IMPERATORE, VALENTINA
 Distribuzione geografica
Continente #
NA - Nord America 126
AS - Asia 123
EU - Europa 73
SA - Sud America 17
AF - Africa 8
Totale 347
Nazione #
US - Stati Uniti d'America 120
SG - Singapore 52
HK - Hong Kong 27
CN - Cina 19
IE - Irlanda 16
RU - Federazione Russa 14
BR - Brasile 13
IT - Italia 12
DE - Germania 9
VN - Vietnam 8
FR - Francia 7
FI - Finlandia 6
KR - Corea 6
CA - Canada 5
IQ - Iraq 4
BE - Belgio 3
KE - Kenya 2
MA - Marocco 2
NL - Olanda 2
UZ - Uzbekistan 2
VE - Venezuela 2
AR - Argentina 1
AT - Austria 1
CL - Cile 1
EG - Egitto 1
GB - Regno Unito 1
GT - Guatemala 1
JO - Giordania 1
JP - Giappone 1
LB - Libano 1
LY - Libia 1
NP - Nepal 1
PH - Filippine 1
PL - Polonia 1
SK - Slovacchia (Repubblica Slovacca) 1
SN - Senegal 1
ZA - Sudafrica 1
Totale 347
Città #
Singapore 37
Hong Kong 27
San Jose 21
Dublin 16
Chandler 8
Boardman 7
The Dalles 7
Ann Arbor 6
Ashburn 6
Seoul 6
Helsinki 5
Perugia 5
West Jordan 5
Beijing 4
Denver 4
Lauterbourg 4
Munich 4
San Mateo 4
Santa Clara 4
Council Bluffs 3
Erbil 3
Frankfurt am Main 3
Ho Chi Minh City 3
Los Angeles 3
Altamura 2
Amsterdam 2
Caracas 2
Hasselt 2
Hefei 2
Lawrence 2
Medford 2
Montreal 2
Moscow 2
Piscataway 2
Princeton 2
Toronto 2
Amman 1
As Samawah 1
Atlanta 1
Benghazi 1
Bologna 1
Bom Jesus de Goiás 1
Boston 1
Botucatu 1
Brasília 1
Brussels 1
Buenos Aires 1
Cairo 1
Campinas 1
Carney 1
Caxias 1
Columbus 1
Da Nang 1
Dakar 1
Ferrara 1
Guangzhou 1
Guatemala City 1
Halifax 1
Itu 1
Johannesburg 1
Juazeiro do Norte 1
Kenitra 1
Lakewood 1
Landshut 1
Las Vegas 1
London 1
Manassas 1
Manaus 1
Manila 1
Marrakesh 1
Marsciano 1
Nairobi 1
New York 1
Ninh Bình 1
Nuremberg 1
Olinda 1
Petrolândia 1
Prievidza 1
Quận Bốn 1
Rio de Janeiro 1
Roubaix 1
San Francisco 1
Santiago 1
Shanghai 1
Suzano 1
Tampa 1
The Bronx 1
Tianjin 1
Tobias Barreto 1
Tokyo 1
Turku 1
Wroclaw 1
Wuhan 1
Xinzhou 1
Yantai 1
Totale 278
Nome #
Identification of a dna methylation episignature in the 22q11.2 deletion syndrome 85
Expanding the genetic and clinical characteristics of Protocadherin 19 gene mutations 83
A rare case of brachyolmia with amelogenesis imperfecta caused by a new pathogenic splicing variant in ltbp3 80
IRF2BPL: A new genotype for progressive myoclonus epilepsies 69
Usmani–Riazuddin Syndrome: Functional Characterization of a Novel c.196G>A Variant in the AP1G1 Gene and Phenotypic Insights Using Zebrafish as a Vertebrate Model 16
Generation of a human induced pluripotent stem cell line (CIBIOi007-A) from a Lafora disease patient 13
Neuronal hyperexcitability: A key to unraveling hippocampal synaptic dysfunction in Lafora disease 12
Epm2b and Epm2b knock-in mouse models of Lafora disease exhibit distinct and pronounced neurological alterations 2
SINEUP-Mediated Overexpression of Endogenous α-Amylase as a Therapeutic Approach in Lafora Disease 1
Totale 361
Categoria #
all - tutte 1.643
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 1.643


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/202215 0 1 1 3 0 0 1 2 0 3 2 2
2022/202337 3 7 2 2 0 3 0 0 18 0 2 0
2023/202434 2 4 1 3 0 0 6 2 4 2 4 6
2024/202580 2 6 5 7 4 5 5 5 9 6 18 8
2025/2026195 22 14 10 16 24 10 32 20 27 20 0 0
Totale 361