IRIS
GRANDONE, ELVIRA
 Distribuzione geografica
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Continente #
NA - Nord America 5.822
EU - Europa 5.719
AS - Asia 4.542
SA - Sud America 1.170
AF - Africa 117
Continente sconosciuto - Info sul continente non disponibili 7
OC - Oceania 5
Totale 17.382
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Nazione #
US - Stati Uniti d'America 5.703
IE - Irlanda 2.357
SG - Singapore 1.994
RU - Federazione Russa 1.141
BR - Brasile 940
CN - Cina 876
HK - Hong Kong 691
SE - Svezia 606
VN - Vietnam 556
FR - Francia 358
IT - Italia 301
UA - Ucraina 282
DE - Germania 225
FI - Finlandia 157
GB - Regno Unito 99
IN - India 92
AR - Argentina 87
TR - Turchia 56
BD - Bangladesh 48
CA - Canada 46
MX - Messico 42
AT - Austria 37
IQ - Iraq 37
PL - Polonia 37
EC - Ecuador 36
NL - Olanda 31
ID - Indonesia 28
AE - Emirati Arabi Uniti 27
ZA - Sudafrica 25
CO - Colombia 24
VE - Venezuela 24
JP - Giappone 22
CL - Cile 19
CZ - Repubblica Ceca 19
MA - Marocco 19
PK - Pakistan 19
PY - Paraguay 16
ES - Italia 14
BE - Belgio 13
IR - Iran 13
UZ - Uzbekistan 13
KE - Kenya 11
UY - Uruguay 11
DZ - Algeria 10
PE - Perù 9
SA - Arabia Saudita 9
TN - Tunisia 9
AL - Albania 8
EG - Egitto 8
SD - Sudan 8
ET - Etiopia 7
JO - Giordania 7
PH - Filippine 6
SN - Senegal 6
AU - Australia 5
DO - Repubblica Dominicana 5
GR - Grecia 5
JM - Giamaica 5
KZ - Kazakistan 5
LB - Libano 5
MD - Moldavia 5
NP - Nepal 5
A2 - ???statistics.table.value.countryCode.A2??? 4
AZ - Azerbaigian 4
BH - Bahrain 4
BO - Bolivia 4
CR - Costa Rica 4
HN - Honduras 4
LT - Lituania 4
PA - Panama 4
PT - Portogallo 4
EU - Europa 3
GT - Guatemala 3
IL - Israele 3
MY - Malesia 3
OM - Oman 3
RO - Romania 3
CG - Congo 2
CH - Svizzera 2
CY - Cipro 2
DK - Danimarca 2
GA - Gabon 2
GE - Georgia 2
HR - Croazia 2
KH - Cambogia 2
KR - Corea 2
MN - Mongolia 2
NG - Nigeria 2
NO - Norvegia 2
RS - Serbia 2
TH - Thailandia 2
AM - Armenia 1
BB - Barbados 1
BF - Burkina Faso 1
BG - Bulgaria 1
BN - Brunei Darussalam 1
BW - Botswana 1
CI - Costa d'Avorio 1
GH - Ghana 1
GN - Guinea 1
Totale 17.370
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Città #
Dublin 2.356
San Jose 1.548
Singapore 831
Hong Kong 691
Ashburn 488
Nyköping 469
Chandler 370
Santa Clara 310
Princeton 277
Lauterbourg 262
Moscow 217
Ho Chi Minh City 209
Wilmington 199
Beijing 195
Dallas 192
Jacksonville 191
Hanoi 124
Dearborn 122
The Dalles 106
Munich 100
Nanjing 86
Helsinki 80
São Paulo 80
New York 78
Des Moines 68
Milan 59
Los Angeles 55
Foggia 42
Turku 42
Boardman 41
Nanchang 34
Warsaw 34
Frankfurt am Main 33
Hillsboro 33
San Mateo 32
Shanghai 30
Ann Arbor 29
Norwalk 28
Nuremberg 28
Vienna 28
Guangzhou 27
Orem 27
Rio de Janeiro 27
San Francisco 24
Da Nang 23
Jiaxing 23
Woodbridge 22
Haiphong 20
Hebei 20
Shenyang 20
Paris 19
Jinan 18
Tokyo 18
Belo Horizonte 17
Porto Alegre 17
Brasília 16
Curitiba 16
London 16
Baghdad 15
Biên Hòa 15
Brno 15
Brooklyn 15
Council Bluffs 15
Pune 15
Hilden 14
Kunming 14
Toronto 14
Charlotte 13
Lanzhou 13
Rome 13
Wuhan 13
Atlanta 12
Boston 12
Quito 12
Bari 11
Changsha 11
Johannesburg 11
Manchester 11
Ninh Bình 11
Salvador 11
Stockholm 11
Tashkent 11
Thái Bình 11
Zhengzhou 11
Amsterdam 10
Chicago 10
Dhaka 10
Guayaquil 10
Montreal 10
Nairobi 10
Osasco 10
Tianjin 10
Washington 10
Brussels 9
Changchun 9
Duque de Caxias 9
Hangzhou 9
Mexico City 9
Montevideo 9
Phủ Lý 9
Totale 11.050
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Nome #
A platelet defect modulates bleeding in mild hemophilia: the tale of 2 brothers. 165
A frameshift mutation in the human fibrinogen Aalpha-chain gene (Aalpha(499)Ala frameshift stop) leading to dysfibrinogen San Giovanni Rotondo 159
Factor XI deficiency: two novel mutations in asymptomatic Italian patients. 153
A polymorfism in VKORC1 gene is associated with an interindividual variability in the dose-anticoagulation effect of warfarin. 152
A G-to A mutation in IVS-3 of the human gamma fibrinogen gene causing afibrinogenemia due to abnormal RNA splicing 152
