Markus Magerl
Charité - Universitätsmedizin Berlin
195 papers found
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F12-46C/T polymorphism as modifier of the clinical phenotype of hereditary angioedema
Download from www.researchgate.netHereditary angioedema: Molecular and clinical differences among European populations
UploadRevisions to the international guidelines on the diagnosis and therapy of chronic urticaria
Download from onlinelibrary.wiley.comHereditary angioedema with C1 inhibitor deficiency: delay in diagnosis in Europe
Download from dx.doi.orgPractical algorithm for diagnosing patients with recurrent wheals or angioedema
Download from www.researchgate.netPractical Approach to Self-Administration of Intravenous C1-INH Concentrate: A Nursing Perspective
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