SCIUTO, LAURA
 Distribuzione geografica
Continente #
NA - Nord America 290
EU - Europa 187
AS - Asia 105
AF - Africa 52
SA - Sud America 46
Totale 680
Nazione #
US - Stati Uniti d'America 288
IT - Italia 103
SG - Singapore 57
BR - Brasile 41
CN - Cina 34
IE - Irlanda 29
CI - Costa d'Avorio 25
SN - Senegal 17
DE - Germania 14
RU - Federazione Russa 11
FI - Finlandia 10
NG - Nigeria 8
IN - India 5
PL - Polonia 5
AR - Argentina 4
FR - Francia 3
GB - Regno Unito 3
KR - Corea 3
AT - Austria 2
CA - Canada 2
MA - Marocco 2
PT - Portogallo 2
CH - Svizzera 1
CO - Colombia 1
CZ - Repubblica Ceca 1
GR - Grecia 1
HK - Hong Kong 1
IQ - Iraq 1
JP - Giappone 1
KG - Kirghizistan 1
NL - Olanda 1
NP - Nepal 1
SE - Svezia 1
TR - Turchia 1
Totale 680
Città #
Santa Clara 61
Chandler 60
Singapore 43
Chicago 31
Dublin 29
Abidjan 25
Bussero 22
Dallas 21
Civitanova Marche 17
Dakar 17
Catania 11
Hefei 10
Los Angeles 10
Boardman 9
Turku 9
Abuja 8
Andover 8
Beijing 8
Cambridge 8
Lawrence 8
Des Moines 7
Lago 7
Ashburn 6
Bremen 6
Munich 5
Rome 5
Boston 3
Rio De Janeiro 3
Saint Petersburg 3
Seoul 3
São Paulo 3
Braga 2
Brooklyn 2
Curitiba 2
Kochi 2
Riposto 2
Seattle 2
Toronto 2
Abakan 1
Alegrete 1
Alvignano 1
Assaí 1
Barbacena 1
Barra Funda 1
Barra do Choça 1
Betim 1
Birmingham 1
Bishkek 1
Brasília 1
Brno 1
Buenos Aires 1
Campinas 1
Caxias 1
Contagem 1
Erbil 1
Esmeraldas 1
Feliz Natal Municipality 1
Gateshead 1
General Roca 1
Glew 1
Gravataí 1
Helsinki 1
Hong Kong 1
Hortolândia 1
Ipatinga 1
Jatai 1
Juiz de Fora 1
Kathmandu 1
Lagoa da Prata 1
Manchester 1
Maracaju 1
Marrakesh 1
Milan 1
Moscow 1
Mumbai 1
New Delhi 1
New York 1
Nocera Inferiore 1
Orobó 1
Ouro Preto 1
Palhoça 1
Paracatu 1
Paraíba do Sul 1
Paris 1
Pereira 1
Phoenix 1
Piracicaba 1
Pittsburgh 1
Port Jefferson 1
Pouso Alegre 1
Pune 1
Quijingue 1
Quilmes 1
Raleigh 1
Santana do Araguaia 1
Santo André 1
Sombrio 1
Sorocaba 1
São Mateus 1
Tappahannock 1
Totale 542
Nome #
Aristaless-related homeobox (ARX): Epilepsy phenotypes beyond lissencephaly and brain malformations 95
SCN1B gene: A close relative to SCN1A 95
DNM1 Gene and Its Related Epileptic Phenotypes 80
KCNT1-Related Epilepsy: A Review 79
MECP2-related disorders and epilepsy phenotypes 69
Deciphering the invdupdel(8p) genotype–phenotype correlation: Our opinion 68
Slc25a22 and its related epileptic encephalopathies 65
PRRT2 Related Epilepsies: A Gene Review 63
Neonatal seizures as onset of Inborn Errors of Metabolism (IEMs): from diagnosis to treatment. A systematic review 60
At the Basis of Brain Malformations: Brain Plasticity, Developmental Neurobiology, and Considerations for Rehabilitation 23
Totale 697
Categoria #
all - tutte 3.410
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 3.410


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20219 0 0 0 0 0 0 1 0 0 0 8 0
2021/202298 2 8 30 1 10 0 20 3 1 4 0 19
2022/2023153 12 16 0 15 12 17 0 39 27 0 3 12
2023/202482 3 10 4 3 4 24 0 4 9 2 15 4
2024/2025281 4 43 16 50 39 32 9 4 15 25 35 9
2025/202674 33 26 15 0 0 0 0 0 0 0 0 0
Totale 697