 60
Lawrence 57
São Paulo 57
Hong Kong 56
The Dalles 54
Boston 52
Cattolica 49
Redwood City 47
Seattle 45
Hanoi 41
Norwalk 41
Bremen 40
Helsinki 40
Buffalo 39
Nanchang 37
Princeton 37
Tokyo 33
Nuremberg 31
Brussels 30
London 30
Redmond 28
Santa Clara 28
Kent 27
Lancaster 26
Seoul 26
Denver 25
Mountain View 24
Detroit 22
San Francisco 22
University Park 22
Brooklyn 21
Council Bluffs 21
Phoenix 21
Stockholm 21
Turku 21
Belo Horizonte 20
Zhengzhou 20
Izmir 18
Tianjin 18
Toronto 18
Boardman 17
Brasília 17
Kunming 17
Vienna 17
Guangzhou 16
Atlanta 15
Cambridge 15
Chicago 15
Hebei 15
Mexico City 15
Nairobi 15
Shenyang 15
Augusta 14
Düsseldorf 14
Elkhart 14
Kish 14
Baghdad 13
Falkenstein 13
Jiaxing 13
Johannesburg 13
Montreal 13
Poplar 13
Portsmouth 13
Prague 13
Changsha 12
Hangzhou 12
Orem 12
Roubaix 12
Amman 11
Dhaka 11
Fremont 11
Manchester 11
Quito 11
Totale 6.287
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Nome #
Chromosome 9p deletion syndrome and sex reversal: novel findings and redefinition of the critically deleted regions 404
Functional hemispherectomy in children with epilepsy and CSWS due to unilateral early brain injury including thalamus: sudden recovery of CSWS 254
Unusual 4p16.3 deletions suggest an additional chromosome region for the Wolf-Hirschhorn syndrome-associated seizures disorder 208
Sleep-potentiated epileptiform activity in early thalamic injuries: Study in a large series (60 cases) 192
Posterior resection for childhood lesional epilepsy: neuropsychological evolution 187
Novel de novo heterozygous loss-of-function variants in MED13L and further delineation of the MED13L haploinsufficiency syndrome 173
Chromosome 9p deletion syndrome and sex reversal: novel findings and redefinition of the critically deleted regions. 171
Early onset myoclonic epilepsy and 15q26 microdeletion: Observation of the first case. 168
Unusual 4p16.3 deletions suggest an additional chromosome region for the Wolf-Hirschhorn syndrome-associated seizures disorder 168
Epilepsy surgery of posterior quadrant dysplasia in the first year of life: experience of a single centre with long term follow-up 163
Electrical and autonomic cardiac function in patients with Dravet syndrome 159
Surgery of children with frontal lobe lesional epilepsy: neuropsychological study 157
Sleep disturbances in preschool age children with cerebral palsy: a questionnaire study 157
Increased sleep spindle activity in patients with Costello syndrome (HRAS gene mutation) 156
Electrical and autonomic cardiac function in patients with Dravet syndrome 147
Pretreatment neuropsychological deficits in children with brain tumors 145
Proposal of a clinical score for the molecular test for Pitt-Hopkins syndrome 145
Wolf-Hirschhorn syndrome-associated chromosome changes are not mediated by olfactory receptor gene clusters nor by inversion polymorphism on 4p16 145
Neuropsychological development in children with Dravet syndrome. 144
Sleep disturbances in preschool age children with cerebral palsy: a questionnaire study 142
Intragenic KANSL1 mutations and chromosome 17q21.31 deletions: broadening the clinical spectrum and genotype-phenotype correlations in a large cohort of patients 142
The Pitt-Hopkins syndrome: report of 16 new patients and clinical diagnostic criteria 135
Early onset myoclonic epilepsy and 15q26 microdeletion: observation of the first case 135
Epilepsy and BRAF mutations: Phenotypes, natural history and genotype-phenotype correlations 133
Pretreatment neuropsychological deficits in children with brain tumors 128
HYPOVENTILATION IN REM SLEEP IN A CASE OF 17p11.2 DELETION (SMITH-MAGENIS SYNDROME) 124
Neuropsychological development in children with Dravet syndrome 123
Disorders of early language development in Dravet syndrome 121
Fighting autoinflammation in FIRES: The role of interleukins and early immunomodulation 119
-Electroclinical patterns and evolution of epilepsy in the 4p- syndrome 118
Clinical-genetic features and peculiar muscle histopathology in infantile DNM1L-related mitochondrial epileptic encephalopathy 118
CHARGE-like presentation, craniosynostosis and mild Mowat-Wilson Syndrome diagnosed by recognition of the distinctive facial gestalt in a cohort of 28 new cases 116
Cognitive-behavioral profiles in teenagers with Dravet syndrome 115
Heart rate variability alterations in Dravet Syndrome: The role of status epilepticus and a possible association with mortality risk 114
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) 113
Role of high-density EEG (hdEEG) in pre-surgical epilepsy evaluation in children: case report and review of the literature 113
Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotype 112
"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 112
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 112
Interactions between antiepileptic and chemoterapeutic drugs in children with brain tumors: is it time to change treatment? 111
Visual and visuoperceptual function in children with Panayiotopoulos syndrome 111
Acneiform eruption induced by ethosuximide 110
Postoperative Epileptic Seizures in Children: Is the Brain Incision a Risk Factor? 110
Cognitive development in Dravet syndrome: a retrospective, multicenter study of 26 patients 109
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 108
Visual Function in Children with GNAO1-Related Encephalopathy 108
Disorders of early language development in Dravet syndrome 107
