IRIS
VENESELLI, EDVIGE MARIA
 Distribuzione geografica
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Continente #
EU - Europa 19.186
AS - Asia 2.101
NA - Nord America 1.535
SA - Sud America 161
Continente sconosciuto - Info sul continente non disponibili 99
AF - Africa 35
OC - Oceania 13
Totale 23.130
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Nazione #
IT - Italia 18.865
US - Stati Uniti d'America 1.428
SG - Singapore 889
CN - Cina 528
VN - Vietnam 338
FR - Francia 177
BD - Bangladesh 133
BR - Brasile 94
HK - Hong Kong 74
FI - Finlandia 49
CA - Canada 46
AR - Argentina 30
IN - India 29
DE - Germania 26
JP - Giappone 25
MX - Messico 20
GB - Regno Unito 17
IQ - Iraq 13
AU - Australia 12
ID - Indonesia 11
JM - Giamaica 11
ZA - Sudafrica 11
CO - Colombia 10
EC - Ecuador 10
PK - Pakistan 10
SA - Arabia Saudita 9
VE - Venezuela 9
CH - Svizzera 8
PH - Filippine 8
RU - Federazione Russa 8
GT - Guatemala 7
TH - Thailandia 7
ES - Italia 6
NL - Olanda 6
CR - Costa Rica 5
KR - Corea 5
MA - Marocco 5
UZ - Uzbekistan 5
AE - Emirati Arabi Uniti 4
DZ - Algeria 4
IE - Irlanda 4
SE - Svezia 4
UA - Ucraina 4
CL - Cile 3
NI - Nicaragua 3
PL - Polonia 3
SN - Senegal 3
TN - Tunisia 3
TR - Turchia 3
BE - Belgio 2
DO - Repubblica Dominicana 2
ET - Etiopia 2
HN - Honduras 2
HT - Haiti 2
MY - Malesia 2
RO - Romania 2
SV - El Salvador 2
TT - Trinidad e Tobago 2
UY - Uruguay 2
AG - Antigua e Barbuda 1
AO - Angola 1
AT - Austria 1
AZ - Azerbaigian 1
BB - Barbados 1
BH - Bahrain 1
BO - Bolivia 1
BY - Bielorussia 1
BZ - Belize 1
CM - Camerun 1
CW - ???statistics.table.value.countryCode.CW??? 1
GE - Georgia 1
GR - Grecia 1
KE - Kenya 1
KG - Kirghizistan 1
KZ - Kazakistan 1
LY - Libia 1
MD - Moldavia 1
MM - Myanmar 1
MU - Mauritius 1
NG - Nigeria 1
NO - Norvegia 1
NZ - Nuova Zelanda 1
PA - Panama 1
PR - Porto Rico 1
PS - Palestinian Territory 1
PY - Paraguay 1
SC - Seychelles 1
SR - Suriname 1
TW - Taiwan 1
Totale 23.032
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Città #
Genova 11.309
Genoa 4.335
Rapallo 1.730
Vado Ligure 1.295
San Jose 445
Singapore 403
Lauterbourg 168
Ashburn 143
Ho Chi Minh City 97
Hanoi 92
Hong Kong 70
Beijing 68
New York 68
Helsinki 49
Bordighera 36
Santa Clara 34
Los Angeles 24
Frankfurt am Main 23
Dallas 22
Tokyo 22
Rome 21
Orem 19
Da Nang 17
Milan 16
São Paulo 14
Tianjin 14
Chicago 12
Council Bluffs 12
Buffalo 11
Atlanta 10
Haiphong 9
Houston 9
Naples 9
Chennai 8
Mexico City 8
Miami 8
Princeton 8
Seattle 8
Bologna 7
Brooklyn 7
Montreal 7
Philadelphia 7
Turin 7
Denver 6
Guatemala City 6
Kingston 6
Mumbai 6
Phoenix 6
Rio de Janeiro 6
Shanghai 6
Zurich 6
Caracas 5
Cardiff 5
Guayaquil 5
Johannesburg 5
Lahore 5
Milwaukee 5
New Delhi 5
San Antonio 5
Summerville 5
Toronto 5
Washington 5
Winnipeg 5
Bangkok 4
Columbus 4
Des Moines 4
Dublin 4
Florence 4
Jacksonville 4
Jeddah 4
Las Vegas 4
Lewiston 4
Nha Trang 4
Porto Alegre 4
Queens 4
Quito 4
Rockledge 4
San Francisco 4
San Tan Valley 4
The Bronx 4
Whitefield 4
Baghdad 3
Baltimore 3
Biên Hòa 3
Catania 3
Dakar 3
Guangzhou 3
Hải Dương 3
Indpls 3
London 3
Managua 3
Manchester 3
Manila 3
Memphis 3
Mount Vernon 3
Newark 3
Ninh Bình 3
Orlando 3
Peoria 3
Phủ Từ Sơn 3
Totale 20.918
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Nome #
Encefalopatia mioclonica (sindrome di Kinsbourne) e neuroblastoma. Aspetti clinico-patologici di nuovi casi 352
Intragenic duplication of KCNQ5 gene results in aberrant splicing leading to a premature termination codon in a patient with intellectual disability 215
Faulty cardiac repolarization reserve in alternating hemiplegia of childhood broadens the phenotype 214
Alternating Hemiplegia of Childhood: Pharmacological treatment of 30 Italian patients 209
Movement lateralization and bimanual coordination in children with Tourette syndrome. 207
CC and CXC chemokines are pivotal mediators of cerebral injury in ischaemic stroke. 206
Su di un caso di distrofia neuroassonale infantile (Malattia di Seitelberger). 204
Are psychobiological markers strongly correlated with allostatic load in population with autism spectrum disorders (ASD)? 201
Hereditary motor and sensory neuropathy with deafness, mental retardation and absence of large myelinated fibers. 196
Anti-N-methyl-D-aspartate-receptor encephalitis in a four-year-old girl. 193
Inferior olivary nucleus involvement in pediatric neurodegenerative disorders: does it play a role in neuroimaging pattern-recognition approach? 190
