GIRELLI, Domenico
 Distribuzione geografica
Continente #
NA - Nord America 19.589
EU - Europa 14.891
AS - Asia 10.529
SA - Sud America 1.535
AF - Africa 141
OC - Oceania 33
Continente sconosciuto - Info sul continente non disponibili 19
Totale 46.737
Nazione #
US - Stati Uniti d'America 19.397
GB - Regno Unito 5.439
SG - Singapore 4.242
CN - Cina 3.662
DE - Germania 1.719
SE - Svezia 1.406
BR - Brasile 1.353
FR - Francia 1.221
HK - Hong Kong 1.197
RU - Federazione Russa 1.161
IE - Irlanda 1.046
FI - Finlandia 1.026
IT - Italia 993
KR - Corea 392
UA - Ucraina 315
VN - Vietnam 284
JP - Giappone 144
TR - Turchia 137
BE - Belgio 136
NL - Olanda 111
CA - Canada 97
IN - India 89
BD - Bangladesh 73
AR - Argentina 62
MX - Messico 59
ID - Indonesia 58
AT - Austria 50
ES - Italia 39
CZ - Repubblica Ceca 35
IQ - Iraq 35
ZA - Sudafrica 32
PL - Polonia 31
AU - Australia 29
VE - Venezuela 26
TG - Togo 23
PK - Pakistan 22
UZ - Uzbekistan 22
RO - Romania 20
EG - Egitto 18
CL - Cile 17
EC - Ecuador 17
LT - Lituania 17
MA - Marocco 17
AZ - Azerbaigian 16
CH - Svizzera 16
IR - Iran 16
PE - Perù 16
AE - Emirati Arabi Uniti 15
CO - Colombia 15
IL - Israele 15
SA - Arabia Saudita 14
TN - Tunisia 14
EU - Europa 13
GR - Grecia 12
HR - Croazia 11
JO - Giordania 11
UY - Uruguay 11
BG - Bulgaria 10
JM - Giamaica 10
KG - Kirghizistan 10
PY - Paraguay 10
PH - Filippine 9
AL - Albania 8
DK - Danimarca 8
HU - Ungheria 8
LU - Lussemburgo 8
NP - Nepal 8
EE - Estonia 7
HN - Honduras 7
KE - Kenya 7
LV - Lettonia 7
BO - Bolivia 6
DZ - Algeria 6
KZ - Kazakistan 6
CI - Costa d'Avorio 5
MY - Malesia 5
NO - Norvegia 5
OM - Oman 5
XK - ???statistics.table.value.countryCode.XK??? 5
AM - Armenia 4
BA - Bosnia-Erzegovina 4
DO - Repubblica Dominicana 4
KW - Kuwait 4
PT - Portogallo 4
RS - Serbia 4
TH - Thailandia 4
TT - Trinidad e Tobago 4
BN - Brunei Darussalam 3
BY - Bielorussia 3
KH - Cambogia 3
LA - Repubblica Popolare Democratica del Laos 3
MD - Moldavia 3
NI - Nicaragua 3
PS - Palestinian Territory 3
AF - Afghanistan, Repubblica islamica di 2
BH - Bahrain 2
BS - Bahamas 2
CR - Costa Rica 2
CY - Cipro 2
GA - Gabon 2
Totale 46.689
Città #
Southend 4.694
Jacksonville 2.819
Chandler 2.805
Singapore 2.102
Woodbridge 1.785
Dallas 1.667
Ann Arbor 1.419
Hong Kong 1.184
Dublin 1.040
Ashburn 1.039
Houston 784
Beijing 509
Wilmington 471
Lawrence 446
Princeton 446
New York 435
Nanjing 321
Verona 316
Munich 296
Jinan 288
Boardman 271
Los Angeles 268
Helsinki 235
The Dalles 227
Shenyang 214
Buffalo 173
Sindelfingen 173
Hebei 155
Lancaster 145
Columbus 140
Redmond 137
Tianjin 137
Brussels 133
Milan 127
Redondo Beach 124
Zhengzhou 122
Nanchang 118
Santa Clara 117
Tokyo 115
Turku 115
Changsha 109
São Paulo 109
Ningbo 97
Jiaxing 86
Seoul 83
Seattle 82
Haikou 81
Taiyuan 81
Falls Church 78
Hangzhou 75
Ho Chi Minh City 74
Guangzhou 72
Nürnberg 69
Norwalk 66
Dong Ket 65
Taizhou 65
Nuremberg 58
San Francisco 58
London 53
Toronto 47
Fuzhou 46
Jakarta 46
Rio de Janeiro 46
Washington 45
Council Bluffs 44
Chicago 43
Moscow 43
Redwood City 41
Brooklyn 39
Fairfield 39
Lanzhou 39
Rome 39
Bologna 37
Falkenstein 34
Hanoi 33
Boston 29
Düsseldorf 29
Frankfurt am Main 27
Belo Horizonte 26
Vienna 26
Lappeenranta 25
Philadelphia 25
Atlanta 24
Auburn Hills 24
Kent 24
Dearborn 23
Detroit 23
Dongguan 23
Lomé 23
Stockholm 23
Warsaw 23
Tashkent 22
Campinas 21
Montreal 21
Phoenix 21
Baghdad 19
Dhaka 19
Brasília 18
Guarulhos 18
Kochi 18
Totale 30.808
Nome #
The European Hematology Association Roadmap for European Hematology Research: a consensus document 559
Fatty acids and antioxidant micronutrients in psoriatic arthritis 279
Altered renal folate handling in hypertensive patients with nephroangiosclerotic damage 245
Low platelet glutathione peroxidase activity and serum selenium concentration in patients with chronic renal failure: relations to dialysis treatments, diet and cardiovascular complications 212
