SFERA Archivio dei prodotti della Ricerca dell'Università di Ferrara

LUNGHI, Barbara
 Distribuzione geografica
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Continente #
NA - Nord America 7.577
AS - Asia 3.756
EU - Europa 2.019
SA - Sud America 586
Continente sconosciuto - Info sul continente non disponibili 145
AF - Africa 96
OC - Oceania 5
Totale 14.184
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Nazione #
US - Stati Uniti d'America 7.405
SG - Singapore 1.372
CN - Cina 901
VN - Vietnam 452
BR - Brasile 437
DE - Germania 370
IT - Italia 363
UA - Ucraina 330
HK - Hong Kong 313
GB - Regno Unito 214
TR - Turchia 186
FR - Francia 126
FI - Finlandia 125
BD - Bangladesh 124
JP - Giappone 113
PL - Polonia 100
CA - Canada 93
SE - Svezia 91
RU - Federazione Russa 78
IN - India 76
ID - Indonesia 56
MX - Messico 56
AR - Argentina 51
NL - Olanda 51
BE - Belgio 35
ZA - Sudafrica 33
IQ - Iraq 31
EC - Ecuador 26
ES - Italia 22
PK - Pakistan 22
CO - Colombia 18
CZ - Repubblica Ceca 18
MY - Malesia 17
AT - Austria 16
VE - Venezuela 16
PH - Filippine 14
CH - Svizzera 13
LT - Lituania 13
CL - Cile 12
DZ - Algeria 12
JO - Giordania 10
MA - Marocco 10
PY - Paraguay 10
SA - Arabia Saudita 9
GR - Grecia 8
IR - Iran 8
RO - Romania 8
NP - Nepal 7
TN - Tunisia 7
UZ - Uzbekistan 7
KE - Kenya 6
PE - Perù 6
UY - Uruguay 6
AU - Australia 5
ET - Etiopia 5
IE - Irlanda 5
JM - Giamaica 5
PT - Portogallo 5
AL - Albania 4
CI - Costa d'Avorio 4
IL - Israele 4
LB - Libano 4
TW - Taiwan 4
AE - Emirati Arabi Uniti 3
AO - Angola 3
BG - Bulgaria 3
BO - Bolivia 3
DO - Repubblica Dominicana 3
EG - Egitto 3
KR - Corea 3
KW - Kuwait 3
NO - Norvegia 3
OM - Oman 3
PR - Porto Rico 3
RS - Serbia 3
SK - Slovacchia (Repubblica Slovacca) 3
SN - Senegal 3
SV - El Salvador 3
AZ - Azerbaigian 2
BH - Bahrain 2
BY - Bielorussia 2
CR - Costa Rica 2
EU - Europa 2
HU - Ungheria 2
SI - Slovenia 2
TH - Thailandia 2
TT - Trinidad e Tobago 2
UG - Uganda 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AG - Antigua e Barbuda 1
BN - Brunei Darussalam 1
BW - Botswana 1
CG - Congo 1
DK - Danimarca 1
EE - Estonia 1
GD - Grenada 1
GH - Ghana 1
HN - Honduras 1
HR - Croazia 1
IS - Islanda 1
Totale 14.025
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Città #
Singapore 845
Ashburn 819
Woodbridge 596
Fairfield 594
San Jose 441
Houston 397
Chandler 369
Santa Clara 347
Jacksonville 345
Hong Kong 306
Beijing 285
Seattle 264
New York 255
Ann Arbor 239
Dallas 224
Wilmington 214
Cambridge 194
Ho Chi Minh City 166
Tokyo 108
Council Bluffs 103
Ferrara 102
Izmir 102
Munich 101
Hanoi 99
Nanjing 99
Warsaw 96
Los Angeles 94
Boardman 93
Princeton 85
The Dalles 77
Lauterbourg 73
San Diego 61
Milan 56
São Paulo 47
Orem 45
Shanghai 40
Helsinki 39
Jakarta 39
Dearborn 37
Buffalo 36
Shenyang 36
Chicago 35
London 35
Mexico City 35
Brussels 34
Bremen 31
Hefei 30
Toronto 29
Tianjin 26
Hebei 24
Frankfurt am Main 23
Chennai 22
Turku 22
Brooklyn 21
Johannesburg 21
Phoenix 21
Rome 21
Jiaxing 20
Nanchang 19
Montreal 18
Nuremberg 18
Redwood City 18
Changsha 16
Da Nang 16
Haiphong 16
Amsterdam 15
Denver 15
Stockholm 15
San Francisco 14
Brno 13
Kunming 13
Mountain View 13
Norwalk 13
Atlanta 12
Auburn Hills 12
Des Moines 12
Düsseldorf 12
Manchester 12
Mcallen 12
Baghdad 11
Curitiba 11
Dong Ket 11
Falkenstein 11
Moscow 11
Vienna 11
Belo Horizonte 10
Hangzhou 10
Poplar 10
Ottawa 9
Redmond 9
Amman 8
Ankara 8
Biên Hòa 8
Boston 8
Charlotte 8
Guayaquil 8
Jinan 8
Kuala Lumpur 8
Lahore 8
Montréal 8
Totale 9.516
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Nome #
C6orf10 low-frequency and rare variants in italian multiple sclerosis patients 361
An integrated genomic-transcriptomic approach supports a role for the proto-oncogene BCL3 in atherosclerosis 304
Activated factor VII-antithrombin complex predicts mortality in patients with stable coronary artery disease: a cohort study 291
A highly polymorphic microsatellite in the factor V gene is an informative tool for the study of factor V-related disorders 263
VITAMIN K-INDUCED MODIFICATION OF COAGULATION PHENOTYPE IN VKORC1 HOMOZYGOUS DEFICIENCY 259
Combinations of 4 mutations (FV R506Q, FV H1299R, FV Y1702C, PT 20210G/A) affecting the prothrombinase complex in a thrombophilic family 257
Changes in expression profiles of internal jugular vein wall and plasma protein levels in multiple sclerosis 252
A novel mutation (Leu817Pro) causing type 2A von Willebrand disease 250
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
Genetic determinants of activated factor VII antithrombin complex plasma concentration include tissue factor, factor VII and endothelial protein C receptor gene variants 248