A successful pregnancy in a woman with late-onset combined homocystinuria and methylmalonic aciduria 146
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 143
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 138
A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarin 131
FXI deficiency: two novel mutations in asymptomatic Italian patients 130
The Italian AICE-Genetics hemophilia A database: results and correlation with clinical phenotype 127
C0268 Higher risk of idiopathic small for gestational age newborns in Italian women carrying the annexin A5 M2 haplotype 125
Acute biocompatibility of hemodiafiltration with endogenous reinfusion (HFR) 124
Venous thromboembolism in assisted reproductive technologies: comparison between unsuccessful versus successful cycles in an Italian cohort. 120
. Adverse pregnancy outcomes are associated with multiple maternal thrombophilic factors. Eur J Obstet Gynecol Reprod Biol. 1;117(2):144-7; 2004 119
Healthy and pro-inflammatory gut ecology plays a crucial role in the digestion and tolerance of a novel Gluten Friendly™ bread in celiac subjects: a randomized, double blind, placebo control in vivo study 116
Identification of 217 unreported mutations in the F8 gene in a group of 1,410 unselected Italian patients with hemophilia A. 116
Identification of fetal gender in maternal blood is a helpful tool in the prenatal diagnosis of haemophilia 115
Inherited abnormalities of fibrinogen: 10-year clinical experience of an Italian group. 113
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 110
Low protein Z levels and risk of occurrence of deep vein thrombosis 109
Expression and hormonal modulation of the thromboxane A2 receptor gene in mammalian testicular arteries 106
Homozygosity by descent of a 3Mb chromosome 17 haplotype causes coinheritance of Glanzmann thrombasthenia and primary ciliary dyskinesia 106
. Acute biocompatibility of hemodiafiltration with endogenous reinfusion (HFR)]G Ital Nefrol.;21 Suppl 30:S185-9; 2004 106
Identification of FVIII gene mutations in patients with hemophilia A using new combinatorial sequencing by hybridization. 105
Clinical histories and molecular characterization of two afibrinogenemic patients: insights into clinical management. 105
Modulation of factors involved in placental haemostasis and angiogenesis by low-molecular-weight-heparins. 105
Hormonal regulation of prostanoids receptors in the testis 104
Factor VII deficiency: a novel missense variant and genotype-phenotype correlation in patients from Southern Italy. 96
Clinical utility of screening for CALR gene exon 9 mutations in patients with splanchnic venous thrombosis 95
Factor XI gene variants in factor XI-deficient patients of Southern Italy: identification of a novel mutation and genotype-phenotype relationship 95
Pregnancy-related venous thrombosis: comparison between spontaneous and ART conception in an Italian cohort 95
A beta3 Asp217-->Val substitution in a patient with variant Glanzmann Thrombasthenia severely affects integrin alphaIIBbeta3 functions 95
Influence of hCG on inducible nitric oxide synthase gene expression in ram testicular arteries 94
.A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarin. Blood. 105(2):645-9; 2005 94
“Correlation between factors invoilved in the local hemostasis and angiogenesis in term human placenta”. 93
Factor VIII gene (F8) mutations as predictors of outcome in immune tolerance induction (ITI) of hemophilia A patients with high-responding inhibitors 93
The curious incident of a cavum velum interpositum cyst in twins of a mother carrying May-Hegglin anomaly: a case report and short literature review 93
Obstetric outcomes in pregnant COVID-19 women: the imbalance of von Willebrand factor and ADAMTS13 axis 92
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 92
2014 Sep 8. A novel congenital dysprothrombinemia leading to defective prothrombin maturation 92
. The Methylenetetrahydrofolate reductase TT677 genotype is associated with venous thrombosis independently of the coexistence of the FV Leiden and the prothrombin A20210 mutations. Thromb Haemost 1998; 79:907-911 91
