D'ONOFRIO, GIANLUCA
 Distribuzione geografica
Continente #
EU - Europa 508
AS - Asia 146
NA - Nord America 89
SA - Sud America 14
AF - Africa 1
OC - Oceania 1
Totale 759
Nazione #
IT - Italia 493
US - Stati Uniti d'America 86
SG - Singapore 64
CN - Cina 43
VN - Vietnam 27
BR - Brasile 6
AR - Argentina 4
FR - Francia 4
DE - Germania 3
HK - Hong Kong 3
GB - Regno Unito 2
JP - Giappone 2
AU - Australia 1
BD - Bangladesh 1
BE - Belgio 1
BH - Bahrain 1
BO - Bolivia 1
BY - Bielorussia 1
CA - Canada 1
CO - Colombia 1
CR - Costa Rica 1
DO - Repubblica Dominicana 1
IN - India 1
KW - Kuwait 1
NL - Olanda 1
PH - Filippine 1
PL - Polonia 1
RU - Federazione Russa 1
SA - Arabia Saudita 1
SI - Slovenia 1
TN - Tunisia 1
TR - Turchia 1
UY - Uruguay 1
VE - Venezuela 1
Totale 759
Città #
Genoa 363
Vado Ligure 71
Rapallo 47
Singapore 33
Ashburn 28
San Jose 24
Ho Chi Minh City 10
Beijing 7
New York 5
Hanoi 4
Los Angeles 4
Bordighera 3
Frankfurt am Main 3
Hong Kong 3
Lauterbourg 3
Santa Clara 3
Atlanta 2
Genova 2
Naples 2
Tianjin 2
Alfortville 1
Amsterdam 1
Bel Air 1
Bogotá 1
Bristol 1
Brussels 1
Buenos Aires 1
Cabo Frio 1
Camboriú 1
Caracas 1
Cerquilho 1
Chicago 1
Fujisawa 1
Golfito 1
Hamad Town 1
Houston 1
Hải Dương 1
Jeddah 1
Kuwait City 1
La Paz 1
Ljubljana 1
Ma'anshan 1
Madurai 1
Makhachkala 1
Manhuaçu 1
Melbourne 1
Minsk 1
Montevideo 1
Montreal 1
Ninh Bình 1
Orem 1
Quezon City 1
Raul Soares 1
Resistencia 1
San Rafael 1
Santa Cruz de Barahona 1
Sousse 1
Stockton-on-Tees 1
Tokyo 1
Viana 1
Vinh 1
Warsaw 1
Wuhan 1
Totale 662
Nome #
Genotype-phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disorders 104
Abnormal course of the corticospinal tracts in KIF5C-related encephalopathy 99
Current and promising therapeutic options for Dravet syndrome 80
Genotype-phenotype correlation in contactin-associated protein-like 2 (CNTNAP-2) developmental disorder 76
Novel biallelic variants expand the phenotype of NAA20-related syndrome 75
Paroxysmal limb dystonias associated with GABBR2 pathogenic variant: A case-based literature review 75
Characterization of rare neurodevelopmental disorders: enhancing diagnosis, providing prognostic insight, and improving treatment 74
A PAK1 Mutational Hotspot Within the Regulatory CRIPaK Domain is Associated With Severe Neurodevelopmental Disorders in Children 72
Pharmacokinetic considerations surrounding the use of levetiracetam for seizure prophylaxis in neurocritical care - an overview 70
Treatment of Refractory Epilepsy With MEK Inhibitor in Patients With RASopathy 48
Totale 773
Categoria #
all - tutte 2.906
article - articoli 2.767
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 5.673


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20224 0 0 0 0 0 0 0 0 0 0 0 4
2022/202359 1 1 0 4 14 5 0 5 10 0 13 6
2023/202468 2 8 1 9 4 15 5 4 0 3 10 7
2024/2025239 11 8 13 16 17 20 11 48 19 15 36 25
2025/2026403 56 14 33 38 68 19 61 26 48 40 0 0
Totale 773