IRIS
NICOTERA, ANTONIO GENNARO
 Distribuzione geografica
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Continente #
EU - Europa 589
NA - Nord America 502
AS - Asia 177
AF - Africa 4
Totale 1.272
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Nazione #
US - Stati Uniti d'America 498
IE - Irlanda 177
IT - Italia 166
SE - Svezia 129
SG - Singapore 90
CN - Cina 51
DE - Germania 38
FI - Finlandia 28
IN - India 26
GB - Regno Unito 14
PL - Polonia 6
UA - Ucraina 6
BE - Belgio 5
AT - Austria 4
CA - Canada 4
FR - Francia 4
RU - Federazione Russa 3
EG - Egitto 2
GH - Ghana 2
GR - Grecia 2
ID - Indonesia 2
JP - Giappone 2
NL - Olanda 2
VN - Vietnam 2
AE - Emirati Arabi Uniti 1
BG - Bulgaria 1
CH - Svizzera 1
EE - Estonia 1
IR - Iran 1
KR - Corea 1
KZ - Kazakistan 1
LV - Lettonia 1
NO - Norvegia 1
Totale 1.272
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Città #
Dublin 177
Chandler 144
Nyköping 81
Singapore 74
Messina 53
Munich 29
Ashburn 22
Hyderabad 22
New York 20
Helsinki 19
Jacksonville 18
Mascali 17
Medford 17
Princeton 17
Ann Arbor 12
Des Moines 12
Lancaster 12
Cambridge 10
Rome 10
Dearborn 9
Shenyang 8
Woodbridge 8
Biancavilla 7
Catania 7
Houston 7
Los Angeles 7
Beijing 6
Palermo 6
Warsaw 6
Brussels 5
Caltanissetta 4
Jinan 4
Ningbo 4
Ottawa 4
Vienna 4
Wilmington 4
Boardman 3
Chelmsford 3
Hangzhou 3
Hefei 3
Nanchang 3
Naples 3
Seattle 3
Accra 2
Athens 2
Auburn Hills 2
Campi Bisenzio 2
Dong Ket 2
Fairfield 2
Foggia 2
Guidonia 2
Jakarta 2
Kurokami 2
Miami 2
Milazzo 2
Mumbai 2
Pune 2
Reggio Calabria 2
San Mateo 2
San Pietro Clarenza 2
Sannicandro Di Bari 2
Santa Teresa Di Riva 2
Shenzhen 2
Sherbin 2
Sortino 2
Strasbourg 2
Tianjin 2
Valguarnera Caropepe 2
Xian 2
Agira 1
Albany 1
Almaty 1
Amsterdam 1
Ardabil 1
Barga 1
Bedford 1
Belpasso 1
Buffalo 1
Changsha 1
Crotone 1
Gela 1
Haikou 1
Hebei 1
Lanzhou 1
Lausanne 1
Levallois-perret 1
Milan 1
Modica 1
Nanjing 1
Noto 1
Nuremberg 1
Nürnberg 1
Phoenix 1
Prineville 1
Ramacca 1
Redwood City 1
Santa Maria Di Licodia 1
Serra D'aiello 1
Sofia 1
Taizhou 1
Totale 970
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Nome #
De novo mutation in SLC25A22 gene: expansion of the clinical and electroencephalographic phenotype 99
Predictive role of early milestones-related psychomotor profiles and long-term neurodevelopmental pitfalls in preterm infants 89
Oxidative Stress in Obesity: A Critical Component in Human Diseases. 83
Idiopathic Bilateral Relapsing-Remitting Painful Ophthalmoplegia co-occurring with Hashimoto thyroiditis and hyperhomocysteinemia 76
Hyperhomocysteinemia and MTHFR polymorphisms as antenatal risk factors of white matter abnormalities in two cohorts of late preterm and full term newborns 75
Primary nocturnal enuresis in children with allergic rhinitis and severe adenotonsillar hypertrophy: a single center pilot study 73
Cognitive Empowerment with New Technologies Improves Neuropsychological and Neurophysiological Parameters in Rett Syndrome 70
Efficacy of Intravenous Hydrocortisone Treatment in Refractory Neonatal Seizures: A Report on Three Cases 58
DECODIFICA DI FILMATI: ATTENZIONE SELETTIVA E INDICI MNESTICI NELLA SINDROME DI RETT . 55
A Focus on the Cerebellum: From Embryogenesis to an Age-Related Clinical Perspective 53
Verifica di un intervento di potenziamento cognitivo con indici neuropsicologici e neurofisiologici. 51
A Novel Homozygous ALG12 Mutation in a Patient with CDG Type Ig: New Report of a Case with a Mild Phenotype 42
Modifica dei parametri neuropsicologici e neurofisiologici nella sindrome di rett 41
Perampanel treatment in Early-onset Epileptic Encephalopathy with infantile movement disorders associated with a de novo GRIN1 gene mutation: a 3-year follow-up. 37
Epileptic Phenotype and Cannabidiol Efficacy in a Williams–Beuren Syndrome Patient With Atypical Deletion: A Case Report 37
null 36
Long-term predictivity of early neurological assessment and developmental trajectories in low-risk preterm infants 30
The Genetics of Sleep Disorders in Children: A Narrative Review 30
Role of COMT V158M polymorphism in the development of dystonia after administration of antipsychotic drugs 29
LONG-TERM NEUROPSYCHIATRIC FOLLOW-UP IN HYPERPROLINEMIA TYPE 1 28
KCNQ2-Related Neonatal Epilepsy Treated With Vitamin B6: A Report of Two Cases and Literature Review 27
Neonatal Seizures: An Overview of Genetic Causes and Treatment Options 27
Identification of a Novel Missense Mutation of POLR3A Gene in a Cohort of Sicilian Patients with Leukodystrophy 25
Semi-Automatic Analysis of Specific Electroencephalographic Patterns during NREM2 Sleep in a Pediatric Population after SARS-CoV-2 Infection. 23
Overview of Guillain-Barrè Syndrome 23
EFFICACY OF BRIVARACETAM IN PEDIATRIC EPILEPSY: AN UP-TO-DATE 21
Treatment of multiple sclerosis in children: A brief overview 21
Synaptopathies in Developmental and Epileptic Encephalopathies: A Focus on Pre-synaptic Dysfunction 19
Neurotrophins: Expression of Brain-Lung Axis Development 14
Impact of respiratory viral infections during pregnancy on the neurological outcomes of the newborn: current knowledge 11
Fibroblast Growth Factor Receptor 2 (FGFR2), a New Gene Involved in the Genesis of Autism Spectrum Disorder 9
null 9
Impact of the Allergic Therapeutic Adherence in Children with Allergic Rhinitis and ADHD: A Pilot Study 6
PHF21A Related Disorder: Description of a New Case 5
Editorial: Neurodevelopment and preterm birth 5
The Impact of Genetics on Cognition: Insights into Cognitive Disorders and Single Nucleotide Polymorphisms 4
Totale 1.341
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Categoria #
all - tutte 7.169
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 7.169
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202055 0 0 0 0 0 0 20 4 4 22 3 2
2020/202199 24 0 18 2 10 3 5 12 7 12 4 2
2021/2022152 4 27 0 3 2 0 9 4 8 42 9 44
2022/2023501 29 52 20 29 33 52 5 34 216 8 13 10
2023/2024167 12 17 4 9 5 33 10 1 4 35 0 37
2024/2025189 19 4 1 40 42 64 19 0 0 0 0 0
Totale 1.341