IRIS
TERRONE, GAETANO
 Distribuzione geografica
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Continente #
AS - Asia 2.942
NA - Nord America 2.429
EU - Europa 2.322
SA - Sud America 374
AF - Africa 72
OC - Oceania 4
Continente sconosciuto - Info sul continente non disponibili 3
AN - Antartide 1
Totale 8.147
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Nazione #
US - Stati Uniti d'America 2.329
SG - Singapore 1.342
IT - Italia 803
RU - Federazione Russa 761
CN - Cina 611
VN - Vietnam 463
BR - Brasile 287
HK - Hong Kong 204
FR - Francia 189
NL - Olanda 124
DE - Germania 113
GB - Regno Unito 68
CA - Canada 64
IN - India 60
JP - Giappone 57
UA - Ucraina 56
BD - Bangladesh 49
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
CO - Colombia 12
ES - Italia 12
PH - Filippine 12
ID - Indonesia 11
PK - Pakistan 11
RO - Romania 11
TR - Turchia 11
EC - Ecuador 10
LT - Lituania 9
SE - Svezia 9
TH - Thailandia 7
UY - Uruguay 7
CL - Cile 6
AZ - Azerbaigian 5
MA - Marocco 5
PE - Perù 5
RS - Serbia 5
TW - Taiwan 5
VE - Venezuela 5
AE - Emirati Arabi Uniti 4
BE - Belgio 4
EG - Egitto 4
NG - Nigeria 4
PY - Paraguay 4
SA - Arabia Saudita 4
SV - El Salvador 4
TN - Tunisia 4
AU - Australia 3
BO - Bolivia 3
HU - Ungheria 3
IL - Israele 3
IR - Iran 3
JO - Giordania 3
KZ - Kazakistan 3
NP - Nepal 3
TT - Trinidad e Tobago 3
TZ - Tanzania 3
AO - Angola 2
BB - Barbados 2
BH - Bahrain 2
BW - Botswana 2
BZ - Belize 2
CD - Congo 2
ET - Etiopia 2
GE - Georgia 2
KH - Cambogia 2
LA - Repubblica Popolare Democratica del Laos 2
LB - Libano 2
MN - Mongolia 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
CR - Costa Rica 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
JM - Giamaica 1
KE - Kenya 1
KG - Kirghizistan 1
KW - Kuwait 1
LV - Lettonia 1
Totale 8.136
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Città #
Singapore 658
San Jose 322
Chandler 269
Ashburn 219
Hong Kong 194
Moscow 186
Beijing 184
Naples 153
Hefei 139
Ho Chi Minh City 138
Hanoi 114
Santa Clara 109
Amsterdam 85
The Dalles 74
Lauterbourg 69
Los Angeles 57
Tokyo 44
Boston 43
Millbury 43
New York 41
Milan 40
Rome 40
São Paulo 38
Des Moines 36
Dallas 35
Redondo Beach 34
Princeton 33
Nanjing 32
Napoli 32
Buffalo 25
Seoul 25
Wilmington 25
Lawrence 23
Orem 22
Da Nang 20
Haiphong 20
Kraków 20
Ottawa 20
Council Bluffs 19
Nuremberg 19
Denver 18
Houston 18
Bologna 16
Frankfurt am Main 16
Norwalk 16
Munich 15
Sofia 15
Hebei 14
Warsaw 14
Boardman 13
Falls Church 13
Florence 12
Montreal 12
Tübingen 12
Brooklyn 11
Nanchang 11
Seattle 11
Toronto 11
Turku 11
Atlanta 10
Chicago 10
Manchester 10
Mexico City 10
Poplar 10
Washington 10
Woodbridge 10
Dublin 9
Johannesburg 9
London 9
Procida 9
Rio de Janeiro 9
Chennai 8
Dong Ket 8
Helsinki 8
Mumbai 8
Phoenix 8
Bari 7
Belo Horizonte 7
Falkenstein 7
Montevideo 7
Palermo 7
Shenyang 7
Stockholm 7
Turin 7
Afragola 6
Columbus 6
Düsseldorf 6
Guangzhou 6
Parma 6
Ankara 5
Baghdad 5
Biên Hòa 5
Buenos Aires 5
Bình Phước 5
Bắc Ninh 5
Chiusano di San Domenico 5
Porto Alegre 5
Pune 5
San Nicola la Strada 5
Tianjin 5
Totale 4.254
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Nome #
Epilessia frontale con bisincronismo secondario in encefalopatia perinatale 420
Short wheat challenge is a reproducible in-vivo assay to detect immune response to gluten. 173
Nutritional assessment and intervention in children with cerebral palsy: a practical approach 170
A case of Lennox-Gastaut syndrome in a patient with FOXG1-related disorder 161
A complicated association between two different genetic rare disorders: Cystic Fibrosis and Spinal Muscular Atrophy 159
Deregulation of microtubule organization and RNA metabolism in Arx models for Lissencephaly and developmental epileptic encephalopathy 159
Respiratory phenotypes of neuromuscular diseases: A challenging issue for pediatricians 151
