DILENA, ROBERTINO
 Distribuzione geografica
Continente #
EU - Europa 906
AS - Asia 142
NA - Nord America 88
SA - Sud America 7
AF - Africa 2
Totale 1.145
Nazione #
IT - Italia 887
US - Stati Uniti d'America 82
SG - Singapore 54
CN - Cina 45
VN - Vietnam 29
FR - Francia 9
BR - Brasile 6
DE - Germania 5
MX - Messico 4
HK - Hong Kong 3
BD - Bangladesh 2
GB - Regno Unito 2
JP - Giappone 2
SE - Svezia 2
CA - Canada 1
EC - Ecuador 1
FI - Finlandia 1
ID - Indonesia 1
IN - India 1
IQ - Iraq 1
JM - Giamaica 1
KH - Cambogia 1
PK - Pakistan 1
SA - Arabia Saudita 1
TH - Thailandia 1
TN - Tunisia 1
ZA - Sudafrica 1
Totale 1.145
Città #
Genoa 356
Genova 298
Rapallo 121
Vado Ligure 98
San Jose 27
Singapore 15
New York 12
Beijing 11
Ho Chi Minh City 9
Lauterbourg 8
Hanoi 7
Frankfurt am Main 5
Bordighera 4
Council Bluffs 4
Haiphong 4
Rome 4
Santa Clara 4
Ashburn 3
Hong Kong 3
Mexico City 3
Atlanta 2
City of London 2
Stockholm 2
Tokyo 2
Ahmedabad 1
Baghdad 1
Biên Hòa 1
Brampton 1
Buffalo 1
Bến Cầu 1
Campinas 1
Campo Grande 1
Cape Town 1
Capim Grosso 1
Da Nang 1
Delano 1
Helsinki 1
Itaocara 1
Jeddah 1
Lagoa Vermelha 1
Lahore 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
San Marzano di San Giuseppe 1
San Tan Valley 1
St Louis 1
Surin 1
Tunis 1
Turin 1
Tân Tiến 1
Tây Ninh 1
Vicenza 1
Virginia Beach 1
Xi'an 1
Totale 1.044
Nome #
STXBP1 Encephalopathy: A Neurodevelopmental Disorder Including Epilepsy 161
Dramatic effect of levetiracetam in early-onset epileptic encephalopathy due to STXBP1 mutation 147
Efficacy of sodium channel blockers in SCN2A early infantile epileptic encephalopathy 126
Epilepsy Course and Developmental Trajectories in STXBP1-DEE 103
“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
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 88
Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders 84
Epilepsy features in ARID1B-related Coffin-Siris syndrome 82
Sleep-related hypermotor epilepsy (SHE): Contribution of known genes in 103 patients 74
Consensus protocol for EEG and amplitude-integrated EEG assessment and monitoring in neonates 58
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 19
Totale 1.173
Categoria #
all - tutte 4.789
article - articoli 4.498
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 9.287


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202122 0 0 0 0 0 0 0 0 0 0 20 2
2021/202287 7 2 4 1 3 9 0 20 10 13 4 14
2022/2023140 13 7 3 10 15 30 0 10 26 1 23 2
2023/202494 6 14 7 20 4 12 2 8 5 1 3 12
2024/2025252 19 13 6 19 21 24 18 33 7 21 36 35
2025/2026367 56 6 16 19 70 32 58 26 28 34 22 0
Totale 1.173