IRIS
DE GRANDIS, ELISA
 Distribuzione geografica
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Continente #
EU - Europa 6.537
AS - Asia 383
SA - Sud America 51
NA - Nord America 25
AF - Africa 1
Totale 6.997
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Nazione #
IT - Italia 6.530
SG - Singapore 156
CN - Cina 110
VN - Vietnam 91
BR - Brasile 32
US - Stati Uniti d'America 14
AR - Argentina 13
HK - Hong Kong 10
MX - Messico 7
ID - Indonesia 5
IN - India 3
IQ - Iraq 3
BD - Bangladesh 2
CA - Canada 2
DO - Repubblica Dominicana 2
NL - Olanda 2
VE - Venezuela 2
BO - Bolivia 1
BY - Bielorussia 1
CL - Cile 1
CO - Colombia 1
DE - Germania 1
EC - Ecuador 1
GE - Georgia 1
IL - Israele 1
MA - Marocco 1
RU - Federazione Russa 1
SE - Svezia 1
UA - Ucraina 1
UZ - Uzbekistan 1
Totale 6.997
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Città #
Genova 3.066
Genoa 2.314
Vado Ligure 614
Rapallo 503
Singapore 44
Ho Chi Minh City 35
Beijing 34
Bordighera 26
Hanoi 21
Hong Kong 10
Tianjin 10
Ashburn 9
Rio de Janeiro 4
Biên Hòa 3
Da Nang 3
Mexico City 3
Ninh Bình 3
Bauru 2
Bắc Ninh 2
Caracas 2
Curitiba 2
Quảng Nam Province 2
Toronto 2
Agadir 1
Ancol 1
Baghdad 1
Bagé 1
Belo Horizonte 1
Bogotá 1
Bắc Giang 1
Campo Novo do Parecis 1
Can Tho 1
Caraúbas 1
Carmópolis de Minas 1
Cañuelas 1
Chicago 1
Cochabamba 1
Coimbatore 1
Concordia 1
Delhi 1
Diyālá 1
Feni 1
Fortaleza 1
Francisco Álvarez 1
Gothenburg 1
Governador Valadares 1
Gresik 1
Guatraché 1
Haiphong 1
Hải Dương 1
Iepê 1
Içara 1
Jakarta 1
Kemerovo 1
Lanús 1
Latacunga 1
León 1
Long An 1
Lấp Vò 1
Maranguape 1
María Juana 1
Marília 1
Milan 1
Morón 1
Nam Định 1
Nantong 1
Naples 1
Nha Trang 1
Nova Iguaçu 1
Orem 1
Orlando 1
Patna 1
Paulista 1
Registro 1
Resistencia 1
Rio Branco 1
Rishon LeTsiyyon 1
Salta 1
San Francisco 1
San Juan Bautista 1
San Justo 1
San Salvador de Jujuy 1
Santiago 1
Santiago de los Caballeros 1
Santo André 1
Santo Domingo 1
Serra 1
Sumy 1
São José dos Campos 1
São Paulo 1
São Sepé 1
Tashkent 1
Tbilisi 1
Teresina 1
Thành Phố Bà Rịa 1
Tijuana 1
Tramandaí 1
Tupã 1
Varjota 1
Veracruz 1
Totale 6.791
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Nome #
Movement lateralization and bimanual coordination in children with Tourette syndrome. 182
Alternating Hemiplegia of Childhood: Pharmacological treatment of 30 Italian patients 178
A novel pathogenic MYH3 mutation in a child with Sheldon–Hall syndrome and vertebral fusions 170
Inferior olivary nucleus involvement in pediatric neurodegenerative disorders: does it play a role in neuroimaging pattern-recognition approach? 168
Response to rituximab in 3 children with opsoclonus-myoclonus syndrome resistant to conventional treatments. 167
Congenital neuroblastoma with symptoms of epidural compression at birth 164
Faulty cardiac repolarization reserve in alternating hemiplegia of childhood broadens the phenotype 156
Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome 156
Efficacious vitamin E treatment in a child with ataxia with isolatedvitamin E deficiency 149
Epileptic Encephalopathy With Continuous Spike and Wave During Sleep Associated to Periventricular Leukomalacia. 145
A UHPLC–MS/MS method for the quantification of Δ9-tetrahydrocannabinol and cannabidiol in decoctions and in plasma samples for therapeutic monitoring of medical cannabis 144
PANDAS and PANS: Clinical, Neuropsychological, and Biological Characterization of a Monocentric Series of Patients and Proposal for a Diagnostic Protocol 143
Early-onset neurodegeneration with brain iron accumulationdue to PANK2 mutation 142
