IRIS
VENESELLI, EDVIGE MARIA
 Distribuzione geografica
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Continente #
EU - Europa 18.704
AS - Asia 85
SA - Sud America 46
NA - Nord America 3
AF - Africa 2
Totale 18.840
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Nazione #
IT - Italia 18.703
CN - Cina 40
BR - Brasile 35
VN - Vietnam 35
AR - Argentina 7
SG - Singapore 3
ID - Indonesia 2
US - Stati Uniti d'America 2
AE - Emirati Arabi Uniti 1
BD - Bangladesh 1
BH - Bahrain 1
BO - Bolivia 1
BY - Bielorussia 1
CL - Cile 1
CO - Colombia 1
EC - Ecuador 1
IQ - Iraq 1
JP - Giappone 1
MA - Marocco 1
MX - Messico 1
SN - Senegal 1
Totale 18.840
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Città #
Genova 11.309
Genoa 4.333
Rapallo 1.730
Vado Ligure 1.295
Bordighera 36
Beijing 18
Hanoi 14
Ho Chi Minh City 12
São Paulo 5
Ashburn 2
Ninh Bình 2
Ribeirão Preto 2
Rio de Janeiro 2
Acopiara 1
Agadir 1
Aquidabã 1
Aristóbulo del Valle 1
Belford Roxo 1
Betim 1
Botucatu 1
Bình Dương 1
Bắc Ninh 1
Cachoeirinha 1
Campo Novo do Parecis 1
Can Tho 1
Candelaria 1
Ciudad Nezahualcoyotl 1
Conceição do Mato Dentro 1
Conselheiro Lafaiete 1
Da Nang 1
Dakar 1
Dourados 1
Dubai 1
Fonseca 1
Formosa 1
Fortaleza 1
Goiânia 1
Haiphong 1
Itumbiara 1
Jacareí 1
La Paz 1
Malang 1
Manama 1
Moreno 1
Nova Lima 1
Ouro Fino 1
Palmeira dos Índios 1
Paraíso do Tocantins 1
Parnaíba 1
Pekanbaru 1
Porto Alegre 1
Quilmes 1
Quito 1
Quảng Nam Province 1
Resistencia 1
Rio Grande 1
Rio Grande da Serra 1
Salto de Pirapora 1
Santa Fe 1
Santa Maria 1
Sete Lagoas 1
Singapore 1
Sulaymaniyah 1
São Luís do Quitunde 1
Thành Phố Bà Rịa 1
Tokyo 1
Vitebsk 1
Ñuñoa 1
Totale 18.815
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Nome #
Encefalopatia mioclonica (sindrome di Kinsbourne) e neuroblastoma. Aspetti clinico-patologici di nuovi casi 321
CC and CXC chemokines are pivotal mediators of cerebral injury in ischaemic stroke. 182
Su di un caso di distrofia neuroassonale infantile (Malattia di Seitelberger). 181
Are psychobiological markers strongly correlated with allostatic load in population with autism spectrum disorders (ASD)? 178
Alternating Hemiplegia of Childhood: Pharmacological treatment of 30 Italian patients 174
Movement lateralization and bimanual coordination in children with Tourette syndrome. 171
Hereditary motor and sensory neuropathy with deafness, mental retardation and absence of large myelinated fibers. 168
Metals, metallothioneins and oxidative stress in blood of autistic children 165
Intragenic duplication of KCNQ5 gene results in aberrant splicing leading to a premature termination codon in a patient with intellectual disability 163
Structural connectivity analysis in children with segmental callosal agenesis 159
Response to rituximab in 3 children with opsoclonus-myoclonus syndrome resistant to conventional treatments. 158
Inferior olivary nucleus involvement in pediatric neurodegenerative disorders: does it play a role in neuroimaging pattern-recognition approach? 158
Anti-Glutamic Acid Decarboxylase Limbic Encephalitis Without Epilepsy Evolving Into Dementia With Cerebellar Ataxia 158
Neuroblastoma with symptomatic spinal cord compression at diagnosis: treatment and results with 76 cases 157
Early-onset cobalamin C/D deficiency: epilepsy and electroencephalographic features. 155
Aicardi-Goutières syndrome presenting atypically as a sub-acute leukoencephalopathy 154
Anti-NMDAR encephalitis misdiagnosed as Hashimoto's encephalopathy. 154
Anti-N-methyl-D-aspartate-receptor encephalitis in a four-year-old girl. 150
Temporal relationship of generalized epileptiform discharges to spindle frequency activity in childhood absence epilepsy 149
Metabolic and genetic risk factors for migraine in children 149
Distribution of epileptiform discharges during nREM sleep in the CSWSS syndrome: relationship with sigma and delta activities 149
Faulty cardiac repolarization reserve in alternating hemiplegia of childhood broadens the phenotype 149
