CATALOGO DEI PRODOTTI DELLA RICERCA

GIRELLI, Domenico
 Distribuzione geografica
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Continente #
NA - Nord America 15.993
EU - Europa 13.851
AS - Asia 5.663
SA - Sud America 88
AF - Africa 41
OC - Oceania 28
Continente sconosciuto - Info sul continente non disponibili 13
Totale 35.677
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Nazione #
US - Stati Uniti d'America 15.925
GB - Regno Unito 5.360
CN - Cina 3.273
SG - Singapore 1.844
SE - Svezia 1.388
DE - Germania 1.368
FR - Francia 1.179
RU - Federazione Russa 1.121
IE - Irlanda 1.042
FI - Finlandia 889
IT - Italia 853
UA - Ucraina 306
BE - Belgio 135
JP - Giappone 96
VN - Vietnam 86
TR - Turchia 82
KR - Corea 69
BR - Brasile 59
CA - Canada 50
IN - India 47
NL - Olanda 38
CZ - Repubblica Ceca 27
HK - Hong Kong 27
AU - Australia 26
ID - Indonesia 25
TG - Togo 23
IR - Iran 15
CH - Svizzera 14
ES - Italia 14
EU - Europa 13
CL - Cile 12
GR - Grecia 12
HR - Croazia 11
IL - Israele 11
PK - Pakistan 11
MX - Messico 10
IQ - Iraq 9
RO - Romania 9
AT - Austria 8
AZ - Azerbaigian 8
LU - Lussemburgo 8
PL - Polonia 8
AR - Argentina 7
BG - Bulgaria 7
EE - Estonia 7
EG - Egitto 7
LT - Lituania 7
PH - Filippine 7
HU - Ungheria 6
SA - Arabia Saudita 6
AE - Emirati Arabi Uniti 5
DK - Danimarca 5
JO - Giordania 5
LV - Lettonia 5
PE - Perù 5
KG - Kirghizistan 4
NO - Norvegia 4
PT - Portogallo 4
TH - Thailandia 4
AL - Albania 3
JM - Giamaica 3
LA - Repubblica Popolare Democratica del Laos 3
MA - Marocco 3
MY - Malesia 3
UZ - Uzbekistan 3
ZA - Sudafrica 3
AM - Armenia 2
BA - Bosnia-Erzegovina 2
BN - Brunei Darussalam 2
BO - Bolivia 2
DO - Repubblica Dominicana 2
GE - Georgia 2
KH - Cambogia 2
LK - Sri Lanka 2
MD - Moldavia 2
ME - Montenegro 2
MT - Malta 2
NP - Nepal 2
NZ - Nuova Zelanda 2
SC - Seychelles 2
SI - Slovenia 2
TW - Taiwan 2
BD - Bangladesh 1
BH - Bahrain 1
BS - Bahamas 1
BT - Bhutan 1
BY - Bielorussia 1
CM - Camerun 1
CO - Colombia 1
CR - Costa Rica 1
CY - Cipro 1
IM - Isola di Man 1
KW - Kuwait 1
KZ - Kazakistan 1
MU - Mauritius 1
PA - Panama 1
PY - Paraguay 1
RS - Serbia 1
TN - Tunisia 1
UY - Uruguay 1
Totale 35.677
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Città #
Southend 4.694
Jacksonville 2.816
Chandler 2.805
Woodbridge 1.785
Singapore 1.503
Ann Arbor 1.419
Dublin 1.037
Ashburn 875
Houston 783
Wilmington 471
Beijing 453
Lawrence 446
Princeton 446
New York 394
Nanjing 319
Jinan 283
Boardman 271
Verona 270
Helsinki 231
Shenyang 212
Sindelfingen 173
Hebei 155
Lancaster 145
Redmond 137
Brussels 132
Tianjin 129
Milan 117
Nanchang 117
Zhengzhou 113
Changsha 105
Ningbo 97
Jiaxing 86
Haikou 81
Santa Clara 80
Taiyuan 79
Falls Church 78
Tokyo 73
Seattle 70
Nürnberg 69
Hangzhou 67
Seoul 67
Norwalk 66
Dong Ket 65
Taizhou 65
Guangzhou 63
Munich 60
Los Angeles 48
Fuzhou 46
Dallas 41
Redwood City 41
Moscow 40
Washington 40
Fairfield 39
Toronto 39
Bologna 36
Lanzhou 36
London 31
Düsseldorf 28
Rome 28
Chicago 25
Auburn Hills 24
Kent 24
San Francisco 24
Dearborn 23
Lomé 23
Detroit 22
Dongguan 22
Falkenstein 22
Jakarta 22
Philadelphia 21
Hong Kong 18
Kochi 18
Mestre 18
Boydton 16
Clearwater 13
Amsterdam 12
San Mateo 12
Frankfurt am Main 11
Leawood 11
San Diego 11
Zurich 11
Cambridge 10
Olomouc 10
Phoenix 10
São Paulo 10
Edinburgh 9
Paris 9
Shanghai 9
Tappahannock 9
Baku 8
Hanover 8
Lappeenranta 8
Mehlingen 8
Ottawa 8
Prague 8
Trento 8
Wuhan 8
Augusta 7
Brno 7
Manila 7
Totale 25.059
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Nome #
The European Hematology Association Roadmap for European Hematology Research: a consensus document 541
Fatty acids and antioxidant micronutrients in psoriatic arthritis 239
Altered renal folate handling in hypertensive patients with nephroangiosclerotic damage 208