Personality profile and health-related quality of life in adults with previous continuous spike-waves during slow sleep syndrome 142
A Personalized Driving Simulator for the Assessment of Adolescents with Attention Deficit Hyperactivity Disorder 137
ATP1A3 spectrum disorders: A video-documented history of 7 genetically confirmed early onset cases 131
De novo mutations in ATP1A3 cause alternating hemiplegia of childhood 128
Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood—a study of 155 patients 127
A case of major form familial hyperekplexia: prenatal diagnosis and effective treatment with clonazepam. 126
Lack of SLC2A1 (Glucose Transporter 1) Mutations in 30 Italian Patients With Alternating Hemiplegia of Childhood. 125
Distinct neurological disorders with ATP1A3 mutations 125
MR imaging findings in 2 cases of late infantile GM1 gangliosidosis. 119
Childhood thalidomide neuropathy: a clinical and neurophysiologic study. 119
Paroxysmal features responding to flunarizine in a child with rapid-onset dystonia-parkinsonism 117
Severe early-onset developmental and epileptic encephalopathy (DEE) associated with novel compound heterozygous pathogenic variants in SLC25A22: Case report and literature review 116
Optic Atrophy and Generalized Chorea in a Patient Harboring an OPA10/RTN4IP1 Pathogenic Variant 115
Pediatric optic neuritis and anti MOG antibodies: a cohort of Italian patients 111
Schimke immuno-osseous dysplasia, two new cases with peculiar EEG pattern 111
Cerebral folate deficiency syndromes in childhood: clinical, analytical, and etiologic aspects. 108
White matter and cerebellar involvement in alternating hemiplegia of childhood 103
Synchronization and continuation: Analysis of repetitive finger movements in patients with Tourette syndrome 102
Pediatric Neuroblastoma-Associated Opsoclonus-Myoclonus-Ataxia Syndrome: Early Diagnosis 99
Cardiac phenotype in ATP1A3-related syndromes: A multicentre cohort study 99
Impact of the COVID-19 Outbreak on the Behavior of Families in Italy: A Focus on Children and Adolescents 98
Cerebrospinal fluid alterations of the serotonin product, 5-hydroxyindolacetic acid, in neurological disorders. 97
Alternating Hemiplegia of Childhood in a Child Harboring a Novel TBC1D24 Mutation: Case Report and Literature Review 97
CEREBRAL FOLATE DEFICIENCY AND DISEASES OF THE CENTRAL NERVOUS SYSTEM IN CHILDHOOD 96
CASK related disorder: Epilepsy and developmental outcome 96
Molecular study and response to levodopa therapy in eight children with tyrosine hydroxylase deficiency 94
Alternating Hemiplegia of Childhood: Genotype–Phenotype Correlations in a Cohort of 39 Italian Patients 93
[Acute urinary retention in a child with acute disseminatedencephalomyelitis] 91
Paroxysmal dyskinesiawith interictal myoclonus and dystonia: a report of two cases. 86
A nationwide study on Sydenham's chorea: Clinical features, treatment and prognostic factors: A multicenter cohort study on Sydenham's chorea 86
USE OF RITUXIMAB IN THE TREATMENT OF THE SYNDROME OPSOMIOCLONIC. EXPERIENCE IN THE G. GASLINI INSTITUTE 79
Secondary dopamine and serotonine deficiencies in children with movement disorders 79
Alternating hemiplegia of childhood: evolution over time and mouse model corroboration 79
Photoparoxysmal response in ADCK3 autosomal recessive ataxia: a case report and literature review 77
Complex cases with Autism Spectrum Disorder (ASD), developmental delay, hyperactivity and sleep disturbance explained by oligogenic mechanisms 75
