GEMMATI, Donato
 Distribuzione geografica
Continente #
NA - Nord America 14.738
EU - Europa 6.380
AS - Asia 3.337
AF - Africa 23
OC - Oceania 16
SA - Sud America 16
Continente sconosciuto - Info sul continente non disponibili 15
Totale 24.525
Nazione #
US - Stati Uniti d'America 14.566
IT - Italia 1.752
CN - Cina 1.658
DE - Germania 1.327
UA - Ucraina 1.169
SG - Singapore 812
PL - Polonia 678
TR - Turchia 615
GB - Regno Unito 595
FI - Finlandia 280
SE - Svezia 225
CA - Canada 168
ID - Indonesia 87
FR - Francia 69
BE - Belgio 59
SM - San Marino 44
IN - India 40
RU - Federazione Russa 40
CZ - Repubblica Ceca 38
VN - Vietnam 38
HK - Hong Kong 26
IR - Iran 25
CH - Svizzera 16
IE - Irlanda 15
RO - Romania 14
BR - Brasile 13
NL - Olanda 13
AU - Australia 11
LT - Lituania 11
EG - Egitto 10
EU - Europa 9
ES - Italia 8
PK - Pakistan 8
A2 - ???statistics.table.value.countryCode.A2??? 6
AL - Albania 5
GR - Grecia 5
JP - Giappone 5
NZ - Nuova Zelanda 5
DK - Danimarca 4
MA - Marocco 4
MY - Malesia 4
SK - Slovacchia (Repubblica Slovacca) 4
KR - Corea 3
ZA - Sudafrica 3
AT - Austria 2
BD - Bangladesh 2
CO - Colombia 2
IL - Israele 2
IQ - Iraq 2
KE - Kenya 2
MG - Madagascar 2
MX - Messico 2
AE - Emirati Arabi Uniti 1
BA - Bosnia-Erzegovina 1
CU - Cuba 1
CY - Cipro 1
DZ - Algeria 1
HN - Honduras 1
HU - Ungheria 1
KZ - Kazakistan 1
MC - Monaco 1
MM - Myanmar 1
NO - Norvegia 1
NP - Nepal 1
PE - Perù 1
PH - Filippine 1
PT - Portogallo 1
RS - Serbia 1
SA - Arabia Saudita 1
SN - Senegal 1
TH - Thailandia 1
TJ - Tagikistan 1
TW - Taiwan 1
VA - Santa Sede (Città del Vaticano) 1
Totale 24.525
Città #
Woodbridge 1.673
Fairfield 1.521
Jacksonville 1.355
Chandler 1.324
Ann Arbor 977
Houston 950
Ashburn 696
Warsaw 674
Santa Clara 634
Singapore 618
Wilmington 613
Seattle 599
Cambridge 445
Izmir 418
Nanjing 388
Beijing 294
Princeton 291
Ferrara 260
Boardman 231
Milan 199
New York 160
Munich 149
San Diego 139
Mcallen 130
Shanghai 129
Montréal 122
Shenyang 117
Dearborn 98
Nanchang 95
Changsha 87
Hebei 86
Jakarta 85
Bremen 81
Jiaxing 70
Los Angeles 65
Rome 65
Tianjin 58
Brussels 57
Redwood City 53
Jinan 52
Greven 51
Bottrop 49
Norwalk 49
Falls Church 48
London 47
Bologna 42
Berlin 39
Dong Ket 37
Düsseldorf 37
Mountain View 37
Kunming 35
San Mateo 32
Guangzhou 31
Zhengzhou 31
Helsinki 30
Orange 30
Brno 28
Des Moines 28
Ningbo 28
Addison 26
Toronto 26
Auburn Hills 25
Hong Kong 23
Augusta 22
Napoli 20
Florence 19
Washington 19
Ottawa 18
Padova 17
Ferrara di Monte Baldo 16
Frankfurt am Main 15
Hangzhou 15
Indiana 13
Leawood 13
Verona 13
Monmouth Junction 12
Meda 11
Ardabil 10
Hefei 10
Bari 9
Changchun 9
Dublin 9
Naples 9
Turin 9
Brescia 8
Catania 8
Chicago 8
Lucknow 8
Philadelphia 8
Domagnano 7
Duncan 7
Genoa 7
Pescara 7
San Francisco 7
Taizhou 7
Tappahannock 7
Ansbach 6
Bonn 6
Dogana 6
Fuzhou 6
Totale 17.268
Nome #
Nanobiomaterials for vascular biology and wound management: a review 1.070
FISIOPATOLOGIA DELL'EMOSTASI E DELLA COAGULAZIONE 454
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. 434
Impact of methylenetetrahydrofolate reductase C677T polymorphism on the efficacy of photodynamic therapy in patients with neovascular age-related macular degeneration 269
Ricerche metodologiche sul dosaggio del cofattore Ristocetinico per la diagnosi di morbo di von Willebrand. 220
C6orf10 low-frequency and rare variants in italian multiple sclerosis patients 189
High throughput array technologies: Expanding applications from clinics to applied research 187
Realizzazione di un DNA-Array di varianti genetiche nelle lesioni croniche di origine vascolare 177
Gene polymorphisms in folate metabolizing enzymes in adult acute lymphoblastic leukemia: effects on methotrexate-related toxicity and survival 171
Gene-gene interactions among coding genes of iron-homeostasis proteins and APOE-alleles in Cognitive Impairment Diseases 168
Sudden sensorineural hearing loss and polymorphisms in iron homeostasis genes: new insights from a case-control study 166
Inherited genetic predispositions in F13A1 and F13B genes predict abdominal adhesion formation: identification of gender prognostic indicators 164
“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 163
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 158
Effect of factor XIII-A G185T polymorphism on visual prognosis after photodynamic therapy for neovascular macular degeneration 156
Fisiopatologia della Coagulazione. 151
