Distribuzione geografica
Continente #
NA - Nord America 3.055
EU - Europa 1.509
AS - Asia 372
AF - Africa 10
SA - Sud America 5
OC - Oceania 2
Totale 4.953
Nazione #
US - Stati Uniti d'America 3.034
IE - Irlanda 1.083
CN - Cina 304
IT - Italia 134
FI - Finlandia 105
DE - Germania 62
BE - Belgio 45
IN - India 34
UA - Ucraina 33
SE - Svezia 24
CA - Canada 16
KR - Corea 15
FR - Francia 9
MU - Mauritius 7
JP - Giappone 6
TR - Turchia 6
GB - Regno Unito 5
MX - Messico 5
AR - Argentina 4
HU - Ungheria 3
NL - Olanda 3
SG - Singapore 3
AU - Australia 2
DZ - Algeria 2
CZ - Repubblica Ceca 1
EG - Egitto 1
ES - Italia 1
FK - Isole Falkland (Malvinas) 1
HK - Hong Kong 1
ID - Indonesia 1
IR - Iran 1
MD - Moldavia 1
TW - Taiwan 1
Totale 4.953
Città #
Dublin 1.078
Chandler 982
Ashburn 293
Princeton 170
Lawrence 165
Wilmington 126
Medford 122
Shanghai 101
Helsinki 85
New York 79
Ann Arbor 53
Nanjing 50
Brussels 45
Jacksonville 45
Seattle 42
Fairfield 33
Pune 28
Beijing 27
Washington 27
Hebei 24
Milan 21
Changsha 20
Falls Church 20
Nanchang 20
Des Moines 17
Rome 17
Shenyang 17
Norwalk 16
Jiaxing 15
Pavia 14
Seongnam-si 14
Philadelphia 13
Toronto 13
Woodbridge 13
Tianjin 10
Cedar Knolls 7
Hangzhou 7
Ankara 6
Boardman 5
Cremona 5
Berlin 4
Chicago 4
Huskvarna 4
Mar del Plata 4
Paris 4
Pieve Emanuele 4
Yokohama 4
Andover 3
Canneto Pavese 3
Como 3
Flushing 3
Mexico City 3
New Delhi 3
North Charleston 3
Redwood City 3
San Diego 3
Seregno 3
Singapore 3
Vicenza 3
Azzano San Paolo 2
Brescia 2
Centrale 2
Feraoun 2
Guangzhou 2
Haranomachi 2
Maniago 2
Naples 2
Napoli 2
Nijmegen 2
Oak Harbor 2
Palermo 2
Pécs 2
Québec 2
San Mateo 2
Secugnago 2
Zhengzhou 2
Anzio 1
Auburn 1
Bottrop 1
Brisbane 1
Budapest 1
Cairo 1
Central 1
Chisinau 1
Ciudad Juárez 1
Colleferro 1
Council Bluffs 1
Fayetteville 1
Fuzhou 1
Genoa 1
Hanam 1
Houston 1
Jinan 1
Kish 1
Kunming 1
Landshut 1
Laurel 1
Lodi 1
London 1
Naaldwijk 1
Totale 3.967
Nome #
Sex-dimorphic pathways in the associations between maternal trait anxiety, infant BDNF methylation and negative emotionality 80
Changes in the optic disc excavation of children affected by cerebral visual impairment: a tomographic analysis. 73
Inverted duplications are recurrent rearrangements always associated with a distal deletion. Description of a new case involving 2q 58
Ketogenic Dietary Therapies in Patients with Autism Spectrum Disorder: Facts or Fads? A Scoping Review and a Proposal for a Shared Protocol 51
Functional Evaluation of Eating Difficulties Scale to predict oral motor skills in infants with neurodevelopmental disorders: a longitudinal study 50
Clinical features of adolescents diagnosed with eating disorders and at risk for psychosis 49
Cryptic telomeric rearrangements in subjects with mental retardation associated with dysmorphism and congenital malformations 48
Frontal nonconvulsive status epilepticus associated with high-dose tiagabine therapy in a child with familial bilateral perisylvian polymicrogyria 47
Prognostic Accuracy of DSM-5 Attenuated Psychosis Symptoms in Adolescents: Prospective Real-World 5-Year Cohort Study 45
Clinical, neuroradiological and molecular characterization of cerebellar dysplasia with cysts (Poretti-Boltshauser syndrome) 44
CASK related disorder: Epilepsy and developmental outcome 44
A 2.3Mb duplication of chromosome 8q24.3 associated with severe mental retardation and epilepsy detected by standard karyotype 43
The spectrum of brainstem malformations associated to mutations of the tubulin genes family: MRI and DTI analysis 43
Anterior Mesencephalic Cap Dysplasia: Novel Brain Stem Malformative Features Associated with Joubert Syndrome 42
Pontine tegmental cap dysplasia: developmental and cognitive outcome in three adolescent patients 42
Bilateral frontoparietal polymicrogyria (BFPP) syndrome secondary to a 16q12.1-q21 chromosome deletion involving GPR56 gene 41
From early stress to 12-month development in very preterm infants: Preliminary findings on epigenetic mechanisms and brain growth 41
Molecular mechanisms generating and stabilizing terminal 22q13 deletions in 44 subjects with Phelan/McDermid syndrome. 40
Feasibility of a home-based computerized cognitive training for pediatric patients with congenital or acquired brain damage: An explorative study 40
Prognostic accuracy and clinical utility of psychometric instruments for individuals at clinical high-risk of psychosis: a systematic review and meta-analysis 40
Corrigendum: Perceived Family Functioning Profile in Adolescents at Clinical High Risk for Psychosis: Rigidity as a Possible Preventive Target 39
