About: Maurizio Margaglione

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researcher (ORCID 0000-0001-5627-9221)

Attributes	Values
rdf:type	Item
description	forskare (sv) ikertzailea (eu) 연구원 (ko) গবেষক (bn) 研究者 (ja) ഗവേഷകൻ (ml) эрдэмтэн (mn) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq) onderzoeker (nl) researcher (ORCID 0000-0001-5627-9221) (en)
rdfs:label	Maurizio Margaglione (en) Maurizio Margaglione (es) Maurizio Margaglione (it) Maurizio Margaglione (nl) Maurizio Margaglione (sl) Maurizio Margaglione (ast)
skos:prefLabel	Maurizio Margaglione (en) Maurizio Margaglione (es) Maurizio Margaglione (it) Maurizio Margaglione (nl) Maurizio Margaglione (sl) Maurizio Margaglione (ast)
name	Maurizio Margaglione (en) Maurizio Margaglione (es) Maurizio Margaglione (it) Maurizio Margaglione (nl) Maurizio Margaglione (sl) Maurizio Margaglione (ast)
given name	wds:Q42638173-F66A25F9-5077-4437-A432-793C06D8EB03
given name	Maurizio
instance of	wds:Q42638173-D16F6FA5-12F3-426B-BC30-D5C4B3C4DA82
instance of	Homo sapiens
occupation	wds:Q42638173-7E543A9D-33E3-40D9-8303-BF8461E247CE
employer	wds:Q42638173-5B355A62-1347-4824-8F15-D8C31AFE0B9C
sex or gender	wds:Q42638173-1D044B8C-D42E-49C7-8A7D-70EAD15AAEA4
educated at	wds:Q42638173-CC4195B1-11C1-457A-9505-9D4C3B393EA9
family name	wds:Q42638173-DC5D94CA-6E2D-4AFC-BBA6-A2F44AE24E88
occupation	researcher
employer	University of Foggia
sex or gender	male
educated at	University of Naples Federico II
family name	Margaglione
ORCID iD	wds:Q42638173-232EC05B-3094-4F0F-86D1-8AA17E6B3824 wds:Q42638173-685061C8-4C9A-47A4-8AA5-6EE781D423D3
ORCID iD	https://orcid.org/0000-0001-5627-9221 https://orcid.org/0000-0001-6178-9939
ORCID iD	0000-0001-5627-9221 0000-0001-6178-9939
is owl:sameAs of	Maurizio Margaglione
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q42638173
is author of	Insight into the nature of the CRP-coronary event association using Mendelian randomization. Increased risk for venous thrombosis in carriers of the prothrombin G-->A20210 gene variant. HLA class II favors clearance of HCV infection and progression of the chronic liver damage Prognostic factors in noncirrhotic patients with splanchnic vein thromboses Coinheritance of the HR2 haplotype in the factor V gene confers an increased risk of venous thromboembolism to carriers of factor V R506Q (factor V Leiden). Prothrombotic genetic risk factors in young survivors of myocardial infarction Identification of 217 unreported mutations in the F8 gene in a group of 1,410 unselected Italian patients with hemophilia A. Methylarginines and mortality in patients with end stage renal disease: a prospective cohort study. The methylenetetrahydrofolate reductase TT677 genotype is associated with venous thrombosis independently of the coexistence of the FV Leiden and the prothrombin A20210 mutation. Genetic susceptibility to pregnancy-related venous thromboembolism: Roles of factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarin. EPCR Ser219Gly: elevated sEPCR, prothrombin F1+2, risk for coronary heart disease, and increased sEPCR shedding in vitro. The role of PC-1 and ACE genes in diabetic nephropathy in type 1 diabetic patients: evidence for a polygenic control of kidney disease progression Eosinophilia and thrombophilia in churg strauss syndrome: a clinical and pathogenetic overview The plasminogen activator inhibitor-1 -675 4G/5G genotype influences the risk of myocardial infarction associated with elevated plasma proinsulin and insulin concentrations in men from Europe: the HIFMECH Study A PC-1 amino acid variant (K121Q) is associated with faster progression of renal disease in patients with type 1 diabetes and albuminuria F8 gene mutation type and inhibitor development in patients with severe hemophilia A: systematic review and meta-analysis Risk of obstetric and thromboembolic complications in family members of women with previous adverse obstetric outcomes carrying common inherited thombophilias Functional and clinical data of Best vitelliform macular dystrophy patients with mutations in the BEST1 gene High prevalence of thrombophilic genotypes in patients with acute mesenteric vein thrombosis. Portal vein thrombosis after variceal endoscopic sclerotherapy in cirrhotic patients: role of genetic thrombophilia Anticardiolipin antibodies in patients with liver disease Risk factors and clinical presentation of portal vein thrombosis in patients with liver cirrhosis. Inherited coagulation disorders in cirrhotic patients with portal vein thrombosis Inherited prothrombotic conditions and premature ischemic stroke: sex difference in the association with factor V Leiden. The PAI-1 Gene Locus 4G/5G Polymorphism Is Associated With a Family History of Coronary Artery Disease Plasminogen Activator Inhibitor-1 (PAI-1) Antigen Plasma Levels in Subjects Attending a Metabolic Ward: Relation to Polymorphisms of PAI-1 and Angiontensin Converting Enzyme (ACE) Genes Abnormally high circulation levels of tissue plasminogen activator and plasminogen activator inhibitor-1 in patients with a history of ischemic stroke Relevance of interleukin-1 receptor antagonist intron-2 polymorphism in ischemic stroke Abnormally high thromboxane biosynthesis in homozygous homocystinuria. Evidence for platelet involvement and probucol-sensitive mechanism Identification of naïve HCV-1 patients with chronic hepatitis who may benefit from dual therapy with peg-interferon and ribavirin Role of thrombophilia in adverse obstetric outcomes and their prevention using antithrombotic therapy The effect of the interleukin-6 c/g-174 polymorphism and circulating interleukin-6 on fibrinogen plasma levels Fibrinogen and mechanisms of thrombosis. A difficult link Plasma fibrinogen concentration predicts the risk of myocardial infarction differently in various parts of Europe: effects of beta-fibrinogen genotype and environmental factors. The HIFMECH Study. The risk of venous thromboembolism in family members with mutations in the genes of factor V or prothrombin or both The Italian AICE-Genetics hemophilia A database: results and correlation with clinical phenotype An alternative method for PAI-1 promoter polymorphism (4G/5G) typing A new JAK2 gene mutation in patients with polycythemia vera and splanchnic vein thrombosis Prevalence of apolipoprotein E alleles in healthy subjects and survivors of ischemic stroke: an Italian Case-Control Study. Deletion polymorphism in the angiotensin-converting enzyme gene in patients with a history of ischemic stroke. Principles of treatment and update of recommendations for the management of haemophilia and congenital bleeding disorders in Italy Perceived challenges and attitudes to regimen and product selection from Italian haemophilia treaters: the 2013 AICE survey. Factor VIII gene (F8) mutations as predictors of outcome in immune tolerance induction of hemophilia A patients with high-responding inhibitors. Inherited Thrombophilic Risk Factors and Venous Thromboembolism

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