IRIS
GRANDONE, ELVIRA
 Distribuzione geografica
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Continente #
EU - Europa 3.184
NA - Nord America 1.804
AS - Asia 259
AF - Africa 17
Continente sconosciuto - Info sul continente non disponibili 5
SA - Sud America 4
OC - Oceania 1
Totale 5.274
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Nazione #
IE - Irlanda 2.216
US - Stati Uniti d'America 1.792
SE - Svezia 512
CN - Cina 190
UA - Ucraina 162
IT - Italia 111
FI - Finlandia 67
IN - India 27
DE - Germania 23
AT - Austria 21
FR - Francia 20
GB - Regno Unito 17
TR - Turchia 16
IR - Iran 8
SD - Sudan 8
CA - Canada 7
MA - Marocco 7
NL - Olanda 7
JP - Giappone 5
MX - Messico 5
A2 - ???statistics.table.value.countryCode.A2??? 4
CL - Cile 4
ES - Italia 4
MD - Moldavia 4
RU - Federazione Russa 4
BD - Bangladesh 3
BE - Belgio 3
RO - Romania 3
CH - Svizzera 2
CZ - Repubblica Ceca 2
EG - Egitto 2
PL - Polonia 2
SG - Singapore 2
AU - Australia 1
AZ - Azerbaigian 1
CY - Cipro 1
DK - Danimarca 1
EU - Europa 1
HR - Croazia 1
IL - Israele 1
KR - Corea 1
LB - Libano 1
MN - Mongolia 1
NO - Norvegia 1
PH - Filippine 1
PK - Pakistan 1
PT - Portogallo 1
Totale 5.274
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Città #
Dublin 2.216
Nyköping 419
Chandler 262
Princeton 262
Wilmington 182
Jacksonville 115
Ashburn 69
Dearborn 63
Des Moines 62
Helsinki 51
Nanjing 49
New York 42
Foggia 35
Norwalk 27
Vienna 21
Beijing 20
Nanchang 16
San Mateo 16
Hebei 14
Ann Arbor 13
Shenyang 12
Woodbridge 12
Pune 11
Lanzhou 10
Boardman 9
Jiaxing 9
Jinan 9
Kunming 9
Zhengzhou 8
Bari 7
Rome 7
Washington 7
Changsha 6
Los Angeles 6
Redmond 6
Falls Church 5
Hanover 5
Lucera 5
Ningbo 5
Pisa 5
Tianjin 5
Borås 4
Chisinau 4
Hangzhou 4
Stevenage 4
Brussels 3
Changchun 3
Fuzhou 3
Hilden 3
Paris 3
Salé 3
Santa Clara 3
Seattle 3
Taizhou 3
Tiflet 3
Turin 3
Auburn Hills 2
Baronissi 2
Bengaluru 2
Coyoacán 2
Cutrofiano 2
Frankfurt am Main 2
Groningen 2
Hefei 2
Kemerovo 2
Latina 2
Mexico 2
Modena 2
Monza 2
Orange 2
Ottawa 2
San Giovanni Rotondo 2
Sangonera la Verde 2
Taranto 2
Tokyo 2
Verona 2
Acate 1
Adana 1
Ardabil 1
Arzano 1
Augusta 1
Baku 1
Barcelona 1
Bassano Del Grappa 1
Beirut 1
Berlin 1
Birmingham 1
Buffalo 1
Caserta 1
Cedar Knolls 1
Cincinnati 1
Clearwater 1
Cupertino 1
Cuttack 1
Dhaka 1
Edinburgh 1
Gazipur 1
Geneva 1
Genoa 1
Gloucester 1
Totale 4.225
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Nome #
Factor XI deficiency: two novel mutations in asymptomatic Italian patients. 101
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 94
FXI deficiency: two novel mutations in asymptomatic Italian patients 86
A successful pregnancy in a woman with late-onset combined homocystinuria and methylmalonic aciduria 84
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 81
Acute biocompatibility of hemodiafiltration with endogenous reinfusion (HFR) 72
Homozygosity by descent of a 3Mb chromosome 17 haplotype causes coinheritance of Glanzmann thrombasthenia and primary ciliary dyskinesia 68
Hormonal regulation of prostanoids receptors in the testis 67
Expression and hormonal modulation of the thromboxane A2 receptor gene in mammalian testicular arteries 61
Venous thromboembolism in assisted reproductive technologies: comparison between unsuccessful versus successful cycles in an Italian cohort. 59
“Correlation between factors invoilved in the local hemostasis and angiogenesis in term human placenta”. 58
Pregnancy-related venous thrombosis: comparison between spontaneous and ART conception in an Italian cohort 58
Fetal sex identification in maternal plasma using short tandem repeats on chromosome X 54
Factor XI gene variants in factor XI-deficient patients of Southern Italy: identification of a novel mutation and genotype-phenotype relationship 53
Factor VII deficiency: a novel missense variant and genotype-phenotype correlation in patients from Southern Italy. 52
Modulation of factors involved in placental haemostasis and angiogenesis by low-molecular-weight-heparins. 51
Sex modulation of the occurrence of jak2 v617f mutation in patients with splanchnic venous thrombosis. 46
Markers of hemostasis and angiogenesis in placentae from gestational vascularcomplications: impairement of mechanisms involved in mantaining intervillous blood flow 45
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. 45
A beta3 Asp217-->Val substitution in a patient with variant Glanzmann Thrombasthenia severely affects integrin alphaIIBbeta3 functions 45
Validation of PLASMIC score and follow-up data in a cohort of patients with suspected microangiopathies from Southern Italy 45
. Acute biocompatibility of hemodiafiltration with endogenous reinfusion (HFR)]G Ital Nefrol.;21 Suppl 30:S185-9; 2004 45
