Emel Aygören-Pürsün, MD

Rare diseases treated or studied

Based on trial PI assignments and publication topics.

• Hereditary angioedema→
• Hereditary angioedema with C1Inh deficiency→
• Hereditary angioedema with normal C1Inh→
• Hereditary angioedema type 2→

Clinical trials (2)

• NCT05047185
• NCT02870972

Verify independently

• ClinicalTrials.gov PI search for Emel Aygören-Pürsün, MD

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