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O nás: Who We Are
Vieš, že...
Približne 1 z 40 ľudí je nositeľom genetickej mutácie, ktorá spôsobuje SMA (spinálnu muskulárnu atrofiu), čo z nej robí jedno z najbežnejších genetických ochorení.
In the MENA region, the lack of standardized referral pathways for Duchenne Muscular Dystrophy (DMD) causes delays in diagnosis and treatment. We aim to build AI-driven software to analyze low MRI muscle tissue scan to provide early detection and comprehensive evaluation of disease management.
OUR MAIN PROJECTS INCLUDE:
medical problem solving contest and summer academy focused on clinical practice
journalism for young scientists with a focus on research
weekend workshops
*European Commission, report on Slovakia 2020
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