CATALOGO DEI PRODOTTI DELLA RICERCA

GIRELLI, Domenico
 Distribuzione geografica
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Continente #
NA - Nord America 31.607
EU - Europa 23.771
AS - Asia 16.096
SA - Sud America 2.260
Continente sconosciuto - Info sul continente non disponibili 502
AF - Africa 388
OC - Oceania 44
Totale 74.668
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Nazione #
US - Stati Uniti d'America 30.626
RU - Federazione Russa 8.176
SG - Singapore 6.755
GB - Regno Unito 5.706
CN - Cina 4.506
IT - Italia 2.026
DE - Germania 1.827
BR - Brasile 1.761
SE - Svezia 1.436
VN - Vietnam 1.394
HK - Hong Kong 1.321
FR - Francia 1.271
FI - Finlandia 1.058
IE - Irlanda 1.057
KR - Corea 544
CA - Canada 452
UA - Ucraina 341
BD - Bangladesh 288
IN - India 223
JP - Giappone 210
TR - Turchia 176
AR - Argentina 173
NL - Olanda 167
BE - Belgio 135
MX - Messico 119
ES - Italia 109
ID - Indonesia 107
IQ - Iraq 92
ZA - Sudafrica 88
PL - Polonia 81
CR - Costa Rica 79
NG - Nigeria 75
EC - Ecuador 72
CO - Colombia 67
AT - Austria 54
PK - Pakistan 54
UZ - Uzbekistan 51
HN - Honduras 49
VE - Venezuela 49
IL - Israele 48
GT - Guatemala 47
JM - Giamaica 47
LT - Lituania 45
SV - El Salvador 45
CW - ???statistics.table.value.countryCode.CW??? 42
CZ - Repubblica Ceca 41
AU - Australia 40
CL - Cile 40
NI - Nicaragua 38
PH - Filippine 35
SA - Arabia Saudita 35
AE - Emirati Arabi Uniti 31
EG - Egitto 30
MA - Marocco 30
TT - Trinidad e Tobago 30
RO - Romania 29
UY - Uruguay 28
PE - Perù 27
PY - Paraguay 27
PR - Porto Rico 26
TN - Tunisia 26
JO - Giordania 25
TG - Togo 24
AZ - Azerbaigian 23
SC - Seychelles 22
CH - Svizzera 20
GR - Grecia 20
KE - Kenya 20
HR - Croazia 19
DK - Danimarca 18
IR - Iran 18
BJ - Benin 17
EE - Estonia 16
MY - Malesia 16
NP - Nepal 16
AL - Albania 15
KG - Kirghizistan 15
GP - Guadalupe 14
BG - Bulgaria 13
DO - Repubblica Dominicana 13
DZ - Algeria 13
EU - Europa 13
BO - Bolivia 12
KZ - Kazakistan 12
LB - Libano 12
OM - Oman 12
LV - Lettonia 11
HU - Ungheria 10
RS - Serbia 10
AM - Armenia 9
ET - Etiopia 9
PS - Palestinian Territory 9
TH - Thailandia 9
BY - Bielorussia 8
LU - Lussemburgo 8
XK - ???statistics.table.value.countryCode.XK??? 8
CI - Costa d'Avorio 7
CY - Cipro 7
NO - Norvegia 7
PT - Portogallo 7
Totale 74.099
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Città #
Southend 4.683
Ashburn 4.226
Singapore 3.723
Jacksonville 2.820
Chandler 2.773
Moscow 2.713
San Jose 2.602
Dallas 1.824
Woodbridge 1.778
Ann Arbor 1.406
Hong Kong 1.296
Dublin 1.049
Council Bluffs 858
Houston 826
Verona 815
The Dalles 731
Beijing 684
New York 653
Ho Chi Minh City 491
Los Angeles 481
Wilmington 471
Princeton 445
Lawrence 443
Nanjing 320
Santa Clara 303
Munich 298
Jinan 289
Hanoi 286
Boardman 279
Helsinki 267
Buffalo 223
São Paulo 221
Shenyang 213
Milan 177
Tokyo 173
Sindelfingen 171
Tianjin 169
Hebei 155
Lancaster 146
Columbus 144
Redondo Beach 144
Orem 140
Redmond 136
Brussels 131
Montreal 127
Zhengzhou 123
Nanchang 117
Turku 115
Changsha 112
London 110
Seattle 99
Ningbo 97
Toronto 96
Chicago 94
Rome 91
Brooklyn 88
Jiaxing 88
Denver 86
Guangzhou 85
Phoenix 83
Atlanta 82
Frankfurt am Main 82
Seoul 82
Haikou 81
Taiyuan 81
Falls Church 79
Hangzhou 77
San Francisco 77
Falkenstein 72
Norwalk 72
Abuja 70
Nürnberg 69
Warsaw 69
Chennai 68
Las Vegas 67
Dong Ket 65
Taizhou 65
Rio de Janeiro 62
Annandale 61
San José 61
Nuremberg 59
Amsterdam 57
Bologna 56
Haiphong 56
Washington 56
Boston 53
Poplar 53
Stockholm 52
Jakarta 51
Johannesburg 51
Philadelphia 49
Manchester 47
North Bergen 47
Fuzhou 46
Tashkent 45
Baghdad 44
Willemstad 42
Redwood City 41
Da Nang 40
Fairfield 39
Totale 46.213
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Nome #
