GEMMATI, Donato
 Distribuzione geografica
Continente #
NA - Nord America 18.731
AS - Asia 9.961
EU - Europa 8.376
SA - Sud America 1.809
AF - Africa 200
OC - Oceania 28
Continente sconosciuto - Info sul continente non disponibili 17
Totale 39.122
Nazione #
US - Stati Uniti d'America 18.195
SG - Singapore 4.032
CN - Cina 2.917
IT - Italia 2.181
DE - Germania 1.813
BR - Brasile 1.540
UA - Ucraina 1.231
HK - Hong Kong 1.048
GB - Regno Unito 776
PL - Polonia 768
TR - Turchia 654
VN - Vietnam 592
FI - Finlandia 407
CA - Canada 317
RU - Federazione Russa 316
SE - Svezia 264
MX - Messico 183
IN - India 146
ID - Indonesia 139
FR - Francia 133
AR - Argentina 114
NL - Olanda 91
ZA - Sudafrica 91
JP - Giappone 80
BE - Belgio 64
ES - Italia 61
BD - Bangladesh 59
SM - San Marino 49
CZ - Repubblica Ceca 47
EC - Ecuador 44
IQ - Iraq 43
IR - Iran 35
LT - Lituania 32
PK - Pakistan 31
MA - Marocco 30
CO - Colombia 29
EG - Egitto 29
AT - Austria 28
CH - Svizzera 28
UZ - Uzbekistan 27
VE - Venezuela 24
PY - Paraguay 23
AU - Australia 21
IE - Irlanda 18
KE - Kenya 17
AE - Emirati Arabi Uniti 16
RO - Romania 16
UY - Uruguay 13
CL - Cile 12
IL - Israele 12
SA - Arabia Saudita 12
TN - Tunisia 12
LK - Sri Lanka 11
MY - Malesia 11
AZ - Azerbaigian 10
NP - Nepal 10
AL - Albania 9
EU - Europa 9
GR - Grecia 9
KR - Corea 8
TW - Taiwan 8
KZ - Kazakistan 7
OM - Oman 7
A2 - ???statistics.table.value.countryCode.A2??? 6
CR - Costa Rica 6
JM - Giamaica 6
LB - Libano 6
PE - Perù 6
SN - Senegal 6
BY - Bielorussia 5
DO - Repubblica Dominicana 5
NZ - Nuova Zelanda 5
TT - Trinidad e Tobago 5
BH - Bahrain 4
BO - Bolivia 4
DK - Danimarca 4
DZ - Algeria 4
HN - Honduras 4
HU - Ungheria 4
JO - Giordania 4
KW - Kuwait 4
PH - Filippine 4
PS - Palestinian Territory 4
PT - Portogallo 4
QA - Qatar 4
SK - Slovacchia (Repubblica Slovacca) 4
TH - Thailandia 4
GT - Guatemala 3
NO - Norvegia 3
LI - Liechtenstein 2
MG - Madagascar 2
NI - Nicaragua 2
PA - Panama 2
TJ - Tagikistan 2
AF - Afghanistan, Repubblica islamica di 1
AM - Armenia 1
AO - Angola 1
BA - Bosnia-Erzegovina 1
BF - Burkina Faso 1
BG - Bulgaria 1
Totale 39.093
Città #
Singapore 2.127
Woodbridge 1.673
Ashburn 1.594
Fairfield 1.521
Jacksonville 1.357
Chandler 1.325
Hong Kong 1.043
Ann Arbor 977
Beijing 974
Houston 973
Santa Clara 954
Warsaw 756
Seattle 617
Wilmington 614
Cambridge 445
Izmir 419
Munich 411
Nanjing 390
Ferrara 311
New York 305
Dallas 302
Los Angeles 297
Princeton 291
Milan 251
Boardman 235
Ho Chi Minh City 209
San Diego 140
Shanghai 137
São Paulo 134
Mexico City 133
Mcallen 130
Montréal 122
Hanoi 117
Shenyang 117
Dearborn 98
Nanchang 96
Jakarta 93
London 92
Rome 92
Buffalo 90
Changsha 88
Turku 88
The Dalles 87
Hebei 86
Tianjin 86
Bologna 83
Bremen 81
Jiaxing 74
Hefei 68
Chicago 67
Montreal 67
Helsinki 66
Tokyo 64
Brussels 61
Toronto 61
Rio de Janeiro 59
Brooklyn 58
Denver 55
Jinan 53
Redwood City 53
Düsseldorf 51
Greven 51
Bottrop 49
Johannesburg 49
Norwalk 49
Orem 49
Falls Church 48
Phoenix 47
Chennai 44
Boston 43
Berlin 41
Belo Horizonte 40
Guangzhou 39
Moscow 39
San Francisco 39
Stockholm 38
Dong Ket 37
Falkenstein 37
Mountain View 37
Atlanta 35
Kunming 35
Nuremberg 35
Zhengzhou 35
San Mateo 32
Brasília 31
Manchester 31
Poplar 31
Frankfurt am Main 30
Ningbo 30
Orange 30
Brno 28
Des Moines 28
Haiphong 27
Addison 26
Naples 26
Auburn Hills 25
Council Bluffs 25
Augusta 24
Curitiba 24
Da Nang 24
Totale 24.806
Nome #
Nanobiomaterials for vascular biology and wound management: a review 1.240
FISIOPATOLOGIA DELL'EMOSTASI E DELLA COAGULAZIONE 623
