Top Tweets for #RareCast
.@ChiesiGRD has evolved through dealmaking, expanding into CRISPR and BBB tech—Giacomo Chiesi shares vision @GlobalGenes #RARECast https://t.co/xDzIzi6Erz
@ChiesiGRD has evolved through dealmaking, expanding into CRISPR and BBB tech—Giacomo Chiesi shares vision @globalgenes #RARECast
https://t.co/YuuwcxcA7m
How do you develop a treatment for a disease with no approved disease-modifying therapies?
Alterity CEO Dr David Stamler joins @globalgenes #RARECast to discuss MSA, ATH434, and the science behind targeting iron dysregulation in neurodegenerative disease
#MSA #RareDisease
David Stamler @AlterityT discusses the biology of multiple system atrophy, the company’s promising clinical results to date, and why its therapeutic approach may also have application in other neurodegenerative diseases. @globalgenes #RARECast
https://t.co/P4xzx4eG6q
David Stamler @AlterityT discusses the biology of multiple system atrophy, the company’s promising clinical results to date, and why its therapeutic approach may also have application in other neurodegenerative diseases. @globalgenes #RARECast
https://t.co/P4xzx4eG6q
.@paulpetertak @CandelTx discusses the company's viral immunotherapy for brain cancer, how it works, and what clinical studies have shown to date. @GlobalGenes #RARECast
https://t.co/DsMOSFXLZf
Steve Mahoney, Viridian’s CEO, sat down w/ @dslevine to talk about the work #TeamViridian is doing to develop potentially new treatment options for people living w/ #ThyroidEyeDisease #TED.
Listen Here > https://t.co/NJMDWHBgvu
@GlobalGenes #RareCast
Our CSO Dr. Arun Upadhyay joins the #RARECast podcast to discuss Ocugen’s modifier #genetherapy and its potential to treat genetically diverse #retinaldiseases. He also co-authored a related study.
🔗 https://t.co/q3QHea629U
📖 https://t.co/71En2Ko9i2
@GlobalGenes @IJMS_MDPI
.@rachnatshroff @UAZCancer discusses biliary tract cancers, the need for biomarker testing, and how to improve outcomes for people with these rare cancers. @Globalgenes #RARECast
https://t.co/ifeP0RkJ3Z
.@rachnatshroff @UAZCancer discusses biliary tract cancers, the need for biomarker testing, and how to improve outcomes for people with these rare cancers. @Globalgenes #RARECast
https://t.co/GusFCi3wFX
Check out @azitrainc's @twhitfill on the #RARECast #podcast - Engineering Skin Bacteria to Be Live Biotherapeutics - digging in on #NethertonSyndrome @lmgbio #precisionderm #dermatology https://t.co/9xfOT1beBT
ICYMI: Engineering Skin Bacteria to Be Live Biotherapeutics - @twhitfill of
@azitrainc discusses #NethertonSyndrome on #RARECast as well as the company’s platform tech @lmgbio #podcast #precisionderm #dermatology https://t.co/YN7CTxpwO5
Liz Thompson, head of research and development for @AcadiaPharma , discusses Rett syndrome, how Daybue has changed the treatment landscape for people with the condition, and the company’s advancing pipeline to treat it. @GlobalGenes #RARECast
https://t.co/qi06IxCR7L
📣 I am delighted to share my discussion with @dslevine on the #RARECast #podcast in the episode : “A Non-Profit Works to Advance a DMD Gene Therapy”.
Listen to the full podcast interview 👇
https://t.co/rnzdcLVUVi
#duchenne #trial #raredisease #commitment
.@NoamBaumatz of Noga Therapeutics discusses his experience with a daughter born with a rare immunodeficiency, how that led to the founding of Noga Therapeutics, and the company’s decision to pursue both rare and common diseases. @GlobalGenes #RARECast
https://t.co/MznMc8UwzY
This past August, Chris Hopkins, CEO of @DevinebioRare, sat down to talk about how the company works with patient organizations, how far it will advance programs, and its exit strategy 🌟🎧: #RARECast
https://t.co/9Il0S75wP9
Monica Coenraads has played a critical role in catalyzing development of therapies to treat Rett Syndrome. She joined us on RARECast this September to talk about what other rare disease organizations can learn from her experience.
🎙️https://t.co/mbsT6sy39M
#RARECast #GlobalGenes
Effie Parks @OnceUponAGene discusses her experience with the diagnostic odyssey for her son Ford, her version of the map to a genetic diagnosis, and what organizations usually get wrong when they seek to map this journey. @GlobalGenes #RARECast
https://t.co/zKNdvBU8SO
Our RAREcast podcast has officially hit 500 episodes! Joining us today is Effie Parks, host of the @OnceUponAGene podcast, to talk about her journey as a mother of a child with a rare disease. Listen now wherever you get your podcasts! 🎙️#CareAboutRare #RareDisease #RAREcast
Brian Strem @KioraPharma discusses inherited retinal diseases, how Kiora’s experimental therapy works to treat these conditions, and a recent collaboration that will help drive clinical development of its lead experimental therapy. @GlobalGenes #RARECast
https://t.co/0HdS8tFfQa
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