SFERA Archivio dei prodotti della Ricerca dell'Università di Ferrara

FERRARESI, Paolo
 Distribuzione geografica
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Continente #
NA - Nord America 4.394
AS - Asia 2.295
EU - Europa 1.157
SA - Sud America 344
AF - Africa 48
OC - Oceania 5
Totale 8.243
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Nazione #
US - Stati Uniti d'America 4.300
SG - Singapore 840
CN - Cina 608
VN - Vietnam 314
BR - Brasile 269
DE - Germania 245
UA - Ucraina 218
HK - Hong Kong 174
IT - Italia 171
GB - Regno Unito 133
TR - Turchia 127
FI - Finlandia 76
FR - Francia 70
JP - Giappone 60
IN - India 55
CA - Canada 52
RU - Federazione Russa 52
SE - Svezia 42
MX - Messico 35
PL - Polonia 34
AR - Argentina 23
BE - Belgio 23
BD - Bangladesh 22
ZA - Sudafrica 22
IQ - Iraq 20
ES - Italia 16
EC - Ecuador 15
ID - Indonesia 14
NL - Olanda 12
PK - Pakistan 12
CO - Colombia 11
LT - Lituania 11
AT - Austria 10
IE - Irlanda 9
MA - Marocco 8
VE - Venezuela 8
CZ - Repubblica Ceca 7
RO - Romania 6
SA - Arabia Saudita 6
UZ - Uzbekistan 6
PE - Perù 5
AL - Albania 4
CL - Cile 4
EG - Egitto 4
JO - Giordania 4
PY - Paraguay 4
AE - Emirati Arabi Uniti 3
AU - Australia 3
CR - Costa Rica 3
IR - Iran 3
MY - Malesia 3
PH - Filippine 3
PT - Portogallo 3
SI - Slovenia 3
TN - Tunisia 3
UY - Uruguay 3
BO - Bolivia 2
DK - Danimarca 2
KE - Kenya 2
LY - Libia 2
NG - Nigeria 2
NZ - Nuova Zelanda 2
QA - Qatar 2
RS - Serbia 2
TH - Thailandia 2
TW - Taiwan 2
AF - Afghanistan, Repubblica islamica di 1
AZ - Azerbaigian 1
BA - Bosnia-Erzegovina 1
BH - Bahrain 1
BN - Brunei Darussalam 1
BW - Botswana 1
BY - Bielorussia 1
CG - Congo 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
ET - Etiopia 1
GE - Georgia 1
GR - Grecia 1
HN - Honduras 1
HR - Croazia 1
HU - Ungheria 1
IL - Israele 1
JM - Giamaica 1
KG - Kirghizistan 1
KH - Cambogia 1
KR - Corea 1
LB - Libano 1
LV - Lettonia 1
MV - Maldive 1
NO - Norvegia 1
NP - Nepal 1
OM - Oman 1
PA - Panama 1
PS - Palestinian Territory 1
SK - Slovacchia (Repubblica Slovacca) 1
SY - Repubblica araba siriana 1
UG - Uganda 1
Totale 8.243
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Città #
Singapore 552
Ashburn 442
Woodbridge 353
Fairfield 313
San Jose 267
Chandler 249
Ann Arbor 224
Jacksonville 223
Houston 221
Beijing 220
Santa Clara 217
Hong Kong 165
Seattle 149
Wilmington 124
Dallas 114
Cambridge 108
Ho Chi Minh City 103
New York 99
Hanoi 80
Ferrara 78
Boardman 74
Izmir 72
Munich 69
Nanjing 67
Los Angeles 66
Tokyo 60
Princeton 48
The Dalles 42
Lauterbourg 40
Warsaw 32
Shanghai 31
Mexico City 26
São Paulo 26
Brussels 23
Buffalo 23
Dearborn 23
San Diego 23
Shenyang 23
Milan 22
Orem 21
Da Nang 20
Chicago 19
Jiaxing 19
Frankfurt am Main 18
Tianjin 18
London 17
Montreal 17
Jinan 16
Nanchang 16
Bremen 15
Helsinki 15
Turku 15
Baghdad 14
Brooklyn 14
Council Bluffs 14
Düsseldorf 13
Hebei 13
Haiphong 12
Auburn Hills 11
Chennai 11
Falls Church 11
Florence 11
Johannesburg 11
Phoenix 11
Rio de Janeiro 11
Toronto 11
Belo Horizonte 10
Denver 10
Hefei 10
Manchester 10
Amsterdam 9
Jakarta 9
Nuremberg 9
Ottawa 9
Redwood City 9
Stockholm 9
Atlanta 8
San Francisco 8
Bologna 7
Boston 7
Curitiba 7
Dortmund 7
Kyiv 7
Mountain View 7
Poplar 7
Porto Alegre 7
San Mateo 7
Vienna 7
Washington 7
Brno 6
Changsha 6
Charlotte 6
Dublin 6
Hải Dương 6
Istanbul 6
Moscow 6
Norwalk 6
Tashkent 6
Thái Nguyên 6
Ankara 5
Totale 5.737
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Nome #
Factor XI rs2036914 gene polymorphism and occurrence of adverse events after percutaneous coronary intervention. A prospective evaluation. 246
A heparin cofactor II mutation (HCII Rimini) combined with factor V Leiden or type I protein C deficiency in two unrelated thrombophilic subjects 242
Angiotensin-converting enzyme insertion/deletion polymorphism and risk of restenosis after directional coronary atherectomy followed by stent implantation 239
Tissue factor and coagulation factor VII levels during acute myocardial infarction: Association with genotype and adverse events 237
Asymptomatic carriership of factor V Leiden and genotypes of the fibrinogen gene cluster 216
Mutation pattern in clinically asymptomatic coagulation factor VII deficiency 212
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 210
Acute Coronaric Syndroms and FVII polymorphisms: different effects in the same gene 200
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 199
Mutations in the R2 FV gene affect the ratio between the two FV isoforms in plasma 198
A family study of FVII genotype, elevated levels of factor VII and arterial thrombotic disease 194
Relationship between paraoxonase Q192R gene polymorphism and on-clopidogrel platelet reactivity over time in patients treated with percutaneous coronary intervention 192
