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         Huntingtons Disease:     more books (100)
  1. Three Models of Huntington's Disease: The Neuropathological Investigations of Transgenic Murine Models of Disease by Aysha S. Raza, 2010-08-02
  2. Huntington's Disease Medical Guide by Qontro Medical Guides, 2008-07-09
  3. Verbal episodic memory declines prior to diagnosis in Huntington's disease [An article from: Neuropsychologia] by the Predict-HD investigators of the Huntington Stu, 2007-01
  4. Remotivation Therapy and Huntington's Disease.: An article from: Journal of Neuroscience Nursing by Florinda R. Sullivan, Edward D. Bird, et all 2001-06-01
  5. Neuroprotection in Huntington's disease.(Second Messenger)(Disease/Disorder overview): An article from: Psychopharmacology Educational Updates (PsychEd Up) by Veronique M. Andre, 2008-10-01
  6. Huntington disease: a nursing perspective.(CE SERIES): An article from: MedSurg Nursing by Heater Skirton, 2005-06-01
  7. A comparison of picture description abilities in individuals with vascular subcortical lesions and Huntington's Disease [An article from: Journal of Communication Disorders] by A.M. Jensen, H.J. Chenery, et all
  8. Sexuality: The impact of Huntington's disease and Multiple Sclerosis on Partnership, Sexual Behavior and Body Image by Eva Schmidt, 2009-04-30
  9. Huntington Disease - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-17
  10. Handbook for Caring in Huntington's Disease
  11. Disgust and Huntington's disease [An article from: Neuropsychologia] by C.J. Hayes, R.J. Stevenson, et all 2007-01
  12. Sirna's collaborator publishes breakthrough research on Huntington's Disease.: An article from: BIOTECH Patent News
  13. Ripples from a stone skipping across the lake: a narrative approach to the meaning of Huntington's disease.: An article from: Journal of Neuroscience Nursing by Rose Rossi Schwartz, 2010-06-01
  14. Huntingtons Disease -- 2006 publication by Knowles, 2006

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Huntington's Disease
C2-8 battles the brain illness, mouse study shows
Dopamine-reducing med shows promise in mice
Finding may spur treatments for fatal nervous system disorder
Progressive neurological illness may stem from lipid overdelivery
Enzyme critical to maintenance of cell health could hold key, study finds
But researcher notes finding is preliminary
Researchers find link between competing theories of brain damage
Turning off gene in mice prevented damage of similar neurological disease How Nerve Cells Grow
Researchers discover protein that could help rebuild nerves after injury, disease Cell Malfunction Clue to Disease Study looks at one way that Huntington's disease affects brain nerve cells ajc.com Web Archives Kudzu.com document.forms[formName].elements['QueryText'].value = queryString; setCheckedValue(document.forms[formName].elements['searchby'], 'ys'); MOST POPULAR STORIES

62. Huntingtons Disease - Patient UK Resources
huntingtons disease also known as or related to huntingdon s, huntingtons, scottish huntington s association, huntington s chorea (disorder),
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huntingtons disease - also known as or related to huntington's chorea, huntington's disease association, huntington's chorea (disorder), huntington, hd - huntington chorea, scottish huntington's association Key = Information Leaflet = Patient Support = Reference Article = Medicine Info = Pharmacy Products = Selected UK Websites = Patient Experience = Book = Guideline = Poem/Story = Diagram = Medical Equipment = Video Links = Audio = News
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63. Huntington's Disease - Movement Disorder Clinic - The Nebraska Medical Center
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Huntington's Disease
Huntington's disease is a progressive, neurodegenerative disease that results in uncontrolled movements, emotional disturbances and mental decline. Huntington's disease always runs in families and does not skip generations. It is associated with a genetic mutation. Individuals have a 50 percent chance to inherit the genetic mutation from their parent, and if they inherit the genetic mutation, they will develop the disease. The disease affects both males and females and symptoms usually begin in middle age. Individuals who develop symptoms at an earlier age, are more likely to have more severe symptoms that progress more quickly.
Treatment
While there is no cure for Huntington's disease and it is ultimately fatal, there are medications that can be used to control some of the symptoms.