Does Anticonvulsant Treatment Influence Pain Perception in Epileptic Children? 106
Early neurodevelopmental characterization in children with cobalamin C/defect 104
Cortical Visual Impairment in CDKL5 Deficiency Disorder 102
Defining the electroclinical phenotype and outcome of PCDH19-related epilepsy: A multicenter study 101
Efficacy and safety of Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: A real-world study 101
Temporal lobe epilepsy surgery in children and adults: A multicenter study 100
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 98
Protocadherin 19 mutations in girls with infantile-onset epilepsy 97
Sleep-potentiated epileptiform activity in early thalamic injuries: Study in a large series (60 cases) 97
Hereditary Hyperekplexia: A New Family and a Systematic Review of GLRA1 Gene-Related Phenotypes 96
A registry for Dravet syndrome: The Italian experience 95
Cortical malformations and COL4A1 mutation: Three new cases 95
The impact of valproic acid treatment on weight gain in pediatric patients with epilepsy 94
Calcified cephalohematoma as an unusual cause of EEG anomalies: Case report 92
Cognitive-behavioral profiles in teenagers with Dravet syndrome 92
Phenomenology and clinical course of movement disorder in GNAO1 variants: Results from an analytical review 90
Chiari 1 Malformation and Epilepsy in Children: A Missing Relationship 89
Congenital immunodeficiency in an individual with Wiedemann–Steiner syndrome due to a novel missense mutation in KMT2A 89
Postoperative Epileptic Seizures in Children 87
Pyridoxine supplementation in PACS2-related encephalopathy: A case report of possible precision therapy 87
Clinical features and genetic analysis of two siblings with startle disease in an Italian family: a case report. 87
Outlining a core neuropsychological phenotype for Dravet syndrome 87
Multimodal assessment of motor pathways and intracortical connections in functional hemispherectomy 87
Sleep disorders in children with cerebral palsy: neurodevelopmental and behavioral correlates 86
Symptomatic and presumed symptomatic focal epilepsies in childhood: An observational, prospective multicentre study 84
A novel homozygous variant in JAM3 gene causing hemorrhagic destruction of the brain, subependymal calcification, and congenital cataracts (HDBSCC) with neonatal onset 84
PRRT2 mutations in familial infantile seizures, paroxysmal dyskinesia, and hemiplegic migraine 83
Dravet syndrome: Early electroclinical findings and long-term outcome in adolescents and adults 82
Multicenter prospective longitudinal study in 34 patients with Dravet syndrome: Neuropsychological development in the first six years of life 82
Glyburide ameliorates motor coordination and glucose homeostasis in a child with diabetes associated with the KCNJ11/S225T, del226-232 mutation 80
Trends in pediatric epilepsy surgery in Europe between 2008 and 2015: Country-, center-, and age-specific variation 80
Pretreatment neuropsychological deficits in children with brain tumors 79
Phosphatase and tensin homolog (PTEN) variants and epilepsy: A multicenter case series 77
Clinical and genetic factors predicting Dravet syndrome in infants with SCN1A mutations 77
Sturge-Weber syndrome: an update on the relevant issues for neurosurgeons 76
Cognitive decline in Dravet syndrome: is there a cerebellar role? 74
Does anticonvulsant treatment influence pain perception in epileptic children? 74
Epileptic children with hemispheres’ asymmetry. Quantitative brain magnetic resonance-based analysis of apparently unaffected hemisphere. Case-control study 74
Rufinamide for the treatment of refractory epilepsy secondary to neuronal migration disorders 73
Outlining a core neuropsychological phenotype for Dravet syndrome 73
Molecular Genetics and Interferon Signature in the Italian Aicardi Goutières Syndrome Cohort: Report of 12 New Cases and Literature Review 73
Non-Stationary Outcome of Alternating Hemiplegia of Childhood into Adulthood 73
Short- vs long-term assessment of heart rate variability: Clinical significance in Dravet Syndrome 72
Survey of rehabilitation approaches and plans for individuals with dravet syndrome (RAPIDS) in Italy: Current practices and strategies to progress 72
Early development in Dravet syndrome; visual function impairment precedes cognitive decline 72
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) 72
Chiari 1 Malformation and Epilepsy in Children: A Missing Relationship 70
Disorders of early language development in Dravet syndrome 70
Increasing volume and complexity of pediatric epilepsy surgery with stable seizure outcome between 2008 and 2014: A nationwide multicenter study 70
Focal seizures with affective symptoms are a major feature of PCDH19 gene-related epilepsy 69
Salivary alpha-amylase: a new non-invasive biomarker for assessment of pain perception in epileptic children 68
Inv dup 15 syndrome: Case report with epilepsy onset in the first year 65
Cognitive decline in Dravet syndrome: is there a cerebellar role? 65
Totale 11.184
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Categoria #
all - tutte 56.850
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 56.850
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021370 0 0 0 0 0 83 56 11 77 21 109 13
2021/2022816 120 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
2025/20263.298 935 174 386 704 1.022 77 0 0 0 0 0 0
Totale 12.688