IRIS
GRANDONE, ELVIRA
 Distribuzione geografica
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Continente #
EU - Europa 4.806
AS - Asia 4.053
NA - Nord America 3.782
SA - Sud America 1.103
AF - Africa 89
Continente sconosciuto - Info sul continente non disponibili 7
OC - Oceania 2
Totale 13.842
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Nazione #
US - Stati Uniti d'America 3.700
IE - Irlanda 2.357
SG - Singapore 1.835
BR - Brasile 900
CN - Cina 743
HK - Hong Kong 673
RU - Federazione Russa 648
SE - Svezia 605
VN - Vietnam 470
UA - Ucraina 280
IT - Italia 265
DE - Germania 190
FI - Finlandia 154
GB - Regno Unito 84
AR - Argentina 80
IN - India 79
FR - Francia 64
TR - Turchia 50
AT - Austria 36
EC - Ecuador 35
CA - Canada 32
BD - Bangladesh 31
MX - Messico 30
AE - Emirati Arabi Uniti 27
ID - Indonesia 27
NL - Olanda 24
IQ - Iraq 23
ZA - Sudafrica 20
CO - Colombia 19
CZ - Repubblica Ceca 19
PL - Polonia 19
MA - Marocco 18
CL - Cile 16
PY - Paraguay 16
VE - Venezuela 16
JP - Giappone 14
IR - Iran 13
ES - Italia 12
BE - Belgio 11
PK - Pakistan 11
UY - Uruguay 10
TN - Tunisia 9
UZ - Uzbekistan 9
PE - Perù 8
SD - Sudan 8
AL - Albania 7
EG - Egitto 7
SA - Arabia Saudita 7
KE - Kenya 6
ET - Etiopia 5
GR - Grecia 5
KZ - Kazakistan 5
LB - Libano 5
A2 - ???statistics.table.value.countryCode.A2??? 4
AZ - Azerbaigian 4
DO - Repubblica Dominicana 4
DZ - Algeria 4
LT - Lituania 4
MD - Moldavia 4
PT - Portogallo 4
BH - Bahrain 3
BO - Bolivia 3
EU - Europa 3
HN - Honduras 3
IL - Israele 3
NP - Nepal 3
OM - Oman 3
RO - Romania 3
SN - Senegal 3
AU - Australia 2
CH - Svizzera 2
DK - Danimarca 2
GT - Guatemala 2
JM - Giamaica 2
JO - Giordania 2
KR - Corea 2
NO - Norvegia 2
PA - Panama 2
PH - Filippine 2
AM - Armenia 1
BB - Barbados 1
BF - Burkina Faso 1
BG - Bulgaria 1
BN - Brunei Darussalam 1
BW - Botswana 1
CG - Congo 1
CI - Costa d'Avorio 1
CR - Costa Rica 1
CY - Cipro 1
GA - Gabon 1
GE - Georgia 1
GH - Ghana 1
GN - Guinea 1
HR - Croazia 1
HU - Ungheria 1
KG - Kirghizistan 1
KH - Cambogia 1
LV - Lettonia 1
LY - Libia 1
MN - Mongolia 1
Totale 13.833
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Città #
Dublin 2.356
Singapore 772
Hong Kong 673
Nyköping 469
Ashburn 393
Chandler 370
Santa Clara 298
Princeton 277
Wilmington 199
Jacksonville 190
Beijing 183
Dallas 180
Ho Chi Minh City 178
Moscow 164
Dearborn 122
Hanoi 99
Munich 99
Nanjing 86
Helsinki 77
São Paulo 75
The Dalles 73
New York 70
Des Moines 68
Milan 58
Los Angeles 52
Foggia 42
Turku 42
Boardman 38
Nanchang 34
San Mateo 32
Shanghai 30
Ann Arbor 29
Norwalk 28
Vienna 28
Guangzhou 27
Rio de Janeiro 27
Jiaxing 23
San Francisco 22
Woodbridge 22
Nuremberg 21
Hebei 20
Shenyang 20
Da Nang 19
Jinan 18
Porto Alegre 17
Belo Horizonte 16
Brasília 16
Curitiba 16
Haiphong 16
Warsaw 16
Brno 15
Brooklyn 15
Biên Hòa 14
Hilden 14
Kunming 14
Pune 14
Lanzhou 13
London 13
Wuhan 13
Frankfurt am Main 12
Quito 12
Bari 11
Boston 11
Charlotte 11
Salvador 11
Thái Bình 11
Tokyo 11
Zhengzhou 11
Baghdad 10
Changsha 10
Chicago 10
Guayaquil 10
Stockholm 10
Tianjin 10
Brussels 9
Changchun 9
Johannesburg 9
Montevideo 9
Montreal 9
Ninh Bình 9
Osasco 9
Phủ Lý 9
Rome 9
Toronto 9
Augusta 8
Duque de Caxias 8
Düsseldorf 8
Hillsboro 8
Jundiaí 8
Manaus 8
Tashkent 8
Atlanta 7
Buffalo 7
Campinas 7
Council Bluffs 7
Guarulhos 7
Ha Long 7
Hangzhou 7
Hải Dương 7
Manchester 7
Totale 8.695
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Nome #
A frameshift mutation in the human fibrinogen Aalpha-chain gene (Aalpha(499)Ala frameshift stop) leading to dysfibrinogen San Giovanni Rotondo 140
A platelet defect modulates bleeding in mild hemophilia: the tale of 2 brothers. 137
