IRIS UniCatt

Battaglia, Domenica Immacolata
 Distribuzione geografica
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Continente #
NA - Nord America 3.466
EU - Europa 3.382
AS - Asia 1.505
SA - Sud America 328
AF - Africa 33
OC - Oceania 12
Continente sconosciuto - Info sul continente non disponibili 3
Totale 8.729
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Nazione #
US - Stati Uniti d'America 3.420
DE - Germania 1.101
SG - Singapore 608
CN - Cina 508
SE - Svezia 484
IT - Italia 391
BR - Brasile 300
UA - Ucraina 292
FR - Francia 258
IE - Irlanda 192
PL - Polonia 150
GB - Regno Unito 133
ID - Indonesia 125
FI - Finlandia 116
RU - Federazione Russa 93
IN - India 79
BE - Belgio 34
CA - Canada 32
TR - Turchia 30
HK - Hong Kong 26
KR - Corea 26
IR - Iran 23
AT - Austria 21
CZ - Repubblica Ceca 20
RO - Romania 19
NL - Olanda 18
VN - Vietnam 15
JP - Giappone 12
MX - Messico 12
ES - Italia 11
LT - Lituania 10
AU - Australia 9
MA - Marocco 9
IQ - Iraq 8
CH - Svizzera 7
CI - Costa d'Avorio 7
IL - Israele 7
AR - Argentina 6
TW - Taiwan 6
EC - Ecuador 5
CL - Cile 4
EG - Egitto 4
GR - Grecia 4
HU - Ungheria 4
KE - Kenya 4
KZ - Kazakistan 4
LV - Lettonia 4
UZ - Uzbekistan 4
VE - Venezuela 4
ZA - Sudafrica 4
A2 - ???statistics.table.value.countryCode.A2??? 3
BD - Bangladesh 3
LK - Sri Lanka 3
NO - Norvegia 3
NZ - Nuova Zelanda 3
PT - Portogallo 3
AE - Emirati Arabi Uniti 2
AL - Albania 2
BG - Bulgaria 2
BO - Bolivia 2
CY - Cipro 2
DZ - Algeria 2
HR - Croazia 2
JO - Giordania 2
KG - Kirghizistan 2
PA - Panama 2
PE - Perù 2
PY - Paraguay 2
TH - Thailandia 2
UY - Uruguay 2
AO - Angola 1
BA - Bosnia-Erzegovina 1
BN - Brunei Darussalam 1
CO - Colombia 1
DK - Danimarca 1
EE - Estonia 1
GE - Georgia 1
IM - Isola di Man 1
IS - Islanda 1
LA - Repubblica Popolare Democratica del Laos 1
LB - Libano 1
LI - Liechtenstein 1
MK - Macedonia 1
MY - Malesia 1
NG - Nigeria 1
PH - Filippine 1
PK - Pakistan 1
RS - Serbia 1
SA - Arabia Saudita 1
SN - Senegal 1
Totale 8.729
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Città #
Chandler 660
Singapore 358
Ashburn 329
Jacksonville 200
Dublin 182
San Mateo 155
New York 153
Warsaw 144
Jakarta 121
Ann Arbor 98
Marseille 84
Nanjing 81
Milan 80
Wilmington 78
Moscow 70
Nürnberg 70
Rome 70
Houston 68
Woodbridge 66
Fairfield 61
Dearborn 60
Los Angeles 60
Lawrence 57
Cattolica 49
Boston 48
Redwood City 47
Munich 41
Norwalk 41
Bremen 40
Helsinki 40
The Dalles 39
Beijing 38
Nanchang 37
Princeton 37
Seattle 35
Frankfurt am Main 34
Hefei 33
Brussels 30
Redmond 28
Nuremberg 26
Seoul 26
Hong Kong 25
Lancaster 25
São Paulo 25
Mountain View 24
University Park 22
Detroit 21
Zhengzhou 20
Izmir 17
Kunming 17
Guangzhou 16
Cambridge 15
Hebei 15
Shenyang 15
Boardman 14
Düsseldorf 14
Kish 14
San Francisco 14
Tianjin 14
Vienna 14
Augusta 13
Falkenstein 13
Jiaxing 13
Portsmouth 13
Prague 13
Belo Horizonte 12
Changsha 12
Hangzhou 12
London 12
Brooklyn 11
Fremont 11
Toronto 11
Council Bluffs 10
Leawood 10
Brasília 9
Costa Mesa 9
Edinburgh 9
Pune 9
Paris 8
Santa Clara 8
Simi Valley 8
Tokyo 8
Turku 8
Abidjan 7
Falls Church 7
Hanoi 7
Lauterbourg 7
Phoenix 7
Rio de Janeiro 7
Timisoara 7
Brno 6
Changchun 6
Porto Alegre 6
Shanghai 6
Shenzhen 6
Washington 6
Amsterdam 5
Campinas 5
Charlotte 5
Colombo 5
Totale 4.662
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Nome #
Chromosome 9p deletion syndrome and sex reversal: novel findings and redefinition of the critically deleted regions 357
Functional hemispherectomy in children with epilepsy and CSWS due to unilateral early brain injury including thalamus: sudden recovery of CSWS 224
Unusual 4p16.3 deletions suggest an additional chromosome region for the Wolf-Hirschhorn syndrome-associated seizures disorder 163
Posterior resection for childhood lesional epilepsy: neuropsychological evolution 162
Sleep-potentiated epileptiform activity in early thalamic injuries: Study in a large series (60 cases) 162
Chromosome 9p deletion syndrome and sex reversal: novel findings and redefinition of the critically deleted regions. 147
Epilepsy surgery of posterior quadrant dysplasia in the first year of life: experience of a single centre with long term follow-up 138
Early onset myoclonic epilepsy and 15q26 microdeletion: Observation of the first case. 137
Novel de novo heterozygous loss-of-function variants in MED13L and further delineation of the MED13L haploinsufficiency syndrome 134
