IRIS UniCatt

Battaglia, Domenica Immacolata
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 5.992
AS - Asia 4.393
EU - Europa 4.093
SA - Sud America 883
AF - Africa 122
OC - Oceania 17
Continente sconosciuto - Info sul continente non disponibili 5
Totale 15.505
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 5.794
SG - Singapore 2.104
DE - Germania 1.208
CN - Cina 963
BR - Brasile 713
IT - Italia 525
SE - Svezia 506
FR - Francia 441
VN - Vietnam 374
UA - Ucraina 296
GB - Regno Unito 227
IE - Irlanda 199
PL - Polonia 182
FI - Finlandia 145
ID - Indonesia 136
IN - India 131
JP - Giappone 128
RU - Federazione Russa 109
CA - Canada 104
BD - Bangladesh 103
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 30
AT - Austria 29
NL - Olanda 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 18
KE - Kenya 18
LT - Lituania 18
VE - Venezuela 17
MA - Marocco 15
AU - Australia 13
EG - Egitto 13
CH - Svizzera 12
CI - Costa d'Avorio 12
IL - Israele 12
JO - Giordania 12
CO - Colombia 11
JM - Giamaica 11
TN - Tunisia 11
KZ - Kazakistan 10
TW - Taiwan 10
PE - Perù 9
PH - Filippine 9
UY - Uruguay 9
MY - Malesia 8
PT - Portogallo 8
AE - Emirati Arabi Uniti 7
AZ - Azerbaigian 7
HN - Honduras 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
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
CY - Cipro 3
KG - Kirghizistan 3
LK - Sri Lanka 3
NO - Norvegia 3
NZ - Nuova Zelanda 3
AO - Angola 2
BH - Bahrain 2
BN - Brunei Darussalam 2
BY - Bielorussia 2
CR - Costa Rica 2
DO - Repubblica Dominicana 2
HR - Croazia 2
MD - Moldavia 2
MN - Mongolia 2
NG - Nigeria 2
PA - Panama 2
RS - Serbia 2
TH - Thailandia 2
TT - Trinidad e Tobago 2
BZ - Belize 1
Totale 15.475
Salva come PNG Salva come JPEG
Città #
Singapore 1.144
Chandler 660
San Jose 647
Ashburn 637
New York 235
Jacksonville 201
Beijing 195
Dublin 186
Los Angeles 172
Warsaw 168
San Mateo 155
Ho Chi Minh City 129
Jakarta 126
Tokyo 124
Lauterbourg 122
Hefei 106
Ann Arbor 98
Hong Kong 95
Milan 91
Rome 90
Dallas 89
Hanoi 89
Munich 86
Frankfurt am Main 85
Marseille 85
Houston 82
Nanjing 81
The Dalles 80
Wilmington 80
Moscow 73
Nürnberg 70
St Louis 67
Woodbridge 66
Buffalo 65
São Paulo 62
Fairfield 61
Council Bluffs 60
Dearborn 60
Lawrence 57
Boston 54
Helsinki 54
Santa Clara 52
Seattle 50
Cattolica 49
Redwood City 47
Norwalk 41
Bremen 40
Nanchang 37
Princeton 37
London 32
Brussels 31
Nuremberg 31
Toronto 29
Boardman 28
Brooklyn 28
Kent 28
Redmond 28
Chicago 27
Denver 27
Lancaster 26
Seoul 26
Mountain View 24
Phoenix 24
Stockholm 24
Detroit 23
Atlanta 22
Guangzhou 22
San Francisco 22
University Park 22
Belo Horizonte 21
Da Nang 21
Montreal 21
Orem 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
Paris 16
Prague 16
Hangzhou 15
Hebei 15
Johannesburg 15
Manchester 15
Shenyang 15
Augusta 14
Chennai 14
Düsseldorf 14
Elkhart 14
Kish 14
Poplar 14
Rio de Janeiro 14
Changsha 13
Totale 8.286
Salva come PNG Salva come JPEG
Nome #
Chromosome 9p deletion syndrome and sex reversal: novel findings and redefinition of the critically deleted regions 449
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 278
Unusual 4p16.3 deletions suggest an additional chromosome region for the Wolf-Hirschhorn syndrome-associated seizures disorder 242
Sleep-potentiated epileptiform activity in early thalamic injuries: Study in a large series (60 cases) 209
Posterior resection for childhood lesional epilepsy: neuropsychological evolution 202
Novel de novo heterozygous loss-of-function variants in MED13L and further delineation of the MED13L haploinsufficiency syndrome 200
Chromosome 9p deletion syndrome and sex reversal: novel findings and redefinition of the critically deleted regions. 195
Increased sleep spindle activity in patients with Costello syndrome (HRAS gene mutation) 183
Early onset myoclonic epilepsy and 15q26 microdeletion: Observation of the first case. 183
Sleep disturbances in preschool age children with cerebral palsy: a questionnaire study 183