Metabolic stroke-like events in a girl with pyruvate dehydrogenase complex deficiency caused by a novel de novo mutation in PDHA1 144
Contribution of Genetic Test to Early Diagnosis of Methylenetetrahydrofolate Reductase (MTHFR) Deficiency: The Experience of a Reference Center in Southern Italy 143
A novel SHANK3 interstitial microdeletion in a family with intellectual disability and brain MRI abnormalities resembling Unidentified Bright Objects. 139
Good cognitive performances in a child with Prader-Willi syndrome. 138
A case of 14q11.2 microdeletion with autistic features, severe obesity and facial dysmorphisms suggestive of Wolf-Hirschhorn syndrome. 137
A small 7q11.23 microduplication involving GTF2I in a family with intellectual disability 137
PP-8 ESOPHAGEAL HIGH RESOLUTION MANOMETRY IN NEUROLOGICALLLY IMPAIRED CHILDREN AND GASTRO-OESOPHAGEAL REFLUX DISEASE 136
X-Linked Epilepsies: A Narrative Review 135
A further contribution to the delineation of the 17q21.31 microdeletion syndrome: Central nervous involvement in two Italian patients. 133
Dual diagnosis in a child with familial SCN8A-related encephalopathy complicated by a 1p13.2 deletion involving NRAS gene 131
COVID-19-associated severe mono-hemispheric encephalitis in a young infant 130
HLA-related genetic risk for celiac disease. 129
Expanding the neurological and behavioral phenotype of White-Sutton syndrome: a case report 127
Early onset Charcot-Marie-Tooth neuropathy type 2A and severe developmental delay: expanding the clinical phenotype of MFN2-related neuropathy 126
Epilessia da deficit di PNPO: follow-up di 5 anni. 122
Safety for Patients With Celiac Disease of Baked Goods Made of Wheat Flour Hydrolyzed During Food Processing 122
Impact and management of drooling in children with neurological disorders: an Italian Delphi consensus 121
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
Epilepsy phenotypes across the different age-ranges in IQSEC2-related encephalopathy: An Italian multicentre retrospective cohort study 119
The Evolving Landscape of Therapeutics for Epilepsy in Tuberous Sclerosis Complex 116
Intrafamilial variability in SPTAN1-related disorder: From benign convulsions with mild gastroenteritis to developmental encephalopathy 115
Bi-allelic loss-of-function variants in PPFIBP1 cause a neurodevelopmental disorder with microcephaly, epilepsy, and periventricular calcifications 112
L-serine treatment in patients with GRIN-related encephalopathy: A phase 2A, non-randomized study 110
Heterozygous KIF1A variants underlie a wide spectrum of neurodevelopmental and neurodegenerative disorders 109
Targeting oxidative stress improves disease outcomes in a rat model of acquired epilepsy 107
Inflammation and Epilepsy: Preclinical Findings and Potential Clinical Translation 107
Variabilità fenotipica intrafamiliare nella miotonia da mutazioni nel gene CLCN1 106
Electroencephalographic findings in ATRX syndrome: A new case series and review of literature 105
Epilepsy in Rett syndrome: can seizures play an encephalopathic effect in this disorder? 104
Developmental and epilepsy spectrum of KCNB1 encephalopathy with long-term outcome 100
Three de novo DDX3X variants associated with distinctive brain developmental abnormalities and brain tumor in intellectually disabled females. 100
Inhibition of monoacylglycerol lipase terminates diazepam-resistant status epilepticus in mice and its effects are potentiated by a ketogenic diet 99
A Novel Splicing SCN2A Mutation in an Adolescent With Low-Functioning Autism, Acute Dystonic Movement Disorder, and Late-Onset Generalized Epilepsy 98
Epilessia strutturale e malformazione corticale complessa 98
Potassium current inactivation as a novel pathomechanism for KCNQ2 developmental and epileptic encephalopathy 97
The Pediatric Symptom Checklist as screening tool for neurological and psychosocial problems in a paediatric cohort of patients with coeliac disease. 91