The carboxyl-terminal region is NOT essential for secreted and functional levels of coagulation factor X 146
Analisi dei multimeri del fattore von Willebrand mediante doppia immunoprecipitazione dopo elettroforesi su gel di agarosio. 145
Factor XIII contrasts the effects of metalloproteinases in human dermal fibroblast cultured cells 144
Serum iron and matrix metalloproteinase-9 variations in limbs affected by chronic venous disease and venous leg ulcers 142
Tissue factor and coagulation factor VII levels during acute myocardial infarction: association with genotype and adverse events. 141
Changes in adipose tissue distribution and association between uric acid and bone health during menopause transition 139
FOLATE GENE VARIANTS AFFECT METHOTREXATE-RELATED TOXICITY IN ADULT ACUTE LYMPHOBLASTIC LEUKEMIA PATIENTS 137
Coexistence of antithrombin deficiency, factor V Leiden and hyperhomocysteinemia in a thrombotic family. 135
Coagulation factor XIIIA (F13A1): Novel perspectives in treatment and pharmacogenetics 133
Methylenetetrahydrofolate reductase C677T and A1298C gene variants in adult non-Hodgkin's lymphoma patients: association with toxicity and survival 130
Factor XIII V34L polymorphism modulates the risk of chronic venous leg ulcer progression and extension 129
Crosstalk between adipokines and paraoxonase 1: A new potential axis linking oxidative stress and inflammation 129
Factor XIII-A dynamics in acute myocardial infarction: a novel prognostic biomarker? 128
Prognostic role of Factor XIII gene variants in nonhealing venous leg ulcers 127
Effects of physical stimulation with electromagnetic field and insulin growth factor-I treatment on proteoglycan synthesis of bovine articular cartilage 125
Genetic predictors of response to photodynamic therapy 125
MTHFR 677C→T polymorphism and risk of coronary heart disease: A meta-analysis 124
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis 124
Redox metals homeostasis in multiple sclerosis and amyotrophic lateral sclerosis: a review 124
A common mutation in the gene for coagulation factor XIII-A (Val34Leu): A risk factor for primary intracerebral hemorrhage is protective against atherothrombotic diseases 123
A novel mutation (Leu817Pro) causing type 2A von Willebrand disease. 123
F13A1 gene variant (V34L) and residual circulating FXIIIA levels predict short-and long-term mortality in acute myocardial infarction after coronary angioplasty 123
Effects of electromagnetic fields on proteoglycan metabolism of bovine articular cartilage explants 121
Meta-analysis of multiple sclerosis microarray data reveals dysregulation in RNA splicing regulatory genes 121
The carboxyl-terminal region is not essential for secreted and functional levels of coagulation factor X 121
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 120
Different anticoagulant response to activated protein C (APC test) and to Agkistrodon Contortix venom (ACV test) in a family with FV-R506Q substitution 120
Influence of gene polymorphisms in ulcer healing process after superficial venous surgery 119
Polymorphisms in the genes coding for iron binding and transporting proteins are Associated with Disability, Severity, and Early Progression in Multiple Sclerosis. 119
A photometric assay for factor-XIII in chronic hepatopathies. 118
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? 118
null 118
DNA-Array of gene variants in venous leg ulcers: detection of prognostic indicators. 117
Molecular defects in CRM+ factor VII deficiencies: modelling of missense mutations in the catalytic domain of FVII 117
Asymptomatic carriership of factor V Leiden and genotypes of the fibrinogen gene cluster 116
Proteoglycan synthesis in bovine articular cartilage explants exposed to different low-frequency low-energy pulsed electromagnetic fields 115
Quantitive evaluation of dentin sialoprotein (DSP) using microbeads - A potential early marker of root resorption 115
A photometric method for the dosage of factor XIII applied to the study of chronic hepatopathies. 113
Detection and characterization of polymorphic markers in the factor-VII gene. 113
Partial gene deletion in a family with factor X deficiency 113
Assessment of the interlaboratory variability and robustness of JAK2V617F mutation assays: A study involving a consortium of 19 Italian laboratories 113
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients. 113