The European Hematology Association Roadmap for European Hematology Research: a consensus document 623
Fatty acids and antioxidant micronutrients in psoriatic arthritis 350
Altered renal folate handling in hypertensive patients with nephroangiosclerotic damage 307
High plasma apolipoprotein C-III levels predict total and cardiovascular mortality in patients with angiographically defined coronary artery disease. 278
A case of congenital dyserythopoietic anaemia with stomatocytosis, reduced bands 7 and 8 and normal cation transport 268
[Effectiveness of loratadine vs. placebo in the treatment of urticaria-angioedema syndrome in patients with food allergy] 263
Global DNA hypomethylation in peripheral blood mononuclear cells as a biomarker of cancer risk 263
Low platelet glutathione peroxidase activity and serum selenium concentration in patients with chronic renal failure: relations to dialysis treatments, diet and cardiovascular complications 262
Associazione di polimorfismi del cluster dei geni FADS1 e FADS2 con i livelli di acidi grassi polinsaturi in malattie coronariche 258
High plasma apolipoprotein C-III levels predict total and cardiovascular mortality in patients with angiographically defined coronary artery disease. 253
ALOX5AP gene variants and risk of coronary artery disease: an angiography-based study 250
A genetic risk factor for vascular disease which leads to mild hyperhomocysteinemia is common in northern Italy. 245
A1298C methylentetrahydrofolate reductase mutation and coronary artery disease:relationship with C677T polymorphysm and homocystein/folate metabolism 242
Promoter methylation in coagulation F7 gene influences plasma FVII concentrations and relates to coronary artery disease. 241
MOLECULARLY IMPRINTED NANOPARTICLES FOR HEPCIDIN CAPTURE: A SYNTHETIC ALTERNATIVE TO NATURAL ANTIBODIES 241
Association of phlebotomy and subcutaneous bolus injection of deferoxamine for treatment of anemic patients with iron overload 240
HEPCIDIN REPRESSION BY PROMOTER DNA HYPERMETHYLATION IN NON-VIRAL HEPATOCELLULAR CARCINOMA 240
[Ion transport in erythrocytes: a universal physiological model. Reflections on the pathogenesis of hypertension (editorial)] 238
A common mutation in the 5, 10-methylenetetrahydrofolate reductase gene affects genomic DNA methylation through an interaction with folate status 237
Activated factor VII-antithrombin complex predicts mortality in patients with stable coronary artery disease: a cohort study 237
Patient Blood Management in chirurgia ortopedica: l'esperienza veronese 235
Novel serum paraoxonase activity assays are associated with coronary artery disease 234
NEXT GENERATION TARGETED DEEP SEQUENCING OF HEMOCHROMATOSIS GENES IN IRON OVERLOADED PATIENTS: A PILOT STUDY 233
Global DNA hypomethylation in peripheral blood mononuclear cells as a biomarker of cancer risk 232
Consensus Statement on the definition and classification of metabolic hyperferritinaemia 231
Alterations of systemic and muscle iron metabolism in human subjects treated with low-dose recombinant erythropoietin 231
Assessment of COVID-19 progression on day 5 from symptoms onset 230
A common polymorphism in low-density lipoprotein receptor gene is a predictor of factor VIII activity levels and is associated with coronary artery disease. 229
Analisi di 51 polimorfismi in 35 geni dell’infiammazione per la valutazione del rischio di coronaropatia e di infarto del miocardio 229
Tarrgeted Exome Sequencing of 5 Hemochromatosis Genes in Iron Overloaded Patients by Next Generation Sequencing (NGS) Platform. 228
A linkage between hereditary hyperferritinaemia not related to iron overload and autosomal dominant congenital cataract 225
Increased serum hepcidin levels in subjects with the metabolic syndrome: a population study. 223
