106 results on '"Serino, Maria Luisa"'
Search Results
2. Gene Dosage of F5 c.3481C>T Stop-Codon (p.R1161Ter) Switches the Clinical Phenotype from Severe Thrombosis to Recurrent Haemorrhage: Novel Hypotheses for Readthrough Strategy
3. miRNAs Epigenetic Tuning of Wall Remodeling in the Early Phase after Myocardial Infarction: A Novel Epidrug Approach
4. Host genetics impact on SARS-CoV-2 vaccine-induced immunoglobulin levels and dynamics: The role of TP53, ABO, APOE, ACE2, HLA-A, and CRP genes
5. A Transition (p.R506Q) in F5 Gene and Selected GWAS Multilocus Approach in Inherited Thrombophilia
6. Cis-Segregation of c.1171C>T Stop Codon (p.R391*) in SERPINC1 Gene and c.1691G>A Transition (p.R506Q) in F5 Gene and Selected GWAS Multilocus Approach in Inherited Thrombophilia
7. Genotype and PK Hemophilia B International Study (GePKHIS) - A progress Report
8. COVID-19 and Individual Genetic Susceptibility/Receptivity: Role of ACE1/ACE2 Genes, Immunity, Inflammation and Coagulation. Might the Double X-Chromosome in Females Be Protective against SARS-CoV-2 Compared to the Single X-Chromosome in Males?
9. Factor XIII Contrasts the Effects of Metalloproteinases in Human Dermal Fibroblast Cultured Cells
10. Blood Group O Protects against Inhibitor Development in Severe Hemophilia A Patients
11. Maternal Haplotypes in DHFR Promoter and MTHFR Gene in Tuning Childhood Acute Lymphoblastic Leukemia Onset-Latency: Genetic/Epigenetic Mother/Child Dyad Study (GEMCDS)
12. F9missense mutations impairing factor IX activation are associated with pleiotropic plasma phenotypes
13. Acquired inhibitors of clotting factors: AICE recommendations for diagnosis and management
14. Gene-gene interactions among coding genes of iron-homeostasis proteins and APOE-alleles in cognitive impairment diseases
15. Assessment of the interlaboratory variability and robustness of JAK2V617F mutation assays: A study involving a consortium of 19 Italian laboratories
16. The Active Metabolite of Warfarin (3'-Hydroxywarfarin) and Correlation with INR, Warfarin and Drug Weekly Dosage in Patients under Oral Anticoagulant Therapy: A Pharmacogenetics Study
17. Malattie emorragiche vascolari
18. Dihydrofolate reductase (DHFR) 19-bp ins/del polymorphism and methylenetetrahydrofolate reductase (MTHFR) C677T in coronary heart disease patients: potential intracellular folate unbalancing
19. FXIII levels and genotypes in myocardial infarction: a potential novel prognostic biomarker?
20. Center-Related Determinants of VKA Anticoagulation Quality: A Prospective, Multicenter Evaluation
21. FXIII Levels in Myocardial Infarction: a Potential Novel Prognostic Biomarker?
22. Spectrum of F8 gene mutations in haemophilia A patients from a region of Italy: Identification of 23 new mutations
23. A web-based clinical record 'xl'Emofilia® 'for outpatients with haemophilia and allied disorders in the region of Emilia-Romagna: Features and pilot use
24. Factor V Levels in a Cohort of Patients Eligible for Oral Anticoagulant Therapy
25. Factor XIIIA-V34L and Factor XIIIB-H95R Gene Variants and Survival after Myocardial Infarction
26. Common Factor XIII Gene Polymorphisms In Venous Leg Ulcers
27. FXIII-A V34L and FXIII-B H95R gene polymorphism: effects on the efficacy of thrombolytic therapy in acute myocardial infarction
28. Common Polymorphisms in the Metabolic Folate Pathway Decrease the Risk of Acute Lymphocitic Leukemia in Adults
29. Common Gene Polymorphisms in the Metabolic Folate and Methylation Pathway and the Risk of Acute Lymphoblastic Leukemia and non-Hodgkin’s Lymphoma
30. Common Polymorphisms in the Metabolic Folate Pathway Decrease the Risk of Acute Lymphocytic Leukemia in Adults
31. Effect of factor XIII Val34Leu polymorphism on plasma clot formation: crosslinking functions and clot longevity properties
32. MTHFR C677T/A1298C, MS A2756G and MTRR A66G Gene Polymorphisms: Effects on Homocysteine Levels and Risk of Miocardial Infarction
33. Low Sensitivity to Endogenous Activated Protein C in Protein S Deficient Subjects Reflects a Reduction in the Thrombotic Risk
34. MTHFR Specific Activity, Homocysteine and Folate Levels in Subjects with Thermolabile MTHFR (C677T)
35. C677T/A1298C MTHFR Gene Mutations, Homocysteine, Folate Levels and MTHFR Activity, in Normal Subjects and Cases with Myocardial Infarction
36. Factor XIII-A Gene Mutation (Val34Leu) and Arterial Vascular Disease
37. A Common mutation in the gene for coagulation factor XIII-A (V34L): a risk factor for hemorrhagic disorders it is protective against atherothrombotic diseases
38. High protein C plasma levels affect the response to exogenous preactivated protein C and enhance that to endogenous Protac-mediated activated protein C
39. A modified functional Global test to measure PC, PS activities and the APC-Resistance phenotype
40. Thrombotic risk in thalassemic patients
41. ProC Global test>ProC Complete test: una modificazione del Global test per la misurazione contemporanea della attività della PC, della PS, e del fenotipo Leiden
42. Low folate levels and thermolabile MTHFR as primary determinant of mild Hyperhomocysteinemia in normal and thromboembolic subjects
43. Different anticoagulant response to activated protein C (APC-test) and to Agkistrodon Contortix Venom (ACV-test) in a family with FV-R506Q substitution
44. Coexistence of antitrhombin deficency, factor V Leiden and hereditary hyperhomocyst(e)inemia in a thrombotic family
45. A de novo antithrombin mutation found in a patient with deep vein thrombosis and vascular abnormalities
46. Conteggio piastrinico e terapia sostitutiva in un paziente con Malattia di von Willebrand tipo 2B
47. Differente risposta alla Proteina C attivata della muatazione R506Q del fattore V della coagulazione (FV Leiden) in due generazioni della stessa famiglia
48. Bassi livelli di Proteina S e Resistenza alla Proteina C attivata in dieci famiglie italiane
49. An Italian Family with a Novel Mutation Causing Type 2A von Willebrand Disease and with Reduced Levels of von Willebrand Factor not Linked with the von Willebrand Factor Gene
50. Piastrinopenia da anticorpi anticardiolipina: remissione persistente dopo splenectomia
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