IRIS
TERRONE, GAETANO
 Distribuzione geografica
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Continente #
AS - Asia 3.004
NA - Nord America 2.582
EU - Europa 2.378
SA - Sud America 384
Continente sconosciuto - Info sul continente non disponibili 123
AF - Africa 73
OC - Oceania 4
AN - Antartide 1
Totale 8.549
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Nazione #
US - Stati Uniti d'America 2.469
SG - Singapore 1.344
IT - Italia 852
RU - Federazione Russa 761
CN - Cina 625
VN - Vietnam 464
BR - Brasile 292
HK - Hong Kong 205
FR - Francia 194
NL - Olanda 124
DE - Germania 113
BD - Bangladesh 85
CA - Canada 72
GB - Regno Unito 69
IN - India 61
JP - Giappone 58
UA - Ucraina 56
FI - Finlandia 47
PL - Polonia 38
AR - Argentina 35
KR - Corea 33
IE - Irlanda 29
MX - Messico 21
CI - Costa d'Avorio 19
IQ - Iraq 18
BG - Bulgaria 16
ZA - Sudafrica 16
AT - Austria 13
EC - Ecuador 13
ID - Indonesia 13
CO - Colombia 12
ES - Italia 12
PH - Filippine 12
RO - Romania 12
TR - Turchia 12
PK - Pakistan 11
LT - Lituania 9
SE - Svezia 9
CL - Cile 7
TH - Thailandia 7
UY - Uruguay 7
PE - Perù 6
AZ - Azerbaigian 5
MA - Marocco 5
RS - Serbia 5
SV - El Salvador 5
TW - Taiwan 5
VE - Venezuela 5
AE - Emirati Arabi Uniti 4
BE - Belgio 4
EG - Egitto 4
NG - Nigeria 4
NP - Nepal 4
PY - Paraguay 4
SA - Arabia Saudita 4
TN - Tunisia 4
AU - Australia 3
BO - Bolivia 3
BZ - Belize 3
HU - Ungheria 3
IL - Israele 3
IR - Iran 3
JO - Giordania 3
KZ - Kazakistan 3
TT - Trinidad e Tobago 3
TZ - Tanzania 3
AO - Angola 2
BB - Barbados 2
BH - Bahrain 2
BW - Botswana 2
CD - Congo 2
CR - Costa Rica 2
ET - Etiopia 2
GE - Georgia 2
JM - Giamaica 2
KH - Cambogia 2
LA - Repubblica Popolare Democratica del Laos 2
LB - Libano 2
MN - Mongolia 2
MY - Malesia 2
PS - Palestinian Territory 2
PT - Portogallo 2
SI - Slovenia 2
UZ - Uzbekistan 2
AL - Albania 1
AM - Armenia 1
AQ - Antartide 1
BJ - Benin 1
BY - Bielorussia 1
CH - Svizzera 1
CV - Capo Verde 1
CW - ???statistics.table.value.countryCode.CW??? 1
EU - Europa 1
GT - Guatemala 1
HN - Honduras 1
HR - Croazia 1
IS - Islanda 1
KE - Kenya 1
KG - Kirghizistan 1
KW - Kuwait 1
Totale 8.415
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Città #
Singapore 659
San Jose 335
Chandler 269
Ashburn 242
Hong Kong 195
Moscow 186
Beijing 185
Naples 154
Hefei 139
Ho Chi Minh City 139
Santa Clara 119
Hanoi 114
Amsterdam 85
The Dalles 74
Lauterbourg 69
Los Angeles 62
Milan 47
Rome 45
Tokyo 44
Boston 43
Millbury 43
New York 43
São Paulo 39
Dallas 37
Des Moines 36
Redondo Beach 34
Princeton 33
Nanjing 32
Napoli 32
Council Bluffs 28
Buffalo 25
Seoul 25
Wilmington 25
Lawrence 23
Orem 22
Da Nang 20
Haiphong 20
Kraków 20
Ottawa 20
Denver 19
Nuremberg 19
Houston 18
Bologna 16
Frankfurt am Main 16
Norwalk 16
Munich 15
Sofia 15
Hebei 14
Warsaw 14
Boardman 13
Falls Church 13
Montreal 13
Toronto 13
Brooklyn 12
Florence 12
Tübingen 12
Atlanta 11
Chicago 11
London 11
Nanchang 11
Seattle 11
Turku 11
Woodbridge 11
Manchester 10
Mexico City 10
Phoenix 10
Poplar 10
Washington 10
Dublin 9
Johannesburg 9
Procida 9
Rio de Janeiro 9
Turin 9
Bari 8
Chennai 8
Dong Ket 8
Helsinki 8
Mumbai 8
Belo Horizonte 7
Falkenstein 7
Guangzhou 7
Montevideo 7
Palermo 7
Shenyang 7
Stockholm 7
Afragola 6
Columbus 6
Düsseldorf 6
Parma 6
Quito 6
Reggio Emilia 6
Tianjin 6
Ankara 5
Baghdad 5
Biên Hòa 5
Buenos Aires 5
Bình Phước 5
Bắc Ninh 5
Chiusano di San Domenico 5
Genoa 5
Totale 4.355
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Nome #
Epilessia frontale con bisincronismo secondario in encefalopatia perinatale 423
Short wheat challenge is a reproducible in-vivo assay to detect immune response to gluten. 175
Nutritional assessment and intervention in children with cerebral palsy: a practical approach 172
A case of Lennox-Gastaut syndrome in a patient with FOXG1-related disorder 163
A complicated association between two different genetic rare disorders: Cystic Fibrosis and Spinal Muscular Atrophy 162
Deregulation of microtubule organization and RNA metabolism in Arx models for Lissencephaly and developmental epileptic encephalopathy 162
Respiratory phenotypes of neuromuscular diseases: A challenging issue for pediatricians 155
