IRIS
TERRONE, GAETANO
 Distribuzione geografica
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Continente #
AS - Asia 2.205
EU - Europa 2.133
NA - Nord America 1.825
SA - Sud America 347
AF - Africa 64
Continente sconosciuto - Info sul continente non disponibili 3
OC - Oceania 3
AN - Antartide 1
Totale 6.581
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Nazione #
US - Stati Uniti d'America 1.749
SG - Singapore 1.201
RU - Federazione Russa 760
IT - Italia 722
CN - Cina 544
BR - Brasile 275
HK - Hong Kong 184
FR - Francia 119
NL - Olanda 118
VN - Vietnam 109
DE - Germania 103
GB - Regno Unito 59
UA - Ucraina 54
CA - Canada 48
FI - Finlandia 47
IN - India 37
PL - Polonia 37
AR - Argentina 31
KR - Corea 28
IE - Irlanda 27
CI - Costa d'Avorio 19
JP - Giappone 19
MX - Messico 19
BG - Bulgaria 15
ZA - Sudafrica 15
BD - Bangladesh 14
AT - Austria 13
CO - Colombia 12
IQ - Iraq 11
RO - Romania 11
EC - Ecuador 10
ES - Italia 10
TR - Turchia 10
LT - Lituania 9
SE - Svezia 9
ID - Indonesia 8
UY - Uruguay 7
MA - Marocco 5
PK - Pakistan 5
RS - Serbia 5
BE - Belgio 4
AE - Emirati Arabi Uniti 3
AZ - Azerbaigian 3
CL - Cile 3
EG - Egitto 3
IL - Israele 3
IR - Iran 3
KZ - Kazakistan 3
NG - Nigeria 3
PE - Perù 3
VE - Venezuela 3
AU - Australia 2
BH - Bahrain 2
BO - Bolivia 2
BW - Botswana 2
CD - Congo 2
ET - Etiopia 2
HU - Ungheria 2
JO - Giordania 2
LA - Repubblica Popolare Democratica del Laos 2
LB - Libano 2
PS - Palestinian Territory 2
PT - Portogallo 2
SA - Arabia Saudita 2
SV - El Salvador 2
TN - Tunisia 2
TT - Trinidad e Tobago 2
UZ - Uzbekistan 2
AO - Angola 1
AQ - Antartide 1
BB - Barbados 1
BJ - Benin 1
BY - Bielorussia 1
BZ - Belize 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
IS - Islanda 1
KE - Kenya 1
KG - Kirghizistan 1
LV - Lettonia 1
LY - Libia 1
MD - Moldavia 1
MK - Macedonia 1
MN - Mongolia 1
MW - Malawi 1
NE - Niger 1
PH - Filippine 1
PY - Paraguay 1
SI - Slovenia 1
SN - Senegal 1
TH - Thailandia 1
TJ - Tagikistan 1
TW - Taiwan 1
TZ - Tanzania 1
WS - Samoa 1
Totale 6.578
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Città #
Singapore 565
Chandler 269
Moscow 186
Hong Kong 184
Beijing 178
Ashburn 160
Naples 140
Hefei 139
Santa Clara 105
Amsterdam 83
Los Angeles 52
Ho Chi Minh City 45
Boston 43
Millbury 43
Rome 37
São Paulo 36
Dallas 35
Des Moines 35
Redondo Beach 34
Princeton 33
Nanjing 32
Napoli 32
Milan 28
New York 25
Seoul 25
Wilmington 25
Buffalo 24
Lawrence 23
The Dalles 22
Kraków 20
Denver 18
Nuremberg 18
Ottawa 18
Norwalk 16
Bologna 15
Hanoi 15
Houston 15
Munich 15
Hebei 14
Sofia 14
Warsaw 14
Boardman 13
Falls Church 13
Orem 12
Tübingen 12
Florence 11
Nanchang 11
Turku 11
Brooklyn 10
Frankfurt am Main 10
Seattle 10
Tokyo 10
Washington 10
Woodbridge 10
Mexico City 9
Montreal 9
Poplar 9
Procida 9
Rio de Janeiro 9
Atlanta 8
Chicago 8
Dong Ket 8
Helsinki 8
Johannesburg 8
London 8
Toronto 8
Belo Horizonte 7
Council Bluffs 7
Dublin 7
Falkenstein 7
Montevideo 7
Shenyang 7
Stockholm 7
Afragola 6
Columbus 6
Da Nang 6
Düsseldorf 6
Guangzhou 6
Haiphong 6
Manchester 6
Parma 6
Phoenix 6
Ankara 5
Bari 5
Chennai 5
Chiusano di San Domenico 5
Mumbai 5
Porto Alegre 5
San Nicola la Strada 5
Tianjin 5
Trieste 5
Ancona 4
Buenos Aires 4
Bắc Ninh 4
Fairfield 4
Francica 4
Genoa 4
Guarulhos 4
Guayaquil 4
Jiaxing 4
Totale 3.258
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Nome #
Epilessia frontale con bisincronismo secondario in encefalopatia perinatale 389
Short wheat challenge is a reproducible in-vivo assay to detect immune response to gluten. 147
Nutritional assessment and intervention in children with cerebral palsy: a practical approach 140
Deregulation of microtubule organization and RNA metabolism in Arx models for Lissencephaly and developmental epileptic encephalopathy 139
A case of Lennox-Gastaut syndrome in a patient with FOXG1-related disorder 137
A complicated association between two different genetic rare disorders: Cystic Fibrosis and Spinal Muscular Atrophy 135
