IRIS UniCatt

Battaglia, Domenica Immacolata
 Distribuzione geografica
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Continente #
NA - Nord America 5.523
AS - Asia 4.331
EU - Europa 3.987
SA - Sud America 869
AF - Africa 122
OC - Oceania 17
Continente sconosciuto - Info sul continente non disponibili 5
Totale 14.854
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Nazione #
US - Stati Uniti d'America 5.352
SG - Singapore 2.100
DE - Germania 1.206
CN - Cina 955
BR - Brasile 708
SE - Svezia 505
IT - Italia 452
FR - Francia 441
VN - Vietnam 374
UA - Ucraina 295
GB - Regno Unito 222
IE - Irlanda 198
PL - Polonia 180
FI - Finlandia 144
ID - Indonesia 136
IN - India 131
JP - Giappone 128
RU - Federazione Russa 109
HK - Hong Kong 94
CA - Canada 86
BD - Bangladesh 61
TR - Turchia 57
MX - Messico 55
AR - Argentina 54
IQ - Iraq 53
BE - Belgio 35
EC - Ecuador 33
PK - Pakistan 33
AT - Austria 28
KR - Corea 28
NL - Olanda 28
ZA - Sudafrica 28
IR - Iran 25
ES - Italia 24
SA - Arabia Saudita 23
CZ - Repubblica Ceca 21
RO - Romania 21
UZ - Uzbekistan 20
CL - Cile 18
KE - Kenya 18
LT - Lituania 17
VE - Venezuela 17
MA - Marocco 15
AU - Australia 13
EG - Egitto 13
CI - Costa d'Avorio 12
JO - Giordania 12
CH - Svizzera 11
CO - Colombia 11
IL - Israele 11
TN - Tunisia 11
KZ - Kazakistan 10
TW - Taiwan 10
PH - Filippine 9
MY - Malesia 8
UY - Uruguay 8
AE - Emirati Arabi Uniti 7
AZ - Azerbaigian 7
HN - Honduras 7
JM - Giamaica 7
PE - Perù 7
PY - Paraguay 7
DZ - Algeria 6
GR - Grecia 6
OM - Oman 6
PT - Portogallo 6
BO - Bolivia 5
BG - Bulgaria 4
ET - Etiopia 4
HU - Ungheria 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
BA - Bosnia-Erzegovina 3
CY - Cipro 3
DK - Danimarca 3
KG - Kirghizistan 3
LK - Sri Lanka 3
NO - Norvegia 3
NZ - Nuova Zelanda 3
AO - Angola 2
BB - Barbados 2
BH - Bahrain 2
BN - Brunei Darussalam 2
BY - Bielorussia 2
DO - Repubblica Dominicana 2
HR - Croazia 2
MN - Mongolia 2
NG - Nigeria 2
PA - Panama 2
RS - Serbia 2
TH - Thailandia 2
TT - Trinidad e Tobago 2
BZ - Belize 1
CG - Congo 1
CR - Costa Rica 1
Totale 14.825
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Città #
Singapore 1.140
Chandler 660
San Jose 591
Ashburn 588
New York 205
Jacksonville 201
Beijing 190
Dublin 186
Warsaw 168
San Mateo 155
Los Angeles 145
Ho Chi Minh City 129
Jakarta 126
Tokyo 124
Lauterbourg 122
Hefei 106
Ann Arbor 98
Hanoi 89
Hong Kong 89
Milan 86
Munich 86
Frankfurt am Main 85
Marseille 85
Houston 81
Nanjing 81
The Dalles 80
Wilmington 78
Rome 75
Dallas 74
Moscow 73
Nürnberg 70
St Louis 66
Woodbridge 66
Fairfield 61
São Paulo 61
Council Bluffs 60
Dearborn 60
Lawrence 57
Helsinki 54
Boston 52
Cattolica 49
Redwood City 47
Seattle 47
Santa Clara 44
Norwalk 41
Bremen 40
Buffalo 40
Nanchang 37
Princeton 37
Nuremberg 31
Brussels 30
London 30
Redmond 28
Denver 27
Kent 27
Lancaster 26
Seoul 26
Mountain View 24
Phoenix 24
Stockholm 23
Toronto 23
Chicago 22
Detroit 22
Guangzhou 22
San Francisco 22
University Park 22
Belo Horizonte 21
Brooklyn 21
Da Nang 21
Orem 21
Turku 21
Mexico City 20
Zhengzhou 20
Atlanta 18
Baghdad 18
Brasília 18
Izmir 18
Tianjin 18
Vienna 18
Boardman 17
Kunming 17
Montreal 17
Nairobi 17
Tashkent 17
Cambridge 16
Paris 16
Hangzhou 15
Hebei 15
Johannesburg 15
Shenyang 15
Augusta 14
Chennai 14
Düsseldorf 14
Elkhart 14
Kish 14
Manchester 14
Poplar 14
Prague 14
Rio de Janeiro 14
Falkenstein 13
Totale 7.983
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Nome #
Chromosome 9p deletion syndrome and sex reversal: novel findings and redefinition of the critically deleted regions 445
Functional hemispherectomy in children with epilepsy and CSWS due to unilateral early brain injury including thalamus: sudden recovery of CSWS 276
Unusual 4p16.3 deletions suggest an additional chromosome region for the Wolf-Hirschhorn syndrome-associated seizures disorder 239
Sleep-potentiated epileptiform activity in early thalamic injuries: Study in a large series (60 cases) 205
Posterior resection for childhood lesional epilepsy: neuropsychological evolution 202
Chromosome 9p deletion syndrome and sex reversal: novel findings and redefinition of the critically deleted regions. 191
Novel de novo heterozygous loss-of-function variants in MED13L and further delineation of the MED13L haploinsufficiency syndrome 191
Unusual 4p16.3 deletions suggest an additional chromosome region for the Wolf-Hirschhorn syndrome-associated seizures disorder 181
