Wed, 04/04/2018 - 15:45 |
Community Route 79, The Duchenne Scholarship Program Clinical Trials Disease Resources Grants and Sponsorships Compassionate Use Policy Managed Access Program |
Sarepta |
Fri, 03/16/2018 - 15:53 |
Human chimeric cells restore crucial protein in Duchenne muscular dystrophy |
UICUniv |
Fri, 03/16/2018 - 11:58 |
How the CPAP machine beats deadly sleep apnoea |
SydneyUniv |
Wed, 03/14/2018 - 13:06 |
Nanostructures created by UCLA scientists could make gene therapies safer, faster and more affordable |
UCLA |
Tue, 03/06/2018 - 10:42 |
Salk Institute for Biological Studies - Ronald Evans |
Salk Institute |
Tue, 03/06/2018 - 09:28 |
Salk scientists find power switch for muscles |
Salk Institute |
Mon, 02/26/2018 - 11:26 |
New health care considerations needed to improve quality of life for Duchenne muscular dystrophy patients |
RTI International |
Fri, 02/23/2018 - 11:23 |
UIC researchers launch company to develop chimeric cell therapy for Duchenne muscular dystrophy |
UICUniv |
Thu, 02/08/2018 - 17:02 |
Device that measures cell strength could help identify drugs for asthma, hypertension and muscular dystrophy |
UCLA |
Mon, 02/05/2018 - 02:36 |
DEEP OSCILLATION® Proves Effective At The Neuromuscular Centre For Muscular Dystrophy |
PhysioPod UK LTD |
Thu, 01/25/2018 - 00:01 |
Kent mother takes fight for fast access to life-saving treatments to parliament |
Muscular Dystro... |
Sun, 01/14/2018 - 05:42 |
Statement on EMAs negative opinion on Raxone |
Muscular Dystro... |
Wed, 12/20/2017 - 13:31 |
Scientists Reprogram Stem Cells to Regenerate Muscle in Muscular Dystrophy |
Northwestern Un... |
Tue, 12/12/2017 - 11:40 |
Research reveals how diabetes in pregnancy affects babys heart |
UCLA |
Thu, 12/07/2017 - 09:59 |
Salk scientists modify CRISPR to epigenetically treat diabetes, kidney disease, muscular dystrophy |
Salk Institute |
Wed, 12/06/2017 - 16:01 |
Founders Council 2017 Grants |
Texas Biomed |
Mon, 12/04/2017 - 16:44 |
STRATEGIC & SCIENTIFIC ADVISORY BOARD |
Sarepta |
Thu, 11/30/2017 - 11:15 |
Designer molecule points to treatment for diseases caused by DNA repeats |
University of W... |
Thu, 11/23/2017 - 03:20 |
All-in-one repair kit makes CRISPR gene editing more precise |
University of W... |
Wed, 11/22/2017 - 10:35 |
AAAS names 8 UW researchers as fellows in 2017 |
UniversityOfWas... |
Wed, 10/25/2017 - 11:34 |
Researchers engineer CRISPR to edit single RNA letters in human cells |
Broad Institute |
Mon, 10/23/2017 - 03:35 |
Families frustration at year-long wait for action on report to tackle treatment delays |
Muscular Dystro... |
Wed, 10/11/2017 - 09:53 |
Moffitt Cancer Center to Partner with VHL Alliance on 2017 Family Weekend |
Moffitt |
Wed, 10/04/2017 - 09:01 |
U-M startup marks milestone in drug therapy for boys with Duchenne muscular dystrophy |
University of M... |
Tue, 10/03/2017 - 10:56 |
CRISPR-Gold fixes Duchenne muscular dystrophy mutation in mice |
University of B... |