Metabolic stroke-like events in a girl with pyruvate dehydrogenase complex deficiency caused by a novel de novo mutation in PDHA1 123
A small 7q11.23 microduplication involving GTF2I in a family with intellectual disability 120
Contribution of Genetic Test to Early Diagnosis of Methylenetetrahydrofolate Reductase (MTHFR) Deficiency: The Experience of a Reference Center in Southern Italy 118
Respiratory phenotypes of neuromuscular diseases: A challenging issue for pediatricians 117
A case of 14q11.2 microdeletion with autistic features, severe obesity and facial dysmorphisms suggestive of Wolf-Hirschhorn syndrome. 116
A novel SHANK3 interstitial microdeletion in a family with intellectual disability and brain MRI abnormalities resembling Unidentified Bright Objects. 116
A further contribution to the delineation of the 17q21.31 microdeletion syndrome: Central nervous involvement in two Italian patients. 114
HLA-related genetic risk for celiac disease. 111
Good cognitive performances in a child with Prader-Willi syndrome. 110
PP-8 ESOPHAGEAL HIGH RESOLUTION MANOMETRY IN NEUROLOGICALLLY IMPAIRED CHILDREN AND GASTRO-OESOPHAGEAL REFLUX DISEASE 110
Early onset Charcot-Marie-Tooth neuropathy type 2A and severe developmental delay: expanding the clinical phenotype of MFN2-related neuropathy 106
COVID-19-associated severe mono-hemispheric encephalitis in a young infant 106
Epilessia da deficit di PNPO: follow-up di 5 anni. 104
Dual diagnosis in a child with familial SCN8A-related encephalopathy complicated by a 1p13.2 deletion involving NRAS gene 103
Bi-allelic loss-of-function variants in PPFIBP1 cause a neurodevelopmental disorder with microcephaly, epilepsy, and periventricular calcifications 101
Low-dose amitriptyline-induced acute dystonia in a patient with metachromatic leukodystrophy. 101
Safety for Patients With Celiac Disease of Baked Goods Made of Wheat Flour Hydrolyzed During Food Processing 100
Expanding the neurological and behavioral phenotype of White-Sutton syndrome: a case report 99
X-Linked Epilepsies: A Narrative Review 98
The Evolving Landscape of Therapeutics for Epilepsy in Tuberous Sclerosis Complex 97
Intrafamilial variability in SPTAN1-related disorder: From benign convulsions with mild gastroenteritis to developmental encephalopathy 97
Epilepsy phenotypes across the different age-ranges in IQSEC2-related encephalopathy: An Italian multicentre retrospective cohort study 95
Approcci diagnostico-terapeutici al dolore cronico delle patologie neurodegenerative: l'esempio delle leucodistrofie. 95
Variabilità fenotipica intrafamiliare nella miotonia da mutazioni nel gene CLCN1 94
L-serine treatment in patients with GRIN-related encephalopathy: A phase 2A, non-randomized study 93
Targeting oxidative stress improves disease outcomes in a rat model of acquired epilepsy 93
Epilepsy in Rett syndrome: can seizures play an encephalopathic effect in this disorder? 90
Impact and management of drooling in children with neurological disorders: an Italian Delphi consensus 88
Heterozygous KIF1A variants underlie a wide spectrum of neurodevelopmental and neurodegenerative disorders 82
Electroencephalographic findings in ATRX syndrome: A new case series and review of literature 82
A Novel Splicing SCN2A Mutation in an Adolescent With Low-Functioning Autism, Acute Dystonic Movement Disorder, and Late-Onset Generalized Epilepsy 81
Potassium current inactivation as a novel pathomechanism for KCNQ2 developmental and epileptic encephalopathy 78
The Pediatric Symptom Checklist as screening tool for neurological and psychosocial problems in a paediatric cohort of patients with coeliac disease. 77
Cholesterol 24-hydroxylase is a novel pharmacological target for anti-ictogenic and disease modification effects in epilepsy 75
Epilessia strutturale e malformazione corticale complessa 75
De novo PIK3R2 variant causes polymicrogyria, corpus callosum hyperplasia and focal cortical dysplasia 75
Three de novo DDX3X variants associated with distinctive brain developmental abnormalities and brain tumor in intellectually disabled females. 75