Low platelet glutathione peroxidase activity and serum selenium concentration in patients with chronic renal failure: relations to dialysis treatments, diet and cardiovascular complications 190
High plasma apolipoprotein C-III levels predict total and cardiovascular mortality in patients with angiographically defined coronary artery disease. 183
High plasma apolipoprotein C-III levels predict total and cardiovascular mortality in patients with angiographically defined coronary artery disease. 177
Renovascular disease: effect of ACE gene deletion polymorphism and endovascular revascularization. 159
Novel serum paraoxonase activity assays are associated with coronary artery disease 141
Association of phlebotomy and subcutaneous bolus injection of deferoxamine for treatment of anemic patients with iron overload 135
Associazione di polimorfismi del cluster dei geni FADS1 e FADS2 con i livelli di acidi grassi polinsaturi in malattie coronariche 134
A case of congenital dyserythopoietic anaemia with stomatocytosis, reduced bands 7 and 8 and normal cation transport 133
Oxidative damage and erythrocyte membrane transport abnormalities in thalassemias 132
Global DNA hypomethylation in peripheral blood mononuclear cells as a biomarker of cancer risk 130
Increased serum hepcidin levels in subjects with the metabolic syndrome: a population study. 129
Global DNA hypomethylation in peripheral blood mononuclear cells as a biomarker of cancer risk 127
Riduzione della emocateresi splenica mediante alte dosi di immunoglobuline in un caso di sferocitosi ereditaria 126
Is the oral methionine loading test insensitive to the methylation pathway of homocysteine? 126
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. 126
Interaction of antibodies against cytomegalovirus with heat-shock protein 60 in pathogenesis of atherosclerosis. 124
Tyr2105Cys mutation in exon 22 of FVIII gene is a risk factor for the development of inhibitors in patients with mild/moderate haemophilia A. 123
Le anemie emolitiche enzimopeniche 122
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 122
A1298C methylentetrahydrofolate reductase mutation and coronary artery disease:relationship with C677T polymorphysm and homocystein/folate metabolism 121
NEXT GENERATION TARGETED DEEP SEQUENCING OF HEMOCHROMATOSIS GENES IN IRON OVERLOADED PATIENTS: A PILOT STUDY 121
Patient Blood Management in chirurgia ortopedica: l'esperienza veronese 120
Identification of novel mutations in hemochromatosis genes by targeted next generation sequencing in Italian patients with unexplained iron overload 119
Interaction between metabolic syndrome and PON 1 polymorphism as a determinant of the risk of coronary artery disease 118
PON2 Ser311Cys polymorphism is a predictor of total and cardiovascular mortality in patients with angiographically proven coronary artery disease. 117
A linkage between hereditary hyperferritinaemia not related to iron overload and autosomal dominant congenital cataract 116
Interaction between folate and MTHFR1298 A/C polymorphism on Genomic DNA Methylation 116
High ferritin and low folate increases PBMCs genomic DNA methylation in association with SHMT1-1420TT variant. 115
Activated factor VII-antithrombin complex predicts mortality in patients with stable coronary artery disease: a cohort study 115
Hepatic venous thrombosis in paroxysmal nocturnal hemoglobinuria: usefulness of ultrasonic scanning monitoring 114
[Effectiveness of loratadine vs. placebo in the treatment of urticaria-angioedema syndrome in patients with food allergy] 113
Clinical and pathological findings in hemochromatosis type 3 due to a novel mutation in transferin receptor 2 gene 113
Promoter methylation in coagulation F7 gene influences plasma FVII concentrations and relates to coronary artery disease. 113
