about
Multiple common variants for celiac disease influencing immune gene expressionThe anti-CD20 monoclonal antibody rituximab to treat acquired haemophilia APreventing adverse obstetric outcomes in women with genetic thrombophiliaMeta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared lociTowards the genetic basis of cerebral venous thrombosis-the BEAST Consortium: a study protocol.Adverse pregnancy outcomes are associated with multiple maternal thrombophilic factors.The G20210A prothrombin variant and the risk of venous thromboembolism or fetal loss in pregnant women: a family study.Clinical utility of antithrombotic prophylaxis in ART procedures: an Italian experience.A novel CISD2 intragenic deletion, optic neuropathy and platelet aggregation defect in Wolfram syndrome type 2.Annexin A5 haplotype M2 is not a risk factor for recurrent spontaneous abortion in Northern Europe: is there sufficient evidence?Pregnancy-related venous thrombosis: comparison between spontaneous and ART conception in an Italian cohortTET2 mutations in Ph-negative myeloproliferative neoplasms: identification of three novel mutations and relationship with clinical and laboratory findings.Low-dose aspirin for in vitro fertilization or intracytoplasmic sperm injection: a systematic review and a meta-analysis of the literature.Liquid chromatography-tandem mass spectrometry method as the golden standard for therapeutic drug monitoring in renal transplant.The Clinical Course of Venous Thromboembolism May Differ According to Cancer Site.Assisted reproductive technologies and thrombosis.Aspirin and heparin in pregnancy.Development of a Risk Prediction Score for Occult Cancer in Patients With VTE.The prevention and treatment of venous thromboembolism in pregnancy.Modulation of factors involved in placental haemostasis and angiogenesis by low-molecular-weight-heparins.Long-term Clinical Outcomes of Splanchnic Vein Thrombosis: Results of an International Registry.Acquired hemophilia a successfully treated with rituximabGain-of-function gene mutations and venous thromboembolism: distinct roles in different clinical settingsInfluence of hCG on inducible nitric oxide synthase gene expression in ram testicular arteries.Antithrombotic prophylaxis during pregnancy in women with deficiency of natural anticoagulants.Adverse outcome in women with thrombophilia and bilateral uterine artery notches.Occurrence of factor V Leiden mutation (Arg506Gln) and anticardiolipin antibodies in migraine patients.Clinical Pregnancies and Live Births in women approaching ART: a follow-up analysis of 157 women after thrombophilia screening.Iron-dependent erythropoiesis in women with excessive menstrual blood losses and women with normal menses.A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarin.Hyperhomocysteinaemia in chronic liver diseases: role of disease stage, vitamin status and methylenetetrahydrofolate reductase genetics.Factor XI deficiency: two novel mutations in asymptomatic Italian patients.Identification of fetal gender in maternal blood is a helpful tool in the prenatal diagnosis of haemophilia.Clinical histories and molecular characterization of two afibrinogenemic patients: insights into clinical management.Venous thrombosis in afibrinogenemia: a successful use of rivaroxaban.Factor VIII gene (F8) mutations as predictors of outcome in immune tolerance induction of hemophilia A patients with high-responding inhibitors.A beta3 Asp217-->Val substitution in a patient with variant Glanzmann Thrombasthenia severely affects integrin alphaIIBbeta3 functions.Homocysteine metabolism in families from southern Italy with neural tube defects: role of genetic and nutritional determinants.Low-molecular -weight heparin in pregnancies after ART -a retrospective study-.Analysis of MTNR1B gene polymorphisms in relationship with IRS2 gene variants, epicardial fat thickness, glucose homeostasis and cognitive performance in the elderly.
P50
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P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Elvira Grandone
@ast
Elvira Grandone
@en
Elvira Grandone
@es
Elvira Grandone
@nl
type
label
Elvira Grandone
@ast
Elvira Grandone
@en
Elvira Grandone
@es
Elvira Grandone
@nl
prefLabel
Elvira Grandone
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Elvira Grandone
@en
Elvira Grandone
@es
Elvira Grandone
@nl
P106
P1153
7006391091
P31
P496
0000-0002-8980-9783