IRIS
TERRONE, GAETANO
 Distribuzione geografica
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Continente #
NA - Nord America 1.135
EU - Europa 923
AS - Asia 304
SA - Sud America 23
AF - Africa 18
Continente sconosciuto - Info sul continente non disponibili 1
Totale 2.404
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Nazione #
US - Stati Uniti d'America 1.106
IT - Italia 535
SG - Singapore 153
CN - Cina 126
FR - Francia 100
NL - Olanda 82
UA - Ucraina 38
DE - Germania 37
FI - Finlandia 29
CA - Canada 28
IE - Irlanda 24
PL - Polonia 21
CI - Costa d'Avorio 18
GB - Regno Unito 15
AR - Argentina 14
BG - Bulgaria 14
IN - India 13
RO - Romania 8
VN - Vietnam 8
CO - Colombia 5
ES - Italia 5
BR - Brasile 4
RS - Serbia 4
SE - Svezia 3
BE - Belgio 2
PT - Portogallo 2
AT - Austria 1
CH - Svizzera 1
EU - Europa 1
HU - Ungheria 1
IL - Israele 1
IR - Iran 1
IS - Islanda 1
JP - Giappone 1
KR - Corea 1
MX - Messico 1
Totale 2.404
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Città #
Chandler 269
Singapore 126
Naples 92
Amsterdam 78
Ashburn 75
Millbury 43
Beijing 39
Boston 36
Des Moines 35
Princeton 33
Napoli 32
Nanjing 31
Rome 29
Wilmington 25
Santa Clara 24
Lawrence 23
Kraków 20
Ottawa 18
Norwalk 16
Milan 15
Hebei 14
Boardman 13
Falls Church 13
Sofia 13
Tübingen 12
Florence 11
Nanchang 11
Houston 10
Woodbridge 10
Bologna 9
Procida 9
Washington 9
Dong Ket 8
Shenyang 7
Parma 6
Chiusano di San Domenico 5
Dublin 5
San Nicola la Strada 5
Trieste 5
Ancona 4
Fairfield 4
Jiaxing 4
Lappeenranta 4
Redwood City 4
Villaricca 4
Capriate San Gervasio 3
Casalnuovo Di Napoli 3
Changsha 3
Dallas 3
Edinburgh 3
Frankfurt am Main 3
Kronberg 3
Medellín 3
Padova 3
Pune 3
Salerno 3
Sasso Marconi 3
Solagna 3
Tianjin 3
Toronto 3
Volla 3
Atlanta 2
Barcelona 2
Basiglio 2
Belgrade 2
Berlin 2
Buenos Aires 2
Cambridge 2
Campobasso 2
Casalecchio di Reno 2
Chicago 2
Council Bluffs 2
Dearborn 2
Denver 2
Federal 2
Fisciano 2
Foggia 2
Guwahati 2
Huizhou 2
Indiana 2
Kraljevo 2
Los Angeles 2
Ludhiana 2
Madrid 2
Marseille 2
Marsico Nuovo 2
Mira 2
Montesilvano Marina 2
Nerviano 2
New Delhi 2
Novi Velia 2
Palermo 2
Parker 2
Pedrengo 2
Pesaro 2
Portici 2
Saint-Martin-d'Hères 2
San Antonio De Areco 2
San Chirico Raparo 2
Santarém 2
Totale 1.384
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Nome #
Epilessia frontale con bisincronismo secondario in encefalopatia perinatale 270
Nutritional assessment and intervention in children with cerebral palsy: a practical approach 70
A novel SHANK3 interstitial microdeletion in a family with intellectual disability and brain MRI abnormalities resembling Unidentified Bright Objects. 63
A case of Lennox-Gastaut syndrome in a patient with FOXG1-related disorder 57
A complicated association between two different genetic rare disorders: Cystic Fibrosis and Spinal Muscular Atrophy 55
A further contribution to the delineation of the 17q21.31 microdeletion syndrome: Central nervous involvement in two Italian patients. 54
A case of 14q11.2 microdeletion with autistic features, severe obesity and facial dysmorphisms suggestive of Wolf-Hirschhorn syndrome. 53
Variabilità fenotipica intrafamiliare nella miotonia da mutazioni nel gene CLCN1 52
Deregulation of microtubule organization and RNA metabolism in Arx models for Lissencephaly and developmental epileptic encephalopathy 49
Good cognitive performances in a child with Prader-Willi syndrome. 48
A small 7q11.23 microduplication involving GTF2I in a family with intellectual disability 47
Early onset Charcot-Marie-Tooth neuropathy type 2A and severe developmental delay: expanding the clinical phenotype of MFN2-related neuropathy 46
PP-8 ESOPHAGEAL HIGH RESOLUTION MANOMETRY IN NEUROLOGICALLLY IMPAIRED CHILDREN AND GASTRO-OESOPHAGEAL REFLUX DISEASE 44
Safety for Patients With Celiac Disease of Baked Goods Made of Wheat Flour Hydrolyzed During Food Processing 44
Approcci diagnostico-terapeutici al dolore cronico delle patologie neurodegenerative: l'esempio delle leucodistrofie. 43
COVID-19-associated severe mono-hemispheric encephalitis in a young infant 42
Low-dose amitriptyline-induced acute dystonia in a patient with metachromatic leukodystrophy. 40
Inhibition of monoacylglycerol lipase terminates diazepam-resistant status epilepticus in mice and its effects are potentiated by a ketogenic diet 40
Targeting oxidative stress improves disease outcomes in a rat model of acquired epilepsy 39
The Pediatric Symptom Checklist as screening tool for neurological and psychosocial problems in a paediatric cohort of patients with coeliac disease. 38
De novo PIK3R2 variant causes polymicrogyria, corpus callosum hyperplasia and focal cortical dysplasia 38
Epilepsy in Rett syndrome: can seizures play an encephalopathic effect in this disorder? 38
A further contribution to the delineation of epileptic phenotype in PACS2-related syndrome 37
Epilessia strutturale e malformazione corticale complessa 35
Short wheat challenge is a reproducible in-vivo assay to detect immune response to gluten. 35
Intrafamilial variability in SPTAN1-related disorder: From benign convulsions with mild gastroenteritis to developmental encephalopathy 35