Leucomalacia periventricolare ed encefalopatia epilettica con punte-onda continue in sonno lento 72
Biallelic ZBTB11 variants associated with complex neuropsychiatric phenotype featuring Tourette syndrome 69
Opsoclonus-myoclonus-atassia syndrome: Neuropsychological and neuroradiological series 69
Influence of isolated low-grade intracranial haemorrhages on the neurodevelopmental outcome of infants born very low birthweight 68
Autism spectrum disorders in a population of very low birth weght: Causes and consequences 66
Restless legs may be associatedwith the post-polio syndrome. 65
Immunological mechanisms inopsoclonus-myoclonus associated neuroblastoma 65
PANDAS e PANS: caratterizzazione clinica e biologica di una coorte di pazienti 64
Correlations between Sleep Features and Iron Status in Children with Neurodevelopmental Disorders: A Cross-Sectional Study 63
Sleep Disturbances in Pediatric Craniopharyngioma: A Systematic Review 61
A novel pathogenic MYH3 mutation in a child with Sheldon-Hall syndrome and vertebral fusion 58
Cardiac autonomic control in Rett syndrome: Insights from heart rate variability analysis 56
Safety and pharmacokinetics of medical cannabis preparation in a monocentric series of young patients with drug resistant epilepsy 55
Erratum: Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome (The American Journal of Human Genetics (2018) 103(3) (431–439), (S0002929718302374), (10.1016/j.ajhg.2018.07.010)) 52
null 51
Cask-Related Disorders: Clinical, Electroencephalographic and Neuroradiological Description of Four Genetically Confirmed Cases 49
Electroclinical Features of Epilepsy in Kleefstra Syndrome 48
Multidirectional Nystagmus as the Presenting Sign of Brain Tumor with Hydrocephalus 45
Impatto della pandemia da COVID-19 sull’andamento dei ricoveri di un reparto di Neuropsichiatria Infantile di terzo livello. 45
LOW-GRADE IVH AND LOW-GRADE CBH: WHICH INFLUENCE ON GRIFFITHS SCORE AT 2 YEARS OF AGE? 42
PATTERN OF NEURODEVELOPMENTAL OUT- COME AT 2 YEARS OF CORRECTED AGE (CA) IN ISOLATED LOW-GRADE INTRA- VENTRICULAR HEMORRHAGES VS LOW- GRADE CEREBELLAR HEMORRHAGES 41
Schimke Immuno-osseous Dysplasia: A Peculiar EEG Pattern 37
Decreased free D-aspartate levels in the blood serum of patients with schizophrenia 36
The Genetic Landscape of Complex Childhood‐Onset Hyperkinetic Movement Disorders 33
Development and testing of methods to record and follow up spells in patients with alternating hemiplegia of childhood 29
Long-term follow-up of neuroblastoma-associated opsoclonus-myoclonus-ataxia syndrome 29
Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene 21
Methodology of a Natural History Study of a Rare Neurodevelopmental Disorder: Alternating Hemiplegia of Childhood as a Prototype Disease 14
Stress symptoms and Coronavirus disease 2019 (COVID-19): a comparative study between Attention Deficit Hyperactivity Disorder and typically developing children and adolescents 7
null 3
Totale 7.160
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Categoria #
all - tutte 26.216
article - articoli 25.162
book - libri 0
conference - conferenze 661
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 393
Totale 52.432
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021261 0 0 0 0 0 15 31 51 21 71 31 41
2021/2022585 20 22 51 56 28 41 24 129 37 68 23 86
2022/2023604 51 62 6 53 107 79 2 54 98 2 77 13
2023/2024590 37 58 28 63 31 126 44 40 32 36 28 67
2024/20251.615 65 89 34 86 232 179 127 265 63 100 168 207
2025/20261.162 361 59 156 196 361 29 0 0 0 0 0 0
Totale 7.160