Owen Donoghue, 44, set out to raise funds for Ella-Rose Kennedy after she was diagnosed with a debilitating progressive brain ...

Researchers have developed a gene editing strategy that can repair the genetic problems that lead to Huntington's disease and Friedreich's ataxia. | Genetics And Genomics ...

Early research shows that editing expanding trinucleotide repeats halts the lengthening process that causes neurological ...

Researchers have developed a way to edit the genetic sequences at the root of Huntington's disease and Friedreich's ataxia. If longer than a certain threshold length, these sequences grow in length ...

After getting a green light from the European Commission, Biogen’s Skyclarys is the first approved medicine for the inherited neurological disease Friedreich ... a range of symptoms, including ...

Larimar is taking part in the pilot with its nomlabofusp protein replacement therapy for Friedreich’s ataxia ... and other neurological symptoms. When START was launched, the FDA said the ...

Figure 5: Sca10 is widely expressed in brain regions that are anatomical substrates for ataxia and epilepsy. We extracted DNA from blood samples of all participating family members after obtaining ...

A Columbia woman is putting a spotlight on a rare, degenerative disease, which targets the nervous system and often impairs ...

Less than one month after his procedure, Charles’ cancer diagnosis was announced. “His Majesty has today commenced a schedule of regular treatments, during which time he has been advised by ...

Understanding how COVID-19 symptoms present can minimize the spread and help you get the right treatment. COVID-19 infection rates have stabilized, but a new Omicron variant driving a surge in ...

Minor cases may not cause any noticeable symptoms. Severe cases often cause severe muscle pain and can be life threatening. The most common cause of rhabdomyolysis is acute skeletal muscle injuries.