Tarrgeted Exome Sequencing of 5 Hemochromatosis Genes in Iron Overloaded Patients by Next Generation Sequencing (NGS) Platform. 113
A genetic risk factor for vascular disease which leads to mild hyperhomocysteinemia is common in northern Italy. 112
Increased erythrocyte membrane arachidonate and platelet malondialdehyde (MDA) production in psoriasis: normalization after fish-oil 111
Homocysteine and atheromatous renal artery stenosis 108
A new mutation in transferrin receptor 2 gene in hemochromatosis type 3 108
Combination of 4 mutations (FV R506Q, FV H1299R,Fv Y1702C, PT 20210)affecting the prothrombinase complex in a thrombophilic family 108
Hyperhomocysteinemia and Mortality after Coronary Artery Bypass Grafting 108
Clinical heterogeneity of acquired hemophilia A: a description of 4 cases. 108
Post-methionine loading hyperhomocysteinemia in patients with angiographically documented coronary artery disease 108
Hyperhomocysteinemia and mortality after coronary artery by-pass grafing. 108
PON2 Ser311Cys polymorphism is a predictor of total and cardiovascular mortality in patients with angiographically confirmed coronary artery disease. 108
Serum levels of the hepcidin-20 isoform in a large general population: The Val Borbera study. 108
[Endogenous erythrocyte proteolysis: a new approach to the study of membrane physiopathology] 107
Reply to Novelli 107
Combined effect of hemostatic gene polymorphisms and the risk of myocardial infarction in patients with advanced coronary atherosclerosis. 107
Genomics of coronary artery disease and myocardial infarction. From Genome Wide Association Studies to the Next-Generation-Sequencing era 107
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 106
Analisi di 51 polimorfismi in 35 geni dell’infiammazione per la valutazione del rischio di coronaropatia e di infarto del miocardio 106
Membrane fatty acids and erythrocyte Li-Na countertransport in nephrotic syndrome and their relationship 105
Elevated D-dimer levels are associated with coronary artery disease and cardiovascular death in an angiographically-studied population 105
Red blood cell cation transports in uraemic anaemia: evidence for an increased K/Cl co-transport activity. Effects of dialysis and erythropoietin treatment. 105
Association of endogenous thrombin potential (ETP) with coronary artery disease. An angiography-based study 105
Thrombotic thrombocytopenic purpura developed during ticlopidine therapy [letter] [see comments] 104
Low plasma vitamin B-6 concentrations and modulation of coronary artery disease risk. 104
PON2 Ser311Cys polymorphism is a predictor of total and cardiovascular mortality in patients with angiographically confirmed coronary artery disease. 104
Paraoxonase-1 status in patients with hereditary hemochromatosis 104
Identification of new BMP6 pro-peptide mutations in patients with iron overload 104
Pancreatic resections in patients who refuse blood transfusions. The application of a perioperative protocol for a true bloodless surgery 104
Assessment of COVID-19 progression on day 5 from symptoms onset 104
Red blood cells and platelet membrane fatty acids in non-dialyzed and dialyzed uremics 103
Omega-3 polyunsaturated fatty acid supplements and ambulatory blood pressure monitoring parameters in patients with mild essential hypertension 103
Epigenetic Regulation Of Hepcidin Expression In Non-Viral Hepatocellular Carcinoma: Results Of A Genome-Wide Study 103
Intravenous immunoglobulins as pre-operative management in a case of hereditary spherocytosis 102
Clinical biochimical and molecular findings in a series of families with hyperferritinemia-cataract syndrome 102
Factor VIII:c Levels in Subjects with the Factor V R2 Polymorphism. 102
Genetic and environmental determinants of hyperhomocysteinemia in subjects with angiographically proven coronary artery disease 102