Epilessia da deficit di PNPO: follow-up di 5 anni. 34
Preventing epileptogenesis: A realistic goal? 34
Inflammation and reactive oxygen species as disease modifiers in epilepsy. 34
Changes of dimension of EEG/ECoG nonlinear dynamics predict epileptogenesis and therapy outcomes 33
Heterozygous KIF1A variants underlie a wide spectrum of neurodevelopmental and neurodegenerative disorders 33
Associazione fra disturbo del movimento di tipo coreico, mioclono non corticale multifocale, epilessia e disabilità intellettiva: descrizione di due casi familiari. 32
HLA-related genetic risk for celiac disease. 32
Neuroinflammatory targets and treatments for epilepsy validated in experimental models 31
Bi-allelic loss-of-function variants in PPFIBP1 cause a neurodevelopmental disorder with microcephaly, epilepsy, and periventricular calcifications 30
Descrizione del fenotipo neuroradiologico in due pazienti con sindrome da microdelezione 17q21.31 30
Polimiosite giovanile: descrizione di un caso 30
Diagnosis delay in West syndrome: misdiagnosis and consequences. 30
Heterozygous missense variants of SPTBN2 are a frequent cause of congenital cerebellar ataxia 30
Reply to letter: "Brain MRI abnormalities resembling unidentified bright objects in a patient with Phelan- McDermid syndrome" 30
Inflammation and reactive oxygen species in status epilepticus: Biomarkers and implications for therapy. 30
Expanding the neurological and behavioral phenotype of White-Sutton syndrome: a case report 30
Inflammation and Epilepsy: Preclinical Findings and Potential Clinical Translation 29
Disturbo complesso dello sviluppo corticale ed epilessia strutturale 28
Three de novo DDX3X variants associated with distinctive brain developmental abnormalities and brain tumor in intellectually disabled females. 28
Effects of antiepileptic therapy on bone mineral status evaluated by phalangeal quantitative ultrasound in pediatric patients with epilepsy and motor impairment. 28
Dual diagnosis in a child with familial SCN8A-related encephalopathy complicated by a 1p13.2 deletion involving NRAS gene 28
Contribution of Genetic Test to Early Diagnosis of Methylenetetrahydrofolate Reductase (MTHFR) Deficiency: The Experience of a Reference Center in Southern Italy 27
Cerebellar dentate nuclei swelling: a new and early magnetic resonance imaging finding of beta-propeller protein-associated neurodegeneration 27
The Pediatric Symptom Checklist as screening tool for neurological and psychosocial problems in celiac disease. 26
Mutations in MAST1 Cause Mega-Corpus-Callosum Syndrome with Cerebellar Hypoplasia and Cortical Malformations 25
Expanding the genetic and phenotypic relevance of KCNB1 variants in developmental and epileptic encephalopathies: 27 new patients and overview of the literature. 25
Electroencephalographic findings in ATRX syndrome: A new case series and review of literature 25
Neurometabolic epilepsies: the experience at a one pediatric centre 24
Low-grade tumour over the left temporal neocortex and ictal asystole: network and surgical implications 23
Clinical evolution and epilepsy outcome in three patients with CDKL5-related developmental encephalopathy 22
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. 22
Mild neurological phenotype in a family carrying a novel N-terminal null GRIN2A variant 22
Respiratory phenotypes of neuromuscular diseases: A challenging issue for pediatricians 20
L-serine treatment in patients with GRIN-related encephalopathy: A phase 2A, non-randomized study 19
X-Linked Epilepsies: A Narrative Review 19
Developmental and epilepsy spectrum of KCNB1 encephalopathy with long-term outcome 18
Metabolic stroke-like events in a girl with pyruvate dehydrogenase complex deficiency caused by a novel de novo mutation in PDHA1 18
High Mobility Group Box 1 is a novel pathogenic factor and a mechanistic biomarker for epilepsy 18
DNA methylation episignature and comparative epigenomic profiling of HNRNPU-related neurodevelopmental disorder 16
The Evolving Landscape of Therapeutics for Epilepsy in Tuberous Sclerosis Complex 16
Cholesterol 24-hydroxylase is a novel pharmacological target for anti-ictogenic and disease modification effects in epilepsy 15
A Novel Splicing SCN2A Mutation in an Adolescent With Low-Functioning Autism, Acute Dystonic Movement Disorder, and Late-Onset Generalized Epilepsy 14
Epilepsy phenotypes across the different age-ranges in IQSEC2-related encephalopathy: An Italian multicentre retrospective cohort study 7
Impact and management of drooling in children with neurological disorders: an Italian Delphi consensus 7
A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease 6
Totale 2.517
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Categoria #
all - tutte 10.697
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 10.697
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020129 0 0 0 8 6 16 4 9 20 17 37 12
2020/2021151 19 11 17 8 8 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
2024/2025239 101 106 30 2 0 0 0 0 0 0 0 0
Totale 2.517