Inhibition of monoacylglycerol lipase terminates diazepam-resistant status epilepticus in mice and its effects are potentiated by a ketogenic diet 74
Effects of antiepileptic therapy on bone mineral status evaluated by phalangeal quantitative ultrasound in pediatric patients with epilepsy and motor impairment. 72
DNA methylation episignature and comparative epigenomic profiling of HNRNPU-related neurodevelopmental disorder 71
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. 71
Disturbo complesso dello sviluppo corticale ed epilessia strutturale 70
Neuroinflammatory targets and treatments for epilepsy validated in experimental models 68
Descrizione del fenotipo neuroradiologico in due pazienti con sindrome da microdelezione 17q21.31 67
Polimiosite giovanile: descrizione di un caso 67
A further contribution to the delineation of epileptic phenotype in PACS2-related syndrome 67
Developmental and epilepsy spectrum of KCNB1 encephalopathy with long-term outcome 66
The Pediatric Symptom Checklist as screening tool for neurological and psychosocial problems in celiac disease. 66
Heterozygous missense variants of SPTBN2 are a frequent cause of congenital cerebellar ataxia 64
Inflammation and reactive oxygen species in status epilepticus: Biomarkers and implications for therapy. 64
Inflammation and reactive oxygen species as disease modifiers in epilepsy. 63
Associazione fra disturbo del movimento di tipo coreico, mioclono non corticale multifocale, epilessia e disabilità intellettiva: descrizione di due casi familiari. 62
Diagnosis delay in West syndrome: misdiagnosis and consequences. 62
Reply to letter: "Brain MRI abnormalities resembling unidentified bright objects in a patient with Phelan- McDermid syndrome" 62
Mutations in MAST1 Cause Mega-Corpus-Callosum Syndrome with Cerebellar Hypoplasia and Cortical Malformations 62
Neurometabolic epilepsies: the experience at a one pediatric centre 61
Preventing epileptogenesis: A realistic goal? 61
Cerebellar dentate nuclei swelling: a new and early magnetic resonance imaging finding of beta-propeller protein-associated neurodegeneration 61
Inflammation and Epilepsy: Preclinical Findings and Potential Clinical Translation 60
Low-grade tumour over the left temporal neocortex and ictal asystole: network and surgical implications 60
Mild neurological phenotype in a family carrying a novel N-terminal null GRIN2A variant 60
Neurological and psychiatric phenotype of a multicenter cohort of patients with SETD5-related neurodevelopmental disorder 59
Changes of dimension of EEG/ECoG nonlinear dynamics predict epileptogenesis and therapy outcomes 59
A novel pathogenic variant causing POU3F3-related neurodevelopmental disorder in a child presenting with infantile epileptic spasms syndrome: Expanding the epileptic phenotype 57
Expanding the genetic and phenotypic relevance of KCNB1 variants in developmental and epileptic encephalopathies: 27 new patients and overview of the literature. 53
Cannabidiol attenuates epileptic phenotype and increases survival in a mouse model of developmental and epileptic encephalopathy type 51
Clinical evolution and epilepsy outcome in three patients with CDKL5-related developmental encephalopathy 47
High Mobility Group Box 1 is a novel pathogenic factor and a mechanistic biomarker for epilepsy 45
A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease 35
Deletion Testing of the DEGS1 Gene Should Be Part of the Diagnostic Pipeline for Hypomyelinating Leukodystrophy (HLD18) 20
Reanalysis of Undiagnosed Neurodevelopmental Disorder Cases: From RNU4-2 Variants to Clinical Phenotypes 11
Totale 6.700
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Categoria #
all - tutte 21.818
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 21.818
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202188 0 0 0 0 0 25 7 11 21 6 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
2025/20262.397 454 345 392 430 643 133 0 0 0 0 0 0
Totale 6.700