Unusual 4p16.3 deletions suggest an additional chromosome region for the Wolf-Hirschhorn syndrome-associated seizures disorder 132
Increased sleep spindle activity in patients with Costello syndrome (HRAS gene mutation) 130
Surgery of children with frontal lobe lesional epilepsy: neuropsychological study 129
Sleep disturbances in preschool age children with cerebral palsy: a questionnaire study 127
Electrical and autonomic cardiac function in patients with Dravet syndrome 123
Neuropsychological development in children with Dravet syndrome. 120
Electrical and autonomic cardiac function in patients with Dravet syndrome 119
Sleep disturbances in preschool age children with cerebral palsy: a questionnaire study 116
Wolf-Hirschhorn syndrome-associated chromosome changes are not mediated by olfactory receptor gene clusters nor by inversion polymorphism on 4p16 113
Early onset myoclonic epilepsy and 15q26 microdeletion: observation of the first case 113
Intragenic KANSL1 mutations and chromosome 17q21.31 deletions: broadening the clinical spectrum and genotype-phenotype correlations in a large cohort of patients 112
Pretreatment neuropsychological deficits in children with brain tumors 111
Pretreatment neuropsychological deficits in children with brain tumors 106
Neuropsychological development in children with Dravet syndrome 105
Proposal of a clinical score for the molecular test for Pitt-Hopkins syndrome 103
HYPOVENTILATION IN REM SLEEP IN A CASE OF 17p11.2 DELETION (SMITH-MAGENIS SYNDROME) 101
The Pitt-Hopkins syndrome: report of 16 new patients and clinical diagnostic criteria 100
CHARGE-like presentation, craniosynostosis and mild Mowat-Wilson Syndrome diagnosed by recognition of the distinctive facial gestalt in a cohort of 28 new cases 97
-Electroclinical patterns and evolution of epilepsy in the 4p- syndrome 96
Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotype 92
Disorders of early language development in Dravet syndrome 90
Cognitive-behavioral profiles in teenagers with Dravet syndrome 90
Postoperative Epileptic Seizures in Children: Is the Brain Incision a Risk Factor? 90
null 89
Interactions between antiepileptic and chemoterapeutic drugs in children with brain tumors: is it time to change treatment? 85
Cognitive development in Dravet syndrome: a retrospective, multicenter study of 26 patients 85
Does Anticonvulsant Treatment Influence Pain Perception in Epileptic Children? 84
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 84
Acneiform eruption induced by ethosuximide 83
"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 83
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) 83
Sleep-potentiated epileptiform activity in early thalamic injuries: Study in a large series (60 cases) 76
Disorders of early language development in Dravet syndrome 76
Cortical Visual Impairment in CDKL5 Deficiency Disorder 75
Efficacy and safety of Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: A real-world study 74
Epilepsy and BRAF mutations: Phenotypes, natural history and genotype-phenotype correlations 72
Heart rate variability alterations in Dravet Syndrome: The role of status epilepticus and a possible association with mortality risk 71
Early neurodevelopmental characterization in children with cobalamin C/defect 70
Outlining a core neuropsychological phenotype for Dravet syndrome 70
Cortical malformations and COL4A1 mutation: Three new cases 69
Cognitive-behavioral profiles in teenagers with Dravet syndrome 68
Clinical-genetic features and peculiar muscle histopathology in infantile DNM1L-related mitochondrial epileptic encephalopathy 68
Clinical features and genetic analysis of two siblings with startle disease in an Italian family: a case report. 67
Calcified cephalohematoma as an unusual cause of EEG anomalies: Case report 66
Multimodal assessment of motor pathways and intracortical connections in functional hemispherectomy 66
Congenital immunodeficiency in an individual with Wiedemann–Steiner syndrome due to a novel missense mutation in KMT2A 65
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 63
PRRT2 mutations in familial infantile seizures, paroxysmal dyskinesia, and hemiplegic migraine 63
Phenomenology and clinical course of movement disorder in GNAO1 variants: Results from an analytical review 63
Symptomatic and presumed symptomatic focal epilepsies in childhood: An observational, prospective multicentre study 62