Influence of hCG on inducible nitric oxide synthase gene expression in ram testicular arteries 44
Obstetric outcomes in pregnant COVID-19 women: the imbalance of von Willebrand factor and ADAMTS13 axis 43
Genetic polymorphism of 5,10-methylenetetrahydrofolate reductase (mthfr) gene in offspring of patients with myocardial infarction. 42
2014 Sep 8. A novel congenital dysprothrombinemia leading to defective prothrombin maturation 42
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 42
.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 41
Validation of PLASMIC score and follow-up data in a cohort of patients with suspected microangiopathies from Southern Italy 39
Acquired hemophilia a successfully treated with rituximab. 37
. 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 37
. Antiphospholipid Antibodies in a General Obstetric Population: Clinical Impact on Pregnancy Outcome and Relationship with the M2 Haplotype in the Annexin A5 (ANXA5) Gene. 36
Abnormally high thromboxane biosynthesis in homozygous homocystinuria. Evidence for platelet involvement and Probucol-sensitive mechanism. J. Clin. Invest. 1993; 92:1400-1406 36
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 34
Mortality and Transfusion Requirements in COVID-19 Hospitalized Italian Patients According to Severity of the Disease 34
Clinical utility of screening for CALR gene exon 9 mutations in patients with splanchnic venous thrombosis. 33
Mortality and Transfusion Requirements in COVID-19 Hospitalized Italian Patients According to Severity of the Disease 31
A Sardinian Family with Factor XI Deficiency 31
A frameshift mutation in the human fibrinogen Aalpha-chain gene (Aalpha(499)Ala frameshift stop) leading to dysfibrinogen San Giovanni Rotondo. Thromb Haemost.;86(6):1483-8. 2001 31
Pulmonary embolism associated with transfusion after severe post-partum haemorrhage: is less more? 30
. 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 30
A new JAK2 gene mutation in patients with polycythemia vera and splanchnic vein thrombosis 29
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 28
Prospective evaluation of pregnancy outcome in an Italian woman with late-onset combined homocystinuria and methylmalonic aciduria 28
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 28
Anemone study: prevalence of risk factors for superficial vein thrombosis in a large Italian population of blood donors 28
Factor XI gene variants in factor XI-deficient patients of Southern Italy: identification of a novel mutation and genotype-phenotype relationship 28
.Adverse outcome in women with thrombophilia and bilateral uterine artery notches. Fertil Steril. 86(3):726-7; 2006 28
. An unreported mutation within protein Z gene is associated with very low protein levels in women with fetal loss.Fertil Steril. 28
Mortality and clinical outcome of Italian patients undergoing orthopaedic surgery: effect of peri-operative blood transfusion 27
. 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. 27
.Expression and hormonal modulation of the thromboxane A2 receptor gene in mammalian testicular arteries. Fertil Steril. 2006; 85 Suppl 1:1276-80 27
Factor VII deficiency: a novel missense variant and genotype-phenotype correlation in patients from Southern Italy 27
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 27
Genome-wide association study identifies first locus associated with susceptibility to cerebral venous thrombosis 26
A novel CISD2 intragenic deletion, optic neuropathy and platelet aggregation defect in Wolfram syndrome type 2. 26
. 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 26
Modulation of factors involved in placental haemostasis and angiogenesis by low-molecular-weight-heparins 26
Abnormally high circulation levels of tissue plasminogen activator inhibitor-1 in patients with a history of hischemic stroke. Arterioscler. Thromb. 1994; 14:1741-1745; 25
.. A G-to-A mutation in IVS-3 of the human gamma fibrinogen gene causing afibrinogenemia due to abnormal RNA splicing. Blood 2000; 96(7):2501-5 25
Long-term clinical outcomes of splanchnic vein thrombosis results of an international registry 25
METHYLENETETRAHYDROFOLATE REDUCTASE (MTHFR) 677T->C MUTATION AND UNEXPLAINED EARLY PREGNANCY LOSS 25
A rapid method for the quantification of the enantiomers of Warfarin, Phenprocoumon and Acenocoumarol by two-dimensional-enantioselective liquid chromatography/electrospray tandem mass spectrometry 25
Long-term Clinical Outcomes of Splanchnic Vein Thrombosis: Results of an International Registry 24
Annexin V expression in human placenta is influenced by the carriership of the common haplotype M2 24