Unusual 4p16.3 deletions suggest an additional chromosome region for the Wolf-Hirschhorn syndrome-associated seizures disorder 182
Surgery of children with frontal lobe lesional epilepsy: neuropsychological study 179
Electrical and autonomic cardiac function in patients with Dravet syndrome 177
Epilepsy surgery of posterior quadrant dysplasia in the first year of life: experience of a single centre with long term follow-up 176
Neuropsychological development in children with Dravet syndrome. 173
Wolf-Hirschhorn syndrome-associated chromosome changes are not mediated by olfactory receptor gene clusters nor by inversion polymorphism on 4p16 169
Proposal of a clinical score for the molecular test for Pitt-Hopkins syndrome 168
Sleep disturbances in preschool age children with cerebral palsy: a questionnaire study 168
Intragenic KANSL1 mutations and chromosome 17q21.31 deletions: broadening the clinical spectrum and genotype-phenotype correlations in a large cohort of patients 167
Electrical and autonomic cardiac function in patients with Dravet syndrome 165
Early neurodevelopmental characterization in children with cobalamin C/defect 164
Pretreatment neuropsychological deficits in children with brain tumors 162
Epilepsy and BRAF mutations: Phenotypes, natural history and genotype-phenotype correlations 158
The Pitt-Hopkins syndrome: report of 16 new patients and clinical diagnostic criteria 154
Fighting autoinflammation in FIRES: The role of interleukins and early immunomodulation 153
Early onset myoclonic epilepsy and 15q26 microdeletion: observation of the first case 151
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
Pretreatment neuropsychological deficits in children with brain tumors 149
Disorders of early language development in Dravet syndrome 146
Clinical-genetic features and peculiar muscle histopathology in infantile DNM1L-related mitochondrial epileptic encephalopathy 146
Heart rate variability alterations in Dravet Syndrome: The role of status epilepticus and a possible association with mortality risk 145
Cortical Visual Impairment in CDKL5 Deficiency Disorder 145
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 140
HYPOVENTILATION IN REM SLEEP IN A CASE OF 17p11.2 DELETION (SMITH-MAGENIS SYNDROME) 138
A registry for Dravet syndrome: The Italian experience 135
Cognitive development in Dravet syndrome: a retrospective, multicenter study of 26 patients 134
Neuropsychological development in children with Dravet syndrome 134
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 133
-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 132
Chiari 1 Malformation and Epilepsy in Children: A Missing Relationship 131
Interactions between antiepileptic and chemoterapeutic drugs in children with brain tumors: is it time to change treatment? 130
Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotype 129
Visual and visuoperceptual function in children with Panayiotopoulos syndrome 129
CHARGE-like presentation, craniosynostosis and mild Mowat-Wilson Syndrome diagnosed by recognition of the distinctive facial gestalt in a cohort of 28 new cases 129
Disorders of early language development in Dravet syndrome 129
"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 128
Cognitive-behavioral profiles in teenagers with Dravet syndrome 128
Postoperative Epileptic Seizures in Children: Is the Brain Incision a Risk Factor? 128
Hereditary Hyperekplexia: A New Family and a Systematic Review of GLRA1 Gene-Related Phenotypes 127
Defining the electroclinical phenotype and outcome of PCDH19-related epilepsy: A multicenter study 126
Acneiform eruption induced by ethosuximide 125
Efficacy and safety of Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: A real-world study 124
Temporal lobe epilepsy surgery in children and adults: A multicenter study 124
Protocadherin 19 mutations in girls with infantile-onset epilepsy 122
Calcified cephalohematoma as an unusual cause of EEG anomalies: Case report 121
Does Anticonvulsant Treatment Influence Pain Perception in Epileptic Children? 120
