293 results on '"Drouet, Christian"'
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2. Hereditary angioedema with normal C1 inhibitor associated with carboxypeptidase N deficiency
3. Hereditary Carboxypeptidase N deficiency, a clinical situation presenting with urticaria and angioedema
4. Complement C3 Deficiency
5. International Consensus on the Use of Genetics in the Management of Hereditary Angioedema
6. Recessive SERPING1 Variant Leads to Kinin–Kallikrein System Control Failure in a Consanguineous Brazilian Family with Hereditary Angioedema
7. S14-3 Effets indésirables receveurs (EIR) après transfusion de plaquettes (CP) 2007-2021
8. Exploration des immunoglobulines
9. Exploration de pathologies impliquant le complément
10. Les anticorps comme réactifs et outils thérapeutiques
11. Exploration du complexe majeur d’histocompatibilité
12. Exploration du complément
13. Introduction générale
14. Immunoinformatique
15. Hypermutations somatiques et translocations chromosomiques
16. Techniques sans traceur
17. Techniques avec traceurs
18. L’antigène comme réactif : définition et propriétés
19. Détection/dosage des cytokines et de leurs récepteurs
20. Techniques de biologie moléculaire
21. Tests cellulaires
22. Modèles et tests in vivo
23. Editorial: Kinin 2022 Meeting, Annecy, France
24. Angioedema attacks in patients with hereditary angioedema: Local manifestations of a systemic activation process
25. C1 Inhibitor
26. List of Contributors
27. The diagnosis of hereditary angioedema with C1 inhibitor deficiency: a survey of Canadian physicians and laboratories
28. In vitro reconstitution of kallikrein-kinin system and progress curve analysis
29. Contact System Activation in Patients with HAE and Normal C1 Inhibitor Function
30. Hypersensitivity transfusion reactions to fresh frozen plasma: a retrospective analysis of the French hemovigilance network
31. International consensus on the diagnosis and management of pediatric patients with hereditary angioedema with C1 inhibitor deficiency
32. Defective glycosylation of coagulation factor XII underlies hereditary angioedema type III
33. Actualités biologiques sur les angioedèmes à kinines
34. SERPING1 Variants and C1-INH Biological Function: A Close Relationship With C1-INH-HAE
35. Kinetic Parameters of Kallikrein-Kinin System Undergoing Cold Activation
36. Complement C3 Deficiency
37. C1 Inhibitor as a glycoprotein: The influence of polysaccharides on its function and autoantibody target
38. Acquired C1-Inhibitor Deficiency: 7 Patients Treated with Rituximab
39. Liste des collaborateurs
40. Liste des collaborateurs
41. Human complement C3 deficiency: Th1 induction requires T cell-derived complement C3a and CD46 activation
42. In Search of an Association Between Genotype and Phenotype in Hereditary Angioedema due to C1-INH Deficiency
43. Intracellular Complement Activation Sustains T Cell Homeostasis and Mediates Effector Differentiation
44. Disease expression in women with hereditary angioedema
45. Plasminogen glycoforms alteration and activation susceptibility associated with the missense variant p.Lys330Glu in HAE-PLG patients
46. Increased activity of coagulation factor XII (Hageman factor) causes hereditary angioedema type III
47. Updated hemovigilance data do not show an increased risk of allergic reactions to methylene blue–treated plasma
48. Characterisation of a new C1 inhibitor mutant in a patient with hepatocellular carcinoma
49. Methylene blue–treated plasma: An increased allergy risk?
50. Hereditary angioedema: Key role for kallikrein and bradykinin in vascular endothelial-cadherin cleavage and edema formation
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