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. 552
Impact of methylenetetrahydrofolate reductase C677T polymorphism on the efficacy of photodynamic therapy in patients with neovascular age-related macular degeneration 341
C6orf10 low-frequency and rare variants in italian multiple sclerosis patients 286
Ricerche metodologiche sul dosaggio del cofattore Ristocetinico per la diagnosi di morbo di von Willebrand. 259
Inherited genetic predispositions in F13A1 and F13B genes predict abdominal adhesion formation: identification of gender prognostic indicators 253
Fisiopatologia della Coagulazione. 244
Gene-gene interactions among coding genes of iron-homeostasis proteins and APOE-alleles in Cognitive Impairment Diseases 243
Gene polymorphisms in folate metabolizing enzymes in adult acute lymphoblastic leukemia: effects on methotrexate-related toxicity and survival 237
Effect of factor XIII-A G185T polymorphism on visual prognosis after photodynamic therapy for neovascular macular degeneration 227
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 226
Methylenetetrahydrofolate reductase C677T and A1298C gene variants in adult non-Hodgkin's lymphoma patients: association with toxicity and survival 226
Serum iron and matrix metalloproteinase-9 variations in limbs affected by chronic venous disease and venous leg ulcers 225
High throughput array technologies: Expanding applications from clinics to applied research 225
Realizzazione di un DNA-Array di varianti genetiche nelle lesioni croniche di origine vascolare 224
Analisi dei multimeri del fattore von Willebrand mediante doppia immunoprecipitazione dopo elettroforesi su gel di agarosio. 223
Sudden sensorineural hearing loss and polymorphisms in iron homeostasis genes: new insights from a case-control study 222
Crosstalk between adipokines and paraoxonase 1: A new potential axis linking oxidative stress and inflammation 222
A De Novo and Heterozygous Gene Deletion Causing a Variant of von Willebrand Disease 208
Tissue factor and coagulation factor VII levels during acute myocardial infarction: Association with genotype and adverse events 206
Coagulation factor XIIIA (F13A1): Novel perspectives in treatment and pharmacogenetics 206
Factor XIII contrasts the effects of metalloproteinases in human dermal fibroblast cultured cells 206
Changes in adipose tissue distribution and association between uric acid and bone health during menopause transition 205
Factor XIII V34L polymorphism modulates the risk of chronic venous leg ulcer progression and extension 204
A novel mutation (Leu817Pro) causing type 2A von Willebrand disease 204
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? 204
FOLATE GENE VARIANTS AFFECT METHOTREXATE-RELATED TOXICITY IN ADULT ACUTE LYMPHOBLASTIC LEUKEMIA PATIENTS 201
“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 200
F13A1 gene variant (V34L) and residual circulating FXIIIA levels predict short-and long-term mortality in acute myocardial infarction after coronary angioplasty 199
DNA-array of gene variants in venous leg ulcers: Detection of prognostic indicators 197
A common mutation in the gene for coagulation factor XIII-A (Val34Leu): A risk factor for primary intracerebral hemorrhage is protective against atherothrombotic diseases 195
Coexistence of antithrombin deficiency, factor V Leiden and hyperhomocysteinemia in a thrombotic family. 195
Factor XIII-A dynamics in acute myocardial infarction: a novel prognostic biomarker? 194
Effects of physical stimulation with electromagnetic field and insulin growth factor-I treatment on proteoglycan synthesis of bovine articular cartilage 192
