RADeep Multicenter European Epidemiological Platform for Patients Diagnosed With Rare Anemia Disorders (RADs)
Conditions
Sickle Cell Disease · Thalassemia · Hemolytic; Anemia, Hereditary, Due to Enzyme Disorder · Anemia Due to Membrane Defect · CDA · Sideroblastic Anemia · Constitutional Aplastic Anemia · Iron Metabolism Disorders · Hereditary Anemia
Simple summaryAI-assisted
This summary is produced by a language model and is experimental. It may be incomplete or inaccurate and is not a substitute for professional medical advice.
Locations
Vall d'hebron Research Institute - Vall d'Hebron Research Institute - University Hospital Vall d'Hebrón (VHIR/HUVH), Barcelona, Catalonia, Spain
Contact: Study coordinator (Victoria Gutiérrez Valle, Msc) · victoria.gutierrez@vhir.org · +34934893000
Study leads
María del Mar Manú Pereira, PhD
Principal Investigator
Vall d'hebron Research Institute - Vall d'Hebron Research Institute - University Hospital Vall d'Hebrón (VHIR/HUVH)
Béatrice Gulbis, MD
Principal Investigator
Hôpital ERASME (ERASME)
Petros Kountouris, PhD
Principal Investigator
Cyprus Institute of Neurology and Genetics (CING)