64. Huntingtons Disease: Term Papers Format, Term Paper Ideas, Term Paper Format, Cu
Ideas and guidelines for writing college term papers, sources for custom term papers topics. Write high quality essay and term paper on different topics.
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Huntingtons Disease This paper will explain what Huntington’s disease is. It will present a new protein treatment used in the disease and discuss its implications. Two sides of this protein treatment will be presented. As well the current controversy over the treatment and its implications on society will be examined. current research and professional articles and sources will be used.
  • Pages: 3 Bibliography: 2 source(s) listed Filename: 20679 Huntington's Disease Protein.doc

65. Huntingtons Disease - Definition From Biology-Online.org
Definition and other additional information on Huntingtons disease from BiologyOnline.org dictionary.
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Huntingtons disease An hereditary disorder with mental and physical deterioration leading to death . Although characterised as an adult-onset disease (as is usually the case), we have seen children with full-blown huntingtons disease
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67. Huntington's Disease News
Sign In; Ecards; Contribute; Contact; About; Health News; Home. Visit the Neurological Disorder News main page for more related topics.
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Huntington's Disease News Visit the Neurological Disorder News main page for more related topics. Our collaborative food blog, Eat This! features everything about food in relation to health, from folk remedies to clinical studies. Latest Story
July 14, 2004
Epilepsy Medicine, Lou Gehrig's Research, Huntington's Research Epilepsy sufferers in the UK were relieved this week to find out an important epilepsy drug would not be withdrawn from the market. Scientists have uncovered evidence that links Lou Gehrig's Disease (ALS) and a problem with the mitochondria Researchers have had some success in silencing a gene in mice that is similar to the one that causes Huntington's Disease in humans. More Recent Stories Web Health Diaries For breast cancer news, visit our Breast Cancer Blog , featuring the latest news and information on breast cancer. For lung cancer news, visit our Lung Cancer Blog , featuring the latest news and information on lung cancer.
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68. Breaking News On Huntingtons Disease
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Mutant Protein In Huntington's Disease Model Mopped Up By 'Intrabody'
published Mon, 26 May 2008 06:00:00 PDT
Scientists have created a tool for mopping up the clumps of mutant protein that drive neurodegeneration in Huntington's disease. Emory University researchers engineered a virus to make an intracellular antibody or "intrabody" against huntingtin, the protein whose mutant forms poison the brain cells of people with Huntington's.
Huntington's Disease: Researchers Develop First Transgenic Monkey Model
published Tue, 20 May 2008 03:00:00 PDT
Scientists have developed the first genetically altered monkey model that replicates some symptoms observed in patients with Huntington's disease, according to a new study funded by the National Institutes of Health. Researchers are now able to better understand this complex, devastating and incurable genetic disorder affecting the brain.
Onset Of Huntington's Delayed By Physical Activity In Mouse Model
published Tue, 01 Apr 2008 04:00:00 PDT

69. Huntingtons Disease
Huntingtons Disease. Q A from our Ask The Doctor Forums chance of having Huntingtons disease (Neurology and Neurosurgery Forum); do all gene carriers
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      Huntington's Disease
      C2-8 battles the brain illness, mouse study shows
      Dopamine-reducing med shows promise in mice
      Finding may spur treatments for fatal nervous system disorder
      Progressive neurological illness may stem from lipid overdelivery
      Enzyme critical to maintenance of cell health could hold key, study finds
      But researcher notes finding is preliminary
      Researchers find link between competing theories of brain damage
      Turning off gene in mice prevented damage of similar neurological disease How Nerve Cells Grow
      Researchers discover protein that could help rebuild nerves after injury, disease Cell Malfunction Clue to Disease
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71. Huntington's Disease T-shirts @ Support Tees - T-shirts And Gifts Of Awareness ¬
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72. Spotjockey.com Web Links Directory- Health > Consumer Support Groups > Huntingto
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73. Huntington's Disease | Evolutionism | Dr. Bob Melamede
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Huntington's Disease
Neurobiology of Disease
Volume 27, Issue 1
, July 2007, Pages 108-116
SummaryPlus
doi:10.1016/j.nbd.2007.04.012
Severe deficiency of the fatty acid amide hydrolase (FAAH) activity segregates with the Huntington's disease mutation in peripheral lymphocytes
Natalia Battista a b , Monica Bari b c , Alessia Tarditi d , Caterina Mariotti e , Anne-Catherine Bachoud-L©vi f , Chiara Zuccato d , Alessandro Finazzi-Agr² c , Silvia Genitrini e , Marc Peschanski g , Stefano Di Donato e , Elena Cattaneo d and Mauro Maccarrone a b
a Department of Biomedical Sciences, University of Teramo, Piazza A. Moro 45, I-64100 Teramo, Italy
b European Center for Brain Research (CERC)/IRCCS S. Lucia Foundation, 00179 Rome, Italy
c Department of Experimental Medicine and Biochemical Sciences, University of Rome √ʬĬúTor Vergata√ʬĬĚ, 00133 Rome, Italy
d Department of Pharmacological Sciences and UniStem √ʬĬď Centre for Stem Cell Research, University of Milan, 20133 Milan, Italy
e Division of Biochemistry and Genetics, Carlo Besta Neurological Institute, 20133 Milan, Italy