Prognostic role of Factor XIII gene variants in nonhealing venous leg ulcers 192
A "de novo" Gene Deletion and New RFLPs Detected by von Willebrand Factor cDNA. 189
A DE NOVO GENE ALTERATION CAUSING VON WILLEBRAND DISEASE 188
Influence of gene polymorphisms in ulcer healing process after superficial venous surgery 188
Genetic predictors of response to photodynamic therapy 187
C677T/A1298C MTHFR Gene Mutations, Homocysteine, Folate Levels and MTHFR Activity, in Normal Subjects and Cases with Myocardial Infarction 186
A photometric assay for factor-XIII in chronic hepatopathies. 184
Asymptomatic carriership of factor V Leiden and genotypes of the fibrinogen gene cluster 183
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 182
The carboxyl-terminal region is NOT essential for secreted and functional levels of coagulation factor X 182
A modified functional Global test to measure protein C, protein S activities and the activated protein C-resistance phenotype. 182
Investigation of in vitro cytotoxicity of the redox state of ionic iron in neuroblastoma cells. 179
The carboxyl-terminal region is not essential for secreted and functional levels of coagulation factor X 178
Effects of electromagnetic fields on proteoglycan metabolism of bovine articular cartilage explants 177
Assessment of the interlaboratory variability and robustness of JAK2V617F mutation assays: A study involving a consortium of 19 Italian laboratories 177
Characterization of polymorphic markers in the von Willebrand factor gene and pseudogene 177
A photometric method for the dosage of factor XIII applied to the study of chronic hepatopathies. 173
FXIII levels and genotypes in myocardial infarction: a potential novel prognostic biomarker? 173
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis 172
Quantitive evaluation of dentin sialoprotein (DSP) using microbeads - A potential early marker of root resorption 172
The factor V Glu1608Lys mutation is recurrent in familial thrombophilia 171
Polymorphisms in the genes coding for iron binding and transporting proteins are Associated with Disability, Severity, and Early Progression in Multiple Sclerosis. 171
Common gene polymorphisms in the metabolic folate and methylation pathway and the risk of acute lymphoblastic leukemia and non-Hodgkin's lymphoma in adults 170
MTHFR 677C→T polymorphism and risk of coronary heart disease: A meta-analysis 170
Fisiopatologia dell'Emostasi e della Coagulazione 168
Redox metals homeostasis in multiple sclerosis and amyotrophic lateral sclerosis: a review 168
Hemochromatosis C282Y gene mutation increases the risk of venous leg ulceration 167
Custom CGH array profiling of copy number variations (CNVs) on chromosome 6p21.32 (HLA locus) in patients with venous malformations associated with multiple sclerosis 167
Influence of Genetic Polymorphisms in Ulcer Healing Process after Superficial Venous Surgery 166
Nanoengineering Approaches to Design Advanced Dental Materials for Clinical Applications. 165
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients 164
Deletion of exons 26-34 (domain D3-A3) of von Willebrand-factor gene in the von Willebrand disease type-II. 163
TIME- AND DOSE-DEPENDENT EFFECTS OF CHRONIC WOUND FLUID ON HUMAN ADULT DERMAL FIBROBLASTS 162
Partial gene deletion in a family with factor X deficiency 160
Rapid detection of a protein C gene mutation present in the asymptomatic and not in the thrombosis‐prone lineage 157
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. 157
