SFERA Archivio dei prodotti della Ricerca dell'Università di Ferrara

FERRARESI, Paolo
 Distribuzione geografica
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Continente #
NA - Nord America 3.807
AS - Asia 1.687
EU - Europa 1.039
SA - Sud America 271
AF - Africa 20
OC - Oceania 4
Totale 6.828
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Nazione #
US - Stati Uniti d'America 3.731
SG - Singapore 663
CN - Cina 546
DE - Germania 240
BR - Brasile 229
UA - Ucraina 213
IT - Italia 159
HK - Hong Kong 155
GB - Regno Unito 125
TR - Turchia 121
VN - Vietnam 97
FI - Finlandia 67
RU - Federazione Russa 51
CA - Canada 42
SE - Svezia 41
PL - Polonia 31
MX - Messico 29
IN - India 27
FR - Francia 26
BE - Belgio 22
AR - Argentina 18
JP - Giappone 17
ES - Italia 12
ZA - Sudafrica 12
EC - Ecuador 11
BD - Bangladesh 10
ID - Indonesia 10
IQ - Iraq 10
NL - Olanda 10
LT - Lituania 9
CZ - Repubblica Ceca 7
AT - Austria 6
RO - Romania 6
IE - Irlanda 5
SA - Arabia Saudita 4
UZ - Uzbekistan 4
AE - Emirati Arabi Uniti 3
IR - Iran 3
JO - Giordania 3
PE - Perù 3
PK - Pakistan 3
TN - Tunisia 3
VE - Venezuela 3
AL - Albania 2
AU - Australia 2
CO - Colombia 2
DK - Danimarca 2
MA - Marocco 2
NZ - Nuova Zelanda 2
PY - Paraguay 2
QA - Qatar 2
UY - Uruguay 2
AF - Afghanistan, Repubblica islamica di 1
AZ - Azerbaigian 1
BN - Brunei Darussalam 1
BO - Bolivia 1
BY - Bielorussia 1
CR - Costa Rica 1
DO - Repubblica Dominicana 1
EG - Egitto 1
HN - Honduras 1
HU - Ungheria 1
IL - Israele 1
JM - Giamaica 1
LB - Libano 1
NG - Nigeria 1
OM - Oman 1
PA - Panama 1
PH - Filippine 1
PT - Portogallo 1
RS - Serbia 1
SK - Slovacchia (Repubblica Slovacca) 1
SY - Repubblica araba siriana 1
TW - Taiwan 1
UG - Uganda 1
Totale 6.828
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Città #
Singapore 385
Woodbridge 353
Ashburn 324
Fairfield 313
Chandler 249
Ann Arbor 224
Jacksonville 223
Houston 221
Santa Clara 212
Beijing 207
Hong Kong 153
Seattle 149
Wilmington 124
Dallas 109
Cambridge 108
New York 83
Ferrara 76
Boardman 74
Izmir 72
Munich 69
Nanjing 67
Los Angeles 54
Princeton 48
Ho Chi Minh City 38
Shanghai 30
Warsaw 29
Mexico City 24
The Dalles 24
Dearborn 23
San Diego 23
Shenyang 23
Brussels 22
Hanoi 22
Milan 22
Buffalo 20
São Paulo 20
Jiaxing 19
Chicago 18
London 17
Tokyo 17
Nanchang 16
Tianjin 16
Bremen 15
Jinan 15
Turku 15
Frankfurt am Main 14
Brooklyn 13
Düsseldorf 13
Hebei 13
Montreal 13
Auburn Hills 11
Falls Church 11
Florence 11
Hefei 10
Phoenix 10
Belo Horizonte 9
Chennai 9
Johannesburg 9
Nuremberg 9
Ottawa 9
Redwood City 9
Rio de Janeiro 9
Amsterdam 8
Baghdad 8
Helsinki 8
Jakarta 8
Manchester 8
San Francisco 8
Stockholm 8
Toronto 8
Bologna 7
Curitiba 7
Denver 7
Dortmund 7
Mountain View 7
Porto Alegre 7
San Mateo 7
Washington 7
Brno 6
Changsha 6
Charlotte 6
Moscow 6
Norwalk 6
Ankara 5
Boston 5
Da Nang 5
Monmouth Junction 5
Ningbo 5
Poplar 5
Zhengzhou 5
Campinas 4
Campo Grande 4
Falkenstein 4
Haiphong 4
Lyon 4
Philadelphia 4
Taizhou 4
Tashkent 4
Thái Nguyên 4
Vienna 4
Totale 4.772
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Nome #
Factor XI rs2036914 gene polymorphism and occurrence of adverse events after percutaneous coronary intervention. A prospective evaluation. 223
Tissue factor and coagulation factor VII levels during acute myocardial infarction: Association with genotype and adverse events 206
A heparin cofactor II mutation (HCII Rimini) combined with factor V Leiden or type I protein C deficiency in two unrelated thrombophilic subjects 204
Angiotensin-converting enzyme insertion/deletion polymorphism and risk of restenosis after directional coronary atherectomy followed by stent implantation 197
Mutation pattern in clinically asymptomatic coagulation factor VII deficiency 184
Asymptomatic carriership of factor V Leiden and genotypes of the fibrinogen gene cluster 183
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 173
Influence of polymorphisms in the factor VII gene promoter on activated factor VII levels and on the risk of myocardial infarction in advanced coronary atherosclerosis 168
Relationship between paraoxonase Q192R gene polymorphism and on-clopidogrel platelet reactivity over time in patients treated with percutaneous coronary intervention 167
Variation of factor VII 140s and 170s loops in fishes: evolutionary aspects and comparison with mutations found in FVII deficiency 165
Mutations in the R2 FV gene affect the ratio between the two FV isoforms in plasma 163
A family study of FVII genotype, elevated levels of factor VII and arterial thrombotic disease 157
Hyperhomocyst(e)inemia and a common methylenetetrahydrofolate reductase mutation (Ala(223)Val MTHFR) in patients with inherited thrombophilic coagulation defects 154