A novel homozygous variant in JAM3 gene causing hemorrhagic destruction of the brain, subependymal calcification, and congenital cataracts (HDBSCC) with neonatal onset 118
Sleep-potentiated epileptiform activity in early thalamic injuries: Study in a large series (60 cases) 117
Postoperative Epileptic Seizures in Children 116
Cortical malformations and COL4A1 mutation: Three new cases 116
The impact of valproic acid treatment on weight gain in pediatric patients with epilepsy 116
Survey of rehabilitation approaches and plans for individuals with dravet syndrome (RAPIDS) in Italy: Current practices and strategies to progress 115
Congenital immunodeficiency in an individual with Wiedemann–Steiner syndrome due to a novel missense mutation in KMT2A 114
Pyridoxine supplementation in PACS2-related encephalopathy: A case report of possible precision therapy 113
Phenomenology and clinical course of movement disorder in GNAO1 variants: Results from an analytical review 113
Multicenter prospective longitudinal study in 34 patients with Dravet syndrome: Neuropsychological development in the first six years of life 112
Phosphatase and tensin homolog (PTEN) variants and epilepsy: A multicenter case series 110
Cognitive-behavioral profiles in teenagers with Dravet syndrome 110
Clinical features and genetic analysis of two siblings with startle disease in an Italian family: a case report. 109
Symptomatic and presumed symptomatic focal epilepsies in childhood: An observational, prospective multicentre study 108
Outlining a core neuropsychological phenotype for Dravet syndrome 108
Dravet syndrome: Early electroclinical findings and long-term outcome in adolescents and adults 106
Trends in pediatric epilepsy surgery in Europe between 2008 and 2015: Country-, center-, and age-specific variation 106
Sturge-Weber syndrome: an update on the relevant issues for neurosurgeons 105
Multimodal assessment of motor pathways and intracortical connections in functional hemispherectomy 105
Sleep disorders in children with cerebral palsy: neurodevelopmental and behavioral correlates 102
Glyburide ameliorates motor coordination and glucose homeostasis in a child with diabetes associated with the KCNJ11/S225T, del226-232 mutation 100
Short- vs long-term assessment of heart rate variability: Clinical significance in Dravet Syndrome 98
PRRT2 mutations in familial infantile seizures, paroxysmal dyskinesia, and hemiplegic migraine 96
Clinical and genetic factors predicting Dravet syndrome in infants with SCN1A mutations 95
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 93
Outlining a core neuropsychological phenotype for Dravet syndrome 92
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
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
Epileptic children with hemispheres’ asymmetry. Quantitative brain magnetic resonance-based analysis of apparently unaffected hemisphere. Case-control study 89
Does anticonvulsant treatment influence pain perception in epileptic children? 88
GABRA1-Related Disorders: From Genetic to Functional Pathways 87
Disorders of early language development in Dravet syndrome 87
Early development in Dravet syndrome; visual function impairment precedes cognitive decline 87
Fatal status epilepticus in dravet syndrome 87
Inv dup 15 syndrome: Case report with epilepsy onset in the first year 86
Cognitive decline in Dravet syndrome: is there a cerebellar role? 86
Pretreatment neuropsychological deficits in children with brain tumors 85
A prospective longitudinal study on visuo-cognitive development in Dravet syndrome: Is there a "dorsal stream vulnerability"? 84
Totale 13.650
Salva come PNG Salva come JPEG
Categoria #
all - tutte 66.829
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 66.829
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
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
2025/20266.276 935 174 386 704 1.022 303 1.063 247 452 447 222 321
2026/202770 70 0 0 0 0 0 0 0 0 0 0 0
Totale 15.736