Hyperhomocyst(e)inemia and a common methylenetetrahydrofolate reductase mutation (Ala(223)Val MTHFR) in patients with inherited thrombophilic coagulation defects 188
Variation of factor VII 140s and 170s loops in fishes: evolutionary aspects and comparison with mutations found in FVII deficiency 187
Factor IX propeptide mutation and life threatening bleeding 184
Modulation of factor VII levels by intron 7 polymorphisms: Population and in vitro studies 182
Factor V gene mutations (R2 gene) are associated with coronary artery disease inelderly people 175
Tissue Factor and Coagulation Factor VII Levels during Acute Myocardial Infarction Contribute to Predict Mortality and re-infarction. 172
Increased factor VIII coagulant activity levels in male carriers of the factor V R2 polymorphism 172
Prospective evaluation of on-clopidogrel platelet reactivity over time in patients treated with percutaneous coronary intervention: Relationship with gene polymorphisms and clinical outcome 171
Next-generation sequencing and recombinant expression characterized aberrant splicing mechanisms and provided correction strategies in factor VII deficiency 166
Polymorphisms in the factor VII gene and the risk of myocardial infarction in patients with coronary artery disease 165
Angiotensin-converting enzyme gene polymorphism made risk of restenosis after coronary stenting 164
Factor XIIIA-V34L and Factor XIIIB-H95R Gene Variants and Survival after Myocardial Infarction. 164
Protein S on the surface of plasma lipoproteins: a potential mechanism for protein S delivery to the atherosclerotic plaques? 162
Non-conventional therapeutic strategies for inherited disorders oh hemostasis 162
Factor V markers for the detection of genetic components of APC resistance in venous thrombosis 162
The F7 p.Val22Ile missense mutation affects splicing and can be counteracted by a compensatory U1snRNA 162
In Situ Endothelial SARS-CoV-2 Presence and PROS1 Plasma Levels Alteration in SARS-CoV-2-Associated Coagulopathies 156
Modulation of FVII levels by intron 7 polymorphisms: population and in vitro studies 154
Factor VIIa levels, gene polymorphism and plasma lipids in subjects with or without angiographically proven coronary artery disease 153
Study of a G/A variation in the 3' untranslated region of prothrombin mRNA in Italian patients with venous thrombosis 152
RNA-based therapeutic approaches for blood coagulation factor deficiencies caused by a splicing mutations 151
Management of Kidney Transplantation in a Factor VII-Deficient Patient: Case Report 151
Hyperhomocysteinemia and a common methylene-tetrahydrofolate reductase mutation (Ala223Val MTHFR) are not associated with a history of thrombosis in patients with inherited thrombophilia 149
Factor V markers for the detection of genetic components of APC resi stance in venous thrombosis. 147
Factor XIIIA-V34L and factor XIIIB-H95R gene variants: effects on survival in myocardial infarction patients. 145
Management of Kidney Transplantation in a Factor VII-Deficient Patient: Case Report 145
Non-conventional therapeutic strategies for inherited disorders of hemostasis 144
Modulation Of Factor VII Expression By Repeat And Sequence Variations In The Intron 7 Of FVII Gene: Population And In Vitro Studies 136
RNA−based therapeutic approaches for blood coagulation factor deficiencies caused by splicing mutations 112
Strong contribution of FVII genotypes to activated FVII levels and differences in genotype frequencies in northern and southern European countries 106
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The heterozygous 20210 G/A genotype prevalence in patients affected by central and branch retinal vein occlusion: a pilot study. 103
The asymptomatic carriership of thrombophilic defects is associated with frequent genotypes of the fibrinogen gene cluster. 101
Idiopathic central retinal vein occlusion in a thrombophilic patient with the heterozygous 20210 G/A prothrombin genotype 94
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Intracellular readthrough of nonsense mutations by aminoglycosides in coagulation factor VII 78
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Rescue of a panel of Hemophilia A-causing 5’ss splicing mutations by unique Exon-specific U1snRNA variants 72
Temporal and genotype-driven variations of factor VII levels in patients with acute myocardial infarction 63
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Totale 8.293
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Categoria #
all - tutte 33.605
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 33.605
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021106 0 0 0 0 0 0 0 0 0 0 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
2025/20263.251 375 131 302 452 534 250 400 192 303 311 1 0
Totale 8.293