IRIS PubliCatt

Battaglia, Domenica Immacolata
 Distribuzione geografica
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Continente #
NA - Nord America 3.121
EU - Europa 2.888
AS - Asia 482
AF - Africa 12
SA - Sud America 9
OC - Oceania 6
Continente sconosciuto - Info sul continente non disponibili 3
Totale 6.521
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Nazione #
US - Stati Uniti d'America 3.106
DE - Germania 993
SE - Svezia 472
CN - Cina 312
IT - Italia 299
UA - Ucraina 289
FR - Francia 211
IE - Irlanda 188
PL - Polonia 146
GB - Regno Unito 101
FI - Finlandia 78
IN - India 69
BE - Belgio 26
TR - Turchia 24
IR - Iran 22
SG - Singapore 19
RO - Romania 18
CA - Canada 14
HK - Hong Kong 13
CZ - Repubblica Ceca 12
NL - Olanda 12
ES - Italia 8
CI - Costa d'Avorio 7
AU - Australia 6
IL - Israele 6
RU - Federazione Russa 6
VN - Vietnam 6
BR - Brasile 5
CH - Svizzera 5
AT - Austria 4
HU - Ungheria 4
JP - Giappone 4
A2 - ???statistics.table.value.countryCode.A2??? 3
CL - Cile 3
EG - Egitto 3
NO - Norvegia 3
BG - Bulgaria 2
GR - Grecia 2
KZ - Kazakistan 2
PT - Portogallo 2
BO - Bolivia 1
EE - Estonia 1
HR - Croazia 1
ID - Indonesia 1
IM - Isola di Man 1
IQ - Iraq 1
IS - Islanda 1
LB - Libano 1
LI - Liechtenstein 1
LT - Lituania 1
MA - Marocco 1
MY - Malesia 1
NG - Nigeria 1
PA - Panama 1
PH - Filippine 1
RS - Serbia 1
Totale 6.521
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Città #
Chandler 660
Ashburn 312
Jacksonville 200
Dublin 179
San Mateo 155
New York 149
Warsaw 143
Ann Arbor 98
Marseille 84
Nanjing 80
Wilmington 78
Nürnberg 70
Milan 69
Houston 66
Woodbridge 66
Fairfield 61
Dearborn 60
Lawrence 57
Cattolica 49
Boston 48
Redwood City 47
Norwalk 41
Bremen 40
Nanchang 37
Princeton 37
Beijing 36
Rome 33
Seattle 31
Redmond 28
Lancaster 25
Mountain View 24
Brussels 22
University Park 22
Detroit 21
Munich 19
Izmir 17
Kunming 16
Cambridge 15
Hebei 15
Shenyang 15
Kish 14
Augusta 13
Helsinki 13
Jiaxing 13
Zhengzhou 13
Changsha 12
Guangzhou 12
Hong Kong 12
Tianjin 12
Fremont 11
Hangzhou 11
Boardman 10
Leawood 10
Prague 10
Costa Mesa 9
Edinburgh 9
Pune 9
San Francisco 8
Simi Valley 8
Abidjan 7
Falls Church 7
Timisoara 7
Washington 6
Brooklyn 5
Changchun 5
Indiana 5
Phoenix 5
Singapore 5
São Paulo 5
Amsterdam 4
Andover 4
Busto Arsizio 4
Clearwater 4
Fuzhou 4
Kocaeli 4
Los Angeles 4
Parma 4
San Jose 4
Toronto 4
Vienna 4
Brescia 3
Budapest 3
Charlotte 3
Falkenstein 3
Frankfurt am Main 3
Jinan 3
Labico 3
Lanzhou 3
Lappeenranta 3
London 3
Madrid 3
Misterbianco 3
Monmouth Junction 3
Montréal 3
Padova 3
Paris 3
Reggio Emilia 3
Shenzhen 3
Tappahannock 3
Waanrode 3
Totale 3.595
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Nome #
Chromosome 9p deletion syndrome and sex reversal: novel findings and redefinition of the critically deleted regions 345
Functional hemispherectomy in children with epilepsy and CSWS due to unilateral early brain injury including thalamus: sudden recovery of CSWS 206
Sleep-potentiated epileptiform activity in early thalamic injuries: Study in a large series (60 cases) 147
Unusual 4p16.3 deletions suggest an additional chromosome region for the Wolf-Hirschhorn syndrome-associated seizures disorder 139
Posterior resection for childhood lesional epilepsy: neuropsychological evolution 135
Chromosome 9p deletion syndrome and sex reversal: novel findings and redefinition of the critically deleted regions. 127
Early onset myoclonic epilepsy and 15q26 microdeletion: Observation of the first case. 122
Epilepsy surgery of posterior quadrant dysplasia in the first year of life: experience of a single centre with long term follow-up 120
Unusual 4p16.3 deletions suggest an additional chromosome region for the Wolf-Hirschhorn syndrome-associated seizures disorder 117
Surgery of children with frontal lobe lesional epilepsy: neuropsychological study 113
Novel de novo heterozygous loss-of-function variants in MED13L and further delineation of the MED13L haploinsufficiency syndrome 111
Increased sleep spindle activity in patients with Costello syndrome (HRAS gene mutation) 110
Sleep disturbances in preschool age children with cerebral palsy: a questionnaire study 110
Electrical and autonomic cardiac function in patients with Dravet syndrome 102
