News
6hon MSN
Cyclists led by Charlie Nuck will arrive in Bar Harbor Saturday to raise awareness and funds for the rare neurogenetic ...
On Friday, Bike 4 Briar had made it’s way to Fulton, NY, where they were welcomed at City Hall . Lunch was provided and a snack donation was made for their journey. Bike 4 Briar is a ...
Maine (WABI) - After 61 days and approximately 4,200 miles, two men have made it to Maine to wrap up an epic journey. At the ...
The General Motors charity car show was held on Sunday in Cheshire, benefitting families with children diagnosed with Angelman Syndrome. Angelman Syndrome affects one in ...
Bike 4 Briar cyclists cross the country to support Angelman syndrome research The Bike for Briar team, consisting of Todd Downey and Charlie Nuck, is biking 4,200 miles across the U.S. and passed ...
Ultragenyx Pharmaceutical Inc. (NASDAQ:RARE) is one of the most promising stocks according to Wall Street analysts.
Oak Hill Bio, a biotechnology company focused on developing life-changing therapies for people with rare diseases, today announced the publication in Nature Medicine of the results of the rugonersen ...
WEWS Cleveland, OH on MSN16d
Ohio uncle goes on cross-country mission to find a cure for rare syndromeAn Ohio uncle on a cross-country mission will be riding through Northeast Ohio this weekend. Charlie Nuck of Cincinnati has a 6-year-old niece named Briar. She has a rare, neurogenetic disorder called ...
Ultragenyx Pharmaceuticals' GTX-102 earns FDA Breakthrough status after early data shows sustained progress in Angelman syndrome patients.
The Hometown Foundation is hosting a car show for Angelman syndrome in Cheshire.
Hosted on MSN28d
Angelman syndrome: the disorder of Colin Farrell's son - MSNIn a conversation with People magazine in 2024, Colin Farrell opened up for the first time about his son's rare condition: Angelman syndrome. Just before his son James’ 21st birthday, the actor ...
2h
KELO Sioux Falls on MSN3-year-old with rare genetic disorder, search for a cureJuly 25 is the awareness day for a very rare syndrome, but one that a local child has. Carter Dreckman is a 3-year-old from ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results