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Clinical Trials

 

The link to the HYP HOP study on clinicaltrials.gov:

http://clinicaltrials.gov/ct/show/NCT00494507?order=1


 

Link to HypHop advertisement in PDF format

Dichlorphenemide for Periodic Paralysis

 


 

ADVERTISEMENTS FOR MUSCULAR DYSTROPHY ASSOCIATION (MDA)

Episodic Ataxia

Subjects 5 years and older with episodic ataxia are being recruited for a 3-year longitudinal, natural history study. This is a multicenter study sponsored by NIH. There is no charge and airfare will be covered. Principal Investigator is Robert C. Griggs, MD, University of Rochester Medical Center, Rochester, NY 14642. For further information, call Kim Hart at 585-275-3767.




Andersen-Tawil Syndrome

Subjects 10 years and older with Andersen-Tawil syndrome are being recruited for a 2-year longitudinal, natural history study. This is a multicenter study sponsored by NIH. 7 centers are participating in the United States, Canada and England. Principal Investigator is Rabi Tawil, MD, University of Rochester Medical Center, Rochester, NY 14642. For further information, call Kim Hart at 585-275-3767.




Nondystrophic Myotonias

Subjects 5 years and older with nondystrophic myotonias are being recruited for a 3-year longitudinal, natural history study. This is a multicenter study sponsored by NIH. There is no charge and airfare will be covered. Principal Investigator is James Cleland, MD, University of Rochester Medical Center, Rochester, NY 14620. For further information, call Kim Hart at 585-275-3767.


 


 

Andersen-Tawil Syndrome Study

 


 

Public Clinical Trials for Periodic Paralysis at Clinical Trials.gov

 


 

NIH has established a new Web page for the Rare Diseases Clinical Research Network. See link to Consortium for Clinical Investigation of Neurological Channelopathies (CINCH) for active Periodic Paralysis Research Projects.



Announcing Studies for Episodic and Neurodegenerative Diseases
Date: 5/2/2004


Dr. Ying-Hui Fu and Dr. Louis Ptacek from the UCSF Department of Neurology are performing studies to learn more about episodic diseases. These studies are aimed at identifying genes causing these diseases. Ultimately we hope to develop more effective patient treatments through a better understanding of the genes associated with these disorders.
We are currently enrolling patients suffering from periodic paralyses, Andersen-Tawil syndrome and restless leg syndrome.

Learn more at: http://www.ucsf.edu/humgene/

Or Contact:
Beatrice Sorensen
Clinical Coordinator
University of California San Francisco
Department of Neurology
1550 4th Street
Mission Bay 19B - Rm #546
San Francisco, CA 94143-2922

Email: bsoren@itsa.ucsf.edu

 

 


 

Andersen-Tawil Syndrome Study (UCSF)
Date: 2/8/2004
ATS is a condition characterized by periodic paralysis, cardiac arrhythmias and occasional other features such as cleft palate and scoliosis. For more information, see: Andersen-Tawil Syndrome in the Judy Tuttle Memorial Research Library.


Dear Patient,
Dr. Grace Yoon, Dr. Joel Kramer, Dr. Bruce Miller, Dr. Magnus Dias Da Silva and Dr. Louis Ptacek of the Neurology Department at the University of California San Francisco (UCSF) are conducting a study to learn more about Andersen Syndrome (also called Andersen-Tawil Syndrome or ATS), and we would like to invite you to participate.

We would like to invite you and one of your siblings to San Francisco for three days for this study, and we will provide travel and accommodation. If you have ATS the study procedures involved are:


A detailed medical and family history, and quality of life assessment using the SF-36 questionnaire.
A detailed external physical examination.
Clinical photographs.
X-rays of your limbs, chest, back and head.
A 24-hour Holter monitor (a small pouch worn around your neck or waist for 24 hours).
EEG with photic stimulation (electrodes attached to the surface of your scalp for 30 minutes). You will be exposed to a flashing light with your eyes closed for several minutes. This does not involve needles or invasive procedures.
Blood tests to evaluate your general health and thyroid function.
If you have not had genetic testing for ATS, we will do this, and will provide you with genetic counseling.
Neuropsychological tests which will test aspects of your memory, cognition and behavior. Some of these will be paper and pencil tests and others may be computerized.
If you are a sibling of someone with ATS you will participate in the neuropsychological testing only.

Participation in this study is completely voluntary, and will require your permission. If you are interested in participating in this study please contact us, and we will send you more information.

Study Contact:

Grace Yoon, MD, FCRP(C), FCCMG
Neurogenetics Fellow
Department of Neurology
505 Parnassus Ave., Box 0114
San Francisco, CA
94143-0114

(415) 502-3976

email: gyoon@itsa.ucsf.edu


 


http://clinicaltrials.gwww.itcmed.com


 

Andersen-Tawil Syndrome Stem Cell Research by Dr. Jonathan Lu

My name is Jonathan Lu and I am a clinical cardiologist who specializes in heart rhythm disorders at Columbia University Medical Center. I am also a scientist with special interests in heritable arrhythmias. I plan to attend the upcoming Periodic Paralysis Association Conference and wanted to let the attendees with ATS know that there will be opportunity to further ATS research by donating some skin cells at the conference. We think this represents an important, unprecedented opportunity to advance our knowledge of ATS!

As most of you know, cardiac arrhythmia (heart beat irregularities) is an important feature of the Andersen-Tawil syndrome that can lead to dizziness, passing out, and even sudden death. Because of this, ATS is also considered one of the Long QT syndromes (LQT7).

Scientific studies have now led us to the knowledge that most ATS are caused by a mutation in a potassium channel called KCNJ2. This discovery has greatly enhanced our understanding of ATS, but many clinical and scientific mysteries remain. For example, why do families members who have the same gene defect present with different constellations of clinical syndromes? How exactly does the mutation cause heart rhythm disorders? What is the best antiarrhythmic drug for the treatment of ATS? How does the KCNJ2 mutation cause problem with muscle and bones?

In the clinical-scientific communities, we have been limited in our ability to research the answer to these questions, in large part due to our lack of access to relevant human tissues. In other words, we simply have not had access to patient’s heart, muscle, and bone tissues that will enable us to look closely at the exact consequences of the gene defects.

The great news is that now we have a way of creating heart, muscle, and bone tissues from skin cells! Some of you may have seen in the news that it is now possible to take skin cells from patients, grow them in a petri dish, and turn them into stem cells. Stem cells, especially patient-specific stem cells, are powerful tools for scientific studies because they have the potential of becoming any tissue in the body. Once we have stem cells generated from skin cells (they are called iPS cells, induced Pluripotent Stem cells), a potentially unlimited supply of heart, muscle, and bone cells will be available for research studies.

In the case of ATS, if you decide to donate some skin cells, we will produce stem cells in the laboratory, then turn them into heart cells. This means that we will be able to directly study your heart cells in the laboratory to ask important clinical and scientific questions that have previously been impossible.

I hope you will consider participating in our effort and I look forward to meeting you all at the conference! Please feel free to contact me with questions at  jl3365@columbia.edu, or 212-305-0055.