Structural connectivity analysis in children with segmental callosal agenesis 190
Anti-Glutamic Acid Decarboxylase Limbic Encephalitis Without Epilepsy Evolving Into Dementia With Cerebellar Ataxia 188
Anti-NMDAR encephalitis misdiagnosed as Hashimoto's encephalopathy. 187
Metals, metallothioneins and oxidative stress in blood of autistic children 185
Response to rituximab in 3 children with opsoclonus-myoclonus syndrome resistant to conventional treatments. 185
Early-onset cobalamin C/D deficiency: epilepsy and electroencephalographic features. 183
Aicardi-Goutières syndrome presenting atypically as a sub-acute leukoencephalopathy 177
Neuroblastoma with symptomatic spinal cord compression at diagnosis: treatment and results with 76 cases 176
Metabolic and genetic risk factors for migraine in children 173
Alternating hemiplegia of childhood: treatment of attacks with chloral hydrate and niaprazine. 171
PANDAS and PANS: Clinical, Neuropsychological, and Biological Characterization of a Monocentric Series of Patients and Proposal for a Diagnostic Protocol 171
Distribution of epileptiform discharges during nREM sleep in the CSWSS syndrome: relationship with sigma and delta activities 170
Epileptic Encephalopathy With Continuous Spike and Wave During Sleep Associated to Periventricular Leukomalacia. 169
Applicability of the 1988 IHS criteria to headache patients under the age of 18 years attending 21 italian headache clinics. 168
Phenylketonuria:diet for life or not? 168
Temporal relationship of generalized epileptiform discharges to spindle frequency activity in childhood absence epilepsy 167
Secondary generalized epilepsy in childhood: EEG patterns and correlation with responsiveness to benzodiazepines or ACTH 166
Five-year follow-up of a cognitive-behavioural lifestyle multidisciplinary programme for childhood obesity outpatient treatment. 166
Hypersomnia in the Prader Willi syndrome: clinical-electrophysiological features and underlying factors. 165
Personality profile and health-related quality of life in adults with previous continuous spike-waves during slow sleep syndrome 165
ATP1A3 spectrum disorders: A video-documented history of 7 genetically confirmed early onset cases 161
Autismo precoce e distrofia muscolare congenita: un caso clinico. 157
Blood oxidative stress and metallothionein expression in Rett syndrome: Probing for markers 157
Clinical and molecular characterization of a patient with interstitial 6q21q22.1 deletion 156
Rapid diazepam introduction (venous or rectal) in childhood epilepsy: taxonomic and therapeutic considerations. 155
Cobalamin (Cbl)C/D deficiency: clinical, neurophysiological and neuroradiologic finding in 14 cases 155
Clinical and electroencephalographic features in patients with CDKL5 mutations: two new Italian cases and review of the literature. 155
Rett networked database: An integrated clinical and genetic network of rett syndrome databases 155
Neuropsychological disorders related to interictal epileptic discharges during sleep in benign epilepsy of childhood with centrotemporal or Rolandic spikes. 154
Cardiac phenotype in ATP1A3-related syndromes: A multicentre cohort study 153
De novo mutations in ATP1A3 cause alternating hemiplegia of childhood 151
Short latency evoked somatosensory potentials after stimulation of the median nerve in children: normative data 149
Variant of Rett Syndrome and CDKL5 Gene: Clinical and Autonomic Description of 10 Cases 148
Outcome of juvenile headache in outpatients attending 23 italian hedeache clinics 147
Epilepsy in Rett syndrome: clinical and genetic features. 147
Severe epilepsy in X-linked creatine transporter defect (CRTR-D) 146
A case of major form familial hyperekplexia: prenatal diagnosis and effective treatment with clonazepam. 146
Chronic inflammatory demyelinating polyneuropathy of childhood: clinical and neuroradiological findings. 146
Diagnosis and treatment of the first epileptic seizure: Guidelines of the Italian League against Epilepsy. 145
Epilepsy in Rett syndrome--lessons from the Rett networked database 145
Type 1 diabetes and epilepsy: more than a casual association? 143
MR imaging findings in 2 cases of late infantile GM1 gangliosidosis. 142
Neuronal ceroid lipofuscinoses: clinical and EEG findings in a large study of italian cases. 141
Occipital cerebral calcifications and celiac disease:an additional case 140
Childhood thalidomide neuropathy: a clinical and neurophysiologic study. 140
