Common genetic cause of autism, epilepsy - UPI.com
Links shared publicly online about this topic.
- 376total visits
Common genetic cause of autism, epilepsy - UPI.com
upi.com —
View full resource at upi.com
Tags: Genetic, Seizure, Epilepsy, Autism Spectrum Disorder, Autism, Genes
Most Recently Shared on April 10, 2011 at 4:10 am By:
Common genetic cause of autism, epilepsy: MONTREAL, April 8 (UPI) -- Researchers in Canada say they discovered a... http://bit.ly/eyuVp7
Also Shared By:
Study In Fruit Flies Has Implications For Autism, Other Cognitive Impairment Syndromes
medicalnewstoday.com — “The most common form of heritable cognitive impairment is Fragile X Syndrome, caused by mutation or malfunction of the FMR1 gene. Loss of FMR1 function is also the most common genetic cause of aut” View full resource at medicalnewstoday.com
Most Recently Shared on November 1, 2011 at 8:06 am By:
Study In Fruit Flies Has Implications For Autism, Other Cognitive Impairment Syndromes: The most common form of ... http://t.co/MLazq4s5
Evidence For The Genetic Basis Of Autism: Mouse Models Show That Gene Copy Number Controls Brain Structure And Behavior
medicalnewstoday.com — “Scientists at Cold Spring Harbor Laboratory (CSHL) have discovered that one of the most common genetic alterations in autism - deletion of a 27-gene cluster on chromosome 16 - causes autism-like f” View full resource at medicalnewstoday.com
Most Recently Shared on October 4, 2011 at 8:05 am By:
Evidence For The Genetic Basis Of Autism: Mouse Models Show That Gene Copy Number Controls Brain Structure And B... http://t.co/0cB7ti1O
Researchers Develop New Drug-Like Molecule to Treat Fragile X Syndrome, the Most Common Genetic Cause of Autism
newswise.com — “Researchers at Vanderbilt University Medical Center, in collaboration with Seaside Therapeutics in Cambridge, Mass., have achieved a milestone in the development of a potential new treatment for fragile X syndrome, the most common genetic cause of autism.” View full resource at newswise.com
Most Recently Shared on September 15, 2011 at 5:04 pm By:
#health news: Researchers Develop New Drug-Like Molecule to Treat Fragile X Syndrome, the Most Common Genetic Ca... http://t.co/wrdXoGjr
New Clinical Trial To Examine Medication To Treat Social Withdrawal In Fragile X And Autism Patients
medicalnewstoday.com — “Children and adults with social withdrawal due to Fragile X syndrome, the most common cause of inherited intellectual disability and the most common known single gene cause of autism, may benefit” View full resource at medicalnewstoday.com
Most Recently Shared on July 20, 2011 at 6:05 pm By:
New Clinical Trial To Examine Medication To Treat Social Withdrawal In Fragile X And Autism Patients http://mnt.to/3Yqj #autism
New Genetic Studies Suggest Why Autism Is More Common In Boys Than Girls | Care2 Causes
care2.com — “Three new studies in Neuron reports that hundreds of spontaneous genetic mutations have been linked to autism. Such CBS News describes the findings as a shocker, previous research has indicated that de novo or spontaneous gene mutations can be linked to the neurodevelopmental disorder. As Time magazine says, the new studies differ from previous genetic studies, which looked at families with at least two autistic children; such families may represent cases in which inherited genetic mutations may” View full resource at care2.com
Most Recently Shared on June 10, 2011 at 5:22 am By:
Seaside Therapeutics Advances Fragile X Drug | The Haystack
cenblog.org — “Some great news out today for parents of kids with Fragile X, a neurological disorder that is also the most common genetic cause of autism: Seaside Therapeutics has begun a Phase III trial of STX209, which could potentially be the first drug available to treat the underlying symptoms of the disorder. Fragile X, a disorder [...]” View full resource at cenblog.org
Most Recently Shared on June 2, 2011 at 7:29 pm By:
Lisa Jarvis Science Enthusiast
Good news in Fragile X & #autism: Seaside Therapeutics starts PhIII trial of STX209. Background on new trial & drug: http://bit.ly/j9RU4J
Autism And Epilepsy Caused By Common Gene | ThirdAge
thirdage.com — “Autism and epilepsy predisposition is connected to a new gene that researchers in Canada say they discovered.” View full resource at thirdage.com
Most Recently Shared on April 24, 2011 at 10:23 pm By:
Autism And Epilepsy Caused By Common Gene: Â Autism and epilepsy predisposition is connected to a new gene that ... http://bit.ly/f10OLO
Autism And Epilepsy Caused By Common Gene | ThirdAge
