175 results on '"Bova, Maria"'
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2. Interplay between C1-inhibitor and group IIA secreted phospholipase A2 impairs their respective function
3. Roles of Immune Cells in Hereditary Angioedema
4. Severely compromised supply of patch test allergens in Europe hampers adequate diagnosis of occupational and non‐occupational contact allergy. A European Society of Contact Dermatitis (ESCD), European Academy of Allergy and Clinical Immunology (EAACI), European Academy of Dermatology and Venereology (EADV) task forces 'Contact Dermatitis' and 'Occupational Skin Disease' position paper
5. The central role of endothelium in hereditary angioedema due to C1 inhibitor deficiency
6. International Consensus on the Use of Genetics in the Management of Hereditary Angioedema
7. Psychological processes in the experience of hereditary angioedema in adult patients: an observational study
8. Neurologic and Psychiatric Manifestations of Bradykinin-Mediated Angioedema: Old and New Challenges
9. Role of Endothelial G Protein-Coupled Receptor Kinase 2 in Angioedema
10. Interplay between C1-inhibitor and group IIA secreted phospholipase A2 impairs their respective function
11. Mutation of the angiopoietin-1 gene (ANGPT1) associates with a new type of hereditary angioedema
12. Value co-creation in healthcare: evidence from innovative therapeutic alternatives for hereditary angioedema
13. Emotional processes and stress in children affected by hereditary angioedema with C1-inhibitor deficiency: a multicenter, prospective study
14. International consensus on the diagnosis and management of pediatric patients with hereditary angioedema with C1 inhibitor deficiency
15. Treatment of ACEI-related angioedema with icatibant: a case series
16. Review for "Negative pressure flash pulmonary edema in a child with hereditary angioedema"
17. Clinical features and burden of genital attacks in hereditary angioedema
18. Interplay between C1-inhibitor and group IIA secreted phospholipase A2 impairs their respective function.
19. Life expectancy in Italian patients with hereditary angioedema due to C1-inhibitor deficiency
20. Orofacial granulomatosis: Clinical and therapeutic features in an Italian cohort and review of the literature
21. Episodic Angioedema with Hypereosinophilia (Gleich’s Syndrome): A Case Report and Extensive Review of the Literature
22. Analysis of Heart-Rate Variability during Angioedema Attacks in Patients with Hereditary C1-Inhibitor Deficiency
23. Prophylaxis of Acute Attacks with a Novel Short-term Protocol in Hereditary Angioedema Patients Requiring Periodontal Treatment
24. Psychology and hereditary angioedema: A systematic review
25. Il Senso di Padronanza della Malattia Cronica: una ricerca mixed Method con adulti affetti da Angioedema Ereditario.
26. Deciphering the Genetics of Primary Angioedema with Normal Levels of C1 Inhibitor
27. Gastrointestinal manifestations of angioedema: a potential area of misdiagnosis
28. A myoferlin gain‐of‐function variant associates with a new type of hereditary angioedema
29. The experience of living with a chronic disease in pediatrics from the mothers’ narratives: The Clinical Interview on Parental Sense of Grip on the Disease
30. International Consensus on the Use of Genetics in the Management of Hereditary Angioedema
31. Impaired control of the contact system in hereditary angioedema with normal C1‐inhibitor
32. Hereditary angioedema attack: what happens to vasoactive mediators?
33. Lanadelumab Injection Treatment For The Prevention Of Hereditary Angioedema (HAE): Design, Development And Place In Therapy
34. Lo Scaffolding psicologico alla Relazione Sanitaria in Pediatria. Alcune proposte metodologiche
35. The role of the meaning-making process in the management of hereditary angioedema
36. Gastrointestinal manifestations of angioedema: a potential area of misdiagnosis.
37. Aspects of hereditary angioedema genotyping in the era of NGS : the case of F12 gene
38. Additional file 1: of Emotional processes and stress in children affected by hereditary angioedema with C1-inhibitor deficiency: a multicenter, prospective study
39. The role of genetics in the current diagnostic workup of idiopathic non‐histaminergic angioedema
40. The Icatibant Outcome Survey: Treatment of laryngeal angioedema attacks
41. Late Breaking Poster Discussion LB 'Emotion Regulation and Stress in Children with Hereditary Angioedema'
42. L'influenza dei fattori psicologici nello sviluppo degli attacchi di Angioedema Ereditario in l'età evolutiva
43. Secreted Phospholipases A2 in Hereditary Angioedema With C1-Inhibitor Deficiency
44. Low functional c1 inhibitor levels and normal c4 levels in patients with idiopathic non-histaminergic angioedema
45. A booklet for the management of pediatric hereditary angioedema due to C1-INH deficiency addressed to parents: an experience of patient engagement
46. Hereditary and Acquired Angioedema: Heterogeneity of Pathogenesis and Clinical Phenotypes
47. A nationwide survey of hereditary angioedema due to C1 inhibitor deficiency in Italy
48. Acquired angioedema due to C1-inhibitor deficiency: a survey of 101 Italian patients
49. Hereditary Angioedema with Normal C1 Inhibitor: An Italian Case Series
50. An International Registry for Angioedema without Urticaria
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