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Funding Awarded
7 awards
Advanced, automated compound screening for the identification of therapeutic agents in Multiple Sulfatase Deficiency.
Multiple Sulfatase Deficiency (MSD) is an extremely rare, fatal, yet untreatable condition. It is caused by the inherited deficiency of an enzyme (called FGE) that activates a whole family of 17 other cellular enzymes named sulfatases. Sulfatases are indispensable for the degradation of a subset of intracellular molecules. Thus,...
Scaling up the Family Carer Decision Support Intervention: A transnational effectiveness-implementation evaluation
The Family Carer Decision Support (FCDS) intervention has been designed to inform family carers about end of life care options available to a person living with advanced dementia. The effect of the FCDS was demonstrated through a study that employed a cluster randomized control trial involving 24 care homes located in the United...
European eHealth care model for rare neurodegenerative diseases
Rare neurodegenerative disorders (RND) like Huntington?s Disease (HD) require multidisciplinary care teams which are in short supply. Given the devastating consequences of RNDs for the individual patient and their families there is an urgent need to develop innovative ways to ensure access to best practices and established care...
Multi-Domain Lifestyle Targets for Improving ProgNOsis in Huntington?s Disease
Huntington?s Disease (HD) is a progressive, life-limiting neurodegenerative disease. It has devastating consequences for the individual and their families. No current treatment to modify the course of the disease exists. Improved evidence-based symptom assessment is crucial to optimising disease management. This project aims to...
Control of neuronal proteostasis by stress-induced transfer RNA fragments (?tiRNA?) as a common stress pathway across neurodegenerative disorders.
This application is for supplemental funding through PA-18-591 for the recently funded grant (1R01AG058476-01), entitled ?Dysfunction of the autophagy-lysosomal pathway as a common mechanism of neurodegeneration,? and the JPND project to support collaborative studies between Dr. Finkbeiner?s lab (Gladstone) and the JPND RNA NEURO...
Biological Resource Analysis to Identify New Mechanisms and phenotypes in Neurodegenerative Diseases "BRAINMEND"
Joint Programme on Neurodegenerative Disease (JPND)
No summary available.Neuroexercise: The effects of an extensive exercise program on the progression of mild cognitive impairment (MCI)
Joint Programme on Neurodegenerative Disease (JPND)
A lack of physical exercise plays a major role in the pathophysiology of vascular, metabolic, and metastatic diseases. Regular physical exercise has been successfully proven to counteract this deconditioning. Human and animal studies have demonstrated that...