MINGOZZI, Federico
 Distribuzione geografica
Continente #
NA - Nord America 570
AS - Asia 142
EU - Europa 138
SA - Sud America 4
Continente sconosciuto - Info sul continente non disponibili 1
OC - Oceania 1
Totale 856
Nazione #
US - Stati Uniti d'America 567
CN - Cina 68
SG - Singapore 55
UA - Ucraina 39
DE - Germania 25
IT - Italia 22
GB - Regno Unito 18
TR - Turchia 13
BE - Belgio 7
FI - Finlandia 7
SE - Svezia 6
BR - Brasile 4
PL - Polonia 4
CA - Canada 3
FR - Francia 3
LT - Lituania 3
AT - Austria 2
ID - Indonesia 2
IN - India 2
VN - Vietnam 2
AU - Australia 1
BY - Bielorussia 1
EU - Europa 1
NL - Olanda 1
Totale 856
Città #
Woodbridge 71
Fairfield 67
Chandler 59
Jacksonville 42
Santa Clara 38
Houston 34
Ashburn 33
Singapore 32
Ann Arbor 31
Seattle 28
Wilmington 23
Cambridge 18
Beijing 17
New York 16
Nanjing 14
Boardman 13
Izmir 10
Milan 9
Princeton 9
Brussels 7
Shanghai 7
Shenyang 7
Ferrara 5
San Diego 5
Dearborn 4
Warsaw 4
Jiaxing 3
Norwalk 3
Augusta 2
Bremen 2
Catania 2
Chicago 2
Dong Ket 2
Düsseldorf 2
Falkenstein 2
Genoa 2
Hebei 2
Hyderabad 2
Jakarta 2
Kunming 2
London 2
Orange 2
Taizhou 2
Tianjin 2
Bacabeira 1
Fiume Veneto 1
Fuzhou 1
Hounslow 1
Islington 1
Los Angeles 1
Minsk 1
Monmouth Junction 1
Mountain View 1
Munich 1
Nanchang 1
Newmarket 1
Ottawa 1
Paraúna 1
Paris 1
Poços de Caldas 1
Redmond 1
Redwood City 1
Saint Louis 1
Santo Antônio do Monte 1
Shenzhen 1
Spresiano 1
Tappahannock 1
Toronto 1
Washington 1
Ürümqi 1
Totale 667
Nome #
A highly polymorphic microsatellite in the factor V gene is an informative tool for the study of factor V-related disorders 148
FV multiallelic marker detects genetic components of APC resistance contributing to venous thromboembolism in FV Leiden carriers 119
Mutations in the R2 FV gene affect the ratio between the two FV isoforms in plasma 111
The factor VIII D I24I E polymorphism is associated with decreased factor VIII activity and not with activated protein C resistance levels 110
Exon-specific U1 snRNAs improve ELP1 exon 20 definition and rescue ELP1 protein expression in a familial dysautonomia mouse model 109
A missense mutation (Y1702C) in the coagulation factor V gene is a frequent cause of factor V deficiency in the Italian population. 106
Factor V gene mutations (R2 gene) are associated with coronary artery disease inelderly people 88
Factor V markers for the detection of genetic components of APC resistance in venous thrombosis 79
Totale 870
Categoria #
all - tutte 4.752
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 4.752


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202039 0 0 0 0 0 0 0 0 0 21 13 5
2020/2021128 8 15 3 10 6 16 4 13 4 25 18 6
2021/202296 2 14 4 7 6 2 4 5 2 5 13 32
2022/2023116 10 18 2 19 16 20 8 3 8 1 7 4
2023/202463 0 8 3 0 5 20 0 1 0 2 1 23
2024/2025123 3 5 19 12 25 29 1 2 26 1 0 0
Totale 870