SFERA Archivio dei prodotti della Ricerca dell'Università di Ferrara

FERRARESI, Paolo
 Distribuzione geografica
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Continente #
NA - Nord America 4.579
AS - Asia 2.360
EU - Europa 1.195
SA - Sud America 348
Continente sconosciuto - Info sul continente non disponibili 50
AF - Africa 49
OC - Oceania 5
Totale 8.586
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Nazione #
US - Stati Uniti d'America 4.470
SG - Singapore 852
CN - Cina 618
VN - Vietnam 314
BR - Brasile 270
DE - Germania 245
UA - Ucraina 219
IT - Italia 200
HK - Hong Kong 174
GB - Regno Unito 133
TR - Turchia 127
FI - Finlandia 76
FR - Francia 71
CA - Canada 65
BD - Bangladesh 64
JP - Giappone 61
IN - India 55
RU - Federazione Russa 52
SE - Svezia 43
MX - Messico 35
PL - Polonia 34
AR - Argentina 23
BE - Belgio 23
ZA - Sudafrica 22
ES - Italia 20
IQ - Iraq 20
EC - Ecuador 15
CO - Colombia 14
ID - Indonesia 14
NL - Olanda 13
LT - Lituania 12
PK - Pakistan 12
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
DZ - Algeria 2
JM - Giamaica 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
BS - Bahamas 1
BW - Botswana 1
BY - Bielorussia 1
CG - Congo 1
DO - Repubblica Dominicana 1
ET - Etiopia 1
GE - Georgia 1
GR - Grecia 1
HN - Honduras 1
HR - Croazia 1
HU - Ungheria 1
IL - Israele 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 8.536
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Città #
Singapore 557
Ashburn 454
Woodbridge 353
Fairfield 313
San Jose 287
Chandler 249
Ann Arbor 224
Houston 224
Jacksonville 223
Beijing 222
Santa Clara 220
Hong Kong 165
Seattle 149
Wilmington 124
Dallas 117
New York 114
Cambridge 108
Ho Chi Minh City 103
Hanoi 80
Ferrara 79
Boardman 74
Izmir 72
Los Angeles 72
Munich 69
Nanjing 67
Tokyo 60
Princeton 48
The Dalles 42
Lauterbourg 40
Council Bluffs 35
Shanghai 32
Warsaw 32
Buffalo 28
Mexico City 26
São Paulo 26
Milan 25
Brussels 23
Dearborn 23
San Diego 23
Shenyang 23
Orem 21
Chicago 20
Da Nang 20
Jiaxing 19
Frankfurt am Main 18
Montreal 18
Tianjin 18
Toronto 18
London 17
Jinan 16
Nanchang 16
Bremen 15
Brooklyn 15
Helsinki 15
Turku 15
Baghdad 14
Düsseldorf 13
Hebei 13
Haiphong 12
Atlanta 11
Auburn Hills 11
Chennai 11
Falls Church 11
Florence 11
Johannesburg 11
Manchester 11
Phoenix 11
Rio de Janeiro 11
Belo Horizonte 10
Denver 10
Hefei 10
Amsterdam 9
Jakarta 9
Nuremberg 9
Ottawa 9
Philadelphia 9
Redwood City 9
San Francisco 9
Stockholm 9
Washington 9
Bologna 8
Boston 7
Curitiba 7
Dortmund 7
Kyiv 7
Mountain View 7
Norwalk 7
Poplar 7
Porto Alegre 7
San Mateo 7
Vienna 7
Brno 6
Changsha 6
Charlotte 6
Dublin 6
Hải Dương 6
Istanbul 6
Moscow 6
Tashkent 6
Thái Nguyên 6
Totale 5.860
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Nome #
A heparin cofactor II mutation (HCII Rimini) combined with factor V Leiden or type I protein C deficiency in two unrelated thrombophilic subjects 249
Factor XI rs2036914 gene polymorphism and occurrence of adverse events after percutaneous coronary intervention. A prospective evaluation. 249
Angiotensin-converting enzyme insertion/deletion polymorphism and risk of restenosis after directional coronary atherectomy followed by stent implantation 248
Tissue factor and coagulation factor VII levels during acute myocardial infarction: Association with genotype and adverse events 244
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 223
Asymptomatic carriership of factor V Leiden and genotypes of the fibrinogen gene cluster 222
Mutation pattern in clinically asymptomatic coagulation factor VII deficiency 220
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 209
Acute Coronaric Syndroms and FVII polymorphisms: different effects in the same gene 204
Hyperhomocyst(e)inemia and a common methylenetetrahydrofolate reductase mutation (Ala(223)Val MTHFR) in patients with inherited thrombophilic coagulation defects 203
Mutations in the R2 FV gene affect the ratio between the two FV isoforms in plasma 200
A family study of FVII genotype, elevated levels of factor VII and arterial thrombotic disease 199
Variation of factor VII 140s and 170s loops in fishes: evolutionary aspects and comparison with mutations found in FVII deficiency 195
Relationship between paraoxonase Q192R gene polymorphism and on-clopidogrel platelet reactivity over time in patients treated with percutaneous coronary intervention 194
Factor IX propeptide mutation and life threatening bleeding 191
