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03/03/2026

Get a quick glimpse into what it’s like to be diagnosed with POLG‑related mitochondrial disease — the sudden symptoms, the life‑changing phone call, and the feeling of navigating a rare condition alone. Watch the full conversation with Jeff to hear his story and learn why awareness and support for POLG disorders matter.

Check the full story: https://youtu.be/H4NvqDp-S2g?si=Mz5ktA76QBj4vhsN

28/02/2026

Today is Rare Disease Day — a moment to recognise the millions of people living with conditions that often remain unseen.
POLG disease affects families, clinicians, and communities in profound ways, and awareness is essential.
To mark Rare Disease Day 2026, we’re launching a new video series sharing lived experiences, expert insights, and the future of POLG research.
Watch the video series in collaboration on YouTube and help shine a light on this rare condition: https://ow.ly/Kn2k50YmP8W

26/02/2026

Discover how research is driving hope for POLG‑related mitochondrial disease — from global collaboration to the rapid progress of gene therapy. Learn why scientists believe breakthroughs for POLG disorders may be closer than ever.
Watch the full interview to explore the future of mitochondrial disease research and treatment.

Get a quick intro to POLG‑related mitochondrial disease — what causes it, how it affects cells, and why early understanding matters. Watch the full expert interview with Dr. Phil West and Prof. Bill Copeland to learn more about the science, symptoms, diagnosis, and future treatment of POLG disorders.

Full episode here: https://youtu.be/Uz47WkX-iYI?si=KhdHTnO6g20RxdsV

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