The BIND project is a EU-funded project that attempts to improve the characterisation of brain involvement in Duchenne and Becker Muscular Dystrophies (DMD and BMD). Here, we present our ongoing work on making multimodal data FAIR, the semantic models, and discuss challenges and opportunities based on our FAIRification experience
The SIR-FMD project is a partnership between the Department of Genetics and Reference Centre for Rar...
peer reviewedDrug development for rare diseases is challenged by small populations and limited data....
Duchenne muscular dystrophy is a rare, progressive, muscle-wasting disease leading to severe disabil...
Duchenne muscular dystrophy (DMD) is an X-linked genetic disease, caused by the absence of the dystr...
International audienceDuchenne muscular dystrophy (DMD) is an X-linked genetic disease, caused by th...
International audienceUMD-DMD France is a knowledgebase developed through a multicenter academic eff...
<p>Duchenne muscular dystrophy (DMD) is an X-linked genetic disease, caused by the absence of ...
Identifying patients with Fibromuscular Dysplasia (FMD) at the international level will have conside...
Duchenne muscular dystrophy is a rare, progressive, muscle-wasting disease leading to severe disabil...
Drug development for rare diseases is challenged by small populations and limited data. This makes d...
The SIR-FMD project is a partnership between the Department of Genetics and Reference Centre for Rar...
peer reviewedDrug development for rare diseases is challenged by small populations and limited data....
Duchenne muscular dystrophy is a rare, progressive, muscle-wasting disease leading to severe disabil...
Duchenne muscular dystrophy (DMD) is an X-linked genetic disease, caused by the absence of the dystr...
International audienceDuchenne muscular dystrophy (DMD) is an X-linked genetic disease, caused by th...
International audienceUMD-DMD France is a knowledgebase developed through a multicenter academic eff...
<p>Duchenne muscular dystrophy (DMD) is an X-linked genetic disease, caused by the absence of ...
Identifying patients with Fibromuscular Dysplasia (FMD) at the international level will have conside...
Duchenne muscular dystrophy is a rare, progressive, muscle-wasting disease leading to severe disabil...
Drug development for rare diseases is challenged by small populations and limited data. This makes d...
The SIR-FMD project is a partnership between the Department of Genetics and Reference Centre for Rar...
peer reviewedDrug development for rare diseases is challenged by small populations and limited data....
Duchenne muscular dystrophy is a rare, progressive, muscle-wasting disease leading to severe disabil...