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Huntingtons Disease:     more books (100)

Cell Transplantation for Huntington's Disease (Medical Intelligence Unit) by Paul R. Sanberg, Klas Wictorin, et all 1994-08 Fetal nerve cells transplanted into brain of Huntington's disease patient appear to have survived.(Brief Article): An article from: Transplant News Huntington disease: An entry from Thomson Gale's <i>Gale Encyclopedia of Neurological Disorders</i> by Deepti, MS, CGC Babu, 2005 The Neurobiology of Huntington's Disease (Frontiers in Neuroscience) by Donald C. Lo, Robert E. Hughes, 2008-09-15 Report : Commission for the Control of Huntington's Disease and Its Consequences Volume I - Overview October, 1977 : DHEW Publication No. (NIH) 78-1501 by Marjorie (Chairperson) & Wexler, Milton (Vice Chairperson) Guthrie, 1977 Speech intelligibility in ALS and HD dysarthria: the everyday listener's perspective.(amyotrophic lateral sclerosis)(Huntington disease): An article from: ... of Medical Speech - Language Pathology by Estelle R. Klasner, Kathryn M. Yorkston, 2005-06-01 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 Arithmetic word-problem-solving in Huntington's disease [An article from: Brain and Cognition] by P. Allain, C. Verny, et all 2005-02-01 Drug for Huntington's-related chorea deemed approvable.(News): An article from: Family Practice News by Elizabeth Mechcatie, 2006-05-15 Drug Combo Studied for Slowing Huntington's.: An article from: Family Practice News by Sherry Boschert, 1999-05-15 Molecular and Cell Biology of Neuropsychiatric Diseases (BT Telecommunications Series) A Manual Of Diseases Of The Throat And Nose by Francke Huntington Bosworth, 2007-07-25 Huntington's disease : hope through research (SuDoc HE 20.3502:H 92/998) by Stephanie E. Clipper, 1998 Huntington's disease: Hope through research (NIH publication ; no. 98-49) by Stephanie E Clipper, 1998

lists with details

61. Huntingtons Disease Association
    huntingtons disease Association 114 Victoria Road Beverley North HumbersideHU17 8BJ Tel 01482 886135 Contact Malcolm Bloomfield  
    http://www.dialdoncaster.co.uk/supgrops/locgroup/loc73.htm

62. Huntingtons Disease
    directory of community organisations. huntingtons disease Association(Dorset) huntingtons disease Association (South East Hampshire).  
    http://www.sswhha.org.uk/istcclr/ixx410.html

63. Research Projects - Huntington Disease -Genetic Testing
    Huntington Disease Testing Centers For more information about testing inyour area contact The huntingtons disease Hotline @ 1800-345-HDSA.  
    http://www.iupui.edu/~medgen/research/hd/genetic_testing/testing_centers1.html

64. Research Projects - Huntington's Disease - Genetic Testing
    More Facts About Finding the HD Gene, DNA Banking and Genetic Testingfor huntingtons disease WHAT DOES THIS MEAN FOR ME? In the  
    http://www.iupui.edu/~medgen/research/hd/genetic_testing/facts_about _testing2.h
    
    Extractions: More Facts About Finding the HD Gene, DNA Banking and Genetic Testing for Huntingtons Disease WHAT DOES THIS MEAN FOR ME? In the immediate future, there will be no changes. The methods for diagnosing and treating HD will remain the same. However, with continued investigation, many new possibilities will arise. Finding the gene is expected to simplify the testing process. Until now, many blood specimens from specific family members were necessary in order for an at-risk person to undergo presymptomatic testing. Now that the gene has been located, a two step testing process has been proposed. First, an affected family member's sample will be tested for the presence of the HD gene. Second, if, in fact, the gene is present (meaning HD was the correct family diagnosis), then the at-risk person who desires to know whether or not he too has inherited the gene, could be tested for its presence. Thus, it is our recommendation that families continue to store DNA on persons who are presumed to have HD. Of course, genetic testing for Huntingtons Disease remains a personal decision which should be considered very carefully. Although the test may be technically less complex, the personal implications remain the same and are substantial. Our recommendation is that anyone seeking genetic testing do so only through programs in which protocols for testing have been submitted to the Huntingtons Disease Society of America and which are known to have reputable pre-test and post-test counseling programs.