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. 221
Hepcidin and DNA promoter methylation in hepatocellular carcinoma 221
Biochemical and genetic markers of iron status and the risk of coronary disease 219
Identification of novel mutations in hemochromatosis genes by targeted next generation sequencing in Italian patients with unexplained iron overload 219
A mutation in the iron responsive element of ferritin L-subunit gene is associated with the recently described ''hereditary hyperferritinemia-cataract syndrome''. 218
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. 217
Identification of new BMP6 pro-peptide mutations in patients with iron overload 217
Genomics of coronary artery disease and myocardial infarction. From Genome Wide Association Studies to the Next-Generation-Sequencing era 216
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? 216
Fatal cytokine release syndrome by an aberrant FLIP/STAT3 axis 216
Epigenetic Regulation Of Hepcidin Expression In Non-Viral Hepatocellular Carcinoma: Results Of A Genome-Wide Study 215
A decade of progress on the genetic basis of coronary artery disease. Practical insights for the internist 215
Renovascular disease: effect of ACE gene deletion polymorphism and endovascular revascularization. 214
Serum levels of the hepcidin-20 isoform in a large general population: The Val Borbera study. 214
Association of endogenous thrombin potential (ETP) with coronary artery disease. An angiography-based study 214
Combined effect of hemostatic gene polymorphisms and the risk of myocardial infarction in patients with advanced coronary atherosclerosis. 213
Acquired form of activated protein C resistance in healthy women taking oestrogen therapy. 211
Elevated D-dimer levels are associated with coronary artery disease and cardiovascular death in an angiographically-studied population 211
[Endogenous erythrocyte proteolysis: a new approach to the study of membrane physiopathology] 210
Long-Term Patient-Centred Follow-up in a Prospective Cohort of Patients with COVID-19 210
A common mutation in the 5,10-methylenetetrahydrofolate reductase gene affects genomic DNA methylation through an interaction with folate status. 209
A common polymorphism in LDL-receptor gene is a predictor of factor VIII activity and is associated with coronary artery disease. 209
Pancreatic resections in patients who refuse blood transfusions. The application of a perioperative protocol for a true bloodless surgery 209
Oxidative damage and erythrocyte membrane transport abnormalities in thalassemias 208
Deep vein thrombosis in SARS-CoV-2 pneumonia-affected patients within standard care units: Exploring a submerged portion of the iceberg 208
ApoC-III gene polymorphisms and risk of coronary artery disease 205
Association of endogenous thrombin potential (ETP) with coronary artery disease. an angiography-based study. 205
Acquired and genetic determinants of homocysteine in atheromatous renel artery stenosis with mild renal insufficiency 204
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 204
Apolipoprotein C-III Strongly Correlates with Activated Factor VII-Anti-Thrombin Complex: An Additional Link between Plasma Lipids and Coagulation 204
Altered iron parameters and hepcidin levels in a general population: lesson from the CHRIS study 204
Erythrocyte and platelet fatty acids in retinitis pigmentosa 203
A new mutation in transferrin receptor 2 gene in hemochromatosis type 3 203
Is the oral methionine loading test insensitive to the methylation pathway of homocysteine? 203
PON2 Ser311Cys polymorphism is a predictor of total and cardiovascular mortality in patients with angiographically proven coronary artery disease. 201