thirdage.com — “Autism and epilepsy predisposition is connected to a new gene that researchers in Canada say they discovered.” View full resource at thirdage.com
Most Recently Shared on April 24, 2011 at 8:44 pm By:
Sandra Cottingham Health Business and Parenting Supporter
Autism And Epilepsy Caused By Common Gene http://bit.ly/homaVD
Health News - A world first: The discovery of a common genetic cause of autism and epilepsy
healthcanal.com — “A world first: The discovery of a common genetic cause of autism and epilepsy” View full resource at healthcanal.com
Most Recently Shared on April 13, 2011 at 2:32 pm By:
SNAPPIN' MINISTRIES Patient Advocate
Health News - A world first: The discovery of a common genetic cause of autism and epilepsy http://j.mp/hIoRbm via @AddToAny
Link Between Fragile X Syndrome And Epilepsy: New Clue Found
medicalnewstoday.com — “Individuals with fragile X syndrome, the most common inherited form of intellectual disability, often develop epilepsy, but so far the underlying causes are unknown. Researchers have now discovere” View full resource at medicalnewstoday.com
Most Recently Shared on April 13, 2011 at 11:05 am By:
Link Between Fragile X Syndrome And Epilepsy: New Clue Found http://mnt.to/3Tzm #epilepsy
A world first: The discovery of a common genetic cause of autism and epilepsy
physorg.com — “Researchers from the CHUM Research Centre (CRCHUM) have identified a new gene that predisposes people to both autism and epilepsy.” View full resource at physorg.com
Most Recently Shared on April 8, 2011 at 11:38 am By:
PhysOrg Health News Health News
A world first: The discovery of a common genetic cause of autism and epilepsy http://tw.physorg.com/221466728
PolygenicBlog: The Causes Of Common Diseases Are Not Genetic Concludes A New Analysis
polygenicpathways.blogspot.com — “Concerning the relationships between genes, risk factors and immunity in Alzheimer's disease, Autism, Bipolar disorder , multiple sclerosis, Parkinson's disease, schizophrenia and chronic fatigue” View full resource at polygenicpathways.blogspot.com
Most Recently Shared on December 7, 2010 at 10:53 pm By:
http://www.linkedin.com/pub/chris-carter/22/560/76a" /> Dr Chris Carter Doctor, Medical Technology, Pharmacist, and PhD
The Causes Of Common Diseases Are Not Genetic Concludes A New Analysis http://goo.gl/fb/OSRin
Secret funding fosters hope for new drugs for autism
eurekalert.org — “Funding from an anonymous wealthy family has been the secret to progress, at long last, in developing drugs that show promise for helping millions of people worldwide with Fragile X syndrome, the most common genetic cause of autism. That's the topic of a fascinating article in the current issue of Chemical & Engineering News, ACS' weekly newsmagazine.” View full resource at eurekalert.org
Most Recently Shared on September 15, 2010 at 6:47 pm By:
Peter H Brown Doctor and Psychologist
Secret funding fosters hope for new drugs for autism http://bit.ly/9Yl4EX #autism
Mutations in STRAD-alpha gene can cause PMSE syndrome in Amish children: Penn researchers
news-medical.net — “So often the rare informs the common. Penn researchers investigating a regulatory protein involved in a rare genetic disease have shown that it may be related to epileptic and autistic symptoms in other more common neurological disorders.” View full resource at news-medical.net
Most Recently Shared on May 12, 2010 at 1:41 pm By:
Epilepsy News: Mutations in STRAD-alpha gene can cause PMSE syndrome in Amish children: Penn researchers: So often... http://bit.ly/abawH4
Rare Disease in Amish Children Sheds Light on Common Neurological Disorders
newswise.com — “Researchers investigating a regulatory protein involved in a rare genetic disease have shown that it may be related to epileptic and autistic symptoms in other more common neurological disorders. A team of researchers demonstrated how mutations in the STRAD-alpha gene can cause a disease called PMSE (polyhydramnios, megalencephaly, and symptomatic epilepsy) syndrome, found in a handful of Amish children.” View full resource at newswise.com
Most Recently Shared on May 11, 2010 at 3:54 pm By:
newswise Health Communicator and Health News
Rare Disease in Amish Children Sheds Light on Common Neurological Disorders: Researchers investigating a regulator... http://bit.ly/b5SRMV
Advertisement
Epilepsy OW
@Epilepsy_Wisdom
Link Between Fragile X Syndrome And Epilepsy: New Clue Found: Individuals with fragile X syndrome, the most comm... http://bit.ly/e81wfy
1 year ago...