Markers of haemostasis and angiogenesis in placentae from gestational vascular complications: impairment of mechanisms involved in maintaining intervillous blood flow 24
Coexistence of factor V Leiden and Factor II A20210 mutations and recurrent venous thromboembolism. Thromb Haemost. 1999; 82(6):1583-7 24
A reliable and rapid tool for plasma quantification of 18 psychotropic drugs by ESI tandem mass spectrometry. J Pharm Biomed Anal. 2012 Aug-Sep;67-68:104-13 23
Venous thromboembolism in assisted reproductive technologies: comparison between unsuccessful versus successful cycles in an Italian cohort 23
Gain-of-function gene mutations and venous thromboembolism: distinct roles in different clinical settings 23
. Identification of fetal gender in maternal blood is a helpful tool in the prenatal diagnosis of haemophilia. Haemophilia. 2006 ;12(4):417-22 23
Factor V Leiden is associated with repeated and recurrent unexplained fetal losses 23
. 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 23
Functional characterization of annexin A5 gene promoter allelic variants. 23
.Does endothelial nitric oxide synthase gene variation play a role in the occurrence of hypertension in pregnancy? Hypertens Pregnancy 2003; 22(2):149-55. 23
STATEMENT CONDIVISO TRA LE SOCIETA’ ITALIANA PER LO STUDIO DELL’ EMOSTASI E DELLA TROMBOSI (SISET) E LA SOCIETA’ ITALIANA DI GINECOLOGIA E OSTETRICIA (SIGO) 23
Linee guida sull’uso dei farmaci anticoagulanti ed antiaggreganti in ostetricia e ginecologia 23
Detection of factor V Leiden Using SSCP. Thromb Haemost 1996; 76:579-583 22
. 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 22
. Genetic polymorhism of 5, 10- MTHFR gene in offspring of patients with myocardial infarction. Thromb Haemost 1999; 82: 19-23 22
A platelet defect modulates bleeding in mild hemophilia: the tale of 2 brothers 22
Validation of PLASMIC score and follow-up data in a cohort of patients with suspected microangiopathies from Southern Italy. 22
. The factor V (FV) gene ASP79HIS polymorphism modulates FV plasma levels and affects the activated protein C resistance phenotype in presence of the FV Leiden mutation. Haematologica 2003; .88(3):286-9. 22
Reduction of ADAMTS13 Levels Predicts Mortality in SARS-CoV-2 Patients. 22
. Impact of prothrombotic mutations and family history on the occurrence of intra-uterine fetal deaths. Haematologica 2002; 87(10):1118-9 22
. Maternal and fetal inherited thrombophilias. Am J Obstet Gynecol. 2002; 186(6):1376 21
Thrombophilia, Inflammation, and Recurrent Pregnancy Loss: A Case-Based Review 21
. 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 21
. Reduction of mononuclear cytokine production in hemodialysis patients treated with steam-sterilized low-flux polysulphone membranes. Int J Artif Organs 1998; 21:210-215 21
A novel congenital dysprothrombinemia leading to defective prothrombin maturation 21
Influence of the Gly1057Asp variant of the insulin receptor substrate 2 (IRS2) on insulin resistance and relationship with epicardial fat thickness in the elderly 21
. Anticardiolipin antibodies in patients with liver disease. Am J Gastroenterol. ;94(10):2983-7; 1999 21
.A new method for determination of plasma homocystine by isotope dilution and electrospray tandem mass spectrometry. J Chromatogr B Analyt Technol Biomed Life Sci. 2006; 842(1):64-9 21
. PAI-1 4G/5G and ACE I/D gene polymorphisms and the occurrence of myocardial infarction in patients on intermittent dialysis. Nephrol Dial Transplant 2003; 18(6):1142-6 21
. Polymorphisms in factor II and factor VII genes modulate oral anticoagulation with warfarin. Haematologica 2004; 89(12):1510-6. 20
. Occurrence of factor V Leiden mutation (Arg506Gln) and anticardiolipin antibodies in migraine patients. Neurol Sci , 2002; 22(6):455-8 20
Factor V Leiden, C>T MTHFR polymorphism and genetic susceptibility to preeclampsia. Thromb Haemost 1997; 77: 1052-1054 20
In vitro inhibition by defibrotide of monocyte superoxide anion generation: a possibile role for the antithrombotic effect of a polydeoxyribonucleotide-derived drug. Haemostasis 1991; 21:98-105 20
Prognostic factors in noncirrhotic patients with splanchnic vein thromboses 20
Protein Z levels and unexplained fetal losses. Fertil Steril.;82(4):982-3; 2004 19
Totale 3.462
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Categoria #
all - tutte 55.472
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 55.472
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201924 0 0 0 0 0 0 0 0 0 0 7 17
2019/2020304 60 21 8 2 38 36 61 9 30 6 29 4
2020/2021214 25 2 23 3 24 9 28 12 55 33 0 0
2021/20221.534 15 0 0 7 726 11 48 117 133 116 19 342
2022/20233.438 409 98 133 74 49 169 11 144 2.269 9 35 38
2023/2024358 62 38 36 18 31 137 17 7 4 8 0 0
Totale 6.121