Increased sleep spindle activity in patients with Costello syndrome (HRAS gene mutation) 180
Sleep disturbances in preschool age children with cerebral palsy: a questionnaire study 180
Early onset myoclonic epilepsy and 15q26 microdeletion: Observation of the first case. 179
Surgery of children with frontal lobe lesional epilepsy: neuropsychological study 178
Electrical and autonomic cardiac function in patients with Dravet syndrome 176
Epilepsy surgery of posterior quadrant dysplasia in the first year of life: experience of a single centre with long term follow-up 174
Sleep disturbances in preschool age children with cerebral palsy: a questionnaire study 167
Neuropsychological development in children with Dravet syndrome. 165
Wolf-Hirschhorn syndrome-associated chromosome changes are not mediated by olfactory receptor gene clusters nor by inversion polymorphism on 4p16 165
Proposal of a clinical score for the molecular test for Pitt-Hopkins syndrome 163
Intragenic KANSL1 mutations and chromosome 17q21.31 deletions: broadening the clinical spectrum and genotype-phenotype correlations in a large cohort of patients 162
Electrical and autonomic cardiac function in patients with Dravet syndrome 161
Pretreatment neuropsychological deficits in children with brain tumors 160
Epilepsy and BRAF mutations: Phenotypes, natural history and genotype-phenotype correlations 156
The Pitt-Hopkins syndrome: report of 16 new patients and clinical diagnostic criteria 152
Fighting autoinflammation in FIRES: The role of interleukins and early immunomodulation 148
Early onset myoclonic epilepsy and 15q26 microdeletion: observation of the first case 148
Pretreatment neuropsychological deficits in children with brain tumors 145
Disorders of early language development in Dravet syndrome 141
Clinical-genetic features and peculiar muscle histopathology in infantile DNM1L-related mitochondrial epileptic encephalopathy 141
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 140
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 139
Cortical Visual Impairment in CDKL5 Deficiency Disorder 139
Heart rate variability alterations in Dravet Syndrome: The role of status epilepticus and a possible association with mortality risk 138
Visual Function in Children with GNAO1-Related Encephalopathy 137
HYPOVENTILATION IN REM SLEEP IN A CASE OF 17p11.2 DELETION (SMITH-MAGENIS SYNDROME) 136
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) 134
-Electroclinical patterns and evolution of epilepsy in the 4p- syndrome 133
Cognitive development in Dravet syndrome: a retrospective, multicenter study of 26 patients 132
Role of high-density EEG (hdEEG) in pre-surgical epilepsy evaluation in children: case report and review of the literature 132
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 130
Interactions between antiepileptic and chemoterapeutic drugs in children with brain tumors: is it time to change treatment? 130
Neuropsychological development in children with Dravet syndrome 130
Cognitive-behavioral profiles in teenagers with Dravet syndrome 127
A registry for Dravet syndrome: The Italian experience 126
Chiari 1 Malformation and Epilepsy in Children: A Missing Relationship 126
Visual and visuoperceptual function in children with Panayiotopoulos syndrome 126
Acneiform eruption induced by ethosuximide 125
CHARGE-like presentation, craniosynostosis and mild Mowat-Wilson Syndrome diagnosed by recognition of the distinctive facial gestalt in a cohort of 28 new cases 125
"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 125
Postoperative Epileptic Seizures in Children: Is the Brain Incision a Risk Factor? 125
Early neurodevelopmental characterization in children with cobalamin C/defect 125
Disorders of early language development in Dravet syndrome 125
Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotype 124
Defining the electroclinical phenotype and outcome of PCDH19-related epilepsy: A multicenter study 124
Efficacy and safety of Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: A real-world study 124
Hereditary Hyperekplexia: A New Family and a Systematic Review of GLRA1 Gene-Related Phenotypes 123
Temporal lobe epilepsy surgery in children and adults: A multicenter study 122
Protocadherin 19 mutations in girls with infantile-onset epilepsy 118
Calcified cephalohematoma as an unusual cause of EEG anomalies: Case report 118