Acute Coronaric Syndroms and FVII polymorphisms: different effects in the same gene 153
Polymorphisms in the factor VII gene and the risk of myocardial infarction in patients with coronary artery disease 152
Tissue Factor and Coagulation Factor VII Levels during Acute Myocardial Infarction Contribute to Predict Mortality and re-infarction. 152
Factor IX propeptide mutation and life threatening bleeding 151
Modulation of factor VII levels by intron 7 polymorphisms: Population and in vitro studies 150
Increased factor VIII coagulant activity levels in male carriers of the factor V R2 polymorphism 141
Next-generation sequencing and recombinant expression characterized aberrant splicing mechanisms and provided correction strategies in factor VII deficiency 141
Factor V gene mutations (R2 gene) are associated with coronary artery disease inelderly people 140
Non-conventional therapeutic strategies for inherited disorders oh hemostasis 138
Prospective evaluation of on-clopidogrel platelet reactivity over time in patients treated with percutaneous coronary intervention: Relationship with gene polymorphisms and clinical outcome 137
Management of Kidney Transplantation in a Factor VII-Deficient Patient: Case Report 136
The F7 p.Val22Ile missense mutation affects splicing and can be counteracted by a compensatory U1snRNA 134
Angiotensin-converting enzyme gene polymorphism made risk of restenosis after coronary stenting 131
Study of a G/A variation in the 3' untranslated region of prothrombin mRNA in Italian patients with venous thrombosis 131
Factor V markers for the detection of genetic components of APC resistance in venous thrombosis 129
Factor XIIIA-V34L and Factor XIIIB-H95R Gene Variants and Survival after Myocardial Infarction. 128
Modulation of FVII levels by intron 7 polymorphisms: population and in vitro studies 126
Protein S on the surface of plasma lipoproteins: a potential mechanism for protein S delivery to the atherosclerotic plaques? 122
Non-conventional therapeutic strategies for inherited disorders of hemostasis 121
Hyperhomocysteinemia and a common methylene-tetrahydrofolate reductase mutation (Ala223Val MTHFR) are not associated with a history of thrombosis in patients with inherited thrombophilia 121
Management of Kidney Transplantation in a Factor VII-Deficient Patient: Case Report 121
RNA-based therapeutic approaches for blood coagulation factor deficiencies caused by a splicing mutations 119
Factor VIIa levels, gene polymorphism and plasma lipids in subjects with or without angiographically proven coronary artery disease 116
Factor V markers for the detection of genetic components of APC resi stance in venous thrombosis. 113
In Situ Endothelial SARS-CoV-2 Presence and PROS1 Plasma Levels Alteration in SARS-CoV-2-Associated Coagulopathies 108
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Modulation Of Factor VII Expression By Repeat And Sequence Variations In The Intron 7 Of FVII Gene: Population And In Vitro Studies 103
Factor XIIIA-V34L and factor XIIIB-H95R gene variants: effects on survival in myocardial infarction patients. 100
Strong contribution of FVII genotypes to activated FVII levels and differences in genotype frequencies in northern and southern European countries 93
RNA−based therapeutic approaches for blood coagulation factor deficiencies caused by splicing mutations 90
The asymptomatic carriership of thrombophilic defects is associated with frequent genotypes of the fibrinogen gene cluster. 89
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The heterozygous 20210 G/A genotype prevalence in patients affected by central and branch retinal vein occlusion: a pilot study. 78
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Idiopathic central retinal vein occlusion in a thrombophilic patient with the heterozygous 20210 G/A prothrombin genotype 70
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Intracellular readthrough of nonsense mutations by aminoglycosides in coagulation factor VII 54
Temporal and genotype-driven variations of factor VII levels in patients with acute myocardial infarction 45
Rescue of a panel of Hemophilia A-causing 5’ss splicing mutations by unique Exon-specific U1snRNA variants 43
Totale 6.878
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Categoria #
all - tutte 30.870
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 30.870
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021352 0 0 0 0 0 61 28 72 14 71 82 24
2021/2022476 21 55 34 23 21 9 24 15 9 32 62 171
2022/2023525 56 53 16 79 75 79 18 41 63 2 23 20
2023/2024354 31 26 7 6 30 78 10 26 9 19 11 101
2024/20251.123 29 20 115 36 147 128 9 24 163 113 184 155
2025/20261.836 375 131 302 452 534 42 0 0 0 0 0 0
Totale 6.878