Contribution of Genetic Test to Early Diagnosis of Methylenetetrahydrofolate Reductase (MTHFR) Deficiency: The Experience of a Reference Center in Southern Italy 148
Metabolic stroke-like events in a girl with pyruvate dehydrogenase complex deficiency caused by a novel de novo mutation in PDHA1 147
X-Linked Epilepsies: A Narrative Review 142
A small 7q11.23 microduplication involving GTF2I in a family with intellectual disability 141
A case of 14q11.2 microdeletion with autistic features, severe obesity and facial dysmorphisms suggestive of Wolf-Hirschhorn syndrome. 140
A novel SHANK3 interstitial microdeletion in a family with intellectual disability and brain MRI abnormalities resembling Unidentified Bright Objects. 140
Good cognitive performances in a child with Prader-Willi syndrome. 138
A further contribution to the delineation of the 17q21.31 microdeletion syndrome: Central nervous involvement in two Italian patients. 137
PP-8 ESOPHAGEAL HIGH RESOLUTION MANOMETRY IN NEUROLOGICALLLY IMPAIRED CHILDREN AND GASTRO-OESOPHAGEAL REFLUX DISEASE 137
Dual diagnosis in a child with familial SCN8A-related encephalopathy complicated by a 1p13.2 deletion involving NRAS gene 133
Expanding the neurological and behavioral phenotype of White-Sutton syndrome: a case report 132
COVID-19-associated severe mono-hemispheric encephalitis in a young infant 132
Early onset Charcot-Marie-Tooth neuropathy type 2A and severe developmental delay: expanding the clinical phenotype of MFN2-related neuropathy 131
HLA-related genetic risk for celiac disease. 129
Intrafamilial variability in SPTAN1-related disorder: From benign convulsions with mild gastroenteritis to developmental encephalopathy 127
Epilepsy phenotypes across the different age-ranges in IQSEC2-related encephalopathy: An Italian multicentre retrospective cohort study 126
Impact and management of drooling in children with neurological disorders: an Italian Delphi consensus 126
Epilessia da deficit di PNPO: follow-up di 5 anni. 125
Safety for Patients With Celiac Disease of Baked Goods Made of Wheat Flour Hydrolyzed During Food Processing 123
Potassium current inactivation as a novel pathomechanism for KCNQ2 developmental and epileptic encephalopathy 121
The Evolving Landscape of Therapeutics for Epilepsy in Tuberous Sclerosis Complex 120
Approcci diagnostico-terapeutici al dolore cronico delle patologie neurodegenerative: l'esempio delle leucodistrofie. 120
Low-dose amitriptyline-induced acute dystonia in a patient with metachromatic leukodystrophy. 120
L-serine treatment in patients with GRIN-related encephalopathy: A phase 2A, non-randomized study 118
Bi-allelic loss-of-function variants in PPFIBP1 cause a neurodevelopmental disorder with microcephaly, epilepsy, and periventricular calcifications 114
Inflammation and Epilepsy: Preclinical Findings and Potential Clinical Translation 113
Heterozygous KIF1A variants underlie a wide spectrum of neurodevelopmental and neurodegenerative disorders 110
Developmental and epilepsy spectrum of KCNB1 encephalopathy with long-term outcome 109
Targeting oxidative stress improves disease outcomes in a rat model of acquired epilepsy 109
Variabilità fenotipica intrafamiliare nella miotonia da mutazioni nel gene CLCN1 106
Epilepsy in Rett syndrome: can seizures play an encephalopathic effect in this disorder? 106
Electroencephalographic findings in ATRX syndrome: A new case series and review of literature 105
Three de novo DDX3X variants associated with distinctive brain developmental abnormalities and brain tumor in intellectually disabled females. 102
A Novel Splicing SCN2A Mutation in an Adolescent With Low-Functioning Autism, Acute Dystonic Movement Disorder, and Late-Onset Generalized Epilepsy 101
Epilessia strutturale e malformazione corticale complessa 100
Inhibition of monoacylglycerol lipase terminates diazepam-resistant status epilepticus in mice and its effects are potentiated by a ketogenic diet 99
Cannabidiol attenuates epileptic phenotype and increases survival in a mouse model of developmental and epileptic encephalopathy type 94
Cholesterol 24-hydroxylase is a novel pharmacological target for anti-ictogenic and disease modification effects in epilepsy 94
