CASTOLDI, Elisabetta
 Distribuzione geografica
Continente #
NA - Nord America 603
EU - Europa 168
AS - Asia 113
OC - Oceania 1
Totale 885
Nazione #
US - Stati Uniti d'America 600
CN - Cina 70
UA - Ucraina 47
IT - Italia 42
DE - Germania 24
TR - Turchia 23
GB - Regno Unito 17
SG - Singapore 13
FI - Finlandia 9
GR - Grecia 7
SE - Svezia 7
FR - Francia 4
IR - Iran 4
BE - Belgio 3
CA - Canada 3
AL - Albania 2
IN - India 2
AU - Australia 1
BY - Bielorussia 1
CH - Svizzera 1
JO - Giordania 1
MK - Macedonia 1
NL - Olanda 1
RO - Romania 1
RU - Federazione Russa 1
Totale 885
Città #
Woodbridge 70
Chandler 68
Fairfield 67
Houston 54
Jacksonville 53
Ann Arbor 31
Ashburn 25
Wilmington 23
Beijing 21
Seattle 21
Boardman 15
Izmir 14
New York 14
Cambridge 13
Nanjing 13
Milan 10
Singapore 10
Princeton 9
Redwood City 8
Falls Church 7
Shenyang 7
Shanghai 6
San Diego 5
Dearborn 4
Mountain View 4
Tianjin 4
Auburn Hills 3
Brussels 3
Hebei 3
Jiaxing 3
Norwalk 3
Rome 3
Athens 2
Bremen 2
Catania 2
Chicago 2
Düsseldorf 2
Genoa 2
Genova 2
Hyderabad 2
Jinan 2
Kunming 2
Nanchang 2
Orange 2
Pavia 2
Redmond 2
Taizhou 2
Tirana 2
Augusta 1
Castelnuovo Rangone 1
Chaniá 1
Eugene 1
Ferrara 1
Fuzhou 1
Hunedoara 1
Leicester 1
Lido Di Camaiore 1
Malatya 1
Martina Franca 1
Minsk 1
Monmouth Junction 1
Munich 1
Newmarket 1
Notaresco 1
Nuraminis 1
Pioltello 1
Portici 1
Sakarya 1
Toronto 1
Trieste 1
Zhengzhou 1
Totale 649
Nome #
Combinations of 4 mutations (FV R506Q, FV H1299R, FV Y1702C, PT 20210G/A) affecting the prothrombinase complex in a thrombophilic family 157
A highly polymorphic microsatellite in the factor V gene is an informative tool for the study of factor V-related disorders 128
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 111
FV multiallelic marker detects genetic components of APC resistance contributing to venous thromboembolism in FV Leiden carriers 108
Mutations in the R2 FV gene affect the ratio between the two FV isoforms in plasma 101
A missense mutation (Y1702C) in the coagulation factor V gene is a frequent cause of factor V deficiency in the Italian population. 81
Factor V gene mutations (R2 gene) are associated with coronary artery disease inelderly people 76
Factor V markers for the detection of genetic components of APC resistance in venous thrombosis 69
Study of a G/A variation in the 3' untranslated region of prothrombin mRNA in Italian patients with venous thrombosis 66
Totale 897
Categoria #
all - tutte 3.605
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 3.605


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020202 29 5 4 31 12 22 16 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
2024/20252 2 0 0 0 0 0 0 0 0 0 0 0
Totale 897