A factor V genetic component differing from factor V R506Q contributes to the activated protein C resistance phenotype 243
Asymptomatic carriership of factor V Leiden and genotypes of the fibrinogen gene cluster 222
Apolipoprotein C-III Strongly Correlates with Activated Factor VII-Anti-Thrombin Complex: An Additional Link between Plasma Lipids and Coagulation 222
Polymorphisms at LDLR locus may be associated with coronary artery disease through modulation of coagulation factor VIII activity and independently from lipid profile 220
Mutation pattern in clinically asymptomatic coagulation factor VII deficiency 220
A missense mutation (Y1702C) in the coagulation factor V gene is a frequent cause of factor V deficiency in the italian population 219
The factor V Glu1608Lys mutation is recurrent in familial thrombophilia 213
A new factor V gene polymorphism (His 1254 Arg) present in subjects of African origin mimics the R2 polymorphism (His 1299 Arg) 209
FV multiallelic marker detects genetic components of APC resistance contributing to venous thromboembolism in FV Leiden carriers 209
Cis-segregation of c.1171c>t stop codon (p.r391*) in serpinc1 gene and c.1691g>a transition (p.r506q) in f5 gene and selected gwas multilocus approach in inherited thrombophilia 205
Molecular bases of CRM+ factor X deficiency: a frequent mutation (Ser334Pro) in the catalytic domain and a substitution (Glul02Lys) in the second EGF‐like domain 203
Performance prediction models based on anthropometric, genetic and psychological traits of Croatian sprinters 202
A novel factor V null mutation detected in a thrombophilic patient with pseudo-homozygous APC resistance and in an asymptomatic unrelated subject 200
Mutations in the R2 FV gene affect the ratio between the two FV isoforms in plasma 200
Interaction of occupational posture, lifestyle and genetic components of thrombophilia 196
The F11 rs2289252 polymorphism is associated with FXI activity levels and APTT ratio in women with thrombosis 194
Prospective evaluation of on-clopidogrel platelet reactivity over time in patients treated with percutaneous coronary intervention: Relationship with gene polymorphisms and clinical outcome 192
Expression Profiles of the Internal Jugular and Saphenous Veins: Focus on Hemostasis Genes 192
Expression profiles of the internal jugular and saphenous veins: Focus on hemostasis genes 190
An Italian Family with a Novel Mutation Causing Type 2A von Willebrand Disease and with Reduced Levels of von Willebrand Factor not Linked with the von Willebrand Factor Gene. 189
An underestimated combination of opposites resulting in enhanced thrombotic tendency 184
The factor VIII D I24I E polymorphism is associated with decreased factor VIII activity and not with activated protein C resistance levels 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
Detection of new polymorphic markers in the factor V gene: Association with factor V levels in plasma 174
Predictive value of D-dimer test for recurrent venous thromboembolism after anticoagulation withdrawal in subjects with a previous idiopathic event and in carriers of congenital thrombophilia 167
Does factor V Asp79His (409 G/C) polymorphism influence factor V and APC resistance levels? 163
New coagulation factor V gene polymorphisms define a single and infrequent haplotype underlying the factor V leiden mutation in Mediterranean populations and Indians 163
Factor V markers for the detection of genetic components of APC resistance in venous thrombosis 163
Hemostasis gene expression of the internal jugular and saphenous veins 158
Resistance to activated protein C, associated with oral contraceptives use; effect of formulations, duration of assumption, and doses of oestro- progestins 153
Modulation of factor V levels in plasma by polymorphisms in the C2 domain 153
Risks factors for highly unstable response to oral anticoagulation: a case-control study 150
Factor V markers for the detection of genetic components of APC resi stance in venous thrombosis. 150
Venous thromboembolism in young women - Role of thrombophilic mutations and oral contraceptive use 150
Novel phenotype and gamma-glutamyl carboxylase mutations in combined deficiency of vitamin K-dependent coagulation factors 149
Contribution of asialoglycoprotein receptor ASGR2 5’ UTR polymorphisms to full-length FVIII concentrate pharmacokinetics 146
The Asialoglycoprotein Receptor Minor Subunit Gene Contributes to Pharmacokinetics of Factor VIII Concentrates in Hemophilia A 146
Factor V Levels in a Cohort of Patients Eligible for Oral Anticoagulant Therapy. 143
Combination of Genomic and Transcriptomic Approaches Highlights Vascular and Circadian Clock Components in Multiple Sclerosis 140