Factor XI deficiency: two novel mutations in asymptomatic Italian patients. 134
A G-to A mutation in IVS-3 of the human gamma fibrinogen gene causing afibrinogenemia due to abnormal RNA splicing 133
A polymorfism in VKORC1 gene is associated with an interindividual variability in the dose-anticoagulation effect of warfarin. 130
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 128
A successful pregnancy in a woman with late-onset combined homocystinuria and methylmalonic aciduria 128
A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarin 118
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 117
FXI deficiency: two novel mutations in asymptomatic Italian patients 110
C0268 Higher risk of idiopathic small for gestational age newborns in Italian women carrying the annexin A5 M2 haplotype 108
The Italian AICE-Genetics hemophilia A database: results and correlation with clinical phenotype 105
Venous thromboembolism in assisted reproductive technologies: comparison between unsuccessful versus successful cycles in an Italian cohort. 105
Identification of 217 unreported mutations in the F8 gene in a group of 1,410 unselected Italian patients with hemophilia A. 103
Acute biocompatibility of hemodiafiltration with endogenous reinfusion (HFR) 102
Inherited abnormalities of fibrinogen: 10-year clinical experience of an Italian group. 99
Identification of fetal gender in maternal blood is a helpful tool in the prenatal diagnosis of haemophilia 99
. Adverse pregnancy outcomes are associated with multiple maternal thrombophilic factors. Eur J Obstet Gynecol Reprod Biol. 1;117(2):144-7; 2004 99
Clinical histories and molecular characterization of two afibrinogenemic patients: insights into clinical management. 96
Modulation of factors involved in placental haemostasis and angiogenesis by low-molecular-weight-heparins. 96
Homozygosity by descent of a 3Mb chromosome 17 haplotype causes coinheritance of Glanzmann thrombasthenia and primary ciliary dyskinesia 93
Low protein Z levels and risk of occurrence of deep vein thrombosis 92
Identification of FVIII gene mutations in patients with hemophilia A using new combinatorial sequencing by hybridization. 91
Expression and hormonal modulation of the thromboxane A2 receptor gene in mammalian testicular arteries 91
Hormonal regulation of prostanoids receptors in the testis 90
. Acute biocompatibility of hemodiafiltration with endogenous reinfusion (HFR)]G Ital Nefrol.;21 Suppl 30:S185-9; 2004 89
Clinical utility of screening for CALR gene exon 9 mutations in patients with splanchnic venous thrombosis 86
Influence of hCG on inducible nitric oxide synthase gene expression in ram testicular arteries 85
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 85
Pregnancy-related venous thrombosis: comparison between spontaneous and ART conception in an Italian cohort 83
“Correlation between factors invoilved in the local hemostasis and angiogenesis in term human placenta”. 82
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 80
Factor VIII gene (F8) mutations as predictors of outcome in immune tolerance induction (ITI) of hemophilia A patients with high-responding inhibitors 79
Factor XI gene variants in factor XI-deficient patients of Southern Italy: identification of a novel mutation and genotype-phenotype relationship 77
A beta3 Asp217-->Val substitution in a patient with variant Glanzmann Thrombasthenia severely affects integrin alphaIIBbeta3 functions 77
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 76
Factor VII deficiency: a novel missense variant and genotype-phenotype correlation in patients from Southern Italy. 76
. 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 76