Prospective evaluation of on-clopidogrel platelet reactivity over time in patients treated with percutaneous coronary intervention: Relationship with gene polymorphisms and clinical outcome 191
Modulation of factor VII levels by intron 7 polymorphisms: Population and in vitro studies 183
Factor V gene mutations (R2 gene) are associated with coronary artery disease inelderly people 179
Increased factor VIII coagulant activity levels in male carriers of the factor V R2 polymorphism 179
Tissue Factor and Coagulation Factor VII Levels during Acute Myocardial Infarction Contribute to Predict Mortality and re-infarction. 176
Factor XIIIA-V34L and factor XIIIB-H95R gene variants: effects on survival in myocardial infarction patients. 175
The F7 p.Val22Ile missense mutation affects splicing and can be counteracted by a compensatory U1snRNA 172
Next-generation sequencing and recombinant expression characterized aberrant splicing mechanisms and provided correction strategies in factor VII deficiency 171
Polymorphisms in the factor VII gene and the risk of myocardial infarction in patients with coronary artery disease 169
Angiotensin-converting enzyme gene polymorphism made risk of restenosis after coronary stenting 168
Factor XIIIA-V34L and Factor XIIIB-H95R Gene Variants and Survival after Myocardial Infarction. 167
Non-conventional therapeutic strategies for inherited disorders oh hemostasis 165
Protein S on the surface of plasma lipoproteins: a potential mechanism for protein S delivery to the atherosclerotic plaques? 164
Factor V markers for the detection of genetic components of APC resistance in venous thrombosis 163
RNA-based therapeutic approaches for blood coagulation factor deficiencies caused by a splicing mutations 161
In Situ Endothelial SARS-CoV-2 Presence and PROS1 Plasma Levels Alteration in SARS-CoV-2-Associated Coagulopathies 159
Factor VIIa levels, gene polymorphism and plasma lipids in subjects with or without angiographically proven coronary artery disease 157
Modulation of FVII levels by intron 7 polymorphisms: population and in vitro studies 156
Management of Kidney Transplantation in a Factor VII-Deficient Patient: Case Report 156
Study of a G/A variation in the 3' untranslated region of prothrombin mRNA in Italian patients with venous thrombosis 155
Management of Kidney Transplantation in a Factor VII-Deficient Patient: Case Report 155
Hyperhomocysteinemia and a common methylene-tetrahydrofolate reductase mutation (Ala223Val MTHFR) are not associated with a history of thrombosis in patients with inherited thrombophilia 152
Factor V markers for the detection of genetic components of APC resi stance in venous thrombosis. 150
Non-conventional therapeutic strategies for inherited disorders of hemostasis 149
Modulation Of Factor VII Expression By Repeat And Sequence Variations In The Intron 7 Of FVII Gene: Population And In Vitro Studies 142
RNA−based therapeutic approaches for blood coagulation factor deficiencies caused by splicing mutations 117
Strong contribution of FVII genotypes to activated FVII levels and differences in genotype frequencies in northern and southern European countries 109
The heterozygous 20210 G/A genotype prevalence in patients affected by central and branch retinal vein occlusion: a pilot study. 107
The asymptomatic carriership of thrombophilic defects is associated with frequent genotypes of the fibrinogen gene cluster. 104
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Idiopathic central retinal vein occlusion in a thrombophilic patient with the heterozygous 20210 G/A prothrombin genotype 94
Rescue of a panel of Hemophilia A-causing 5’ss splicing mutations by unique Exon-specific U1snRNA variants 85
Intracellular readthrough of nonsense mutations by aminoglycosides in coagulation factor VII 83
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Temporal and genotype-driven variations of factor VII levels in patients with acute myocardial infarction 65
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Totale 8.586
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Categoria #
all - tutte 36.205
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 36.205
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
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
2025/20263.469 375 131 302 452 534 250 400 192 303 311 119 100
2026/202775 75 0 0 0 0 0 0 0 0 0 0 0
Totale 8.586