166 results on '"Suffritti, Chiara"'
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2. Hereditary Deficiency of C1 Inhibitor and Angioedema
3. Hereditary angioedema due to C1 inhibitor deficiency in Belarus: epidemiology, access to diagnosis and seven novel mutations in SERPING1 gene
4. Anti-C1-Inhibitor Autoantibody Detection by ELISA
5. Clinical efficiency of the cleaved high-molecular-weight kininogen detection in the diagnosis of hereditary angioedema
6. Characterization of Immunogenicity and Safety of COVID-19 mRNA-1273 in HIV-Positive Italian Patients with Hemophilia: A Prospective Single-Center Cohort Study
7. Diagnosis, Course, and Management of Angioedema in Patients With Acquired C1-Inhibitor Deficiency
8. Risk of relapse after SARS-CoV-2 vaccine in the Milan cohort of thrombotic thrombocytopenic purpura patients
9. Plasmin is a natural trigger for bradykinin production in patients with hereditary angioedema with factor XII mutations
10. Efficacy of lanadelumab in angioedema due to acquired C1 inhibitor deficiency
11. Efficacy of lanadelumab in angioedema due to acquired C1 inhibitor deficiency
12. Updates on Novel Non-Replacement Drugs for Hemophilia
13. Splenic marginal zone lymphomas in acquired C1-inhibitor deficiency: clinical and molecular characterization
14. Real-Life Experience With Subcutaneous Plasma-Derived C1-Inhibitor for Long-Term Prophylaxis in Patients With Hereditary Angioedema: A Case Series
15. Hereditary Deficiency of C1 Inhibitor and Angioedema
16. Cleaved kininogen as a biomarker for bradykinin release in hereditary angioedema
17. High prevalence of splenic marginal zone lymphoma among patients with acquired C1 inhibtor deficiency
18. Anti-Emicizumab Antibodies Do Not Cross-React with Mim8 in Vitro
19. Lung Ultrasound Findings and Endothelial Perturbation in a COVID-19 Low-Intensity Care Unit.
20. List of Contributors
21. C1 Inhibitor Autoantibodies
22. The Histopathological Landscape of Synovitis in Hemophilic Arthropathy
23. Mutation screening of C1 inhibitor gene in 108 unrelated families with hereditary angioedema: Functional and structural correlates
24. Pharmacokinetics of plasma-derived C1-esterase inhibitor after subcutaneous versus intravenous administration in subjects with mild or moderate hereditary angioedema: the PASSION study
25. Quantitative multiplex profiling of the complement system to diagnose complement-mediated diseases
26. Decreasing Attacks and Improving Quality of Life through a Systematic Management Program for Patients with Hereditary Angioedema
27. Deciphering the Genetics of Primary Angioedema with Normal Levels of C1 Inhibitor
28. Understanding the Pathophysiology of COVID-19: Could the Contact System Be the Key?
29. Hereditary angioedema due to C1 inhibitor In Belarus: epidemiology, access to diagnosis and seven novel mutations in SERPING1 gene
30. Hereditary angioedema in Belarus: epidemiology, genetics, access to diagnosis and therapy
31. Impaired control of the contact system in hereditary angioedema with normal C1‐inhibitor
32. Quantitative multiplex profiling of the complement system to diagnose complement‐mediated diseases
33. Immune response covaries with corticosterone plasma levels under experimentally stressful conditions in nestling barn swallows (Hirundo rustica)
34. Aspects of hereditary angioedema genotyping in the era of NGS : the case of F12 gene
35. Current and emerging biologics for the treatment of hereditary angioedema
36. Short term prophylaxis in patients with hereditary angioedema undergoing dental procedures
37. Two Cases Of Peculiar Hypereosinophilic Syndrome Treated With Mepolizumab
38. Cleaved High Molecular Weight Kininogen Correlates With Hereditary Angioedema Due To C1-Inhibitor Deficiency
39. A transcriptomics study of hereditary angioedema attacks
40. Secreted Phospholipases A2 in Hereditary Angioedema With C1-Inhibitor Deficiency
41. Intermittent C1-Inhibitor Deficiency Associated with Recessive Inheritance: Functional and Structural Insight
42. Hereditary angioedema: Assessing the hypothesis for underlying autonomic dysfunction
43. Catabolism of C1 inhibitor influences the response to replacement therapy in hereditary angioedema
44. Reply
45. Hereditary Angioedema with Normal C1 Inhibitor: An Italian Case Series
46. Autonomic Modulation and Contact System in Patients with Hereditary Angioedema Due to C1 Inhibitor Deficiency
47. A case of remittent C1-inhibitor deficiency
48. Plasmin is a natural trigger for bradykinin production in patients with hereditary angioedema with factor XII mutations
49. Secreted Phospholipases A2 in Hereditary Angioedema With C1-Inhibitor Deficiency.
50. High Prevalence of Marginal ZONE Lymphoma Among Patients with Acquired C1- Inhibtor Deficiency
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