Obstetric outcomes in pregnant COVID-19 women: the imbalance of von Willebrand factor and ADAMTS13 axis 73
Fetal sex identification in maternal plasma using short tandem repeats on chromosome X 73
Factor XI gene variants in factor XI-deficient patients of Southern Italy: identification of a novel mutation and genotype-phenotype relationship 73
.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 73
Validation of PLASMIC score and follow-up data in a cohort of patients with suspected microangiopathies from Southern Italy 73
Sex modulation of the occurrence of jak2 v617f mutation in patients with splanchnic venous thrombosis. 72
Acquired hemophilia a successfully treated with rituximab. 72
2014 Sep 8. A novel congenital dysprothrombinemia leading to defective prothrombin maturation 72
. An unreported mutation within protein Z gene is associated with very low protein levels in women with fetal loss.Fertil Steril. 72
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 71
. Antiphospholipid Antibodies in a General Obstetric Population: Clinical Impact on Pregnancy Outcome and Relationship with the M2 Haplotype in the Annexin A5 (ANXA5) Gene. 71
A Sardinian Family with Factor XI Deficiency 70
. 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 68
. 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 67
Markers of hemostasis and angiogenesis in placentae from gestational vascularcomplications: impairement of mechanisms involved in mantaining intervillous blood flow 66
.Does endothelial nitric oxide synthase gene variation play a role in the occurrence of hypertension in pregnancy? Hypertens Pregnancy 2003; 22(2):149-55. 66
Validation of PLASMIC score and follow-up data in a cohort of patients with suspected microangiopathies from Southern Italy 65
Mortality and Transfusion Requirements in COVID-19 Hospitalized Italian Patients According to Severity of the Disease 64
Genome-wide association study identifies first locus associated with susceptibility to cerebral venous thrombosis 64
A novel CISD2 intragenic deletion, optic neuropathy and platelet aggregation defect in Wolfram syndrome type 2. 64
Influence of the Gly1057Asp variant of the insulin receptor substrate 2 (IRS2) on insulin resistance and relationship with epicardial fat thickness in the elderly 63
OLD AND NEW INHERITED THROMBOPHILIAS IN THE OCCURRENCE OF PREGNANCY LOSSES 63
Genetic modulation of oral anticoagulation with warfarin. Thromb Haemost. 2000; 84(5):775-8 61
Validation of the ISTH/SSC bleeding assessment tool for inherited platelet disorders: A communication from the Platelet Physiology SSC 61
Factor V Leiden, C>T MTHFR polymorphism and genetic susceptibility to preeclampsia. Thromb Haemost 1997; 77: 1052-1054 61
. Impact of prothrombotic mutations and family history on the occurrence of intra-uterine fetal deaths. Haematologica 2002; 87(10):1118-9 61
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. 60
Genetic polymorphism of 5,10-methylenetetrahydrofolate reductase (mthfr) gene in offspring of patients with myocardial infarction. 60
Mortality and clinical outcome of Italian patients undergoing orthopaedic surgery: effect of peri-operative blood transfusion 60
The JAK2 V617F mutation frequently occurs in patients with portal and mesenteric venous thrombosis 60
METHYLENETETRAHYDROFOLATE REDUCTASE (MTHFR) 677T->C MUTATION AND UNEXPLAINED EARLY PREGNANCY LOSS 60
Searching for the thrombogenic mechanism(s) of fibrinogen. Thromb Res, ; 1990; 61-67 60
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 59
Mortality and Transfusion Requirements in COVID-19 Hospitalized Italian Patients According to Severity of the Disease 59