Neuropsychological development in children with Dravet syndrome. 101
Electrical and autonomic cardiac function in patients with Dravet syndrome 100
Early onset myoclonic epilepsy and 15q26 microdeletion: observation of the first case 99
Sleep disturbances in preschool age children with cerebral palsy: a questionnaire study 98
Wolf-Hirschhorn syndrome-associated chromosome changes are not mediated by olfactory receptor gene clusters nor by inversion polymorphism on 4p16 92
Neuropsychological development in children with Dravet syndrome 92
Pretreatment neuropsychological deficits in children with brain tumors 90
Pretreatment neuropsychological deficits in children with brain tumors 90
Intragenic KANSL1 mutations and chromosome 17q21.31 deletions: broadening the clinical spectrum and genotype-phenotype correlations in a large cohort of patients 90
HYPOVENTILATION IN REM SLEEP IN A CASE OF 17p11.2 DELETION (SMITH-MAGENIS SYNDROME) 87
Proposal of a clinical score for the molecular test for Pitt-Hopkins syndrome 85
Visual and visuoperceptual function in children with Panayiotopoulos syndrome 81
The Pitt-Hopkins syndrome: report of 16 new patients and clinical diagnostic criteria 80
-Electroclinical patterns and evolution of epilepsy in the 4p- syndrome 77
Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotype 76
CHARGE-like presentation, craniosynostosis and mild Mowat-Wilson Syndrome diagnosed by recognition of the distinctive facial gestalt in a cohort of 28 new cases 76
Cognitive-behavioral profiles in teenagers with Dravet syndrome 74
Cognitive development in Dravet syndrome: a retrospective, multicenter study of 26 patients 73
Interactions between antiepileptic and chemoterapeutic drugs in children with brain tumors: is it time to change treatment? 72
Postoperative Epileptic Seizures in Children: Is the Brain Incision a Risk Factor? 71
Acneiform eruption induced by ethosuximide 70
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) 70
Does Anticonvulsant Treatment Influence Pain Perception in Epileptic Children? 68
Sleep-potentiated epileptiform activity in early thalamic injuries: Study in a large series (60 cases) 68
"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 65
Disorders of early language development in Dravet syndrome 63
Disorders of early language development in Dravet syndrome 57
Outlining a core neuropsychological phenotype for Dravet syndrome 56
Cortical malformations and COL4A1 mutation: Three new cases 55
Protocadherin 19 mutations in girls with infantile-onset epilepsy 53
Pretreatment neuropsychological deficits in children with brain tumors 53
Congenital immunodeficiency in an individual with Wiedemann–Steiner syndrome due to a novel missense mutation in KMT2A 53
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 53
Clinical features and genetic analysis of two siblings with startle disease in an Italian family: a case report. 51
Cognitive-behavioral profiles in teenagers with Dravet syndrome 51
Sturge-Weber syndrome: an update on the relevant issues for neurosurgeons 51
PRRT2 mutations in familial infantile seizures, paroxysmal dyskinesia, and hemiplegic migraine 49
Salivary alpha-amylase: a new non-invasive biomarker for assessment of pain perception in epileptic children 49
Calcified cephalohematoma as an unusual cause of EEG anomalies: Case report 49
Efficacy and safety of Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: A real-world study 49
Sleep disorders in children with cerebral palsy: neurodevelopmental and behavioral correlates 48
Early neurodevelopmental characterization in children with cobalamin C/defect 48
Multimodal assessment of motor pathways and intracortical connections in functional hemispherectomy 48
Cortical Visual Impairment in CDKL5 Deficiency Disorder 48
Symptomatic and presumed symptomatic focal epilepsies in childhood: An observational, prospective multicentre study 47
Clinical-genetic features and peculiar muscle histopathology in infantile DNM1L-related mitochondrial epileptic encephalopathy 46
Does anticonvulsant treatment influence pain perception in epileptic children? 45
Epilepsy and BRAF mutations: Phenotypes, natural history and genotype-phenotype correlations 45