CYBRD1 as a modifier gene that modulates iron phenotype in HFE p.c282y homozygous patients. 102
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. 101
DISHphagia: An Unusual Cause of Dysphagia. J Clin Endocrinol Metab. 101
Erythrocyte and platelet fatty acids in retinitis pigmentosa 100
Alterations of systemic and muscle iron metabolism in human subjects treated with low-dose recombinant erythropoietin 100
Hepcidin and DNA promoter methylation in hepatocellular carcinoma 100
Anti-oxidant status and lipid peroxidation in patients with essential hypertension 99
Potassium loss and cellular dehydration of stored erythrocytes following incubation in autologous plasma: role of the KCl cotransport system 99
ALOX5AP gene variants and risk of coronary artery disease: an angiography-based study 99
Association of phlebotomy and subcutaneous bolus injection of deferoxamine for the treatment of anemic patients with iron overload 98
Polymorphisms in the Hemostatic Pathway Genes and the Risk of Myocardial infarction in Patients with Advanced Coronary Artery Disease. Results from the Verona Heart Project. 98
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 98
HEPCIDIN REPRESSION BY PROMOTER DNA HYPERMETHYLATION IN NON-VIRAL HEPATOCELLULAR CARCINOMA 98
Molecular basis for the recently described hereditary hyperferritinemia-cataract syndrome: A mutation in the iron-responsive element of ferritin L-subunit gene 97
Evidence of heterogenicity of hemochromatosis in Italy 97
Apolipoprotein C-III predicts cardiovascular mortality in severe coronary artery disease and is associated with an enhanced plasma thrombin generation 97
Serum uric acid, but not rs7442295 polymorphism of SCL2A9 gene, predicts total and cardiovascular mortality in severe coronary artery disease. 97
Red blood cell molecular abnormalities in non haematological diseases 96
Methylenetetrahydrofolate reductase C677 T mutation, plasma homocysteine, and folate in subjects from northern Italy with or without angiographically documented severe coronary atherosclerotic disease: evidence for an important genetic-environmental interaction. 96
Neutrophil arachidonic acid level and adhesive capability are increased in essential hypertension 96
Acquired form of activated protein C resistance in healthy women taking oestrogen therapy. 96
High levels of homocysteine are associated with small number of traditional cardiovascular risk factors in patients with similar degree of coronary atherosclerosis. 96
Serum uric acid, but not rs7442295 polymorphism of SCL2A9 gene, predicts total and cardiovascular mortality in advanced coronary artery disease. 96
Genetic risk score from GWA studies is strongly associated with angiographically-defined coronary artery disease but not with mortality in the setting of secondary prevention 96
Hepcidin Inhibition by Modified Heparins without Anticoagulant Activity 96
Altered iron parameters and hepcidin levels in a general population: lesson from the CHRIS study 96
[Ion transport in erythrocytes: a universal physiological model. Reflections on the pathogenesis of hypertension (editorial)] 95
A common mutation in the 5, 10-methylenetetrahydrofolate reductase gene affects genomic DNA methylation through an interaction with folate status 95
Totale 11.806
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Categoria #
all - tutte 123.755
article - articoli 94.605
book - libri 0
conference - conferenze 28.398
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 752
Totale 247.510
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20202.489 0 0 0 0 0 496 465 363 151 433 139 442
2020/20213.928 298 627 173 402 520 467 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
2024/20253.989 583 707 356 1.569 441 333 0 0 0 0 0 0
Totale 36.036