Service de presse : nos actus, le #Téléthon, la recherche sur les maladies rares (thérapie génique, cellulaire...). Contact 01 69 47 12 78 / 06 45 15 95 87
https://www.afm-telethon.fr/fr/espace-presse
Compte officiel
L'AFM-Téléthon est une association de malades et parents de malades
Retrouvez-nous sur https://www.afm-telethon.fr
📆 #Téléthon2025 : 5 & 6 déc.
Dad of 3, Geospatial Analyst, looking for a cure for Duchenne Muscular Dystrophy.
Our mission is to cure Duchenne muscular dystrophy with our innovative venture philanthropy model that funds groundbreaking research, early diagnosis and treatment access.
Vecht voor genezing of behandeling van spierziekte Duchenne, betere zorg & hulpmiddelen! Doe mee via http://duchenne.nl NL15INGB0000818818
Trusted knowledge base of practical information and resources focused on treating and diagnosing #RareDisease.
https://www.rarediseaseadvisor.com/
Scientist @UniMelb 🇦🇺 focusing on #proteomics, signaling and metabolism. Loves 🏄♂️⛷️⛰️
Geneticist, Skeletal Muscle, Drug development, Gene therapies. Non-coding RNA, and Zebrafish Aficionado. Lover of all things muscle. All posts are my own. Instagram @thealexanderlab
Lab website: https://www.uab.edu/medicine/peds/research/division-researc
Senior Scientist that investigates the molecular mechanisms that regulate skeletal muscle mass and function in health and in various disease states. Protein synthesis, ubiquitin biology.
https://scholar.google.com.au/citations?user=ICAcUqUAAAAJ&hl=en
Director: Muscle Health Research Centre
Professor: muscle disorders and the metabolic basis of muscle fitness. Translating mitochondrial bioenergetics and redox biology to health/disease
http://health.yorku.ca/health-profiles/index.php?mid=1068349
official Bluesky account (check username👆)
Bugs, feature requests, feedback: support@bsky.app