Sudden sensorineural hearing loss and polymorphisms in iron homeostasis genes. 156
Factor XIIIA V34L and Factor XIIIB H95R Gene Polymorphisms: Effects on the Risk of Myocardial Infarction and on Survival. 154
Meta-analysis of multiple sclerosis microarray data reveals dysregulation in RNA splicing regulatory genes 154
The reduced sensitivity of the ProC (R) Global test in protein S deficient subjects reflects a reduction in the associated thrombotic risk 153
C677T Substitution in the Methylenetetrahydrofolate Reductase Gene as a Risk Factor for Venous Thrombosis and Arterial Disease in Selected Patients. 153
Acute Coronaric Syndroms and FVII polymorphisms: different effects in the same gene 153
Molecular defects in CRM+ factor VII deficiencies: modelling of missense mutations in the catalytic domain of FVII 153
Folate: metabolism, biochemistry and role in disease processes. 152
Tissue Factor and Coagulation Factor VII Levels during Acute Myocardial Infarction Contribute to Predict Mortality and re-infarction. 152
Expression Profiles of the Internal Jugular and Saphenous Veins: Focus on Hemostasis Genes 152
Proteoglycan synthesis in bovine articular cartilage explants exposed to different low-frequency low-energy pulsed electromagnetic fields 151
Different anticoagulant response to activated protein C (APC test) and to Agkistrodon Contortix venom (ACV test) in a family with FV-R506Q substitution 151
A deep vein thrombosis in an adolescent diabetic boy: A case report | [Descrizione di un caso di trombosi venosa profonda in un adolescente diabetico] 147
Expression profiles of the internal jugular and saphenous veins: Focus on hemostasis genes 147
Clinical observations on the relationship between idiopathic thrombocytopenic purpura lupus anticoagulant and anticardio-lipin antibody syndrome. 146
A de novo antithrombin mutation found in a patient with deep vein thrombosis and vascular abnormalities 146
Dihydrofolate reductase (DHFR) 19-bp ins/del polymorphism and methylenetetrahydrofolate reductase (MTHFR) C677T in coronary heart disease patients: potential intracellular folate unbalancing. 145
Functional properties of factor V and factor Va encoded by the R2-gene 143
Detection of new polymorphic markers in the factor V gene: Association with factor V levels in plasma 143
A modified functional global test to measure PC, PS activities and the APC-resistance phenotype 143
Clinical implications of gene polymorphisms in venous leg ulcer: A model in tissue injury and reparative process 142
GENETIC SUSCEPTIBILITY IN VENOUS LEG ULCER 142
Detection and characterization of polymorphic markers in the factor-VII gene. 142
Common Polymorphisms in the Metabolic Folate Pathway Decrease the Risk of Acute Lymphocytic Leukemia in Adults 140
What is potentially the right factor XIII for venous leg ulcer treatment? 139
Common Gene Polymorphisms in the Metabolic Folate and Methylation Pathway and the Risk of Acute Lymphoblastic Leukemia and non-Hodgkin’s Lymphoma 139
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 139
Una "rete" per proteggere il cuore. (FAR 2013) 137
Factor XIII-A Gene Mutation (Val34Leu) and Arterial Vascular Disease 136
Totale 20.031
Categoria #
all - tutte 173.860
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 7.773
Totale 181.633


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20212.274 0 0 0 0 0 424 181 420 105 494 476 174
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
2025/20269.675 1.665 860 1.622 2.538 2.632 358 0 0 0 0 0 0
Totale 39.552