Phenylketonuria:diet for life or not? 148
Five-year follow-up of a cognitive-behavioural lifestyle multidisciplinary programme for childhood obesity outpatient treatment. 147
Alternating hemiplegia of childhood: treatment of attacks with chloral hydrate and niaprazine. 144
Applicability of the 1988 IHS criteria to headache patients under the age of 18 years attending 21 italian headache clinics. 142
Epileptic Encephalopathy With Continuous Spike and Wave During Sleep Associated to Periventricular Leukomalacia. 140
Rapid diazepam introduction (venous or rectal) in childhood epilepsy: taxonomic and therapeutic considerations. 139
Hypersomnia in the Prader Willi syndrome: clinical-electrophysiological features and underlying factors. 138
Personality profile and health-related quality of life in adults with previous continuous spike-waves during slow sleep syndrome 138
Neuropsychological disorders related to interictal epileptic discharges during sleep in benign epilepsy of childhood with centrotemporal or Rolandic spikes. 137
Autismo precoce e distrofia muscolare congenita: un caso clinico. 133
Secondary generalized epilepsy in childhood: EEG patterns and correlation with responsiveness to benzodiazepines or ACTH 133
PANDAS and PANS: Clinical, Neuropsychological, and Biological Characterization of a Monocentric Series of Patients and Proposal for a Diagnostic Protocol 133
Short latency evoked somatosensory potentials after stimulation of the median nerve in children: normative data 132
Rett networked database: An integrated clinical and genetic network of rett syndrome databases 131
Severe epilepsy in X-linked creatine transporter defect (CRTR-D) 130
Clinical and electroencephalographic features in patients with CDKL5 mutations: two new Italian cases and review of the literature. 130
Blood oxidative stress and metallothionein expression in Rett syndrome: Probing for markers 130
Occipital cerebral calcifications and celiac disease:an additional case 128
Outcome of juvenile headache in outpatients attending 23 italian hedeache clinics 125
Cobalamin (Cbl)C/D deficiency: clinical, neurophysiological and neuroradiologic finding in 14 cases 125
ATP1A3 spectrum disorders: A video-documented history of 7 genetically confirmed early onset cases 125
Lack of SLC2A1 (Glucose Transporter 1) Mutations in 30 Italian Patients With Alternating Hemiplegia of Childhood. 124
De novo mutations in ATP1A3 cause alternating hemiplegia of childhood 124
Neuronal ceroid lipofuscinoses: clinical and EEG findings in a large study of italian cases. 124
Type 1 diabetes and epilepsy: more than a casual association? 123
Epilepsy in Rett syndrome: clinical and genetic features. 122
Epilepsy in Rett syndrome--lessons from the Rett networked database 122
Epilepsia partialis continua in type 1 diabetes: evolution into epileptic encephalopathy with continuous spike-waves during slow sleep 121
Variant of Rett Syndrome and CDKL5 Gene: Clinical and Autonomic Description of 10 Cases 121
A case of major form familial hyperekplexia: prenatal diagnosis and effective treatment with clonazepam. 120
Clinical and molecular characterization of a patient with interstitial 6q21q22.1 deletion 120
Chronic inflammatory demyelinating polyneuropathy of childhood: clinical and neuroradiological findings. 120
MR imaging findings in 2 cases of late infantile GM1 gangliosidosis. 118
Variant late infantile neuronal ceroid lipofuscinosis because of CLN1 mutations 118
Malignant migrating partial seizures in infancy 118
Unusually prolonged survival and childhood-onset epilepsy in a case of alobar holoprosencephaly. 118
Effect of steroid and high-dose immunoglobulin therapy on opsoclonus-myoclonus syndrome occurring in neuroblastoma. 118
null 116
Childhood thalidomide neuropathy: a clinical and neurophysiologic study. 116
Paroxysmal features responding to flunarizine in a child with rapid-onset dystonia-parkinsonism 115
