opener

Walk
Contact Registry
News
Blog

Search for:

DOnate

What is Angelman Syndrome
For Parents
Research
Make an Impact
Clinics
Resources
Events
About

articles and announcements

2010: Clinical Trials Act

September 9, 2010

2010: Clinical Trials Act Timelines: The History of Angelman Syndrome and the ASF

Ultragenyx Announces Positive Interim Phase 1/2 Data from GTX-102
Family Advocates Urge Congress’ Support During Inaugural Angelman Syndrome (AS) Congressional Advocacy Day
Angelman Clinic opens at Cedars-Sinai Guerin Children’s
Angelman Clinic opens at Children’s Hospital of Philadelphia (CHOP)
ASF and .PROT partner to launch new Angelman Center for families in Poland
Roche Clinical Trial of Rugonersen in Angelman Syndrome
ASF Opens Application for its Inaugural Jacob Pritzker Fellowship
Canadian Angelman Syndrome Society is now ASF Canada
GFAS Ukraine and ASF partner to Launch Clinic in Ukraine
AngelmanUK and ASF partner to launch clinics in the UK
LADDER Database Receives Transformational Dataset from Ovid Therapeutics
ASF Partners with Families in UAE to Expand Clinical Network
ASF to Host Screening of Caregiver Documentary, Unseen
Angelman Syndrome Foundation and Dup15q Alliance partner to launch the LADDER Learning Network, showing continued dedication to research
Newborn Screening Grant for Early Check
ASF Funded Research on Gene Therapy in AS Published in JCI Insight
ASF and Angelman UK Partner to Expand Family Support
ASF and FAST Unite for Legislative Working Group
Joint Initiative between ASA and ASF
Groundbreaking ASF Funded Research on Gene Therapy in AS Published in Nature

Browse

What is Angelman Syndrome
For Parents
ASF Funded Research
Make an Impact
Events
About
Angelman Resources & Education
Contact Registry
News

Address Angelman Syndrome Foundation
3015 E. New York Street
Suite A2 #285
Aurora, IL 60504 Phone800.432.6435 Emailinfo@angelman.org

Connect

facebook
twitter
linkedin
instagram
pinterest
rss
youtube

The Mission

The mission of the Angelman Syndrome Foundation is to advance the awareness and treatment of Angelman syndrome through education and information, research, and support for individuals with Angelman syndrome, their families and other concerned parties. We exist to give all of them a reason to smile, with the ultimate goal of finding a cure.

Copyright © 2024 Angelman Syndrome Foundation. ALL Rights Reserved. | Site design: BRAND INSPIRATION, LLC