Effects of antiepileptic therapy on bone mineral status evaluated by phalangeal quantitative ultrasound in pediatric patients with epilepsy and motor impairment. 91
Cannabidiol attenuates epileptic phenotype and increases survival in a mouse model of developmental and epileptic encephalopathy type 88
Mutations in MAST1 Cause Mega-Corpus-Callosum Syndrome with Cerebellar Hypoplasia and Cortical Malformations 87
Cholesterol 24-hydroxylase is a novel pharmacological target for anti-ictogenic and disease modification effects in epilepsy 86
Neuroinflammatory targets and treatments for epilepsy validated in experimental models 86
DNA methylation episignature and comparative epigenomic profiling of HNRNPU-related neurodevelopmental disorder 85
A novel pathogenic variant causing POU3F3-related neurodevelopmental disorder in a child presenting with infantile epileptic spasms syndrome: Expanding the epileptic phenotype 84
De novo PIK3R2 variant causes polymicrogyria, corpus callosum hyperplasia and focal cortical dysplasia 84
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. 84
Disturbo complesso dello sviluppo corticale ed epilessia strutturale 82
Inflammation and reactive oxygen species as disease modifiers in epilepsy. 82
Descrizione del fenotipo neuroradiologico in due pazienti con sindrome da microdelezione 17q21.31 81
A further contribution to the delineation of epileptic phenotype in PACS2-related syndrome 81
Low-grade tumour over the left temporal neocortex and ictal asystole: network and surgical implications 81
Mild neurological phenotype in a family carrying a novel N-terminal null GRIN2A variant 81
Preventing epileptogenesis: A realistic goal? 79
Reply to letter: "Brain MRI abnormalities resembling unidentified bright objects in a patient with Phelan- McDermid syndrome" 77
Heterozygous missense variants of SPTBN2 are a frequent cause of congenital cerebellar ataxia 76
Inflammation and reactive oxygen species in status epilepticus: Biomarkers and implications for therapy. 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
The Pediatric Symptom Checklist as screening tool for neurological and psychosocial problems in celiac disease. 74
Changes of dimension of EEG/ECoG nonlinear dynamics predict epileptogenesis and therapy outcomes 74
Neurological and psychiatric phenotype of a multicenter cohort of patients with SETD5-related neurodevelopmental disorder 73
Cerebellar dentate nuclei swelling: a new and early magnetic resonance imaging finding of beta-propeller protein-associated neurodegeneration 73
Diagnosis delay in West syndrome: misdiagnosis and consequences. 71
Neurometabolic epilepsies: the experience at a one pediatric centre 70
Expanding the genetic and phenotypic relevance of KCNB1 variants in developmental and epileptic encephalopathies: 27 new patients and overview of the literature. 67
Clinical evolution and epilepsy outcome in three patients with CDKL5-related developmental encephalopathy 64
High Mobility Group Box 1 is a novel pathogenic factor and a mechanistic biomarker for epilepsy 58
Deletion Testing of the DEGS1 Gene Should Be Part of the Diagnostic Pipeline for Hypomyelinating Leukodystrophy (HLD18) 58
A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease 56
Reanalysis of Undiagnosed Neurodevelopmental Disorder Cases: From RNU4-2 Variants to Clinical Phenotypes 23
Single nucleotide variants in UNC13C associated with neurodevelopmental disorders affect ethanol sensitivity in Drosophila 10
Totale 8.267
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Categoria #
all - tutte 25.481
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 25.481
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202118 0 0 0 0 0 0 0 0 0 0 7 11
2021/2022364 3 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
2025/20263.964 454 345 392 430 643 181 364 358 426 226 145 0
Totale 8.267