IRIS
VENESELLI, EDVIGE MARIA
 Distribuzione geografica
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Continente #
EU - Europa 14.531
Totale 14.531
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Nazione #
IT - Italia 14.531
Totale 14.531
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Città #
Genova 11.309
Rapallo 1.730
Genoa 1.384
Vado Ligure 72
Bordighera 36
Totale 14.531
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Nome #
Encefalopatia mioclonica (sindrome di Kinsbourne) e neuroblastoma. Aspetti clinico-patologici di nuovi casi 283
Su di un caso di distrofia neuroassonale infantile (Malattia di Seitelberger). 158
CC and CXC chemokines are pivotal mediators of cerebral injury in ischaemic stroke. 151
Movement lateralization and bimanual coordination in children with Tourette syndrome. 147
Are psychobiological markers strongly correlated with allostatic load in population with autism spectrum disorders (ASD)? 147
Neuroblastoma with symptomatic spinal cord compression at diagnosis: treatment and results with 76 cases 141
Hereditary motor and sensory neuropathy with deafness, mental retardation and absence of large myelinated fibers. 139
Alternating Hemiplegia of Childhood: Pharmacological treatment of 30 Italian patients 134
Phenylketonuria:diet for life or not? 132
Metabolic and genetic risk factors for migraine in children 131
Response to rituximab in 3 children with opsoclonus-myoclonus syndrome resistant to conventional treatments. 131
Inferior olivary nucleus involvement in pediatric neurodegenerative disorders: does it play a role in neuroimaging pattern-recognition approach? 130
Five-year follow-up of a cognitive-behavioural lifestyle multidisciplinary programme for childhood obesity outpatient treatment. 128
Temporal relationship of generalized epileptiform discharges to spindle frequency activity in childhood absence epilepsy 128
Anti-NMDAR encephalitis misdiagnosed as Hashimoto's encephalopathy. 125
Early-onset cobalamin C/D deficiency: epilepsy and electroencephalographic features. 125
Structural connectivity analysis in children with segmental callosal agenesis 124
Rapid diazepam introduction (venous or rectal) in childhood epilepsy: taxonomic and therapeutic considerations. 122
Aicardi-Goutières syndrome presenting atypically as a sub-acute leukoencephalopathy 122
Neuropsychological disorders related to interictal epileptic discharges during sleep in benign epilepsy of childhood with centrotemporal or Rolandic spikes. 121
Faulty cardiac repolarization reserve in alternating hemiplegia of childhood broadens the phenotype 118
Intragenic duplication of KCNQ5 gene results in aberrant splicing leading to a premature termination codon in a patient with intellectual disability 118
Applicability of the 1988 IHS criteria to headache patients under the age of 18 years attending 21 italian headache clinics. 117
Autismo precoce e distrofia muscolare congenita: un caso clinico. 116
Metals, metallothioneins and oxidative stress in blood of autistic children 116
null 116
Anti-Glutamic Acid Decarboxylase Limbic Encephalitis Without Epilepsy Evolving Into Dementia With Cerebellar Ataxia 114
Alternating hemiplegia of childhood: treatment of attacks with chloral hydrate and niaprazine. 112
Secondary generalized epilepsy in childhood: EEG patterns and correlation with responsiveness to benzodiazepines or ACTH 112
Anti-N-methyl-D-aspartate-receptor encephalitis in a four-year-old girl. 112
Distribution of epileptiform discharges during nREM sleep in the CSWSS syndrome: relationship with sigma and delta activities 112
Rett networked database: An integrated clinical and genetic network of rett syndrome databases 111
Hypersomnia in the Prader Willi syndrome: clinical-electrophysiological features and underlying factors. 109
De novo mutations in ATP1A3 cause alternating hemiplegia of childhood 109
Type 1 diabetes and epilepsy: more than a casual association? 109
Occipital cerebral calcifications and celiac disease:an additional case 108
Blood oxidative stress and metallothionein expression in Rett syndrome: Probing for markers 108
Unusually prolonged survival and childhood-onset epilepsy in a case of alobar holoprosencephaly. 108
Clinical and electroencephalographic features in patients with CDKL5 mutations: two new Italian cases and review of the literature. 106
Epileptic Encephalopathy With Continuous Spike and Wave During Sleep Associated to Periventricular Leukomalacia. 106
MR imaging findings in 2 cases of late infantile GM1 gangliosidosis. 105
Epilepsia partialis continua in type 1 diabetes: evolution into epileptic encephalopathy with continuous spike-waves during slow sleep 105
Lack of SLC2A1 (Glucose Transporter 1) Mutations in 30 Italian Patients With Alternating Hemiplegia of Childhood. 105
Diagnosis and treatment of the first epileptic seizure: Guidelines of the Italian League against Epilepsy. 105
Chronic inflammatory demyelinating polyneuropathy of childhood: clinical and neuroradiological findings. 105
Effect of steroid and high-dose immunoglobulin therapy on opsoclonus-myoclonus syndrome occurring in neuroblastoma. 104
