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         Huntingtons Disease:     more books (100)
  1. Walking the tightrope: Living at risk for Huntington's Disease by Randi Jones, 1996
  2. Toward a fuller life: A guide to everyday living with Huntington's disease by Eileen Werbel, 1990
  3. Hanging in the Balance: In Search of My Inner Soul, Living with Huntington's Disease by ArvaD. Brackins, 1998
  4. Advances in Neurology Volume 23 Huntington's Disease by Thomas N./Wexler, Nancy S./Barbeau, Andre Chase, 1979
  5. Afraid: A book for children "at risk" for Huntington's disease by Michelle Hardt Thompson, 2002
  6. A description of selected speech characteristics in Huntington's disease by Douglas J Anderson, 1988
  7. Metamemory in Parkinson's Disease by Lynn DellaPietra, 1995
  8. The history of Huntington's chorea in the United States of America by Russell N DeJong, 1973
  9. Great Britain and the early history of Huntington's chorea by Macdonald Critchley, 1973
  10. Huntington's chorea: A booklet for the families and friends of patients with the disease by David Lawrence Stevens, 1975
  11. Plasma choline and cholinergic mechanisms in the brain: Methods, functions and role in Huntington's chorea (Acta physiologica scandinavica. Supplementum) by Sven-Åke Eckernäs, 1977
  12. The form and functions of the central nervous system. An introduction to the study of nervous diseases. Foreword by George S. Huntington. by Frederick (1875-1938) & Henry Alsop RILEY (1887-1966). TILNEY, 1923
  13. Huntington's Chorea by Michael R. Hayden, 1981-10
  14. Man, Moral And Physical Or, The Influence Of Health And Disease On Religious Experience by Joseph Huntington Jones, 2007-07-25

101. Huntington's Disease Links
Ask Jeeves Links to Huntington s disease Resources is an outstanding compilation of Huntington s disease Advocacy Center is a wonderful new site by HD
http://carmenleal.com/WS/Faces/hdlinks.html
Huntington's Disease Links

102. New Insights Into How Huntington's Disease Attacks The Brain
Scientific theory holds that Huntington s disease (HD) is caused by a mutant protein that arises within brain cells and kills them, triggering the genetic
http://www.medicalnewstoday.com/medicalnews.php?newsid=23855

103. Molecular Trigger For Huntington's Disease Found
Researchers have discovered a key regulatory molecule whose overactivation by the abnormal protein produced in Huntington s disease (HD) causes the central
http://www.medicalnewstoday.com/medicalnews.php?newsid=27037

104. CureHD Foundation; Creating Awareness And Fund-raising To Cure Huntington's Dise
Help eradicate Huntington s disease by funding research to cure this genetic illness; killing over 100000 people and destroying their families.
http://www.curehd.org/
- CureHD Foundation -
Dedicated to funding a cure for Huntington's Disease.
Robert Bishop
Introduction

HD family tree

Why I do this

Family photos

What is HD?
Definition

The HD secret

How many have HD

The cruelest illness
The HD nightmare My experience Other experiences HD research Hope for a cure North America How can I help? Make a donation Contact the media Ask legislators... I need your help Contact info CureHD Foundation CureHD sponsors HD web sites Other info Content © 1999-2003 CureHD Foundation www.curehd.org Last updated: Mar 13, 2003 huntington's disease huntington's disease huntington's disease huntington's chorea huntington's chorea huntington's chorea huntingtons disease huntingtons disease huntingtons disease huntingtons chorea huntingtons chorea huntingtons chorea huntington disease huntington disease huntington chorea huntington chorea hd, hd, hd, hd, hd hd, hd, hd, hd, hd (50% at-risk for HD) (50% at-risk for HD) (50% at-risk for HD) (50% at-risk for HD) (50% at-risk for HD) (Bishop Family) PLEASE HELP ME SAVE MY KIDS!!!

105. Huntington's Disease ACEi Treatment
We report on a woman with Huntington s disease whose condition deteriorated dramatically during treatment with the angiotensin converting enzyme inhibitor
http://hdlighthouse.org/treatment-care/treatment/drugs/related/updates/0056acei.
New to the Huntington's Disease Lighthouse:
Welcome, start here
Beginners Search Treatment Now ... EPA-DHA
Drugs Related
Haldol
bench
human
...
human
Huntington's disease ACEi Treatment HD Lighthouse Contributing Editor's Comment: GenoMed is currently recruiting HD patients for trials of it's angiotensin converting enzyme inhibitor (ACEi). A drug that is generally safe may not be safe for Huntington's disease (HD). It is good science to test candidate drugs for the treatment of HD with lab animals first . Jerry
Posted to the HDL: 10 Jul 2003
Huntingtons disease: deterioration in clinical state: during treatment with angiotensin converting enzyme inhibitor
We report on a woman with Huntington's disease whose condition deteriorated dramatically during treatment with the angiotensin converting enzyme inhibitor captopril and improved on withdrawal of the drug.
Case report
A 47 year old woman who had been diagnosed eight years earlier as suffering from Huntington's disease was admitted to hospital, for control of newly diagnosed hypertension (210/120 mm Hg). She had previously been managed at home with haloperidol l'5 mg.thrice daily. On examination she walked without help and had typical features of Huntington's disease, with diffuse involuntary choreiform movements, facial apraxia, and inability to protrude her tongue for longer than five seconds. Her higher mental functions were impaired, although she could communicate and follow simple commands. She was otherwise medically well and had no clinical features of end organ damage due to hypertension.