Rufinamide for the treatment of refractory epilepsy secondary to neuronal migration disorders 44
Dravet syndrome: Early electroclinical findings and long-term outcome in adolescents and adults 44
Glyburide ameliorates motor coordination and glucose homeostasis in a child with diabetes associated with the KCNJ11/S225T, del226-232 mutation 43
Cognitive decline in Dravet syndrome: is there a cerebellar role? 42
Duchenne muscular dystrophy and epilepsy 42
Early development in Dravet syndrome; visual function impairment precedes cognitive decline 42
Trends in pediatric epilepsy surgery in Europe between 2008 and 2015: Country-, center-, and age-specific variation 42
Role of high-density EEG (hdEEG) in pre-surgical epilepsy evaluation in children: case report and review of the literature 42
Heart rate variability alterations in Dravet Syndrome: The role of status epilepticus and a possible association with mortality risk 42
Cognitive decline in Dravet syndrome: is there a cerebellar role? 41
Molecular Genetics and Interferon Signature in the Italian Aicardi Goutières Syndrome Cohort: Report of 12 New Cases and Literature Review 41
Focal seizures with affective symptoms are a major feature of PCDH19 gene-related epilepsy 40
Phenomenology and clinical course of movement disorder in GNAO1 variants: Results from an analytical review 39
Clinical and genetic factors predicting Dravet syndrome in infants with SCN1A mutations 38
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) 38
Non-Stationary Outcome of Alternating Hemiplegia of Childhood into Adulthood 38
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 37
Outlining a core neuropsychological phenotype for Dravet syndrome 37
Epileptic children with hemispheres’ asymmetry. Quantitative brain magnetic resonance-based analysis of apparently unaffected hemisphere. Case-control study 37
Duchenne muscular dystrophy and epilepsy 36
A novel homozygous variant in JAM3 gene causing hemorrhagic destruction of the brain, subependymal calcification, and congenital cataracts (HDBSCC) with neonatal onset 36
Temporal lobe epilepsy surgery in children and adults: A multicenter study 36
Defining the electroclinical phenotype and outcome of PCDH19-related epilepsy: A multicenter study 34
Multicenter prospective longitudinal study in 34 patients with Dravet syndrome: Neuropsychological development in the first six years of life 34
Does anticonvulsant treatment influence pain perception in epileptic children? 31
Increasing volume and complexity of pediatric epilepsy surgery with stable seizure outcome between 2008 and 2014: A nationwide multicenter study 31
The impact of valproic acid treatment on weight gain in pediatric patients with epilepsy 30
Spectral Domain Optical Coherence Tomography of Choroidal and Outer Retinal Layer Thickness in the Sturge Weber Syndrome 28
Fatal status epilepticus in dravet syndrome 27
A registry for Dravet syndrome: The Italian experience 26
Results From an Italian Expanded Access Program on Cannabidiol Treatment in Highly Refractory Dravet Syndrome and Lennox–Gastaut Syndrome 25
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 23
Hereditary Hyperekplexia: A New Family and a Systematic Review of GLRA1 Gene-Related Phenotypes 23
Reply to dravet, c. Different outcomes of acute encephalopathy after status epilepticus in patients with dravet syndrome. how to avoid them? comment on “de liso et al. fatal status epilepticus in dravet syndrome. brain sci. 2020, 10, 889” 22
Phosphatase and tensin homolog (PTEN) variants and epilepsy: A multicenter case series 20
Chiari 1 Malformation and Epilepsy in Children: A Missing Relationship 19
Delineating SPTAN1 associated phenotypes: From isolated epilepsy to encephalopathy with progressive brain atrophy 19
Pyridoxine supplementation in PACS2-related encephalopathy: A case report of possible precision therapy 18
Totale 6.503
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Categoria #
all - tutte 25.959
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 25.959
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019130 0 0 0 0 0 0 0 0 0 34 44 52
2019/2020881 163 65 68 57 43 72 102 37 61 43 104 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
2023/2024897 35 274 35 143 61 226 61 36 19 7 0 0
Totale 6.689