SFERA Archivio dei prodotti della Ricerca dell'Università di Ferrara

GEMMATI, Donato
 Distribuzione geografica
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Continente #
NA - Nord America 22.635
AS - Asia 13.879
EU - Europa 9.672
SA - Sud America 2.262
AF - Africa 320
OC - Oceania 33
Continente sconosciuto - Info sul continente non disponibili 18
Totale 48.819
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Nazione #
US - Stati Uniti d'America 21.959
SG - Singapore 5.146
CN - Cina 3.363
IT - Italia 2.659
DE - Germania 1.874
BR - Brasile 1.784
VN - Vietnam 1.549
UA - Ucraina 1.248
HK - Hong Kong 1.167
GB - Regno Unito 860
PL - Polonia 786
TR - Turchia 698
FI - Finlandia 541
FR - Francia 451
BD - Bangladesh 438
CA - Canada 388
JP - Giappone 387
RU - Federazione Russa 334
IN - India 301
SE - Svezia 276
MX - Messico 210
AR - Argentina 176
ID - Indonesia 172
NL - Olanda 127
ZA - Sudafrica 117
IQ - Iraq 101
ES - Italia 79
BE - Belgio 71
PK - Pakistan 70
EC - Ecuador 67
CO - Colombia 66
VE - Venezuela 60
UZ - Uzbekistan 58
CZ - Repubblica Ceca 51
MA - Marocco 51
SA - Arabia Saudita 51
SM - San Marino 49
EG - Egitto 41
CH - Svizzera 40
MY - Malesia 40
AT - Austria 39
LT - Lituania 38
PH - Filippine 38
AE - Emirati Arabi Uniti 36
IR - Iran 36
CL - Cile 33
PY - Paraguay 33
IE - Irlanda 30
AU - Australia 26
KE - Kenya 26
NP - Nepal 26
TN - Tunisia 24
UY - Uruguay 21
RO - Romania 20
AZ - Azerbaigian 17
IL - Israele 17
JO - Giordania 17
TH - Thailandia 15
JM - Giamaica 14
KZ - Kazakistan 14
GR - Grecia 13
LK - Sri Lanka 13
PT - Portogallo 13
TW - Taiwan 13
CR - Costa Rica 12
DZ - Algeria 12
KR - Corea 12
LB - Libano 12
PE - Perù 12
PS - Palestinian Territory 12
SN - Senegal 12
DO - Repubblica Dominicana 11
OM - Oman 11
AL - Albania 10
BO - Bolivia 9
EU - Europa 9
DK - Danimarca 8
ET - Etiopia 8
GT - Guatemala 8
SK - Slovacchia (Repubblica Slovacca) 8
BG - Bulgaria 7
BY - Bielorussia 7
GE - Georgia 7
KW - Kuwait 7
QA - Qatar 7
RS - Serbia 7
TT - Trinidad e Tobago 7
A2 - ???statistics.table.value.countryCode.A2??? 6
HN - Honduras 6
HU - Ungheria 6
BH - Bahrain 5
KG - Kirghizistan 5
NZ - Nuova Zelanda 5
NG - Nigeria 4
NI - Nicaragua 4
NO - Norvegia 4
PA - Panama 4
AO - Angola 3
CG - Congo 3
GD - Grenada 3
Totale 48.751
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Città #
Singapore 3.018
Ashburn 2.323
Woodbridge 1.674
Fairfield 1.521
San Jose 1.435
Jacksonville 1.364
Chandler 1.325
Hong Kong 1.149
Beijing 1.047
Santa Clara 1.021
Houston 989
Ann Arbor 977
Warsaw 773
Seattle 623
Wilmington 614
Ho Chi Minh City 499
New York 469
Cambridge 445
Izmir 422
Munich 411
Los Angeles 401
Nanjing 390
Tokyo 365
Dallas 360
Hanoi 359
Ferrara 334
Milan 298
Princeton 291
Lauterbourg 273
Boardman 238
Helsinki 191
São Paulo 159
Council Bluffs 150
Orem 147
Mexico City 144
Rome 144
Shanghai 142
San Diego 141
Mcallen 130
Buffalo 124
Montréal 122
Bologna 118
The Dalles 118
Shenyang 117
London 116
Dearborn 99
Jakarta 98
Nanchang 96
Montreal 91
Changsha 90
Tianjin 89
Da Nang 88
Turku 88
Hebei 86
Toronto 83
Chicago 82
Bremen 81
Chennai 80
Denver 76
Jiaxing 74
Brooklyn 73
Hefei 69
Frankfurt am Main 68
Haiphong 68
Rio de Janeiro 67
Brussels 65
Phoenix 63
Johannesburg 61
Boston 55
Jinan 53
Redwood City 53
Naples 52
Düsseldorf 51
Greven 51
Belo Horizonte 50
Tashkent 50
Bottrop 49
Guangzhou 49
Norwalk 49
Stockholm 49
Falls Church 48
San Francisco 48
Atlanta 47
Berlin 47
Baghdad 46
Manchester 43
Moscow 41
Brasília 39
Nuremberg 39
Poplar 38
Dong Ket 37
Falkenstein 37
Mountain View 37
Amsterdam 36
Kunming 35
Zhengzhou 35
San Mateo 32
Des Moines 31
Mumbai 31
Ningbo 30
Totale 30.694
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Nome #
Nanobiomaterials for vascular biology and wound management: a review 1.301
FISIOPATOLOGIA DELL'EMOSTASI E DELLA COAGULAZIONE 726
ProC Global test>ProC Complete test: una modificazione del Global test per la misurazione contemporanea della attività della PC, della PS, e del fenotipo Leiden. 586
