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AngelmanSyndrome news

Enabling and empowering: Absent state support, local agencies fill the gap for people with disabilities


Frederick News Post (subscription) - Sep 17, 2017
Michelle Sclater and her son Jake, 14, work with Mariah Tarboro, a support staff worker of the Arc of Frederick County. Jake has Angelman syndrome, a rare neuro-genetic disorder that causes developmental delays, balance problems, speech difficulty and ...
 

Colin Farrell Shares the Touching Moment His Son with Special Needs Took His First Steps: 'It Was Humbling to See'


PEOPLE.com - Sep 9, 2017
The actor's firstborn son, who turns 14 next week, has a rare genetic disorder called Angelman syndrome, which causes motor and developmental disabilities, among other symptoms.. Farrell says that while any child taking their first steps is a momentous ...
 

ACHV Focuses On Achievement, IMGN Strikes Chord With JAZZ, FDA Snubs ACOR


Nasdaq - Aug 30, 2017
The top line data from the phase I trial evaluating OV101 in adolescents diagnosed with Angelman syndrome or Fragile X syndrome are expected to be available in the second half of 2017. -- Data from the phase 1b/2a clinical trial of TAK-935/OV935 are ...
 

Angelman Syndrome - premium items on eBay

USED (VG) The Official Parent's Sourcebook on Angelman Syndrome: A Revised and U


 

The Official Parent's Sourcebook on Angelman Syndrome Revised Updated James Park


 

Angelman Syndrome by Bernard Dan (English) Paperback Book


 

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What does Angelman Syndrome look like?


Angelman Syndrome (AS) is a rare condition with different genotypes and varying degrees of severity affecting approximately 1:15000 births. Around 490000 ...
 

4 siblings with Angelman Syndrome


 

Jacob's Story: Angelman Syndrome | Studio 10


Young Jacob suffers from a rare disease that affects 1 in 20000 children. Studio 10 | 8:30am on TEN.
 

A Story about Angelman Syndrome


Angelman Syndrome is a rare genetic condition. You can read the clinical characteristics and what individuals and their families may go through, however it is ...
 

Angelman Syndrome interview with Tanya O'Rourke


Angelman Syndrome Walk on May 17.