What does DBDD mean in DATABASES

The Developmental Brain Disorders Database (DBDD) is a repository of brain imaging data collected from individuals affected by neurodevelopmental disorders. DBDD provides researchers access to brain images and clinical data related to various neurological conditions, including autism, Fragile X syndrome, ADHD, and other conditions. This resource enables the study of patterns of brain dysfunction in these populations through statistical analyses across large datasets.

The DBDD is available to any researcher who has an approved research project using the database. Access is granted after submitting an application form which will be reviewed by a committee of experts who decide whether or not to grant access to the database.

The database contains brain imaging scans and associated demographic information about participants with neurodevelopmental disorders divided into four broad categories; structural MRI, functional MRI, diffusion-weighted MRI, and single photon emission computed tomography (SPECT) images. Additionally, the database also includes clinical information such as medical history data, mental health status assessment results, parental/guardian reports on learning disabilities or social behaviour patterns and other pertinent information.

Access to the DBDD requires registration via an online application form and approval from a committee responsible for overseeing this process. Applications are typically processed within two weeks depending on availability of necessary documentation and approval from participating institutions involved in this project.

Currently several countries are already involved in this initiative including USA, Canada , Finland , Spain , France , Italy , Israel , Japan , China , Turkey and many more. Additional countries can apply for inclusion in future updates of the project according to their scientific interests and resources availability.

All users must agree to abide by a Distribution License Agreement before accessing any data within the database. Furthermore, all usage must conform with local laws governing research ethics for each country involved.

Patient real names are never disclosed in any way through reports or publications derived from using this resource but instead pseudonyms are used that maintain patient confidentiality while allowing full disclosure of demographic variables such as age or gender which may be relevant for analysis purposes.

All published work based on experimenting with DBDB data should be credited back to it with clear reference provided as well as any applicable restrictions stated regarding usage rights detailed in its distribution license agreement. Furthermore authors have responsibility over intellectual property rights related with their own publications.