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Posts Tagged ‘tourette’s syndrome’
Friday, October 10th, 2008
Tourette syndrome experts in genetics and pediatric neurology to discuss research and treatment on November 22
FOR IMMEDIATE RELEASE
October 9, 2008 — Somerville, N.J.–New Jersey Center for Tourette Syndrome and Associated Disorders, the group behind the world’s first TS DNA sharing repository, will feature an event on November 22 in Voorhees, N.J. Experts in genetics and pediatric neurology will present discussions on the diagnosis and treatment of TS.
Pediatric Neurologist Dr. Larry Brown of Children’s Hospital of Philadelphia will discuss state-of-the-art treatments for TS and associated disorders including attention deficit, attention deficit hyperactivity and obsessive compulsive disorders; depression and rage.
Dr. Jay Tischfield, Director of the NJ Center for Tourette Syndrome TS Sharing Repository at Rutgers will present information on TS genetics research. Research has revealed that Tourette Syndrome (TS) has a strong inherited component, and in recent years, the disorder has been linked to specific genes but these may account for only rare forms of TS. The repository gathers information and samples from those who have TS and/or relatives of those with TS to make this research possible. For more information on the TS Sharing Repository visit http://www.tourettesyndromeresearch.org
The November 22 event will take place at Virtua West Jersey Hospital in Voorhees, NJ. Registration is required by calling 908-575-7350.
Tags: add, adhd, depression, DNA research, DNA sharing repository, genetic research, Jay Tischfield, Larry Brown, NJCTS, ocd, pediatric neurology, rage, Tourette Syndrome, tourette syndrome research, tourette's syndrome, tourette's syndrome research, TS, TS genetic research, TS research
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Friday, October 3rd, 2008
Group behind Tourette Syndrome Sharing Repository offers webinar on treatment options for those with TS and associated disorders.
October 3, 2008
FOR IMMEDIATE RELEASE
Contact: NJCTS 908-575-7350
Somerville, NJ–New Jersey Center for Tourette Syndrome and Associated Disorders host “Mental Health Treatment for Individuals with Tourette Syndrome: Does it Work?” a free webinar on Wednesday, Oct. 29.
The presentation will be led by Lori Rockmore, Psy.D, Clinical Director: NJCTS Tourette Syndrome Program, Rutgers University Graduate School of Professional Psychology. The program will run from 7:30- 8:30 p.m. All are welcome to join this informative webinar. The discussion will focus on Tourette Syndrome and its associated disorders including attendion deficit disorder, obsessive compulsive disorder, depression and rage. To register or to learn more about NJCTS, please visit www.tourettesyndromeresearch.org.
New Jersey Center for Tourette Syndrome is non-profit organization behind the world’s first Tourette Syndrome DNA Sharing Repository at Rutgers University. The goal of the research is to help qualified scientists further the study of the genetic links to TS and ultimately lead to more comprehensive treatments.
For more information on the Sharing Repository or NJCTS, please visit www.tourettesyndromeresearch.org.
Tags: add, adhd, depression, DNA, genetic research, genetics, ocd, rage, repository, research, tourette syndrome research, tourette's research, tourette's syndrome, TS, TS research
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Wednesday, October 1st, 2008
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TS DNA SHARING REPOSITORY HOSTS STATE-OF-THE-ART TREATMENT TALK ABOUT TOURETTE SYNDROME
TS DNA Sharing Repository hosts a presentation on “State-of-the-art treatments for Tourette Syndrome and assocciated conditions” by Dr. Robert King as part of NJCTS ongoing genetic research project.
Sep 10, 2008 – FOR IMMEDIATE RELESE
Contact: Nicole Greco- NJCTS- 908.575.7350
Somerville, N.J.- New pathways to treating Tourette Syndrome and its associated neurological disorders will be discussed by Robert A. King, MD on September 19, from 5-6 p.m. at Rutgers University in Piscataway. Dr. King is part of New Jersey Center for Tourette Syndrome- a partnership between the Tourette Syndrome Association of New Jersey, Rutgers University and medical professionals throughout New Jersey.
Tourette Syndrome is a neurological disorder, most commonly expressed in motor of vocal tics that affects as many as 28,000 children and families throughout New Jersey. Aside from providing support to those with TS, NJCTS has established the world’s first TS DNA Sharing Repository, and the world’s first student-run stand-alone TS Clinic- both at Rutgers University.
Dr. King is taking part in the genetic study of Tourette Syndrome and on September 19th he will present recent clinical advances in medication and other state-of-the-art treatments for Tourette Syndrome and other associated disorders. Dr. King will answer questions and describe the ongoing genetic research study by NJCTS.
Dr. King wills Medical Director of Tourette/OCD/Anxiety Disorder Clinic at the Yale University Child Study Center where he is also Professor of Child Psychiatry. He is the author of numerous scientific papers and wrote the American Academy of Child and Adolescent Psychiatry’s Practice Parameter on Assessment and Treatment of Childhood OCD.
Visit www.tourettesyndromeresearch.org for more information.
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Tags: add, adhd, DNA, genetic research, neurological disorder, new jersey center tourette syndrome, ocd, Robert A. King, sharing repository, Tourette Syndrome, tourette syndrome nj, tourette syndrome treatments, tourette's syndrome, TS
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