Functional genetics 139
F9 missense mutations impairing factor IX activation are associated with pleiotropic plasma phenotypes 139
Phenotype and genotype expression in pseudohomozygous factor V-LEIDEN - The need for phenotype analysis 138
Resistance to activated protein C in healthy women taking oral contraceptives 138
CMR+ Factor V deficiency Arg2080Cys: A model to investigate altered C2 domain-membrane interaction. 137
Phenotypic homozygous activated protein C resistance associated with compound heterozygosity for Arg506Gln (factor V Leiden) and His1299 Arg substitutions in factor V 136
Combination of CLEC4M rs868875 G-Carriership and ABO O Genotypes May Predict Faster Decay of FVIII Infused in Hemophilia A Patients 135
Molecular basis of coagulation factor V deficiency caused by the R1698W inter-domain mutation. 134
Aptamer-modified FXa generation assays to investigate hypercoagulability in plasma from patients with ischemic heart disease 130
Expression of the normal factor V allele modulates the APC resistance phenotype in heterozygous carriers of the factor V Leiden mutation 129
In vivo modulation of a dominant-negative variant in mouse models of von Willebrand disease type 2A 125
Polimorfismi funzionali e terapia anticoagulante 124
Increased Susceptibility to Proteases in Type 2A von Willebrand Disease Associated with two Novel Mutations (Val 867 Glu, Pro 864 His). 123
Molecular bases of pseudo-homozygous APC resistance: The compound heterozygosity for FV R506Q and a FV null mutation results in the exclusive presence of FV Leiden molecules in plasma 121
Severe bleeding and absent ADP-induced platelet aggregation associated with inherited combined CalDAG-GEFI and P2Y12 deficiencies 111
Contribution of low density lipoprotein receptor-related protein genotypes to coagulation factor VIII levels in thrombotic women 109
Functional polymorphisms in the LDLR and pharmacokinetics of Factor VIII concentrates 106
The p.P1127S pathogenic variant lowers von Willebrand factor levels through higher affinity for the macrophagic scavenger receptor LRP1: Clinical phenotype and pathogenic mechanisms 106
Whole-Exome Sequencing in a Family with an Unexplained Tendency for Venous Thromboembolism: Multicomponent Prediction of Low-Frequency Variant Deleteriousness and of Individual Protein Interaction 105
The asymptomatic carriership of thrombophilic defects is associated with frequent genotypes of the fibrinogen gene cluster. 104
The asialoglycoprotein receptor ASGR2 5’ UTR polymorphisms influence several parameters of full-length FVIII concentrate pharmacokinetics 103
Evaluation of FV mRNA to define the residual FV expression levels in severe FV deficiency 96
null 95
Expression and characterization of a factor V mutation (E1608K) detected in familial thrombophilia. 95
Lesioni molecolari ricorrenti sono responsabili di difetti funzionali del fattore VII. 90
Studio di mutazioni in geni dell’emostasi. 90
Detection of New Polymorphic Markers in the Factor V Gene. 89
null 88
Studio di Mutazioni in Geni dell'Emostasi. 86
Selected cell receptor genotypes differentially modulate the ABO blood group influence on Factor VIII levels in severe aortic stenosis 83
In vitro and ex vivo rescue of a nonsense mutation responsible for severe coagulation factor V deficiency 78
Modulation of factor VIII pharmacokinetics by genetic components in factor VIII receptors 67
Association of membranous nephropathy with familial resistance to activated protein C 65
Influence of low-density lipoprotein (LDL) receptor-related protein and ABO blood group genotypes on factor XI levels. 64
null 63
Factor V Kuwait alias factor V R3: A rare polymorphism of uncertain functional significance 53
Genetic components in factor VIII receptors for individual and genotype-modeled hemophilia A treatment 32
Genetic determinants of activated factor VII-antithrombin plasma levels and mortality in patients with coronary artery disease 21
Reduced inhibition of activated prothrombin by heparin and venous thromboembolism: heparin resistance revisited 21
Totale 14.184
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Categoria #
all - tutte 64.719
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 64.719
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022903 96 87 47 71 50 18 54 47 21 59 83 270
2022/2023902 93 78 24 109 130 130 67 76 100 15 46 34
2023/2024563 34 39 18 20 36 183 9 26 17 7 13 161
2024/20251.870 44 31 172 66 243 169 46 77 316 219 275 212
2025/20265.510 524 222 523 704 758 356 620 311 547 537 277 131
2026/2027148 148 0 0 0 0 0 0 0 0 0 0 0
Totale 14.184