Identification of 217 unreported mutations in the F8 gene in a group of 1,410 unselected Italian patients with hemophilia A 59
Homozygosity by descent of a 3Mb chromosome 17 haplotype causes coinheritance of Glanzmann thrombasthenia and primary ciliary dyskinesia. 58
. New epidemiological risk factors for venous thromboembolism (VTE) after menopause. J Thromb Haemost. 2006; 4(1):70. 58
. 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 58
. 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 57
Role of thrombophilia in adverse obstetric outcomes and their prevention using antithrombotic therapy 57
Factor VII deficiency: a novel missense variant and genotype-phenotype correlation in patients from Southern Italy 57
Inherited thrombophilia and gestational vascular complications. Best Pract Res Clin Haematol. 2003; 16(2):321 57
PROTHROMBOTIC GENETIC RISK FACTORS AND THE OCCURRENCE OF GESTATIONAL HYPERTENSION WITH OR WITHOUT PROTEINURIA 57
. Genetic polymorhism of 5, 10- MTHFR gene in offspring of patients with myocardial infarction. Thromb Haemost 1999; 82: 19-23 56
Abnormally high thromboxane biosynthesis in homozygous homocystinuria. Evidence for platelet involvement and Probucol-sensitive mechanism. J. Clin. Invest. 1993; 92:1400-1406 56
. 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. 55
Stable-isotope dilution LC-ESI-MS/MS techniques for the quantification of total homocysteine in human plasma 55
.Expression and hormonal modulation of the thromboxane A2 receptor gene in mammalian testicular arteries. Fertil Steril. 2006; 85 Suppl 1:1276-80 55
.Adverse outcome in women with thrombophilia and bilateral uterine artery notches. Fertil Steril. 86(3):726-7; 2006 55
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 55
Setting up a 2D-LC/MS/MS method for the rapid quantitation of the prostanoid metabolites 6-oxo-PGF(1alpha) and TXB2 as markers for hemostasis assessment 55
Clinical utility of screening for CALR gene exon 9 mutations in patients with splanchnic venous thrombosis. 54
New TET2 gene mutations in patients with myeloproliferative neoplasms and splanchnic vein thrombosis 54
The Clinical Course of Venous Thromboembolism May Differ According to Cancer Site 54
FEDERAZIONE CENTRI PER LA DIAGNOSI DELLA TROMBOSI E LA SORVEGLIANZA DELLE TERAPIE ANTITROMBOTICHE FCSA TERAPIA ANTICOAGULANTE E GRAVIDANZA RACCOMANDAZIONI DELLA FCSA 54
. Maternal and fetal inherited thrombophilias. Am J Obstet Gynecol. 2002; 186(6):1376 53
Recommendations for prophylaxis of pregnancy-related venous thromboembolism in carriers of inherited thrombophilia. Comment on the 2012 ACCP guidelines. 53
. Reduction of mononuclear cytokine production in hemodialysis patients treated with steam-sterilized low-flux polysulphone membranes. Int J Artif Organs 1998; 21:210-215 53
. Identification of fetal gender in maternal blood is a helpful tool in the prenatal diagnosis of haemophilia. Haemophilia. 2006 ;12(4):417-22 53
Findings from a multicentre, observational study on reproductive outcomes in women with unexplained recurrent pregnancy loss: the OTTILIA registry 53
Anemone study: prevalence of risk factors for superficial vein thrombosis in a large Italian population of blood donors 52
Low-molecular -weight heparin in pregnancies after ART -a retrospective study-. 52
Totale 7.577
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Categoria #
all - tutte 115.504
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 115.504
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021214 0 0 0 0 0 23 48 14 70 58 1 0
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
2025/20263.517 315 500 907 1.555 225 15 0 0 0 0 0 0
Totale 14.773