While Illinois joins states challenging cuts to medical research funding, an Illinois State University lab supported by the ...
Less than half of patients had undergone bone monitoring, suggesting a need for better clinical guidance and management of ...
Duchenne muscular dystrophy (DMD) is a rare hereditary disease that is associated with progressive muscle wasting. The ...
Enrolment in this trial is expected to continue through the first quarter of 2025. Satellos is on track to submit a Phase II ...
Learn More Genetic Causes of Muscular Dystrophy Is muscular dystrophy fatal? Some types of muscular dystrophy can be fatal. Certain types, including Duchenne muscular dystrophy, can lead to problems ...
NEW YORK – Belief BioMed announced Wednesday that the US Food and Drug Administration has cleared its investigational new drug application enabling it to begin testing its gene therapy candidate for ...
Get Instant Summarized Text (Gist) Muscular strength and cardiorespiratory fitness are significantly linked to a lower risk of death in cancer patients. A pooled analysis of 42 studies involving ...
J35, also known as Tahlequah, is seen pushing her dead calf, J61, near Seattle, Wash., on Jan. 1. (NOAA Fisheries) The post detailing the sighting says observers "were not seeing much of the ...
There is a simple discount patient access scheme for vamorolone. NHS organisations can get details on the Commercial Access and Pricing (CAP) Portal. Non-NHS organisations can contact ...
DM1 is a form of muscular dystrophy where mutations in the DMPK gene lead to the production of an abnormal version of RNA, a template molecule used to make protein. This abnormal RNA accumulates and ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results