Hereditary angioedema with C1 inhibitor deficiency: Delay in diagnosis in Europe

Allergy, Asthma and Clinical Immunology

Volumn 9, Issue 1, 2013, Pages 1-4

  Zanichelli, Andrea ^a   Magerl, Markus ^b   Longhurst, Hilary ^c   Fabien, Vincent ^d   Maurer, Marcus ^b  

^a UNIVERSITY OF MILAN   (Italy)

^b CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

^c ROYAL LONDON HOSPITAL   (United Kingdom)

^d Shire Human Genetic Therapies Inc   (Switzerland)

Author keywords

Bradykinin; C1 inhibitor; Diagnosis; Hereditary angioedema; Icatibant

Indexed keywords

COMPLEMENT COMPONENT C1S INHIBITOR; ICATIBANT;

ADULT; AGED; ANGIONEUROTIC EDEMA; ANGIONEUROTIC EDEMA TYPE I; ANGIONEUROTIC EDEMA TYPE II; ARTICLE; COMPLEMENT COMPONENT C1S INHIBITOR DEFICIENCY; COMPLEMENT DEFICIENCY; DELAYED DIAGNOSIS; EUROPE; FEMALE; HEALTH SURVEY; HUMAN; MAJOR CLINICAL STUDY; MALE; OBSERVATIONAL STUDY; OUTCOME ASSESSMENT;

EID: 84882666263     PISSN: 17101484     EISSN: 17101492     Source Type: Journal    
DOI: 10.1186/1710-1492-9-29     Document Type: Article

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