Cerebellar Damage Affects Contextual Priors for Action Prediction in Patients with Childhood Brain Tumor 39
Effectiveness of Computerized Cognitive Training Programs (CCTP) with Game-like Features in Children with or without Neuropsychological Disorders: a Meta-Analytic Investigation 39
Perceived Family Functioning Profile in Adolescents at Clinical High Risk for Psychosis: Rigidity as a Possible Preventive Target 39
Alone With the Kids: Tele-Medicine for Children With Special Healthcare Needs During COVID-19 Emergency 38
Tubulin genes and malformations of cortical development 38
A de-novo STXBP1 gene mutation in a patient showing the Rett syndrome phenotype 38
Measuring the Outcomes of Maternal COVID-19-related Prenatal Exposure (MOM-COPE): Study protocol for a multicentric longitudinal project 38
Challenges and resources in adult life with Joubert syndrome: issues from an international classification of functioning (ICF) perspective 38
Cognitive rehabilitation in a child with Joubert Syndrome: Developmental trends and adaptive changes in a single case report 37
A novel mutation in the beta-tubulin gene TUBB2B associated with complex malformation of cortical development and deficits in axonal guidance 37
Virtual Reality Social Prediction Improvement and Rehabilitation Intensive Training (VR-SPIRIT) for paediatric patients with congenital cerebellar diseases: Study protocol of a randomised controlled trial 37
The phenotypic spectrum of WWOX -related disorders: 20 additional cases of WOREE syndrome and review of the literature 37
Longitudinal outcome of attenuated positive symptoms, negative symptoms, functioning and remission in people at clinical high risk for psychosis: a meta-analysis 37
Perceived and observed family functioning in adolescents affected by restrictive eating disorders 37
Premature birth affects visual body representation and body schema in preterm children 36
Early brain damage affects body schema and person perception abilities in children and adolescents with spastic diplegia 36
Remote technology-based training programs for children with acquired brain injury: A systematic review and a meta-analytic exploration 36
Basal Ganglia Dysmorphism in Patients With Aicardi Syndrome 36
Refining the mutational spectrum and gene-phenotype correlates in pontocerebellar hypoplasia: Results of a multicentric study 36
ITAlian partnership for psychosis prevention (ITAPP): Improving the mental health of young people 35
Maternal caregiving and DNA methylation in human infants and children: Systematic review 35
Early parenting intervention promotes 24-month psychomotor development in preterm children 35
How social is the cerebellum? Exploring the effects of cerebellar transcranial direct current stimulation on the prediction of social and physical events 35
Facial emotion recognition in Williams syndrome and Down syndrome: A matching and developmental study 35
Aberrant supracallosal longitudinal bundle: MR features, pathogenesis and associated clinical phenotype 35
Visual perception and spatial transformation of the body in children and adolescents with brain tumor 35
Novel TMEM67 Mutations and Genotype-phenotype Correlates in Meckelin-related Ciliopathies 34
Maternal sensitivity is associated with configural processing of infant's cues in preterm and full-term mothers 34
Clinical Characterization, Genetics, and Long-Term Follow-up of a Large Cohort of Patients with Agenesis of the Corpus Callosum 34
Cognitive functioning of pediatric patients with brain tumor: an investigation of the role of gender 34
Diagnostic yield and cost-effectiveness of “dynamic” exome analysis in epilepsy with neurodevelopmental disorders: A tertiary-center experience in Northern Italy 34
Assessing Family Functioning Before and After an Integrated Multidisciplinary Family Treatment for Adolescents With Restrictive Eating Disorders 34
A wide spectrum of clinical, neurophysiological and neuroradiological abnormalities in a family with a novel CACNA1A mutation 33
Non-invasive brain stimulation for the rehabilitation of children and adolescents with neurodevelopmental disorders: A systematic reviewnon-invasive brain stimulation for the rehabilitation of children and adolescents with neurodevelopmental disorders: A systematic review 33
Effectiveness of short-term psychodynamic psychotherapy in preadolescents and adolescents affected by psychiatric disorders 33
Impaired urinary concentration ability is a sensitive predictor of renal disease progression in Joubert syndrome 32
Age and sex prevalence estimate of Joubert syndrome in Italy 32
