Specialists for Hereditary angioedema with C1Inh deficiency

8 physicians and care centers identified from ClinicalTrials.gov trial PIs, PubMed publications, and the NPPES NPI registry.

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Specialists are identified from ClinicalTrials.gov principal investigators, PubMed publications, and the NPI registry, then ranked through an automated scoring pipeline.

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Mikhail Rojavin
Rare Disease / Clinical Research
CSL Behring
QC-verified PI×1
Marcus Maurer, MD
Charite University, Berlin, Germany
PI×6
Program Director
Rare Disease / Clinical Research
CSL Behring
PI×9
Anurag Relan, MD
Rare Disease / Clinical Research
VP Clinical Research & Medical Affairs at Pharming
SANTA MONICA, CA
PI×4
Jonathan Bernstein, MD
Rare Disease / Clinical Research
Bernstein Clinical Research Center
PI×2
Emel Aygören-Pürsün, MD
Rare Disease / Clinical Research
University Hospital Frankfurt - Goethe University, Frankfurt, Germany
PI×2
Wolfhart Kreuz, PD Phd
Rare Disease / Clinical Research
Centre of Paediatrics III, Department of Haematology, Haemostaseology and Oncology, Comprehensive Care Centre for Thrombosis and Haemostasis, Johann-Wolfgang-Goethe-University Hospital
PI×1
Marc Riedl, MD, MD
Rare Disease / Clinical Research
UC San Diego, La Jolla, California, United States
SAN DIEGO, CA
PI×1

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