The VASCERN Registry is an essential tool that offers a centralized repository for clinical data and information related to rare vascular diseases. By gathering clinical data, the registry aims to improve research, diagnosis, and care for patients. With standardized data collection and collaboration among healthcare professionals, researchers, and patients, the registry empowers personalized treatment, fosters innovation, and enhances patient care.
The NEUROVASC Registry project consists of the creation of a FAIR registry dedicated to the diseases covered by the NEUROVASC-WG. It has been designed to include the European core dataset as well as set of data specific to the rare diseases of NEUROVASC.
More information on the NEUROVASC-WG registry is available on the Registry page here.