Trends in pediatric epilepsy surgery in Europe between 2008 and 2015: Country-, center-, and age-specific variation 61
Role of high-density EEG (hdEEG) in pre-surgical epilepsy evaluation in children: case report and review of the literature 61
Protocadherin 19 mutations in girls with infantile-onset epilepsy 60
Sturge-Weber syndrome: an update on the relevant issues for neurosurgeons 60
Sleep disorders in children with cerebral palsy: neurodevelopmental and behavioral correlates 59
Pretreatment neuropsychological deficits in children with brain tumors 59
Dravet syndrome: Early electroclinical findings and long-term outcome in adolescents and adults 59
Clinical and genetic factors predicting Dravet syndrome in infants with SCN1A mutations 58
Defining the electroclinical phenotype and outcome of PCDH19-related epilepsy: A multicenter study 58
Does anticonvulsant treatment influence pain perception in epileptic children? 56
Temporal lobe epilepsy surgery in children and adults: A multicenter study 56
A registry for Dravet syndrome: The Italian experience 55
Molecular Genetics and Interferon Signature in the Italian Aicardi Goutières Syndrome Cohort: Report of 12 New Cases and Literature Review 55
Multicenter prospective longitudinal study in 34 patients with Dravet syndrome: Neuropsychological development in the first six years of life 55
Fighting autoinflammation in FIRES: The role of interleukins and early immunomodulation 54
Salivary alpha-amylase: a new non-invasive biomarker for assessment of pain perception in epileptic children 54
Outlining a core neuropsychological phenotype for Dravet syndrome 54
A novel homozygous variant in JAM3 gene causing hemorrhagic destruction of the brain, subependymal calcification, and congenital cataracts (HDBSCC) with neonatal onset 54
Hereditary Hyperekplexia: A New Family and a Systematic Review of GLRA1 Gene-Related Phenotypes 54
Glyburide ameliorates motor coordination and glucose homeostasis in a child with diabetes associated with the KCNJ11/S225T, del226-232 mutation 53
Cognitive decline in Dravet syndrome: is there a cerebellar role? 53
Early development in Dravet syndrome; visual function impairment precedes cognitive decline 53
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) 53
Non-Stationary Outcome of Alternating Hemiplegia of Childhood into Adulthood 51
Rufinamide for the treatment of refractory epilepsy secondary to neuronal migration disorders 50
Focal seizures with affective symptoms are a major feature of PCDH19 gene-related epilepsy 50
Epileptic children with hemispheres’ asymmetry. Quantitative brain magnetic resonance-based analysis of apparently unaffected hemisphere. Case-control study 50
Visual Function in Children with GNAO1-Related Encephalopathy 49
Duchenne muscular dystrophy and epilepsy 49
Cognitive decline in Dravet syndrome: is there a cerebellar role? 47
Increasing volume and complexity of pediatric epilepsy surgery with stable seizure outcome between 2008 and 2014: A nationwide multicenter study 46
Results From an Italian Expanded Access Program on Cannabidiol Treatment in Highly Refractory Dravet Syndrome and Lennox–Gastaut Syndrome 46
Postoperative Epileptic Seizures in Children 45
The impact of valproic acid treatment on weight gain in pediatric patients with epilepsy 45
Functional characterization of a novel KCNJ11 in frame mutation-deletion associated with infancy-onset diabetes and a mild form of intermediate DEND: a battle between K(ATP) gain of channel activity and loss of channel expression 44
Phosphatase and tensin homolog (PTEN) variants and epilepsy: A multicenter case series 43
Duchenne muscular dystrophy and epilepsy 43
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 42
Chiari 1 Malformation and Epilepsy in Children: A Missing Relationship 41
Fatal status epilepticus in dravet syndrome 40
Pyridoxine supplementation in PACS2-related encephalopathy: A case report of possible precision therapy 39
Totale 8.233
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Categoria #
all - tutte 44.079
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 44.079
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020170 0 0 0 0 0 0 0 0 0 0 104 66
2020/2021670 29 71 7 113 80 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
2024/20251.949 36 62 162 122 228 96 99 116 383 192 453 0
Totale 8.912