High plasma apolipoprotein C-III levels predict total and cardiovascular mortality in patients with angiographically defined coronary artery disease. 204
High plasma apolipoprotein C-III levels predict total and cardiovascular mortality in patients with angiographically defined coronary artery disease. 203
A case of congenital dyserythopoietic anaemia with stomatocytosis, reduced bands 7 and 8 and normal cation transport 174
Renovascular disease: effect of ACE gene deletion polymorphism and endovascular revascularization. 173
A genetic risk factor for vascular disease which leads to mild hyperhomocysteinemia is common in northern Italy. 167
Associazione di polimorfismi del cluster dei geni FADS1 e FADS2 con i livelli di acidi grassi polinsaturi in malattie coronariche 165
[Effectiveness of loratadine vs. placebo in the treatment of urticaria-angioedema syndrome in patients with food allergy] 163
A1298C methylentetrahydrofolate reductase mutation and coronary artery disease:relationship with C677T polymorphysm and homocystein/folate metabolism 163
Novel serum paraoxonase activity assays are associated with coronary artery disease 163
Association of phlebotomy and subcutaneous bolus injection of deferoxamine for treatment of anemic patients with iron overload 158
MOLECULARLY IMPRINTED NANOPARTICLES FOR HEPCIDIN CAPTURE: A SYNTHETIC ALTERNATIVE TO NATURAL ANTIBODIES 158
ALOX5AP gene variants and risk of coronary artery disease: an angiography-based study 157
Global DNA hypomethylation in peripheral blood mononuclear cells as a biomarker of cancer risk 156
Oxidative damage and erythrocyte membrane transport abnormalities in thalassemias 155
Global DNA hypomethylation in peripheral blood mononuclear cells as a biomarker of cancer risk 155
NEXT GENERATION TARGETED DEEP SEQUENCING OF HEMOCHROMATOSIS GENES IN IRON OVERLOADED PATIENTS: A PILOT STUDY 155
A linkage between hereditary hyperferritinaemia not related to iron overload and autosomal dominant congenital cataract 153
Activated factor VII-antithrombin complex predicts mortality in patients with stable coronary artery disease: a cohort study 153
[Ion transport in erythrocytes: a universal physiological model. Reflections on the pathogenesis of hypertension (editorial)] 152
Increased serum hepcidin levels in subjects with the metabolic syndrome: a population study. 149
A common mutation in the 5, 10-methylenetetrahydrofolate reductase gene affects genomic DNA methylation through an interaction with folate status 147
Tarrgeted Exome Sequencing of 5 Hemochromatosis Genes in Iron Overloaded Patients by Next Generation Sequencing (NGS) Platform. 147
Analisi di 51 polimorfismi in 35 geni dell’infiammazione per la valutazione del rischio di coronaropatia e di infarto del miocardio 145
Patient Blood Management in chirurgia ortopedica: l'esperienza veronese 145
The -1131 T > C and S19W APOA5 gene polymorphisms are associated with high levels of triglycerides and apolipoprotein C-III, but not with coronary artery disease: an angiographic study 145
Genetic risk score from GWA studies is strongly associated with angiographically-defined coronary artery disease, but not with mortalilty in the setting of secondary prevention. 144
Analysis of ferritins in lymphoblastoid cell lines and in the lens of subjects with hereditary hyperferritinemia-cataract syndrome 143
Promoter methylation in coagulation F7 gene influences plasma FVII concentrations and relates to coronary artery disease. 143
Hepatic venous thrombosis in paroxysmal nocturnal hemoglobinuria: usefulness of ultrasonic scanning monitoring 142
A new mutation in transferrin receptor 2 gene in hemochromatosis type 3 142
Interaction of antibodies against cytomegalovirus with heat-shock protein 60 in pathogenesis of atherosclerosis. 141
High ferritin and low folate increases PBMCs genomic DNA methylation in association with SHMT1-1420TT variant. 141
[Endogenous erythrocyte proteolysis: a new approach to the study of membrane physiopathology] 140