The Pediatric Symptom Checklist as screening tool for neurological and psychosocial problems in a paediatric cohort of patients with coeliac disease. 93
Effects of antiepileptic therapy on bone mineral status evaluated by phalangeal quantitative ultrasound in pediatric patients with epilepsy and motor impairment. 93
A novel pathogenic variant causing POU3F3-related neurodevelopmental disorder in a child presenting with infantile epileptic spasms syndrome: Expanding the epileptic phenotype 92
Mutations in MAST1 Cause Mega-Corpus-Callosum Syndrome with Cerebellar Hypoplasia and Cortical Malformations 90
DNA methylation episignature and comparative epigenomic profiling of HNRNPU-related neurodevelopmental disorder 87
Neurological and psychiatric phenotype of a multicenter cohort of patients with SETD5-related neurodevelopmental disorder 86
Neuroinflammatory targets and treatments for epilepsy validated in experimental models 86
Inflammation and reactive oxygen species as disease modifiers in epilepsy. 86
Use of nutritional supplements based on melatonin, tryptophan and vitamin B6 in children with primary chronic headache, with or without sleep disorders: a pilot study. 86
De novo PIK3R2 variant causes polymicrogyria, corpus callosum hyperplasia and focal cortical dysplasia 85
Disturbo complesso dello sviluppo corticale ed epilessia strutturale 84
Mild neurological phenotype in a family carrying a novel N-terminal null GRIN2A variant 84
Descrizione del fenotipo neuroradiologico in due pazienti con sindrome da microdelezione 17q21.31 83
A further contribution to the delineation of epileptic phenotype in PACS2-related syndrome 83
Low-grade tumour over the left temporal neocortex and ictal asystole: network and surgical implications 81
Preventing epileptogenesis: A realistic goal? 80
Heterozygous missense variants of SPTBN2 are a frequent cause of congenital cerebellar ataxia 79
The Pediatric Symptom Checklist as screening tool for neurological and psychosocial problems in celiac disease. 78
Reply to letter: "Brain MRI abnormalities resembling unidentified bright objects in a patient with Phelan- McDermid syndrome" 77
Changes of dimension of EEG/ECoG nonlinear dynamics predict epileptogenesis and therapy outcomes 77
Inflammation and reactive oxygen species in status epilepticus: Biomarkers and implications for therapy. 77
Cerebellar dentate nuclei swelling: a new and early magnetic resonance imaging finding of beta-propeller protein-associated neurodegeneration 76
Associazione fra disturbo del movimento di tipo coreico, mioclono non corticale multifocale, epilessia e disabilità intellettiva: descrizione di due casi familiari. 75
Polimiosite giovanile: descrizione di un caso 74
Diagnosis delay in West syndrome: misdiagnosis and consequences. 74
Deletion Testing of the DEGS1 Gene Should Be Part of the Diagnostic Pipeline for Hypomyelinating Leukodystrophy (HLD18) 74
Expanding the genetic and phenotypic relevance of KCNB1 variants in developmental and epileptic encephalopathies: 27 new patients and overview of the literature. 71
Clinical evolution and epilepsy outcome in three patients with CDKL5-related developmental encephalopathy 70
Neurometabolic epilepsies: the experience at a one pediatric centre 70
A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease 66
High Mobility Group Box 1 is a novel pathogenic factor and a mechanistic biomarker for epilepsy 59
Reanalysis of Undiagnosed Neurodevelopmental Disorder Cases: From RNU4-2 Variants to Clinical Phenotypes 27
Single nucleotide variants in UNC13C associated with neurodevelopmental disorders affect ethanol sensitivity in Drosophila 19
Totale 8.549
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Categoria #
all - tutte 27.556
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 27.556
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022361 0 1 21 17 8 16 13 11 26 34 76 138
2022/2023680 66 31 35 79 87 84 1 57 110 88 33 9
2023/2024469 26 70 69 27 25 45 13 51 12 14 73 44
2024/20252.025 101 106 30 35 73 117 205 158 155 255 593 197
2025/20264.088 454 345 392 430 643 181 364 358 426 226 149 120
2026/2027158 133 25 0 0 0 0 0 0 0 0 0 0
Totale 8.549