The reduced sensitivity of the ProC (R) Global test in protein S deficient subjects reflects a reduction in the associated thrombotic risk 111
A "de novo" Gene Deletion and New RFLPs Detected by von Willebrand Factor cDNA. 111
Investigation of in vitro cytotoxicity of the redox state of ionic iron in neuroblastoma cells. 111
A De Novo and Heterozygous Gene Deletion Causing a Variant of von Willebrand Disease 110
Tissue Factor and Coagulation Factor VII Levels during Acute Myocardial Infarction Contribute to Predict Mortality and re-infarction. 109
Clinical observations on the relationship between idiopathic thrombocytopenic purpura lupus anticoagulant and anticardio-lipin antibody syndrome. 109
A modified functional Global test to measure protein C, protein S activities and the activated protein C-resistance phenotype. 109
TIME- AND DOSE-DEPENDENT EFFECTS OF CHRONIC WOUND FLUID ON HUMAN ADULT DERMAL FIBROBLASTS 109
Characterization of polymorphic markers in the von Willebrand factor gene and pseudogene 108
Custom CGH array profiling of copy number variations (CNVs) on chromosome 6p21.32 (HLA locus) in patients with venous malformations associated with multiple sclerosis 107
Folate: metabolism, biochemistry and role in disease processes. 106
Nanoengineering Approaches to Design Advanced Dental Materials for Clinical Applications. 106
Functional properties of factor V and factor Va encoded by the R2-gene 105
Hemochromatosis C282Y gene mutation increases the risk of venous leg ulceration 105
Karyotype-Phenotype Correlation in Partial Trisomies of the Short Arm of Chromosome 6: A Family Case Report and Review of the Literature. 102
Low folate levels and thermolabile methylenetetrahydrofolate reductase as primary determinant of mild hyperhomocystinemia in normal and thromboembolic subjects 102
Clinical implications of gene polymorphisms in venous leg ulcer: A model in tissue injury and reparative process 101
Reference materials (RMs) for analysis of the human factor II (prothrombin) gene G20210A mutation. 101
Symptomatic type II protein C deficiency caused by a missense mutation (Gly 381-->Ser) in the substrate-binding pocket 101
FXIII levels and genotypes in myocardial infarction: a potential novel prognostic biomarker? 101
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 101
The role of the MTHFR 677C>T polymorphism in methotrexate-induced liver toxicity: a meta-analysis in patients with cancer 101
null 100
Influence of Genetic Polymorphisms in Ulcer Healing Process after Superficial Venous Surgery 99
Rapid detection of a protein C gene mutation present in the asymptomatic and not in the thrombosis‐prone lineage 99
A DE NOVO GENE ALTERATION CAUSING VON WILLEBRAND DISEASE 98
The factor V Glu1608Lys mutation is recurrent in familial thrombophilia 98
Deletion of exons 26-34 (domain D3-A3) of von Willebrand-factor gene in the von Willebrand disease type-II. 98
null 97
PCR and specific oligonucleotide hybridization for the molecular characterization and carrier detection of hemophilia A. 97
null 97
null 97
Expression profiles of the internal jugular and saphenous veins: Focus on hemostasis genes 97
null 96
C677T/A1298C MTHFR Gene Mutations, Homocysteine, Folate Levels and MTHFR Activity, in Normal Subjects and Cases with Myocardial Infarction 95
Detection of two missense mutations and characterization of a repeat polymorphism in the factor VII gene (F7) 94
Common gene polymorphisms in the metabolic folate and methylation pathway and the risk of acute lymphoblastic leukemia and non-Hodgkin's lymphoma in adults 92
null 91
TRAIL, OPG, and TWEAK in kidney disease: biomarkers or therapeutic targets? 91
In-Frame Deletion of von Willebrand Factor Exons 26-34 (D3-A3 Domains) in Type II von Willebrand Disease. 90
Sudden sensorineural hearing loss and polymorphisms in iron homeostasis genes. 90
Sublocalization of von Willebrand Factor Pseudogene in 22q11.22-q11.23 and Detection of two TaqI RFLPs. 89
Totale 13.764
Categoria #
all - tutte 106.286
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 4.383
Totale 110.669


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20203.104 0 0 0 0 341 602 415 507 321 555 248 115
2020/20213.771 362 343 201 365 226 424 181 420 105 494 476 174
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
2024/20251.960 204 157 543 215 841 0 0 0 0 0 0 0
Totale 24.914