DILENA, ROBERTINO
 Distribuzione geografica
Continente #
EU - Europa 855
AS - Asia 149
NA - Nord America 91
SA - Sud America 7
AF - Africa 2
Totale 1.104
Nazione #
IT - Italia 836
US - Stati Uniti d'America 82
SG - Singapore 51
CN - Cina 42
VN - Vietnam 28
BD - Bangladesh 16
FR - Francia 9
BR - Brasile 6
DE - Germania 5
MX - Messico 4
CA - Canada 3
HK - Hong Kong 3
GB - Regno Unito 2
JM - Giamaica 2
JP - Giappone 2
SE - Svezia 2
EC - Ecuador 1
FI - Finlandia 1
ID - Indonesia 1
IN - India 1
IQ - Iraq 1
KH - Cambogia 1
PK - Pakistan 1
SA - Arabia Saudita 1
TH - Thailandia 1
TN - Tunisia 1
ZA - Sudafrica 1
Totale 1.104
Città #
Genoa 336
Genova 277
Rapallo 111
Vado Ligure 92
San Jose 25
Singapore 15
New York 12
Beijing 10
Ho Chi Minh City 9
Lauterbourg 8
Hanoi 7
Rome 6
Frankfurt am Main 5
Ashburn 4
Haiphong 4
Santa Clara 4
Hong Kong 3
Mexico City 3
Atlanta 2
Bordighera 2
Buffalo 2
City of London 2
Council Bluffs 2
Stockholm 2
Tokyo 2
Turin 2
Ahmedabad 1
Baghdad 1
Bari 1
Biên Hòa 1
Brampton 1
Bến Cầu 1
Campinas 1
Campo Grande 1
Canton 1
Cape Town 1
Capim Grosso 1
Da Nang 1
Delano 1
Gricignano di Aversa 1
Helsinki 1
Itaocara 1
Jeddah 1
Kingston 1
Lagoa Vermelha 1
Lahore 1
Los Angeles 1
Macerata 1
Martínez de la Torre 1
Monroe 1
Myrtle Beach 1
Naples 1
Neptune City 1
Parambu 1
Paris 1
Phnom Penh 1
Phú Thọ 1
Quito 1
Rach Gia 1
Reno 1
Saint John 1
Salerno 1
San Donà di Piave 1
San Marzano di San Giuseppe 1
San Tan Valley 1
Spring 1
St Louis 1
Surin 1
Trento 1
Tunis 1
Tân Tiến 1
Vicenza 1
Virginia Beach 1
Warrenton 1
Winnipeg 1
Xi'an 1
Totale 997
Nome #
STXBP1 Encephalopathy: A Neurodevelopmental Disorder Including Epilepsy 161
Dramatic effect of levetiracetam in early-onset epileptic encephalopathy due to STXBP1 mutation 150
Efficacy of sodium channel blockers in SCN2A early infantile epileptic encephalopathy 126
Epilepsy Course and Developmental Trajectories in STXBP1-DEE 106
“EPINEO” Monocentric Retrospective Study on Neonatal Seizures: Incidence, ILAE Seizure Type, Epileptic Syndrome, EEG and Etiology 97
Contribution of ultrarare variants in mTOR pathway genes to sporadic focal epilepsies 90
Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders 90
Early Treatment with Quinidine in 2 Patients with Epilepsy of Infancy with Migrating Focal Seizures (EIMFS) Due to Gain-of-Function KCNT1 Mutations: Functional Studies, Clinical Responses, and Critical Issues for Personalized Therapy 89
Epilepsy features in ARID1B-related Coffin-Siris syndrome 82
Consensus protocol for EEG and amplitude-integrated EEG assessment and monitoring in neonates 59
Case Report: Effect of Targeted Therapy With Carbamazepine in KCNQ2 Neonatal Epilepsy 44
DNA-binding affinity and specificity determine the phenotypic diversity in BCL11B-related disorders 37
Totale 1.131
Categoria #
all - tutte 4.478
article - articoli 4.185
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 8.663


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202120 0 0 0 0 0 0 0 0 0 0 20 0
2021/202276 7 2 2 1 3 7 0 18 7 12 4 13
2022/2023127 12 7 3 9 15 26 0 10 22 1 21 1
2023/202487 4 14 7 19 4 12 2 6 4 1 3 11
2024/2025238 18 12 6 18 19 23 17 33 7 20 32 33
2025/2026381 54 5 16 18 66 31 55 24 25 34 53 0
Totale 1.131