LE WE PMID CA
Angioedema hereditary151Angiooedem (hereditaer)

Angioedema hereditary

Bradykinin

C1 esterase inhibitor deficiency

Conestat alfa ttC1INH

2010  
1
Hereditary angioedema: current and emerging treatment options.
[20418292] Anesth Analg 110(5): 1271-80 (2010)
2007  
2
Nonallergic angioedema: role of bradykinin.
[17620062] Allergy 62(8): 842-56 (2007)
2009  
3
Clinical Immunology Review Series: An approach to the patient with angio-oedema.
[19220828] Clin Exp Immunol 155(3): 367-77 (2009)
2005  
4
C1 inhibitor deficiency: consensus document.
[15730382] Clin Exp Immunol 139(3): 379-94 (2005)
2002  
5
Current management of hereditary angio-oedema (C'1 esterase inhibitor deficiency).
[11919209] J Clin Pathol 55(4): 266-70 (2002)
2006  
6
Genetic test indications and interpretations in patients with hereditary angioedema.
[16835976] Mayo Clin Proc 81(7): 958-72 (2006)
2007  
7
Management of hereditary angioedema in pediatric patients.
[17724112] Pediatrics 120(3): e713-22 (2007)
2010  
8
Diagnosis and management of angioedema with abdominal involvement: a gastroenterology perspective.
[20954277] World J Gastroenterol 16(39): 4913-21 (2010)
2008  
9
Hereditary angioedema: new hopes for an orphan disease.
[19160940] Isr Med Assoc J 10(12): 850-5 (2008)
2011  
10
Conestat alfa for the treatment of angioedema attacks.
[21753889] Ther Clin Risk Manag 7(-): 265-73 (2011)
2011  
11
Consensus statement on the diagnosis, management, and treatment of angioedema mediated by bradykinin. Part II. Treatment, follow-up, and special situations.
[21995176] J Investig Allergol Clin Immunol 21(6): 422-41; quiz 442-3 (2011)
2011  
12
Consensus statement on the diagnosis, management, and treatment of angioedema mediated by bradykinin. Part I. Classification, epidemiology, pathophysiology, genetics, clinical symptoms, and diagnosis.
[21905496] J Investig Allergol Clin Immunol 21(5): 333-47; quiz follow 347 (2011)

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  • Angiooedem (hereditaer)

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