The Generative Brain

Atlas

The Atlas is the reference section of the site. It collects trials, tests, therapies, organizations, regulations, papers, funding programs and events on CJD and prion diseases, each with its sources and the date it was checked.

What the Atlas holds today

The Atlas holds the detailed records behind the rest of the site. Each entry names its sources, the date it was last checked and a status, so you can see how current it is. Families can start with the plain-language pages on the home page. Clinicians, researchers and partners can go straight to the sections below.

Prion diseases are caused by misfolded prion protein. The best known human form is Creutzfeldt-Jakob disease, which can be sporadic, genetic or acquired through healthcare exposure. Diagnosis combines clinical assessment with tests, and confirmation needs brain tissue. No treatment has yet been shown to cure these diseases, so many entries describe research that is still early.

What does the Atlas contain?

SectionWhat you will find
TrialsClinical studies, with sponsor-stated eligibility and the date it was read
Tests and assaysDiagnostic and research tests, from spinal fluid assays to blood and imaging markers
Therapies in developmentApproaches under study, by stage
OrganizationsSurveillance centres, labs, clinics, foundations, companies, regulators and funders
RegulationsLaws and guidance that affect prion disease, blood, tissue, medicines and genetic testing
Key papersStudies the Atlas relies on
Funding programsGrants and awards that support prion research
Events and conferencesScientific and family meetings
GlossaryShort definitions of terms used across the site
SourcesThe sources the Atlas draws on

How current is an entry?

Each entry shows when it was last checked. Trial and therapy status changes often, so confirm it with the sponsor or the registry before relying on it. The About page explains how the site works, and Partners is for organizations that want to contribute.

Can I use the Atlas to decide something about my own care?

No. The Atlas gives general information. A doctor or genetic counsellor can talk through symptoms, tests and family questions with you.

Explore

Sources for this page