Riduzione della emocateresi splenica mediante alte dosi di immunoglobuline in un caso di sferocitosi ereditaria 140
Le anemie emolitiche enzimopeniche 140
Tyr2105Cys mutation in exon 22 of FVIII gene is a risk factor for the development of inhibitors in patients with mild/moderate haemophilia A. 140
Is the oral methionine loading test insensitive to the methylation pathway of homocysteine? 140
PON2 Ser311Cys polymorphism is a predictor of total and cardiovascular mortality in patients with angiographically proven coronary artery disease. 140
Identification of new BMP6 pro-peptide mutations in patients with iron overload 140
Identification of novel mutations in hemochromatosis genes by targeted next generation sequencing in Italian patients with unexplained iron overload 139
Interaction between folate and MTHFR1298 A/C polymorphism on Genomic DNA Methylation 138
Pancreatic resections in patients who refuse blood transfusions. The application of a perioperative protocol for a true bloodless surgery 138
Reply to Novelli 137
A mutation in the iron responsive element of ferritin L-subunit gene is associated with the recently described ''hereditary hyperferritinemia-cataract syndrome''. 137
Clinical and pathological findings in hemochromatosis type 3 due to a novel mutation in transferin receptor 2 gene 136
Interaction between metabolic syndrome and PON 1 polymorphism as a determinant of the risk of coronary artery disease 136
Combined effect of hemostatic gene polymorphisms and the risk of myocardial infarction in patients with advanced coronary atherosclerosis. 136
Assessment of COVID-19 progression on day 5 from symptoms onset 136
Erythrocyte and platelet fatty acids in retinitis pigmentosa 135
Hepcidin and DNA promoter methylation in hepatocellular carcinoma 135
A decade of progress on the genetic basis of coronary artery disease. Practical insights for the internist 135
A common mutation in the 5,10-methylenetetrahydrofolate reductase gene affects genomic DNA methylation through an interaction with folate status. 133
A common polymorphism in LDL-receptor gene is a predictor of factor VIII activity and is associated with coronary artery disease. 133
Association of endogenous thrombin potential (ETP) with coronary artery disease. An angiography-based study 133
Hyperhomocysteinemia and Mortality after Coronary Artery Bypass Grafting 132
Additive effect of LRP8/APOER2 R952Q variant to APOE epsilon2/epsilon3/epsilon4 genotype in modulating apolipoprotein E concentration and the risk of myocardial infarction: a case-control study. 132
Genomics of coronary artery disease and myocardial infarction. From Genome Wide Association Studies to the Next-Generation-Sequencing era 132
Increased erythrocyte membrane arachidonate and platelet malondialdehyde (MDA) production in psoriasis: normalization after fish-oil 131
Thrombotic thrombocytopenic purpura developed during ticlopidine therapy [letter] [see comments] 131
Hyperhomocysteinemia and mortality after coronary artery by-pass grafing. 131
Acquired and genetic determinants of homocysteine in atheromatous renel artery stenosis with mild renal insufficiency 130
Deep vein thrombosis in SARS-CoV-2 pneumonia-affected patients within standard care units: Exploring a submerged portion of the iceberg 130
Homocysteine and atheromatous renal artery stenosis 129
Epigenetic Regulation Of Hepcidin Expression In Non-Viral Hepatocellular Carcinoma: Results Of A Genome-Wide Study 129
Intravenous immunoglobulins as pre-operative management in a case of hereditary spherocytosis 128
Membrane fatty acids and erythrocyte Li-Na countertransport in nephrotic syndrome and their relationship 128
Elevated D-dimer levels are associated with coronary artery disease and cardiovascular death in an angiographically-studied population 128
Serum levels of the hepcidin-20 isoform in a large general population: The Val Borbera study. 128