106. LAX-101 AND HUNTINGTON'S DISEASE: QUESTIONS AND ANSWERS
Huntington s disease Questions and answers about LAX101, the first statistically significant treatment for Huntington s disease in phase 3 clinical
http://hdlighthouse.org/treatment-care/treatment/drugs/lax101/human/updates/0033
New to the Huntington's Disease Lighthouse:
Welcome, start here
Beginners Search
Treatment Now
... EPA-DHA
Drugs Related
Haldol
bench
human
...
human
HD Lighthouse Editor's Comment: LAX-101 treats HD, not just the symptoms but the disease itself. The active molecule in LAX-101 is Eicosapentaenoic Acid (EPA). All molecules of EPA are identical. The molecules of EPA found in LAX-101 are identical to the molecules of EPA found in fish oil food supplements. There is no scientific support for the belief that any molecule produced by a cold water fish is harmful to humans. There is scientific support that other molecules in fish oil are beneficial to humans. The importance of essential poly-unsaturated fatty acids (PUFA’s), found in fish oil, as dietary supplement has become well established since their beneficial effects were described in the late 1920’s. Unlike the bread mold Penicillium, fish oil supplements are available in commercially pure and assayed form. LAX-101 bears the same sort of relationship to fish oil as does pure vitamin C to oranges, in the sense that LAX-101 and vitamin C each represent a purified, refined and tested pharmaceutical product derived from a natural source. Laxdale has developed and proven a prescription drug to treat HD. With FDA approval this will enable medical workers and insurance companies to bring treatment to suffers of HD. This is great news for the HD community. See

107. SupportPath.com: Huntington's Disease
SupportPath.com leads you to Internet resources for supportrelated information on hundreds of health, personal, and relationship topics.
http://www.supportpath.com/sl_h/huntingtons_disease.htm
Huntington's Disease
Also called: HD, Huntington's Chorea Other topics of interest on SupportPath.com:
Dementia
Rare Disorders About Us Add-A-Link ... here
Online Communities / Message Boards...
  • Braintalk Communities: Huntingtons Disease
    Website:
    Description:
    A part of the BrainTalk Communities website. Registration is required to post to this message board.
    Date Added: 06/06/2002
Online Chats...
Note: Regularly scheduled chats are listed on our NEW Online Events Calendar
Links in this section are primarily to chat rooms open 24/7 which may or may not be moderated.
  • None Listed
Usenet Groups...
Note: Your browser must be properly configured to access Usenet groups from this site.
  • None Listed
Mailing Lists...
  • None Listed
National / International Organizations...
  • INTERNATIONAL
    International Huntington Association (IHA)
    Website:
    Description:
    The IHA is "a federation of national voluntary health agencies that share common concern for individuals with Huntington's Disease (HD) and their families". Website had numerous HD articles
    Date Added: 07/11/2002
  • BELGIUM
    HUNTINGTON LIGA Website:
    http://www.huntingtonliga.be/

108. Huntington's Disease - Swedish Medical Center, Seattle, Washington
Huntington s disease Swedish Medical Center, Seattle, Washington.
http://www.swedish.org/14448.cfm
PDF Version Search Send-to-Friend Health Library Home ... Conditions InBrief
Huntington's Disease
(Huntington's Chorea)
by Rick Alan Definition Causes Risk Factors ... Organizations
Definition
Huntington's disease (HD) is an inherited disorder that affects the brain. HD causes slow, progressive degeneration of nerve cells in certain areas of the brain. Eventually, HD results in:
  • Abnormal body movements Gradual deterioration or loss of intellectual abilities (dementia) Behavior problems
The disease is named for George Huntington, the physician who first described the condition in the 1870s.
Causes
HD is caused by a faulty gene on the #4 chromosome. All people who inherit the faulty gene will eventually develop HD.
Risk Factors
A risk factor is something that increases your chances of getting a disease or condition.
  • Family members with HD. Each person whose parent has HD has a 50% chance of inheriting the disorder. Age: Onset of symptoms on average 35-50.
Symptoms
Symptoms are mild at first and are often barely noticeable. Symptoms usually worsen over a 15-20 year period. Physical symptoms may include:
  • Abnormal body movements that worsen over time, including:

109. Huntington Disease
Huntington disease is going to serve as our prototype. Huntington is a dominantly inherited disorder. It is a disease of brain cells, a loss of neurons,
http://www.accessexcellence.org/AE/AEPC/BE02/zanko/huns3.html
Huntington Disease is going to serve as our prototype...
for more discussion into the nuances of what we're here for today because it is a single gene disorder for which we have DNA prediction of a disease in a healthy individual. You're going to hear me say the prediction word throughout the afternoon because that is the difference. Huntington is a dominantly inherited disorder. It is a disease of brain cells, a loss of neurons, which results in an array of changes. You have a handout that lists many of the changes, looking at the physical changes, the intellectual and the emotional/behavioral. I try to present many things, which unfortunately may change the essence of the person over time. In fact, the physical changes are often the things that the people find the least disturbing. It's the dementia and most of all the behavioral and emotional changes that are so disturbing to my families. The causative gene is at the distal end of the short arm of chromosome 4. It is one of the CAG-trinucleotide repeat mutations. If there are less than 30 repeats, that's OK. 40 or more, absolutely, without question if you live long enough, you will get Huntington. It's not a susceptibility, it's not a percentage, it's an absolute. Again, the

110. Huntington Disease Unit
Hartwyck Centers Nursing, Convalescent Rehabilitation center is a network of three nonprofit, long-term care facilities located in central New Jersey
http://www.solarishs.org/hartwyck/hun_disease_unit.html
Huntington's Disease Unit
Solaris Health System

e-mail: webmaster@solarishs.org
Hartwyck Home
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