CASTOLDI, Elisabetta
 Distribuzione geografica
Continente #
NA - Nord America 653
EU - Europa 181
AS - Asia 139
SA - Sud America 2
OC - Oceania 1
Totale 976
Nazione #
US - Stati Uniti d'America 649
CN - Cina 74
UA - Ucraina 47
IT - Italia 45
SG - Singapore 35
DE - Germania 25
TR - Turchia 23
GB - Regno Unito 18
FI - Finlandia 9
BE - Belgio 7
GR - Grecia 7
SE - Svezia 7
CA - Canada 4
FR - Francia 4
IR - Iran 4
LT - Lituania 3
AL - Albania 2
BR - Brasile 2
IN - India 2
NL - Olanda 2
AU - Australia 1
BY - Bielorussia 1
CH - Svizzera 1
JO - Giordania 1
MK - Macedonia 1
RO - Romania 1
RU - Federazione Russa 1
Totale 976
Città #
Woodbridge 70
Chandler 68
Fairfield 67
Houston 54
Jacksonville 53
Santa Clara 43
Singapore 32
Ann Arbor 31
Ashburn 25
Wilmington 23
Beijing 21
Seattle 21
Boardman 15
Izmir 14
New York 14
Cambridge 13
Nanjing 13
Milan 10
Princeton 9
Redwood City 8
Brussels 7
Falls Church 7
Shenyang 7
Shanghai 6
San Diego 5
Dearborn 4
Mountain View 4
Tianjin 4
Auburn Hills 3
Hebei 3
Jiaxing 3
Kunming 3
Norwalk 3
Rome 3
Athens 2
Bremen 2
Catania 2
Chicago 2
Düsseldorf 2
Genoa 2
Genova 2
Hyderabad 2
Jinan 2
Nanchang 2
Orange 2
Pavia 2
Redmond 2
Taizhou 2
Tirana 2
Turin 2
Augusta 1
Castelnuovo Rangone 1
Chaniá 1
Diamantina 1
Eugene 1
Falkenstein 1
Ferrara 1
Fuzhou 1
Hunedoara 1
Leicester 1
Lido Di Camaiore 1
London 1
Los Angeles 1
Malatya 1
Martina Franca 1
Minsk 1
Monmouth Junction 1
Munich 1
Newmarket 1
Notaresco 1
Nuraminis 1
Ottawa 1
Pioltello 1
Portici 1
Sakarya 1
Santo Antônio do Monte 1
Toronto 1
Trieste 1
Zhengzhou 1
Ürümqi 1
Totale 728
Nome #
Combinations of 4 mutations (FV R506Q, FV H1299R, FV Y1702C, PT 20210G/A) affecting the prothrombinase complex in a thrombophilic family 167
A highly polymorphic microsatellite in the factor V gene is an informative tool for the study of factor V-related disorders 139
The heterozygous 20210 G/A prothrombin genotype is associated with early venous thrombosis in inherited thrombophilias and is not increased in frequency in artery disease 119
FV multiallelic marker detects genetic components of APC resistance contributing to venous thromboembolism in FV Leiden carriers 118
Mutations in the R2 FV gene affect the ratio between the two FV isoforms in plasma 110
A missense mutation (Y1702C) in the coagulation factor V gene is a frequent cause of factor V deficiency in the Italian population. 97
Factor V gene mutations (R2 gene) are associated with coronary artery disease inelderly people 87
Factor V markers for the detection of genetic components of APC resistance in venous thrombosis 78
Study of a G/A variation in the 3' untranslated region of prothrombin mRNA in Italian patients with venous thrombosis 73
Totale 988
Categoria #
all - tutte 4.854
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 4.854


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202083 0 0 0 0 0 0 0 20 14 27 16 6
2020/2021118 11 13 2 12 6 17 5 14 1 15 18 4
2021/2022121 3 13 6 12 10 5 5 10 2 7 13 35
2022/2023130 11 18 4 18 21 22 7 7 13 1 5 3
2023/202464 2 10 2 0 3 15 2 0 0 3 1 26
2024/202593 2 2 20 11 28 25 1 4 0 0 0 0
Totale 988