Gene-gene interactions among coding genes of iron-homeostasis proteins and APOE-alleles in Cognitive Impairment Diseases 487
Impact of methylenetetrahydrofolate reductase C677T polymorphism on the efficacy of photodynamic therapy in patients with neovascular age-related macular degeneration 371
C6orf10 low-frequency and rare variants in italian multiple sclerosis patients 358
Gene polymorphisms in folate metabolizing enzymes in adult acute lymphoblastic leukemia: effects on methotrexate-related toxicity and survival 288
Inherited genetic predispositions in F13A1 and F13B genes predict abdominal adhesion formation: identification of gender prognostic indicators 288
Fisiopatologia della Coagulazione. 283
Ricerche metodologiche sul dosaggio del cofattore Ristocetinico per la diagnosi di morbo di von Willebrand. 279
Methylenetetrahydrofolate reductase C677T and A1298C gene variants in adult non-Hodgkin's lymphoma patients: association with toxicity and survival 270
Effect of factor XIII-A G185T polymorphism on visual prognosis after photodynamic therapy for neovascular macular degeneration 269
Coagulation factor XIIIA (F13A1): Novel perspectives in treatment and pharmacogenetics 265
The active metabolite of warfarin (3′-hydroxywarfarin) and correlation with INR, warfarin and drug weekly dosage in patients under oral anticoagulant therapy: A pharmacogenetics study 265
Sudden sensorineural hearing loss and polymorphisms in iron homeostasis genes: new insights from a case-control study 264
Serum iron and matrix metalloproteinase-9 variations in limbs affected by chronic venous disease and venous leg ulcers 262
Crosstalk between adipokines and paraoxonase 1: A new potential axis linking oxidative stress and inflammation 260
COVID-19 and individual genetic susceptibility/receptivity: Role of ACE1/ACE2 genes, immunity, inflammation and coagulation. might the double x-chromosome in females be protective against SARS-COV-2 compared to the single x-chromosome in males? 258
Realizzazione di un DNA-Array di varianti genetiche nelle lesioni croniche di origine vascolare 256
F13A1 gene variant (V34L) and residual circulating FXIIIA levels predict short-and long-term mortality in acute myocardial infarction after coronary angioplasty 255
Changes in adipose tissue distribution and association between uric acid and bone health during menopause transition 255
A De Novo and Heterozygous Gene Deletion Causing a Variant of von Willebrand Disease 252
Factor XIII V34L polymorphism modulates the risk of chronic venous leg ulcer progression and extension 251
Factor XIII contrasts the effects of metalloproteinases in human dermal fibroblast cultured cells 251
Hemochromatosis C282Y gene mutation increases the risk of venous leg ulceration 249
FOLATE GENE VARIANTS AFFECT METHOTREXATE-RELATED TOXICITY IN ADULT ACUTE LYMPHOBLASTIC LEUKEMIA PATIENTS 249
A novel mutation (Leu817Pro) causing type 2A von Willebrand disease 247
High throughput array technologies: Expanding applications from clinics to applied research 245
Tissue factor and coagulation factor VII levels during acute myocardial infarction: Association with genotype and adverse events 241
Analisi dei multimeri del fattore von Willebrand mediante doppia immunoprecipitazione dopo elettroforesi su gel di agarosio. 241
Factor XIII-A dynamics in acute myocardial infarction: a novel prognostic biomarker? 240
A common mutation in the gene for coagulation factor XIII-A (Val34Leu): A risk factor for primary intracerebral hemorrhage is protective against atherothrombotic diseases 237
Assessment of the interlaboratory variability and robustness of JAK2V617F mutation assays: A study involving a consortium of 19 Italian laboratories 236
“Bridging the Gap” Everything that Could Have Been Avoided If We Had Applied Gender Medicine, Pharmacogenetics and Personalized Medicine in the Gender-Omics and Sex-Omics Era 236
