Alessandro Casini, MD

Rare diseases treated or studied

Based on trial PI assignments and publication topics.

• Familial dysfibrinogenemia→
• Congenital fibrinogen deficiency→
• Congenital short bowel syndrome→
• Multiple epiphyseal dysplasia→

Clinical trials (3)

• NCT03962335
• NCT03920332
• NCT02641834

Verify independently

• ClinicalTrials.gov PI search for Alessandro Casini, MD

Other specialists for Familial dysfibrinogenemia

Peers ranked by clinical-trial PI role, publications, and verification quality.

• Aurélien LEBRETON
  University Hospital, Clermont-Ferrand
• Justine Hugon-Rodin, MD, PHD
  APHP

See all specialists for Familial dysfibrinogenemia →