65. Huntington's Disease Advocacy Center - Community Calendar
    Each Tuesday, 800pm EST the wee hours of the morning, huntingtons disease SupportClub. Each Saturday, 500pm-800pm EST, huntingtons disease Support Club.  
    http://www.hdac.org/calendar/index.php
    
    Extractions: Web Site: www.bikeforthecure.org This year's ride will be "HD Ramble 'Round the Colonies," a bike tour through New England into Ohio. It will start in New Hampshire on Friday, April 26 and end Thursday, May 30 in Columbus, Ohio. We will ride through Boston, New York City, Philadelphia, Baltimore, and Pittsburgh as main cities. Want more information? 5th annual Trapshoot for Huntington.

66. Genometech.com - View Article
    The query I used for this article is huntingtons disease AND (mice Title/Abstract OR mouse Title/Abstract OR murine Title/Abstract).  
    http://www.reeltwo.com/news/genomeTech2.html
    
    Extractions: Article Date: 1/1/2003 Text Mining: Help is On the Way Poor Dataslave. We’ve all been there, trying to cull a few interesting documents from a large pile of boring ones. The only solution, until recently, was brain grease: read every document — the abstracts, anyway — and make a judgment call. But that’s starting to change. Software vendors have felt our pain and are busily at work crafting new products that automate literature searching. There are many choices: Some products try to understand the content; others try to learn what you’re looking for by watching you classify a small number of examples; some analyze the entire literature, creating yet another database for you to search; others work on subsets that you select; others build on top of these products and let you combine analyses from multiple tools. There are some open-source packages, as well. Dataslave needed some help, so I grabbed one product and two open- source tools and went to work. Before long, I had the answer and some confidence that it was right. The software helped and I’m glad I had it, but it wasn’t as easy as I hoped.

67. Huntington's Disease Memorial Quilt
    transporting the quilt. For information on obtaining the quilt for ahuntingtons disease event, please contact Jean Miller. A Display  
    http://endoflifecare.tripod.com/huntdisscholarshipfund/id15.html

68. Research - Where Are Your $$ Going?
    protein. Cell Death in HD huntingtons disease, Current Research. Scientists HD.huntingtons disease, Current Research continued. Imaging  
    http://endoflifecare.tripod.com/huntingtondiseasesupport/id177.html
    
    Extractions: Huntington's Disease Support Information Research - Where Are Your $$ Going? Home Index~HD Search Section 1 General Information Section 2 HD Specific ... Index~HD Search For any one who may wonder what is being done with all the $$$ donated for Huntington's Disease research, you might just want to check out a few of the areas where those hard earned dollars/donations have been spent in the past 5 years. but for therapeutic treatment for the symptoms of Huntington's Disease too. The links on the right is only one website's listing on Huntington's Disease research. I know there has been a lot more research which may not be included here. I, for one, will continue to support HD RESEARCH.....as well as Family services! Five Years of Research Please note that in most of the categories included on the following links the ref-erences are sorted with respect to publication date, and are listed from the latest to 1998.

69. Inspiration 2002 Event - About Huntingtons Disease
    Select a link.  
    http://www.v-net.com/haltipper/inspiration2002/html/about_huntingtons_disease.ht
    
    Extractions: Canadian Association of Professional Speakers Click here to Play - Real Player Windows Media Quick Site Navigation Select a link Home About Huntingtons Disease 6 Speakers Program Information Become an Official Sponsor Register Media Information Volunteer Opportunities Organizing Commitee Official Sponsors June 14th - Click Here To Register Now Warren and Arlene Evans’ daughter Laura lost her battle with Juvenile Huntington disease in Oct. 2001, at 28 years old. Huntington’s is an inherited, ‘neuro-degenerative’ genetic brain disorder, impacting about 185,000 people in North America. It causes brain cells to start dying around age 30. This leads to a steady deterioration in both mental and physical abilities, ending eventually in total incapacitation. There is no treatment, and it always proves fatal, usually by the mid-40’s. The Laura’s Hope Fund: Early in 2001, Warren and Arlene realized that a series of recent research breakthroughs had brought the dream of finding a treatment within reach in the immediate future.