Fetal sex identification in maternal plasma using short tandem repeats on chromosome X 89
Factor XI gene variants in factor XI-deficient patients of Southern Italy: identification of a novel mutation and genotype-phenotype relationship 89
. An unreported mutation within protein Z gene is associated with very low protein levels in women with fetal loss.Fertil Steril. 89
Validation of PLASMIC score and follow-up data in a cohort of patients with suspected microangiopathies from Southern Italy 88
. C-reactive protein in offspring is associated with the occurrence of myocardial infarction in first-degree relatives. Arterioscler Thromb Vasc Biol. 2000; 20(1):198-203 86
. Antiphospholipid Antibodies in a General Obstetric Population: Clinical Impact on Pregnancy Outcome and Relationship with the M2 Haplotype in the Annexin A5 (ANXA5) Gene. 86
Sex modulation of the occurrence of jak2 v617f mutation in patients with splanchnic venous thrombosis. 85
Validation of PLASMIC score and follow-up data in a cohort of patients with suspected microangiopathies from Southern Italy 83
. Compound heterozygosity (554-589 del, C515-T transition) in the platelet glycoprotein Ib gene in a patient with a severe bleeding tendency. Thromb Haemost 1999, 81(4): 486-92 82
Markers of hemostasis and angiogenesis in placentae from gestational vascularcomplications: impairement of mechanisms involved in mantaining intervillous blood flow 81
A Sardinian Family with Factor XI Deficiency 81
Acquired hemophilia a successfully treated with rituximab. 80
. Impact of prothrombotic mutations and family history on the occurrence of intra-uterine fetal deaths. Haematologica 2002; 87(10):1118-9 79
Mortality and Transfusion Requirements in COVID-19 Hospitalized Italian Patients According to Severity of the Disease 78
Genome-wide association study identifies first locus associated with susceptibility to cerebral venous thrombosis 78
. Molecular characterization of a factor VII deficient patient supports the importance of the second epidermal growth factor-like domain. Haematologica. 89(8):979-84; 2004 78
.Expression and hormonal modulation of the thromboxane A2 receptor gene in mammalian testicular arteries. Fertil Steril. 2006; 85 Suppl 1:1276-80 77
. Maternal and fetal inherited thrombophilias. Am J Obstet Gynecol. 2002; 186(6):1376 76
.Adverse outcome in women with thrombophilia and bilateral uterine artery notches. Fertil Steril. 86(3):726-7; 2006 76
. FV HR2 haplotype as additional inherited risk factor for deep vein thrombosis in individuals with a high-risk profile. Thromb Haemost. 2002; 87(1):32-6. 75
. Anticardiolipin antibodies in patients with liver disease. Am J Gastroenterol. ;94(10):2983-7; 1999 75
Mortality and Transfusion Requirements in COVID-19 Hospitalized Italian Patients According to Severity of the Disease 74
Validation of the ISTH/SSC bleeding assessment tool for inherited platelet disorders: A communication from the Platelet Physiology SSC 74
Influence of the Gly1057Asp variant of the insulin receptor substrate 2 (IRS2) on insulin resistance and relationship with epicardial fat thickness in the elderly 74
.Does endothelial nitric oxide synthase gene variation play a role in the occurrence of hypertension in pregnancy? Hypertens Pregnancy 2003; 22(2):149-55. 74
. Determining sulphur-containing aminoacids by capillary electrophoresis. A fast novel method for total homocyst(e)ine in human plasma. Electrophoresis 1999; 20: (3): 569-74 73
. Genetic polymorhism of 5, 10- MTHFR gene in offspring of patients with myocardial infarction. Thromb Haemost 1999; 82: 19-23 73
A novel CISD2 intragenic deletion, optic neuropathy and platelet aggregation defect in Wolfram syndrome type 2. 73
OLD AND NEW INHERITED THROMBOPHILIAS IN THE OCCURRENCE OF PREGNANCY LOSSES 72
Anemone study: prevalence of risk factors for superficial vein thrombosis in a large Italian population of blood donors 71
