#ICYMI: Lindsey Lee Lair, MD, MBA, FAAN, VP of Clinical Development, spoke with Daniel Levine on a Global Genes #RARECast #podcast about #SMA, the progress we’ve seen in treating the condition, and Biohaven’s efforts to develop a therapy to stimulate the growth of muscle mass and strength in people with the disease. Listen to the podcast here: https://brnw.ch/21wGq8V #DaysMatter
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🎙️ ICYMI: In a new podcast episode of Mind Moments, Cathleen Lutz, PhD, of The Jackson Laboratory, provided comment on a recently published study on the role of stathmin-2 loss leads to in patients with #ALS. Lutz offered insight on the role stathmin-2 may have in this disease, the questions that still remain, and whether restoration of stathmin-2 may be an attractive therapeutic approach. Furthermore, she spoke on the potential of this protein as a disease-modifying biomarker and whether it may be incorporated in trials in the near future. 🎧 Listen here: https://lnkd.in/ehP8AXr6
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#podcast Dr. Sherif Idriss is the CEO of Elastin Biosciences, a company focused on targeting aging-related diseases by restoring elastin, a key protein in the extracellular matrix that provides elasticity and resilience to organs and tissues. They are developing small molecule therapies for diseases linked to elastin deficiency, including Williams syndrome and abdominal aortic aneurysm. As elastin degrades over time due to aging, it leads to loss of tissue structural integrity and function, contributing to numerous age-related diseases. #ElastinBiosciences #Aging #AgingRelatedDiseases #Elastin #WilliamsSyndrome elastin-biosciences.com https://lnkd.in/gE8b8a4d
Empowered Patient Podcast: Addressing Extracellular Matrix Breakdown That Leads to Age-Related Diseases with Dr. Sherif Idriss Elastin Biosciences
empoweredpatientradio.com
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[Podcast] Dr. Zuhal Butuner OD, MSc, MBA, Chief Medical Officer at Sepul Bio, recently joined Ben Shaberman on the Eye on The Cure podcast to discuss the future of our innovative therapies, sepofarsen for LCA10 and ultevursen for USH2A. To listen to the podcast, link in comment 👇🏽 #RNAtherapies #GeneticEyeDiseases #Podcast #LCA10 #UsherSyndrome #InheritedRetinalDiseases”
On this week's episode of the Eye on The Cure podcast, Dr. Zuhal Butuner, Chief Medical Officer at Sepul Bio, speaks with Ben Shaberman about the future of two innovative RNA therapies – sepofarsen (for LCA10) and ultevursen (for USH2A). From early clinical trials to plans for new studies, this episode dives deep into cutting-edge treatments for inherited retinal diseases. Learn more about streaming at: https://gag.gl/HJ4Riu #VisionRestoration #ClinicalTrials #RNAtherapies #LCA10 #USH2A #EyeHealth #InnovativeMedicine Image Description: Dark blue background with Foundation Fighting Blindness logo in the top left and Eye on the Cure Podcast logo in the top right. Teal half circle at the top center with "Ep. 73" inside. Below, text reads, "Listen to the latest podcast episode out now. September 20, 2024." To the left is Ben Shaberman's headshot with "Ben Shaberman, Host" beneath. To the right is Zuhal Butuner's headshot with "Dr. Zuhal Butuner, Guest" below.
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#podcast Dahlia Attia-King, CEO of Panacea, is bringing whole exome sequencing to a broader audience and promoting the value of this data for disease prevention and making smarter lifestyle choices. She highlights the differences between whole exome sequencing and whole genome sequencing, noting that whole exome sequencing can be conducted more cost-effectively and provide information about the genes most likely to impact health. #SeekPanacea #WholeExomeSequencing #WholeGenomeSequencing #Genome #PreventativeMedicine seekpanacea.com https://lnkd.in/dyVE8VG8
Empowered Patient Podcast: Making Whole Exome Sequencing Affordable Accessible Interpretable with Dahlia Attia-King Panacea
empoweredpatientradio.com
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Are you aware that the frequencies in our body can impact our health? Discover how vibration therapy could be the key to preventing serious diseases. Join Stephen Bland as he chats with Iman Antonious PMP,LSSGB,SAFe Agilist, Owner/Managing Director of Global Genesis LLC on this Wytpod episode. They delve into how our body's frequency can detect and combat low-frequency diseases like cancer. Don't miss out on this enlightening episode - tune in now! https://lnkd.in/gdkJjitd #healthtech #vibrationtherapy #innovativehealth #biofrequency #healthawareness #podcast
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Check out this incredible discussion on the research behind longevity, quantifying the aging process, and understanding how our past experiences and traumas are stored in our DNA through an extraordinary mind-body connection. In this Data-Driven Health Radio podcast episode, TruDiagnostic Founder and VP, Ryan Smith with Dave Korsunsky of Heads Up also talked about advancements in research that can help us accurately predict biological outcomes and detect diseases such as cancer at an earlier rate. Take a listen: https://lnkd.in/g9pAqjgx
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With a PH diagnosis, I didn't think of myself as passing away. I don't know if it has to do with me being a mom or not, but I just could not fathom not being here. Pulmonary Hypertension and Lung Transplant patient, Brittany Valim. phaware® podcast ep 458 Like and Subscribe. Link in bio #phaware #pulmonaryhypertension #podcast #pulmonary #lungs #pah
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Encouraging your patients to get their screenings can make all the difference in early detection and treatment. With the new guidelines, starting mammograms at 40 and colon cancer screenings at 45 is more important than ever. Stress the importance of these screenings during visits, and remind them that proactive care leads to better health outcomes. Like Dr. Tiffany Troso-Sandoval, MD, be the voice that motivates them to stay on top of their health. 🎙️ Watch Ep. 35 w/ Dr. Troso on YouTube, Spotify, and Apple Podcasts! ▶️ https://lnkd.in/eqB7Y_3E #EarlyDetection #PreventiveCare #StayHealthy #Mammograms #ColonCancerAwareness #HealthcareUpdates
Mammograms & Colon Cancer Screening Ages Lowered
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Psychologist || Building THE CSHAPED NETWORK for sickle cell disease awareness, warriors empowerment, and to support caregivers || UNDP-NJFP Fellow ‘23/24 || UN-SDG 3 Advocate || Data Annotator (AI Ops)
I will keep talking about it because it’s possible. Achieving a generation free from sickle cell disease is POSSIBLE. It is important to prevent more babies from being born with this challenging condition. Sickle cell anemia is inherited from parents with incompatible genotypes. Knowing your genotype is the first step toward a solution. #positivechange begins with YOU and I. ♻️Turn on post notifications 🔔 to receive insightful content that raises awareness about sickle cell disease. ♻️Repost and share to inform your network about THE C-SHAPED PODCAST. Do you know your genotype? Are you sure? Let me know in the comments. #20daylinkedinchallengewithhaoma #sicklecellawareness #sdg3 #thecshapedpodcast #thoughtleader #healthadvocacy
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Charcot-Marie-Tooth Disease, also known as peroneal muscular atrophy, is a common autosomal dominant hereditary motor sensory neuropathy, caused by abnormal peripheral myelin protein, that presents with muscles weakness and sensory changes which can lead to cavovarus feet, scoliosis, and claw foot deformities. Diagnosis is made with nerve conduction studies showing low nerve conduction velocities with prolonged distal latencies in the peroneal, ulnar, and median nerves. Learn more high-yield concepts about Charcot-Marie-Tooth Disease on our DAILY Orthobullets podcast. Listen wherever you listen to podcasts! https://bit.ly/3Qm53uO
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