Air particulate matter and cardiovascular disease: a narrative review. 201
Hyperhomocysteinemia in relation to total and cardiovascular death after coronary bypass grafting. 200
Activation of K+/Cl- cotransport in human erythrocytes exposed to oxidative agents 200
Clinical, pathological, and molecular correlates in ferroportin disease: a study of two novel mutations. 200
Clinical biochimical and molecular findings in a series of families with hyperferritinemia-cataract syndrome 199
Interaction of antibodies against cytomegalovirus with heat-shock protein 60 in pathogenesis of atherosclerosis. 199
Reply to Novelli 198
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 198
["Hyperferritinemia-cataract syndrome". Description of a new hereditary disease, from anamnesis to molecular diagnosis] 197
Hepatic venous thrombosis in paroxysmal nocturnal hemoglobinuria: usefulness of ultrasonic scanning monitoring 197
Clinical and pathological findings in hemochromatosis type 3 due to a novel mutation in transferin receptor 2 gene 197
Determinants of serum ferritin and prevalence of iron overload in the Metabolic (Insulin Resistance). 197
Altered paraoxonase expression in patients with genetic haemochromatosis. 197
Hyperhomocysteinemia and Mortality after Coronary Artery Bypass Grafting 196
PON2 Ser311Cys polymorphism is a predictor of total and cardiovascular mortality in patients with angiographically confirmed coronary artery disease. 196
Nervous system: subclinical target of SARS-CoV-2 infection 196
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 195
Increased Incidence of Ischemic Cerebrovascular Events in Cardiovascular Patients With Elevated Apolipoprotein CIII 195
Tyr2105Cys mutation in exon 22 of FVIII gene is a risk factor for the development of inhibitors in patients with mild/moderate haemophilia A. 194
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 194
Low circulating vitamin B6 markers of inflammation, and risk of coronary artery disease. 194
Apolipoprotein C-III predicts cardiovascular mortality in severe coronary artery disease and is associated with an enhanced plasma thrombin generation 194
Association of endogenous thrombin potential (ETP) with coronary artery disease. An angiography-based study. 193
Hyperhomocysteinemia and mortality after coronary artery by-pass grafing. 192
High ferritin and low folate increases PBMCs genomic DNA methylation in association with SHMT1-1420TT variant. 192
Aceruloplasminemia: A Severe Neurodegenerative Disorder Deserving an Early Diagnosis 192
Asthmatic patients in COVID-19 outbreak: Few cases despite many cases 192
Anti-oxidant status and lipid peroxidation in patients with essential hypertension 191
Determinants of serum ferritin in the metabolic syndrome. 191
Low vitamin B6, markers of inflammation, and risk of coronary artery disease. 191
Neurological symptoms and axonal damage in COVID-19 survivors: are there sequelae? 191
Le anemie emolitiche enzimopeniche 190
Interaction between folate and MTHFR1298 A/C polymorphism on Genomic DNA Methylation 190
Totale 22.121
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Categoria #
all - tutte 247.198
article - articoli 190.785
book - libri 0
conference - conferenze 54.852
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.561
Totale 494.396
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.976 0 0 0 0 174 169 70 192 146 99 331 795
2022/20237.663 550 740 731 1.323 735 1.746 92 537 896 32 179 102
2023/20243.624 157 302 272 364 437 640 124 236 29 134 571 358
2024/20259.377 575 701 352 1.545 427 347 458 364 1.299 573 809 1.927
2025/202626.900 2.005 1.400 1.874 4.459 6.906 1.783 2.598 1.354 1.971 1.452 435 663
2026/20276.530 370 786 1.438 3.699 237 0 0 0 0 0 0 0
Totale 74.668