Lack of SLC2A1 (Glucose Transporter 1) Mutations in 30 Italian Patients With Alternating Hemiplegia of Childhood. 138
Epilepsia partialis continua in type 1 diabetes: evolution into epileptic encephalopathy with continuous spike-waves during slow sleep 137
Antiepileptic drugs in Rett Syndrome 137
Affezioni neurologiche infantili a decorso lento e indagini immunologiche. 134
Variant late infantile neuronal ceroid lipofuscinosis because of CLN1 mutations 134
Aspetti elettroclinici e neuropsicologici delle epilessie focali idiopatiche del bambino (BFCE) che evolvono in stato di male elettrico in sonno (ESES) 134
Unusually prolonged survival and childhood-onset epilepsy in a case of alobar holoprosencephaly. 134
NOVEL MUTATIONS IN CDKL5 GENE, PREDICTED EFFECTS AND ASSOCIATED PHENOTYPES 133
Neonatal diabetes mellitus due to pancreatic agenesis and pervasive developmental disorder 132
Effect of steroid and high-dose immunoglobulin therapy on opsoclonus-myoclonus syndrome occurring in neuroblastoma. 131
Paroxysmal features responding to flunarizine in a child with rapid-onset dystonia-parkinsonism 129
Malignant migrating partial seizures in infancy 129
Cerebrospinal fluid alterations of the serotonin product, 5-hydroxyindolacetic acid, in neurological disorders. 128
Congenital muscular dystrophy and epileptic syndromes in infancy and childhood. 127
Mutations in MFSD8/CLN7 are a frequent cause of variant-late infantile neuronal ceroid lipofuscinosis 127
White matter and cerebellar involvement in alternating hemiplegia of childhood 127
Narcolessia in età pediatrica: un caso clinico. 126
Neuroblastic tumors associated with opsoclonus-myoclonus syndrome: histological, immunohistochimical and molecular features of 15 italian cases 125
Le mioclonie non epilettiche nell'età evolutiva 121
Cytochrome-coxidase deficiency in three patients with Leigh's disease 121
Corpus callosum abnormalities: neuroimaging, cytogenetics and clinical characterization of a very large multicenter Italian series 119
Patologia metabolica. Inquadramento clinico neurologico. 119
Epilessie infantili farmacoresistenti e forme rare di neurolipidosi. 119
Leucoencefalopatie su base genetica in età pediatrica 119
Inquadramento nosografico delle atrofie muscolari spinali nell'età evolutiva: studio su 120 casi. 118
Aspetti clinici generali 118
Synchronization and continuation: Analysis of repetitive finger movements in patients with Tourette syndrome 117
null 116
Sjogren-Larsson syndrome: nuclear magnetic resonance imaging of the brein in a 4-years-old boy. 115
Criteri diagnostici delle encefalopatie progressive e/o metaboliche 115
Convulsioni e stato di male epilettico 115
Autismo infantile: aspetti neurofisiologici. 114
L'acido dipropilacetico e il clonazepam nel trattamento dell'epilessia infantile 114
Childhood sarcoidosis presenting with prevalent muscolar symptoms: report of a case. 114
Contributo della Computed EEG Topography (CET) allo studio delle epilessie infantili. 113
Introduzione alla elettroencefalografia dell'Età Evolutiva 112
A double-blind, parallel, multicenter comparison of L-acetylcarnitine with placebo on the attention deficit hyperactivity disorder in fragile X syndrome boys. 112
Attention-deficit/hyperactivity disorder drugs and growth: an Italian prospective observational study. 112
L'acropatia ulcero-mutilante in età pediatrica. Descrizione di un caso e sue complicazioni ortopedioche. 109
I mezzi di investigazione elettrofisiologica del Sistema Nervoso Centrale 109
MICROCEPHALY AND HEAD GROWTH DECREASE IN RETT SYNDROME 109
Aspetti EEG di tipo epilettico senza epilessia in età pediatrica. 109
Novel mutations in the CDKL5 gene, predicted effects and associated phenotypes 109
Indirizzi precoci di trattamento delle paralisi ostetriche del plesso brachiale. 107
Totale 14.948
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Categoria #
all - tutte 70.285
article - articoli 60.352
book - libri 338
conference - conferenze 1.368
curatela - curatele 0
other - altro 312
patent - brevetti 0
selected - selezionate 0
volume - volumi 7.915
Totale 140.570
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20222.108 35 152 112 333 70 158 84 568 53 226 41 276
2022/20232.070 212 126 39 218 363 401 9 146 345 14 172 25
2023/20241.061 48 168 45 110 70 235 38 58 47 35 86 121
2024/20252.896 82 248 113 143 469 322 239 443 94 140 250 353
2025/20265.159 532 225 241 495 694 533 892 247 339 393 262 306
2026/2027547 547 0 0 0 0 0 0 0 0 0 0 0
Totale 23.130