858 results on '"Margaglione, Maurizio"'
Search Results
2. Homozygous MTHFR C677T carriers develop idiopathic portal vein thrombosis 20 years earlier than wild type
3. Prevalence of Blastocystis sp. and other gastrointestinal pathogens among diarrheic COVID-19 patients in Italy
4. Prevalence and genetic diversity of Blastocystis sp. among autochthonous and immigrant patients in Italy
5. Italian experience with rVIII-single chain: a survey of patients with haemophilia A and their physicians
6. Obstetric outcomes in pregnant COVID-19 women: the imbalance of von Willebrand factor and ADAMTS13 axis
7. Coma in adult cerebral venous thrombosis: The BEAST study.
8. Investigation of a Large Kindred Reveals Cardiac Calsequestrin (CASQ2) as a Cause of Brugada Syndrome.
9. Real‐world experience of rIX‐FP prophylaxis at dosing intervals of 14 days or more in adult patients with haemophilia B in Italy – Results from IDEAL Part B.
10. De Novo p.Asp3368Gly Variant of Dystrophin Gene Associated with X-Linked Dilated Cardiomyopathy and Skeletal Myopathy: Clinical Features and In Silico Analysis
11. Gene-Gene Interaction Between Factor-XI and ABO Genes in Cerebral Venous Thrombosis: The BEAST Study.
12. Pattern of use and clinical outcomes with rIX‐FP in pediatric/adolescent patients with haemophilia B in Italy: Results from IDEAL real‐world study.
13. International Consensus on the Use of Genetics in the Management of Hereditary Angioedema
14. The Role of Genetics in the Management of Heart Failure Patients
15. De Novo p.Asp3368Gly Variant of Dystrophin Gene Associated with X-Linked Dilated Cardiomyopathy and Skeletal Myopathy: Clinical Features and In Silico Analysis.
16. 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
17. A Novel KCNN2 Variant in a Family with Essential Tremor Plus: Clinical Characteristics and In Silico Analysis
18. Venous Thromboembolism in Women of Childbearing Age: Insights from the START Registry
19. Age of onset of cerebral venous thrombosis: the BEAST study
20. Venous thromboembolism in assisted reproductive technologies: comparison between unsuccessful versus successful cycles in an Italian cohort
21. A Novel DLG1 Variant in a Family with Brugada Syndrome: Clinical Characteristics and In Silico Analysis
22. Age of onset of cerebral venous thrombosis: the BEAST study
23. Novel AKAP9 mutation and long QT syndrome in a patient with torsades des pointes
24. Prospective evaluation of pregnancy outcome in an Italian woman with late-onset combined homocystinuria and methylmalonic aciduria
25. A Novel KCNN2 Variant in a Family with Essential Tremor Plus: Clinical Characteristics and In Silico Analysis.
26. Characterization of patients with angioedema without wheals: The importance of F12 gene screening
27. 416 DESMOPLAKIN CARDIOMYOPATHY PRESENTING WITH CARDIAC ARREST IN A PATIENT WITH MYOCARDIAL NON-COMPACTION AND LEFT ACCESSORY PATHWAY
28. IDEAL study: A real‐world assessment of pattern of use and clinical outcomes with recombinant coagulation factor IX albumin fusion protein (rIX‐FP) in patients with haemophilia B in Italy
29. Modulation of factors involved in placental haemostasis and angiogenesis by low-molecular-weight-heparins
30. A novel congenital dysprothrombinemia leading to defective prothrombin maturation
31. Homozygous Mthfr C677t Carriers Develop Idiopathic Portal Vein Thrombosis Twenty Years Earlier Than Wild Type
32. A Report on a Targeted Screening Population for Alpha-1-Antitrypsin Deficiency (AATD) in Central-Southern Italy
33. Mutation of the angiopoietin-1 gene (ANGPT1) associates with a new type of hereditary angioedema
34. Pain assessment and management in Italian Haemophilia Centres
35. Identification of the Novel G250R Variant Indicates a Role for Thrombomodulin in Modulating the Risk for Venous Thromboembolism
36. Outcome of patients with splanchnic venous thrombosis presenting without overt MPN: A role for the JAK2 V617F mutation re-evaluation
37. Mechanisms of fibrinolysis and clinical use of thrombolytic agents
38. Influence of the Gly1057Asp variant of the insulin receptor substrate 2 (IRS2) on insulin resistance and relationship with epicardial fat thickness in the elderly
39. A Novel DLG1 Variant in a Family with Brugada Syndrome: Clinical Characteristics and In Silico Analysis.
40. IDEAL study: A real‐world assessment of pattern of use and clinical outcomes with recombinant coagulation factor IX albumin fusion protein (rIX‐FP) in patients with haemophilia B in Italy.
41. A reliable and rapid tool for plasma quantification of 18 psychotropic drugs by ESI tandem mass spectrometry
42. F8 gene mutation type and inhibitor development in patients with severe hemophilia A: systematic review and meta-analysis
43. Fatal pulmonary thromboembolism. A retrospective autopsy study: Searching for genetic thrombophilias (Factor V Leiden (G1691A) and FII (G20210A) gene variants) and dating the thrombus
44. Psychosomatic syndromes are associated with IL-6 pro-inflammatory cytokine in heart failure patients
45. Lack of plasma viremia in SARS-CoV-2 seropositive blood donors carrying the virus in nasopharyngeal swabs argues against potential transmission of COVID-19 through blood
46. Congenital Platelet Disorders
47. Genetic Polymorphisms and Arterial Thrombosis
48. The risk of occurrence of venous thrombosis: focus on protein Z
49. Sex modulation of the occurrence of jak2 v617f mutation in patients with splanchnic venous thrombosis
50. Increased warfarin consumption and residual fibrin turnover in thrombotic patients with primary antiphospholipid syndrome
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