The carboxyl-terminal region is not essential for secreted and functional levels of coagulation factor X 233
Coexistence of antithrombin deficiency, factor V Leiden and hyperhomocysteinemia in a thrombotic family. 232
Genetic predictors of response to photodynamic therapy 231
DNA-array of gene variants in venous leg ulcers: Detection of prognostic indicators 229
A DE NOVO GENE ALTERATION CAUSING VON WILLEBRAND DISEASE 228
Prognostic role of Factor XIII gene variants in nonhealing venous leg ulcers 228
Influence of gene polymorphisms in ulcer healing process after superficial venous surgery 227
Fisiopatologia dell'Emostasi e della Coagulazione 227
A deep vein thrombosis in an adolescent diabetic boy: A case report | [Descrizione di un caso di trombosi venosa profonda in un adolescente diabetico] 226
A "de novo" Gene Deletion and New RFLPs Detected by von Willebrand Factor cDNA. 226
Asymptomatic carriership of factor V Leiden and genotypes of the fibrinogen gene cluster 221
C677T/A1298C MTHFR Gene Mutations, Homocysteine, Folate Levels and MTHFR Activity, in Normal Subjects and Cases with Myocardial Infarction 220
A photometric assay for factor-XIII in chronic hepatopathies. 218
Coexistence of factor V G1691A and factor II G20210A gene mutations in a thrombotic family is associated with recurrence and early onset of venous thrombosis 216
Common gene polymorphisms in the metabolic folate and methylation pathway and the risk of acute lymphoblastic leukemia and non-Hodgkin's lymphoma in adults 215
Effects of physical stimulation with electromagnetic field and insulin growth factor-I treatment on proteoglycan synthesis of bovine articular cartilage 215
Effects of electromagnetic fields on proteoglycan metabolism of bovine articular cartilage explants 214
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis 213
The factor V Glu1608Lys mutation is recurrent in familial thrombophilia 211
Polymorphisms in the genes coding for iron binding and transporting proteins are Associated with Disability, Severity, and Early Progression in Multiple Sclerosis. 211
FXIII levels and genotypes in myocardial infarction: a potential novel prognostic biomarker? 211
MTHFR 677C→T polymorphism and risk of coronary heart disease: A meta-analysis 210
A modified functional Global test to measure protein C, protein S activities and the activated protein C-resistance phenotype. 210
The carboxyl-terminal region is NOT essential for secreted and functional levels of coagulation factor X 209
Quantitive evaluation of dentin sialoprotein (DSP) using microbeads - A potential early marker of root resorption 209
Influence of Genetic Polymorphisms in Ulcer Healing Process after Superficial Venous Surgery 208
Custom CGH array profiling of copy number variations (CNVs) on chromosome 6p21.32 (HLA locus) in patients with venous malformations associated with multiple sclerosis 208
Investigation of in vitro cytotoxicity of the redox state of ionic iron in neuroblastoma cells. 206
Acute Coronaric Syndroms and FVII polymorphisms: different effects in the same gene 204
Redox metals homeostasis in multiple sclerosis and amyotrophic lateral sclerosis: a review 203
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 202
Characterization of polymorphic markers in the von Willebrand factor gene and pseudogene 201
A photometric method for the dosage of factor XIII applied to the study of chronic hepatopathies. 199
TIME- AND DOSE-DEPENDENT EFFECTS OF CHRONIC WOUND FLUID ON HUMAN ADULT DERMAL FIBROBLASTS 199
GENETIC SUSCEPTIBILITY IN VENOUS LEG ULCER 198
Nanoengineering Approaches to Design Advanced Dental Materials for Clinical Applications. 198
Factor XIIIA V34L and Factor XIIIB H95R Gene Polymorphisms: Effects on the Risk of Myocardial Infarction and on Survival. 194
C677T Substitution in the Methylenetetrahydrofolate Reductase Gene as a Risk Factor for Venous Thrombosis and Arterial Disease in Selected Patients. 193