. Reduction of mononuclear cytokine production in hemodialysis patients treated with steam-sterilized low-flux polysulphone membranes. Int J Artif Organs 1998; 21:210-215 71
. New epidemiological risk factors for venous thromboembolism (VTE) after menopause. J Thromb Haemost. 2006; 4(1):70. 71
Factor VII deficiency: a novel missense variant and genotype-phenotype correlation in patients from Southern Italy 71
Obstetric complications and pregnancy-related venous thromboembolism: the effect of low molecular weight heparin on their prevention in carriers of factor V leiden or prothrombin G20210A mutation. 70
The curious incident of a cavum velum interpositum cyst in twins of a mother carrying May-Hegglin anomaly: a case report and short literature review 70
Genetic modulation of oral anticoagulation with warfarin. Thromb Haemost. 2000; 84(5):775-8 70
. Identification of fetal gender in maternal blood is a helpful tool in the prenatal diagnosis of haemophilia. Haemophilia. 2006 ;12(4):417-22 70
Factor V Leiden, C>T MTHFR polymorphism and genetic susceptibility to preeclampsia. Thromb Haemost 1997; 77: 1052-1054 70
Inherited thrombophilia and gestational vascular complications. Best Pract Res Clin Haematol. 2003; 16(2):321 70
. Plasminogen activator inhibitor-1 (PAI-1) plasma levels in a general population without clinical evidence of atherosclerosis. Relation to environmental and genetic determinants. Arterioscler. Thromb. Vasc. Biol. 18:562-567; 1998 69
Genetic polymorphism of 5,10-methylenetetrahydrofolate reductase (mthfr) gene in offspring of patients with myocardial infarction. 68
. Polymorphisms in factor II and factor VII genes modulate oral anticoagulation with warfarin. Haematologica 2004; 89(12):1510-6. 68
The JAK2 V617F mutation frequently occurs in patients with portal and mesenteric venous thrombosis 68
Homozygosity by descent of a 3Mb chromosome 17 haplotype causes coinheritance of Glanzmann thrombasthenia and primary ciliary dyskinesia. 68
METHYLENETETRAHYDROFOLATE REDUCTASE (MTHFR) 677T->C MUTATION AND UNEXPLAINED EARLY PREGNANCY LOSS 68
Searching for the thrombogenic mechanism(s) of fibrinogen. Thromb Res, ; 1990; 61-67 68
Abnormally high thromboxane biosynthesis in homozygous homocystinuria. Evidence for platelet involvement and Probucol-sensitive mechanism. J. Clin. Invest. 1993; 92:1400-1406 68
Coma in adult cerebral venous thrombosis: The BEAST study 67
Mortality and clinical outcome of Italian patients undergoing orthopaedic surgery: effect of peri-operative blood transfusion 67
A novel congenital dysprothrombinemia leading to defective prothrombin maturation 67
PROTHROMBOTIC GENETIC RISK FACTORS AND THE OCCURRENCE OF GESTATIONAL HYPERTENSION WITH OR WITHOUT PROTEINURIA 67
Identification of 217 unreported mutations in the F8 gene in a group of 1,410 unselected Italian patients with hemophilia A 67
Blood Loss in Women of Childbearing Potential Taking Oral Anticoagulants for Venous Thromboembolism (The BLEED Study) 66
. Occurrence of factor V Leiden mutation (Arg506Gln) and anticardiolipin antibodies in migraine patients. Neurol Sci , 2002; 22(6):455-8 65
Clinical utility of screening for CALR gene exon 9 mutations in patients with splanchnic venous thrombosis. 65
Role of thrombophilia in adverse obstetric outcomes and their prevention using antithrombotic therapy 65
Plasma lipoprotein(a) in subjects attending a metabolic ward. Comparisons between individuals with and without a history of ischemic stroke. Arteriosc. Thromb. Vasc. Biol. 1996; 16:120-128 65
Age of onset of cerebral venous thrombosis: the BEAST study 64
Totale 9.082
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Categoria #
all - tutte 128.742
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 128.742
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.613 31 1 0 9 735 12 48 122 140 126 28 361
2022/20233.864 447 116 152 102 82 207 11 183 2.450 12 45 57
2023/2024503 76 41 38 20 34 149 32 7 4 11 8 83
2024/20253.872 307 65 72 136 54 451 552 149 1.115 283 281 407
2025/20267.063 315 500 907 1.555 225 249 1.198 881 528 393 159 153
Totale 18.319