PANDAS and PANS: Clinical, Neuropsychological, and Biological Characterization of a Monocentric Series of Patients and Proposal for a Diagnostic Protocol 104
Variant late infantile neuronal ceroid lipofuscinosis because of CLN1 mutations 103
Neonatal diabetes mellitus due to pancreatic agenesis and pervasive developmental disorder 101
Paroxysmal features responding to flunarizine in a child with rapid-onset dystonia-parkinsonism 101
Malignant migrating partial seizures in infancy 101
Epilepsy in Rett syndrome: clinical and genetic features. 101
Epilepsy in Rett syndrome--lessons from the Rett networked database 101
Personality profile and health-related quality of life in adults with previous continuous spike-waves during slow sleep syndrome 99
Outcome of juvenile headache in outpatients attending 23 italian hedeache clinics 97
Childhood thalidomide neuropathy: a clinical and neurophysiologic study. 97
ATP1A3 spectrum disorders: A video-documented history of 7 genetically confirmed early onset cases 96
Variant of Rett Syndrome and CDKL5 Gene: Clinical and Autonomic Description of 10 Cases 95
Short latency evoked somatosensory potentials after stimulation of the median nerve in children: normative data 94
Severe epilepsy in X-linked creatine transporter defect (CRTR-D) 93
Cobalamin (Cbl)C/D deficiency: clinical, neurophysiological and neuroradiologic finding in 14 cases 92
Neuroblastic tumors associated with opsoclonus-myoclonus syndrome: histological, immunohistochimical and molecular features of 15 italian cases 90
Neuronal ceroid lipofuscinoses: clinical and EEG findings in a large study of italian cases. 90
Cytochrome-coxidase deficiency in three patients with Leigh's disease 90
Congenital muscular dystrophy and epileptic syndromes in infancy and childhood. 89
NOVEL MUTATIONS IN CDKL5 GENE, PREDICTED EFFECTS AND ASSOCIATED PHENOTYPES 87
Patologia metabolica. Inquadramento clinico neurologico. 86
Antiepileptic drugs in Rett Syndrome 84
A case of major form familial hyperekplexia: prenatal diagnosis and effective treatment with clonazepam. 83
Synchronization and continuation: Analysis of repetitive finger movements in patients with Tourette syndrome 82
Attention-deficit/hyperactivity disorder drugs and growth: an Italian prospective observational study. 81
Mutations in MFSD8/CLN7 are a frequent cause of variant-late infantile neuronal ceroid lipofuscinosis 80
Cerebrospinal fluid alterations of the serotonin product, 5-hydroxyindolacetic acid, in neurological disorders. 80
Clinical and molecular characterization of a patient with interstitial 6q21q22.1 deletion 80
L'acido dipropilacetico e il clonazepam nel trattamento dell'epilessia infantile 77
The relationship between group A streptococcal infections and Tourette syndrome: a study on a large service-based cohort. 76
L'acropatia ulcero-mutilante in età pediatrica. Descrizione di un caso e sue complicazioni ortopedioche. 75
Affezioni neurologiche infantili a decorso lento e indagini immunologiche. 73
Childhood sarcoidosis presenting with prevalent muscolar symptoms: report of a case. 73
Sjogren-Larsson syndrome: nuclear magnetic resonance imaging of the brein in a 4-years-old boy. 72
Proposta di un protocollo per l'identificazione della Sindrome dell'X-Fragile. 72
MICROCEPHALY AND HEAD GROWTH DECREASE IN RETT SYNDROME 72
Novel mutations in the CDKL5 gene, predicted effects and associated phenotypes 72
Le mioclonie non epilettiche nell'età evolutiva 70
Narcolessia in età pediatrica: un caso clinico. 69
La psichiatria del bambino e dell'adolescente all'interno della Neuropsichiatria Infantile. 68
Clinical and EEG findings of 18 cases of late infantile neuronal ceroid lipofuscunosis 68
Increased levels of metal trace elements and metallothionein expression in blood of children with autism 68
Aspetti elettroclinici e neuropsicologici delle epilessie focali idiopatiche del bambino (BFCE) che evolvono in stato di male elettrico in sonno (ESES) 67
Indirizzi precoci di trattamento delle paralisi ostetriche del plesso brachiale. 66
Attualità nella Patologia Neurologica dell'età evolutiva. Paralisi cerebrali. 66
Inquadramento nosografico delle atrofie muscolari spinali nell'età evolutiva: studio su 120 casi. 64
Epilessia e calcificazione cortico-sottocorticali bilaterali senza angiomatosi: sindrome di SturgeWeber atipica? 64
Secondary dopamine and serotonine deficiencies in children with movement disorders 64
Leucoencefalopatie su base genetica in età pediatrica 64
Problematiche e contributi nella presa in carico dei pazienti affetti da Sclerosi Tuberosa. 63
La determinazione della morte cerebrale in età evolutiva. 61
Farmaci anti-epilettici 61
La sclerosi tuberosa 61
Metabolic myopathies: general aspect and clinical approach. 61
Totale 10.029
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Categoria #
all - tutte 37.138
article - articoli 32.275
book - libri 184
conference - conferenze 751
curatela - curatele 0
other - altro 142
patent - brevetti 0
selected - selezionate 0
volume - volumi 3.786
Totale 74.276
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20204.204 0 85 166 168 374 336 903 223 319 818 626 186
2020/2021986 57 71 51 76 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
2024/2025100 82 18 0 0 0 0 0 0 0 0 0 0
Totale 14.628