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      Huntington's Disease
      C2-8 battles the brain illness, mouse study shows
      Dopamine-reducing med shows promise in mice
      Finding may spur treatments for fatal nervous system disorder
      Progressive neurological illness may stem from lipid overdelivery
      Enzyme critical to maintenance of cell health could hold key, study finds
      But researcher notes finding is preliminary
      Researchers find link between competing theories of brain damage
      Turning off gene in mice prevented damage of similar neurological disease How Nerve Cells Grow
      Researchers discover protein that could help rebuild nerves after injury, disease Cell Malfunction Clue to Disease
      Study looks at one way that Huntington's disease affects brain nerve cells ctxt_ad_interface = 'http://cm.npc-cox.overture.com/js_1_0/'; ctxt_ad_width = 336; ctxt_ad_height = 280; ctxt_ad_source = 'npc_coxnews_wacotribuneherald_t1_ctxt'; ctxt_ad_config = '1435184754'; ctxt_ad_id = 'health'; ctxt_ad_type = ctxt_ad_id; /* ctxt_ad_url is set in the "yahoourl.js" script */ ctxt_ad_css = 'http://alt.coxnewsweb.com/wacotrib/css/yahoo_contentmatch.css'; HELPFUL TOOLS
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77. Huntington's Disease - Drug Companies - Pipeline Drugs -- Clinical Trials
pipeline drugs clinical trials - Biotechnology Stocks.
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A Resource Guide to Investing in Biotechnology Directory Encyclopedia Stock Index Pipeline Drugs Biotechnology Encyclopedia Huntington's Disease Huntington's disease or Huntington's chorea is an inherited disorder characterized by abnormal body movements called chorea , and loss of memory . The incidence is 5 to 8 per 100,000.
Short Summary
Genetics
The causative gene (one of the first identified to cause an inherited disease) is located on chromosome 4. Huntington's disease is inherited in an autosomal dominant fashion. The autosomal dominant fashion means that the a recipient of the gene only needs one allele to inherit the disease. Most genetic diseases are autosomal recessive meaning that they need two alleles to inherit the disease. The dominant nature of Huntington's disease increases the chance of the disease occuring in offspring. A parent who has the disorder have a 50% chance of passing on the gene with each child. The product of this gene is a 350KDa cytoplasmic protein called huntingtin . The continuous aggregation of huntingtin molecules in neuronal cells gives rise to cell death , especially in the frontal lobes and the basal ganglia (mainly in the caudate nucleus ) by some unknown mechanism. Huntingtin has a characteristic sequence of 40 or fewer

78. Huntington's Disease : More Conditions H : Conditions H - Mega Net
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Login Search Mega Net: Home Personal Health Conditions A-Z ... http://glaxocentre.merseyside.org/huntingtons.html Univ. of Chicago librarian offers a personal collection of HD resources. Link to documents, tips for daily living, support groups and recipes. http://www.lib.uchicago.edu/~rd13/hd/index.html Find chapter news and event announcements, as well as support group schedules. Shares a newsletter. http://www.geocities.com/hdsarmc/index.html http://www.angelfire.com/al/leonc/
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79. My ASEBP November Is Huntington√ʬĬôs Disease Awareness Month
November is Huntington’s disease Awareness Month. Huntington’s disease (HD) is an inherited neurological disorder named after the physician who first
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November is Huntington√ʬĬôs disease Awareness Month
Huntington√ʬĬôs disease (HD) is an inherited neurological disorder named after the physician who first described it in 1872. HD causes cells in specific areas of the brain to degenerate and die. These brain cells connect with other parts of the brain to help control body movements, emotions, thinking, behaviour and perception. As these brain cells die, people with HD are less able to control movements, recall recent events, make decisions and control emotions. Eventually this disease leads to disability and eventually death. Healthcare providers usually diagnose HD using neurological and psychological tests. Some use various brain scans, while others look to genetic testing to confirm diagnosis.

80. Huntington's Disease Health Topic - Medicine Online
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Attention, chocolate lovers: You may not be able to help yourselves. Swiss and British scientists have linked the widespread love of chocolate to a chemical "signature" that may be programmed into our metabolic systems.
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