Clinical heterogeneity of acquired hemophilia A: a description of 4 cases. 127
ApoC-III gene polymorphisms and risk of coronary artery disease 126
Association of endogenous thrombin potential (ETP) with coronary artery disease. an angiography-based study. 126
PON2 Ser311Cys polymorphism is a predictor of total and cardiovascular mortality in patients with angiographically confirmed coronary artery disease. 126
PON2 Ser311Cys polymorphism is a predictor of total and cardiovascular mortality in patients with angiographically confirmed coronary artery disease. 126
Paraoxonase-1 status in patients with hereditary hemochromatosis 126
A single dialysis session of hemodiafiltration with sorbent-regenerated endogenous ultrafiltrate reinfusion (HFR) removes hepcidin more efficiently than bicarbonate hemodialysis: a new approach to containing hepcidin burden in dialysis patients? 126
Activation of K+/Cl- cotransport in human erythrocytes exposed to oxidative agents 125
Homozygosity for APOCIII variant at position 455 of insulin responsive element promoter region is associated with increased APOC-III levels and risk of coronary artery disease 125
Acquired form of activated protein C resistance in healthy women taking oestrogen therapy. 125
Clinical, pathological, and molecular correlates in ferroportin disease: a study of two novel mutations. 125
A common polymorphism in low-density lipoprotein receptor gene is a predictor of factor VIII activity levels and is associated with coronary artery disease. 125
Alterations of systemic and muscle iron metabolism in human subjects treated with low-dose recombinant erythropoietin 125
A common polymorphism in low-density lipoprotein receptor gene is a predictor of factor VIII activity levels and is associated with coronary artery disease. 125
CYBRD1 as a modifier gene that modulates iron phenotype in HFE p.c282y homozygous patients. 125
Targeted Next Generation Sequencing of the Five Hemochromatosis Genes in Italian Patients with Iron Overload and Non-Diagnostic First Level Genetic Test: A Pilot Study 125
Red blood cells and platelet membrane fatty acids in non-dialyzed and dialyzed uremics 124
HEPCIDIN REPRESSION BY PROMOTER DNA HYPERMETHYLATION IN NON-VIRAL HEPATOCELLULAR CARCINOMA 124
Clinical biochimical and molecular findings in a series of families with hyperferritinemia-cataract syndrome 123
Combination of 4 mutations (FV R506Q, FV H1299R,Fv Y1702C, PT 20210)affecting the prothrombinase complex in a thrombophilic family 123
Post-methionine loading hyperhomocysteinemia in patients with angiographically documented coronary artery disease 123
Low plasma vitamin B-6 concentrations and modulation of coronary artery disease risk. 123
Altered paraoxonase expression in patients with genetic haemochromatosis. 123
Altered iron parameters and hepcidin levels in a general population: lesson from the CHRIS study 123
Fatal cytokine release syndrome by an aberrant FLIP/STAT3 axis 123
Factor VIII:c Levels in Subjects with the Factor V R2 Polymorphism. 122
Factors affecting the thiobarbituric acid test as index of red blood cell susceptibility to lipid peroxidation: a multivariate analysis 121
Apolipoprotein C-III, n-3 Polyunsaturated Fatty Acids, and “Insulin-Resistant” T-455C APOC3 gene polymorphism in heart disease patients: example of gene-diet interaction 121
Totale 14.613
Categoria #
all - tutte 170.439
article - articoli 131.159
book - libri 0
conference - conferenze 38.287
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 993
Totale 340.878


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20212.830 0 0 0 402 520 467 91 322 285 75 483 185
2021/20223.404 191 884 60 272 174 170 70 193 151 100 332 807
2022/20237.739 557 749 742 1.338 735 1.763 92 543 905 32 180 103
2023/20243.644 159 305 274 367 440 641 125 237 29 135 573 359
2024/20259.508 583 707 356 1.569 441 357 466 370 1.321 578 821 1.939
2025/20265.606 2.025 1.407 1.887 287 0 0 0 0 0 0 0 0
Totale 47.161