Antiepileptic drugs in Rett Syndrome 115
Neonatal diabetes mellitus due to pancreatic agenesis and pervasive developmental disorder 114
Diagnosis and treatment of the first epileptic seizure: Guidelines of the Italian League against Epilepsy. 114
Congenital muscular dystrophy and epileptic syndromes in infancy and childhood. 111
Affezioni neurologiche infantili a decorso lento e indagini immunologiche. 107
Neuroblastic tumors associated with opsoclonus-myoclonus syndrome: histological, immunohistochimical and molecular features of 15 italian cases 106
Patologia metabolica. Inquadramento clinico neurologico. 105
Cytochrome-coxidase deficiency in three patients with Leigh's disease 104
NOVEL MUTATIONS IN CDKL5 GENE, PREDICTED EFFECTS AND ASSOCIATED PHENOTYPES 103
Mutations in MFSD8/CLN7 are a frequent cause of variant-late infantile neuronal ceroid lipofuscinosis 103
Aspetti elettroclinici e neuropsicologici delle epilessie focali idiopatiche del bambino (BFCE) che evolvono in stato di male elettrico in sonno (ESES) 102
Childhood sarcoidosis presenting with prevalent muscolar symptoms: report of a case. 102
Narcolessia in età pediatrica: un caso clinico. 100
Synchronization and continuation: Analysis of repetitive finger movements in patients with Tourette syndrome 100
White matter and cerebellar involvement in alternating hemiplegia of childhood 99
Attention-deficit/hyperactivity disorder drugs and growth: an Italian prospective observational study. 98
L'acido dipropilacetico e il clonazepam nel trattamento dell'epilessia infantile 97
Epilessie infantili farmacoresistenti e forme rare di neurolipidosi. 97
Cerebrospinal fluid alterations of the serotonin product, 5-hydroxyindolacetic acid, in neurological disorders. 95
Cardiac phenotype in ATP1A3-related syndromes: A multicentre cohort study 94
Sjogren-Larsson syndrome: nuclear magnetic resonance imaging of the brein in a 4-years-old boy. 92
Autismo infantile: aspetti neurofisiologici. 92
L'acropatia ulcero-mutilante in età pediatrica. Descrizione di un caso e sue complicazioni ortopedioche. 92
Le mioclonie non epilettiche nell'età evolutiva 92
Novel mutations in the CDKL5 gene, predicted effects and associated phenotypes 92
Inquadramento nosografico delle atrofie muscolari spinali nell'età evolutiva: studio su 120 casi. 91
The relationship between group A streptococcal infections and Tourette syndrome: a study on a large service-based cohort. 90
Indirizzi precoci di trattamento delle paralisi ostetriche del plesso brachiale. 89
Problems and suggestions in handling patients with tuberous sclerosis 89
Aspetti EEG di tipo epilettico senza epilessia in età pediatrica. 89
Leucoencefalopatie su base genetica in età pediatrica 89
Corpus callosum abnormalities: neuroimaging, cytogenetics and clinical characterization of a very large multicenter Italian series 88
Aspetti clinici generali 88
MICROCEPHALY AND HEAD GROWTH DECREASE IN RETT SYNDROME 87
Criteri diagnostici delle encefalopatie progressive e/o metaboliche 86
A double-blind, parallel, multicenter comparison of L-acetylcarnitine with placebo on the attention deficit hyperactivity disorder in fragile X syndrome boys. 86
La psichiatria del bambino e dell'adolescente all'interno della Neuropsichiatria Infantile. 85
Epilessia e calcificazione cortico-sottocorticali bilaterali senza angiomatosi: sindrome di SturgeWeber atipica? 85
Totale 12.476
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Categoria #
all - tutte 58.184
article - articoli 50.096
book - libri 285
conference - conferenze 1.124
curatela - curatele 0
other - altro 249
patent - brevetti 0
selected - selezionate 0
volume - volumi 6.430
Totale 116.368
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021731 0 0 0 0 45 111 56 111 87 98 110 113
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
2025/20261.514 532 225 241 495 21 0 0 0 0 0 0 0
Totale 18.938