Scientist with rare ALS genetic mutation looks to experimental treatment
Scientist with rare ALS genetic mutation looks to experimental treatment
1 month ago
MSNJon LaPook
Novel ALS Variants ID'ed, Now 1 in 4 Patients Have Genetic Cause | Genetics And Genomics
Novel ALS Variants ID'ed, Now 1 in 4 Patients Have Genetic Cause | Genetics And Genomics
1 month ago
labroots.com
Penn medical student, who is genetic carrier of rare form of ALS, on mission to develop gene therapy | Ry Leahy
Penn medical student, who is genetic carrier of rare form of ALS, on mission to develop gene therapy | Ry Leahy
27.4K views1 month ago
linkedin.com
Amyotrophic lateral sclerosis (ALS) is a universally devastating disease in all its forms. Close to 15% of all ALS cases are associated with a known genetic mutation. Learn more about genetic ALS this ALS Awareness Month: http://ow.ly/IfZA50Oosgj | Biogen
0:26
Amyotrophic lateral sclerosis (ALS) is a universally devastating disease in all its forms. Close to 15% of all ALS cases are associated with a known genetic mutation. Learn more about genetic ALS this ALS Awareness Month: http://ow.ly/IfZA50Oosgj | Biogen
220 viewsMay 15, 2023
FacebookBiogen
Experimental gene therapy shows promise in preventing ALS symptoms
1:00
Experimental gene therapy shows promise in preventing ALS symptoms
1 month ago
MSNKYTX-TV Tyler-Longview
Learn About How the Gene Mutation Works
Learn About How the Gene Mutation Works
Apr 30, 2025
thoughtco.com
What is inversion 3 mutation? Inside Tatiana Schlossberg’s rare genetic anomaly
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What is inversion 3 mutation? Inside Tatiana Schlossberg’s rare genetic anomaly
5 months ago
nypost.com
6:36
90% of ALS diagnoses are considered sporadic. So that means just a small percentage of ALS patients have inherited a genetic form of this disease. While it seems unlikely to have a genetic onset of ALS, it’s really important to discover the type of onset we have as it relates to immediate treatment options, but most importantly, future generations. There is a 50% chance of future generations inheriting this genetic disposition. It can help prepare better for the future of this disease as it will
8K views6 months ago
FacebookDeanna Cotten
1:26
Superoxide dismutase 1 (SOD1) amyotrophic lateral sclerosis (ALS) progressively robs people of their ability to move, speak, swallow and breathe. It is a rare, genetic form of the disease that makes up about 2% of global ALS cases. Learn more about the role of the SOD1 gene mutation in ALS. | Biogen
1.1K viewsDec 2, 2022
FacebookBiogen
1:30:53
ALS (Amyotrophic Lateral Sclerosis) and Frontotemporal Degeneration | AFTD
Feb 25, 2019
theaftd.org
Investigational drug for genetic form of ALS improves disease’s molecular signs | Newswise
Sep 16, 2022
newswise.com
New ALS Gene and Signaling Pathways Identified
Feb 19, 2015
columbia.edu
Scientists Discover a Genetic Variant That Enables ALS Recovery | Genetics And Genomics
Aug 5, 2024
labroots.com
1:02
If you have #ALS, a genetic test can determine if you have a known ALS-associated genetic mutation, as well as the risk of disease in your family members. Learn more: https://bit.ly/ALSGeneticTesting | The ALS Association
1.1K viewsMar 13, 2024
FacebookThe ALS Association
ALS is only 50% genetic – identifying DNA regions affected by lifestyle and environmental risk factors could help pinpoint avenues for treatment
Feb 12, 2025
theconversation.com
What causes ALS?⎜Your ALS Guide
Mar 18, 2021
youralsguide.com
Harvard scientists identify gut-brain connection in ALS
May 13, 2020
harvard.edu
4.10: Mutation Effects
Jul 20, 2023
libretexts.org
1:07
In the quest for a cure for ALS, there’s a new reason for hope. Thanks to new genetic tools, scientists can now target the exact neurons impacted by amyotrophic lateral sclerosis (ALS). These tools give researchers the ability to zero in on these neurons and could provide a way for gene therapies to be delivered. | Allen Institute
98K views7 months ago
FacebookAllen Institute
Mayo Clinic: New Mouse Model for ALS and Frontotemporal Dementia Gene Offers Hope for Potential Therapies - Mayo Clinic News Network
May 13, 2015
mayoclinic.org
3:14
At 29, Lee is planning for her future while facing the harsh reality of ALS. With a family history of the disease and testing positive for the genetic mutation of ALS, she’s determined to raise awareness and fight for a cure. Learn more about Lee's journey, genetic testing, and how you can support the fight against ALS. https://bit.ly/Lees-Story | The ALS Association
164K viewsFeb 15, 2025
FacebookThe ALS Association
7:02
How Familial ALS Helps Scientists Understand Sporadic ALS
1 month ago
YouTubeALS.community
6:37
Precision Medicine: Personalized Treatment, Genetic Testing, and ALS Clinical Trials Explained
4 views1 month ago
YouTubeALS.community
7:08
Familial ALS: Understanding the Genetic Form of ALS
1 views1 month ago
YouTubeALS.community
2:37
Dr. Rosa Rademakers explains ALS-dementia gene research and discovery
2.2K views3 weeks ago
YouTubeMayo Clinic
4:59
Episode 4: I'm a genetic carrier for ALS/FTD: what is my risk?
2 views1 month ago
YouTubeYentli Soto Albrecht, PhD
0:16
Scientist with rare ALS genetic mutation explores experimental treatment options
61 views1 month ago
YouTubeStateside Now
7:20
C9orf72 and ALS: The Most Common Genetic Cause of Familial ALS Explained
1 month ago
YouTubeALS.community
11:29
Overview of Amyotrophic lateral sclerosis
4.4K views2 weeks ago
YouTubeLectures on Human Diseases and Genes
5:26
One year ago today, I found out I carry a genetic mutation linked to ALS and FTD. A moment like that changes the way you see your future, your time, and the people you love. This past year has been a mix of fear, gratitude, learning, and purpose. I’ve learned more about ALS than I ever imagined, connected with an incredible community, and realized how many families are facing this disease every single day. Living with this knowledge isn’t easy, but it has also made me appreciate the present more
431 views2 months ago
TikToklivingwiththegene
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