Luca Sangiorgi, MD, PhD

Rare diseases treated or studied

Based on trial PI assignments and publication topics.

• Rare genetic bone development disorder→
• Multiple osteochondromas→
• Ollier disease→
• Rare genetic movement disorder→
• Metabolic disease with skin involvement→
• Rare developmental defect with connective tissue involvement→
• Mucopolysaccharidosis with skin involvement→
• Schwartz-Jampel syndrome→
• Rare bone tumor→
• Rare bone development disorder→
• Lysosomal storage disease with skeletal involvement→
• Rare rheumatologic disease→

Clinical trials (2)

• NCT05247645
• NCT06397443

Verify independently

• ClinicalTrials.gov PI search for Luca Sangiorgi, MD, PhD

Other specialists for Rare genetic bone development disorder

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

• Dag Malm, MD
  Department of Medicine, University of Tromsoe
• Michael Beck, MD
  Children's Hospital, University of Mainz
• Jiri Zeman, MD
  Department of Pediatrics, Charles University
• Alessandro Pini, MD
  Cardiovascular-Gentic Centre, IRCCS Policlinico San Donato
  Lombardy
• Carlos R Ferreira Lopez, M.D.
  Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
  Maryland
• Sophie DUPUIS-GIROD, MD
  Service de Génétique - Hôpital Femme-Mère-Enfant - HCL
• Ed Wraith, MD
  Willink Biochemical Genetics Unit, Royal Manchester Childern's Hospital
• Luca Sangiorgi, MD, Phd
  IRCCS Istituto ORtopedico Rizzoli

See all specialists for Rare genetic bone development disorder →