Sudden sensorineural hearing loss and polymorphisms in iron homeostasis genes. 190
Expression profiles of the internal jugular and saphenous veins: Focus on hemostasis genes 190
Expression Profiles of the Internal Jugular and Saphenous Veins: Focus on Hemostasis Genes 190
Partial gene deletion in a family with factor X deficiency 188
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. 188
Risk of venous thromboembolism associated with single and combined effects of Factor V Leiden, Prothrombin 20210A and Methylenetethraydrofolate reductase C677T: a meta-analysis involving over 11,000 cases and 21,000 controls 187
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients 186
The reduced sensitivity of the ProC (R) Global test in protein S deficient subjects reflects a reduction in the associated thrombotic risk 185
Folate: metabolism, biochemistry and role in disease processes. 184
A de novo antithrombin mutation found in a patient with deep vein thrombosis and vascular abnormalities 184
Genetics and epigenetics of one-carbon metabolism pathway in autism spectrum disorder: A sex-specific brain epigenome? 184
Dihydrofolate reductase (DHFR) 19-bp ins/del polymorphism and methylenetetrahydrofolate reductase (MTHFR) C677T in coronary heart disease patients: potential intracellular folate unbalancing. 181
Meta-analysis of multiple sclerosis microarray data reveals dysregulation in RNA splicing regulatory genes 181
Low folate levels and thermolabile methylenetetrahydrofolate reductase as primary determinant of mild hyperhomocystinemia in normal and thromboembolic subjects 178
Deletion of exons 26-34 (domain D3-A3) of von Willebrand-factor gene in the von Willebrand disease type-II. 177
circRNAs as Epigenetic Regulators of Integrity in Blood–Brain Barrier Architecture: Mechanisms and Therapeutic Strategies in Multiple Sclerosis 176
Different anticoagulant response to activated protein C (APC test) and to Agkistrodon Contortix venom (ACV test) in a family with FV-R506Q substitution 176
Rapid detection of a protein C gene mutation present in the asymptomatic and not in the thrombosis‐prone lineage 176
Maternal Haplotypes in DHFR Promoter and MTHFR Gene in Tuning Childhood Acute Lymphoblastic Leukemia Onset-Latency: Genetic/Epigenetic Mother/Child Dyad Study (GEMCDS) 175
Molecular defects in CRM+ factor VII deficiencies: modelling of missense mutations in the catalytic domain of FVII 175
Tissue Factor and Coagulation Factor VII Levels during Acute Myocardial Infarction Contribute to Predict Mortality and re-infarction. 174
A modified functional global test to measure PC, PS activities and the APC-resistance phenotype 174
Factor XIIIA-V34L and factor XIIIB-H95R gene variants: effects on survival in myocardial infarction patients. 174
Common Polymorphisms in the Metabolic Folate Pathway Decrease the Risk of Acute Lymphocytic Leukemia in Adults 174
Common Polymorphisms in the Metabolic Folate Pathway Decrease the Risk of Acute Lymphocitic Leukemia in Adults 173
Factor XIII-A Gene Mutation (Val34Leu) and Arterial Vascular Disease 173
The eclipse effect: the overlapping of varicose vein and C282Y heterozygous gene mutation 173
Detection of new polymorphic markers in the factor V gene: Association with factor V levels in plasma 172
Totale 24.162
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Categoria #
all - tutte 200.670
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 9.143
Totale 209.813
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021174 0 0 0 0 0 0 0 0 0 0 0 174
2021/20223.009 210 380 272 98 247 124 118 116 101 253 301 789
2022/20233.069 328 212 78 377 496 507 167 279 317 32 174 102
2023/20241.611 148 190 69 46 162 247 49 110 34 53 75 428
2024/20256.923 204 157 543 215 892 500 239 423 1.180 902 945 723
2025/202619.381 1.665 860 1.622 2.538 2.632 1.286 2.192 1.137 1.847 2.037 1.092 473
Totale 49.258