Brain injury in a healthy child one year after periureteral injection of Teflon 32
Functional genome-wide siRNA screen identifies KIAA0586 as mutated in Joubert syndrome 32
Learning to live without the cerebellum 32
COMTval158met polymorphism is associated with behavioral response and physiologic reactivity to socio-emotional stress in 4-month-old infants 32
Impact of the inversion time on regional brain perfusion estimation with clinical arterial spin labeling protocols 32
Family Dysfunctional Interactive Patterns and Alexithymia in Adolescent Patients with Restrictive Eating Disorders 31
Behavioural features of Italian infants and young adults with Williams-Beuren syndrome 31
Long-term neuropsychological deficits after cerebellar infarctions in two young adult twins 31
Home-based cognitive training in pediatric patients with acquired brain injury: preliminary results on efficacy of a randomized clinical trial 31
Characterizingwhite matter tract organization in polymicrogyria and lissencephaly: A multifiber diffusion mri modeling and tractography study 31
Telomere length and salivary cortisol stress reactivity in very preterm infants 31
A different brain: Anomalies of functional and structural connections in williams syndrome 31
Very preterm birth is associated with PLAGL1 gene hypomethylation at birth and discharge 31
Tubulin-related cerebellar dysplasia: definition of a distinct pattern of cerebellar malformation 30
Infant's emotional variability associated to interactive stressful situation: A novel analysis approach with Sample Entropy and Lempel-Ziv Complexity 30
Pain-related increase in serotonin transporter gene methylation associates with emotional regulation in 4.5-year-old preterm-born children 30
Rating behavioral problems in adolescent eating disorders: Parent-child differences 30
A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardation 29
Checklist for the evaluation of low vision in uncooperative patients 29
Learning and using abstract words: Evidence from clinical populations 29
A categorical approach to infants' individual differences during the Still-Face paradigm 29
SLC6A4 promoter region methylation and socio-emotional stress response in very preterm and full-term infants 29
When one is Enough: Impaired Multisensory Integration in Cerebellar Agenesis 29
Phonological memory updating and developmental dyslexia: The role of long-term knowledge 29
Hidden pandemic: COVID-19-related stress, SLC6A4 methylation, and infants’ temperament at 3 months 29
Neurodevelopmental outcome of Italian preterm ELBW infants: an eleven years single center cohort 28
Retrospective diagnosis of congenital cytomegalovirus infection and cortical maldevelopment - Reply 28
Migraine Symptoms Improvement During the COVID-19 Lockdown in a Cohort of Children and Adolescents 28
Role of the cerebellum in high stages of motor planning hierarchy 28
Mutations in α- and β-tubulin encoding genes: implications in brain malformations 28
Get Your Molar Tooth Right: Joubert Syndrome Misdiagnosis Unmasked by Whole-Exome Sequencing 28
Phenotypic spectrum and prevalence of INPP5E mutations in Joubert Syndrome and related disorders 27
Characterization of mutations in the gene doublecortin in patients with double cortex syndrome 27
Neurological soft signs feature a double dissociation within the language system in Williams syndrome 27
Seizures and EEG patterns in Pallister-Killian syndrome: 13 New Italian patients. 27
Finding a common path to the assessment of persons with intellectual development disorders 27
Does quality of developmental care in NICUs affect health-related quality of life in 5-y-old children born preterm? 27
Pain exposure associates with telomere length erosion in very preterm infants 27
Heterozygous KIF1A variants underlie a wide spectrum of neurodevelopmental and neurodegenerative disorders 27
Maternal and infant NR3C1 and SLC6A4 epigenetic signatures of the COVID-19 pandemic lockdown: when timing matters 26
Sequence memory skills in Spastic Bilateral Cerebral Palsy are age independent as in normally developing children 26
Language and social communication in children with cerebellar dysgenesis 26
Totale 3.543
Categoria #
all - tutte 24.115
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 24.115

Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/20196 0 0 0 0 0 0 0 2 4 0 0 0
2019/2020198 77 93 0 4 0 4 0 4 0 13 2 1
2020/2021303 5 4 1 5 0 83 67 79 11 10 20 18
2021/2022699 7 7 6 3 32 19 12 47 44 10 115 397
2022/20232.852 254 171 40 234 226 273 5 190 1.289 37 83 50
2023/20241.000 93 146 58 58 129 311 115 90 0 0 0 0
Totale 5.150