Does Anticonvulsant Treatment Influence Pain Perception in Epileptic Children? 115
The impact of valproic acid treatment on weight gain in pediatric patients with epilepsy 115
A novel homozygous variant in JAM3 gene causing hemorrhagic destruction of the brain, subependymal calcification, and congenital cataracts (HDBSCC) with neonatal onset 114
Cortical malformations and COL4A1 mutation: Three new cases 113
Pyridoxine supplementation in PACS2-related encephalopathy: A case report of possible precision therapy 112
Sleep-potentiated epileptiform activity in early thalamic injuries: Study in a large series (60 cases) 111
Congenital immunodeficiency in an individual with Wiedemann–Steiner syndrome due to a novel missense mutation in KMT2A 109
Clinical features and genetic analysis of two siblings with startle disease in an Italian family: a case report. 109
Postoperative Epileptic Seizures in Children 108
Phenomenology and clinical course of movement disorder in GNAO1 variants: Results from an analytical review 108
Multicenter prospective longitudinal study in 34 patients with Dravet syndrome: Neuropsychological development in the first six years of life 108
Cognitive-behavioral profiles in teenagers with Dravet syndrome 107
Symptomatic and presumed symptomatic focal epilepsies in childhood: An observational, prospective multicentre study 106
Trends in pediatric epilepsy surgery in Europe between 2008 and 2015: Country-, center-, and age-specific variation 106
Outlining a core neuropsychological phenotype for Dravet syndrome 105
Multimodal assessment of motor pathways and intracortical connections in functional hemispherectomy 104
Survey of rehabilitation approaches and plans for individuals with dravet syndrome (RAPIDS) in Italy: Current practices and strategies to progress 103
Dravet syndrome: Early electroclinical findings and long-term outcome in adolescents and adults 103
Phosphatase and tensin homolog (PTEN) variants and epilepsy: A multicenter case series 102
Sturge-Weber syndrome: an update on the relevant issues for neurosurgeons 100
Sleep disorders in children with cerebral palsy: neurodevelopmental and behavioral correlates 98
Short- vs long-term assessment of heart rate variability: Clinical significance in Dravet Syndrome 94
PRRT2 mutations in familial infantile seizures, paroxysmal dyskinesia, and hemiplegic migraine 94
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) 94
Glyburide ameliorates motor coordination and glucose homeostasis in a child with diabetes associated with the KCNJ11/S225T, del226-232 mutation 93
Chiari 1 Malformation and Epilepsy in Children: A Missing Relationship 92
Outlining a core neuropsychological phenotype for Dravet syndrome 91
Increasing volume and complexity of pediatric epilepsy surgery with stable seizure outcome between 2008 and 2014: A nationwide multicenter study 91
Clinical and genetic factors predicting Dravet syndrome in infants with SCN1A mutations 91
KETASER01 protocol: What went right and what went wrong 88
Epileptic children with hemispheres’ asymmetry. Quantitative brain magnetic resonance-based analysis of apparently unaffected hemisphere. Case-control study 88
Non-Stationary Outcome of Alternating Hemiplegia of Childhood into Adulthood 88
Does anticonvulsant treatment influence pain perception in epileptic children? 87
Molecular Genetics and Interferon Signature in the Italian Aicardi Goutières Syndrome Cohort: Report of 12 New Cases and Literature Review 86
GABRA1-Related Disorders: From Genetic to Functional Pathways 85
Early development in Dravet syndrome; visual function impairment precedes cognitive decline 85
Pretreatment neuropsychological deficits in children with brain tumors 85
Inv dup 15 syndrome: Case report with epilepsy onset in the first year 84
Disorders of early language development in Dravet syndrome 83
Cognitive decline in Dravet syndrome: is there a cerebellar role? 83
Fatal status epilepticus in dravet syndrome 82
Early thalamic injury associated with epilepsy and continuous spike-wave during slow sleep 81
Totale 13.130
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Categoria #
all - tutte 62.048
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 62.048
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021143 0 0 0 0 0 0 0 0 0 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
2025/20265.687 935 174 386 704 1.022 303 1.063 247 452 401 0 0
Totale 15.077