70. SpotJockey.co.uk - The UKs Co-op Search Engine And Directory
    DIRECTORY, add your website to this category. Sites listed in Health ConsumerSupport Groups huntingtons disease . No links in this category at the moment.  
    http://www.spotjockey.co.uk/portal/html/Health/Consumer_Support_Groups/Huntingto

71. Huntingtons Disease
    The Geoff Brown Charitable Trust donated £500 to huntingtons disease Asscociation(Cumbria Branch) and wishes them well for the future. Back to Home Page.  
    http://freespace.virgin.net/iain.r/Johnh.html
    
    Extractions: The Geoff Brown Charitable Trust "here to help local people with local money" The game played was the first volume in a series of five adventures, which together form the Doomstones Campaign. The adventure is a search to find the resting place for an ancient magical artefact and then to stop the forces of evil from uniting the artefacts and using them to overrun the world. The game was played from 10.00am to 4.30pm and the chill of the day kept everyone focused on the job in hand. John Horner, the organiser said " A big thanks also to all the players that gave up their time not only on the day but also in the planning of the day ." Back to Home Page

72. Mioti: Medical Condition
    Condition huntingtons disease. BrainTalk Communities. huntingtons diseaseMenu. This is a webforum to discuss and comment on huntingtons disease.  
    http://www.mioti.com/cat/condition/condition.asp?Cat=Huntingtons

73. Huntington And Disease
    Updated 200206-20 huntingtons disease Society of America 158 West 29thStreet, 7th (800) 345-HDSA FAX (212) 239-3430 The Huntingtons  
    http://www.childplacementhelp.com/history-book-from-penguin-book.htm

74. Scirus.com
    huntingtons disease. S. Results and Future Research The signaling compound,chitosan, stops pathogen and activates the plant immune system.  
    http://www.scirus-topics.com/huntingtons_disease_ole.html

75. FAST: Organisation Details
    Organisation Details. Organisation Name, huntingtons disease Association. OrganisationType, Societies/Associations. Address, 108 Battersea High Street. Town, London.  
    http://www.fastuk.org/organisation_details.php3?Ref=1855

76. Huntington Disease Resource Centre
    Camps huntingtons disease; Crisis intervention - huntingtons disease; Huntingtonsdisease; huntingtons disease - Recreation; Residential camps; Summer camps.  
    http://www.harmreduction.ca/services/H_813.html
    
    Extractions: Access Wheelchair accessible building including main entrance but not washrooms Description Referrals for medical diagnosis and treatment, psychological and psychiatric counselling assists in arranging social, recreation and support services to help individuals remain in the community assists in arranging long term care education, consultation, literature newsletter counselling crisis intervention discussion groups day program of social activities summer camp program for persons residing in community operated by Huntington Society of Canada local volunteer chapters including Toronto Subjects Home Index First Previous ... Search the site Harm Reduction Recent Changes Site Warnings Who are we info@harmreduction.ca

77. PALS
    Room 10 41 Bridge Street Hereford, Tel 01432 270050. TO TOP. HuntingtonsDisease National huntingtons disease Association, Tel 0207 2237000. TO TOP.  
    http://www.infoinherefordshire.org.uk/pals/h.htm

78. Map Of Huntingtons Disease Association CH646UY
    QUICKSEARCH. Albania.  
    http://uke.multimap.com/map/browse.cgi?pc=CH64 6UY&title=Huntingtons Disease Ass

79. [AP-Bio] Huntingtons Disease-casey
    APBio huntingtons disease-casey. Casey 0600 Previous message AP-BioQuizes; Next message AP-Bio huntingtons disease-casey;  
    http://lists.isd197.org/pipermail/apbio/2002-December/000175.html

80. [AP-Bio] Huntingtons Disease-casey
    APBio huntingtons disease-casey. Meg 0600 Previous message AP-Biohuntingtons disease-casey; Next message AP-Bio steroids-casey;  
    http://lists.isd197.org/pipermail/apbio/2002-December/000180.html
    
    Extractions: Mon, 23 Dec 2002 23:18:23 -0600 Previous message: [AP-Bio] huntingtons disease-casey Next message: [AP-Bio] steroids-casey Messages sorted by: [ date ] [ thread ] [ subject ] [ author ] Previous message: [AP-Bio] huntingtons disease-casey Next message: [AP-Bio] steroids-casey Messages sorted by: [ date ] [ thread ] [ subject ] [ author ]

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