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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. Stem Cell Symphony: A Novel by Ricki Lewis, 2008-01-03
  3. Disgust in pre-clinical Huntington's disease: A longitudinal study [An article from: Neuropsychologia] by R. Sprengelmeyer, U. Schroeder, et all
  4. A Caregiver's Handbook for Advanced-Stage Huntington's Disease by Jim Pollard, 1999
  5. Huntington disease: An entry from Thomson Gale's <i>Gale Encyclopedia of Science, 3rd ed.</i> by Liz Marshall, 2004
  6. Fetal striatal cell transplants feasible for Huntington's disease but may not be helpful.(Brief Article): An article from: Transplant News
  7. Report: Commission for the Control of Huntington's Disease and Its Consequences. Volume II: Technical Report, October, 1977
  8. Media by Topic: Media About Zhou Tong, Media About Yue Fei, List of Dwarfism Media Depictions, List of Huntington's Disease Media Depictions
  9. A home program of speech therapy in Huntington's disease.(Clinical report): An article from: Journal of Medical Speech - Language Pathology by Cheryl L. Giddens, Anton E. Coleman, et all 2010-06-01
  10. Metabolon collaborates on biomarker study for Huntington's Disease.(High Q Foundation): An article from: BIOTECH Patent News
  11. Case studies: the price of silence. (Huntington's disease and ethics; includes commentaries): An article from: The Hastings Center Report by John C. Fletcher, Dorothy Wertz, et all 1990-05-01
  12. Gale Encyclopedia of Medicine: Huntington disease by Laith Farid Gulli M.D., 2002-01-01
  13. 21st Century Ultimate Medical Guide to Huntington's Disease - Authoritative Clinical Information for Physicians and Patients (Two CD-ROM Set) by PM Medical Health News, 2009-05-12
  14. Nutrition and Huntington's Disease, A practical guide--A multidisciplinary approach. (Book Reviews).(Book Review): An article from: Nutrition & Dietetics: ... of the Dieticians Association of Australia by Beth Rohrlach, 2002-12-01

41. Huntingtons Disease Association (South East Hampshire)
Organisation huntingtons disease Association (South East Hampshire) ContactMrs Trudi Smith Phone 01489 893842 Address 8 Bank Street Bishops Waltham
http://www.hants.gov.uk/istcclr/cch10820.html
Home Search Contacts A-Z Index ... Cousin is Hampshire County Council's directory of community organisations.
Want more information? Please contact the organisation direct.
About our maintenance policy Top of this page Hantsweb Homepage Search Cousin ...
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This page produced by the Hantsweb Team . Comments on Hantsweb should be sent to the Hantsweb Manager For more information on our services please contact Hampshire County Council Information Centres This page last updated on 25 March 2003. Hampshire County Council 2003. and Privacy Statement

42. ALS Treatment: Amyotrophic Lateral Sclerosis Lou Gehrigs Disease
muscular dystrophy treatment amyotrophic lateral sclerosis lou gehrigs disease musculardystrophy lou gehrig disease huntingtons disease als treatment als cure
http://www.enhancedlifesciences.com/index.shtml
Home Neuraegis Creatine Co Q10 ... Message Board
Enhanced Life Sciences is the nutritional leader in the fight against neurological and neuromuscular disorders. Our products are based on the latest clinical research developments and they have shown significant potential or proven benefit to neurological/neuromuscular wellness and longevity. This endeavor was undertaken due to an intimate experience with ALS and the accompanying awareness of the challenges and frustrations patients face. The founders of this company truly believe that their years and technical knowledge in a closely related industry could be brought together to generate a meaningful benefit to those who are interested in nutritional products with superior quality. Enhanced Life Sciences has pledged to contribute financially a portion of the revenue generated by the sale of every product to organizations dedicated to the search for cures of neurological/neuromuscular disorders. They include but are not limited to the following: the ALS Association, MSA, HDSA and the MDA. 75 Farmington Valley Drive Plainville, CT 06062

43. Re: Come Join Our New Huntingtons Disease Group -- H.D. Folks
Next Message Previous Message Date Posted 183333 12/03/02 Tue Author ShellyWendt Subject Re come join our new huntingtons disease group In reply to
http://www.voy.com/24875/14.html
VoyForums Homepage Create a New Forum Owner Login VoyForums News Help Desk VoyForums Exchange FAQ - Frequently Asked Questions Directory/Categories Search VoyForums Contribute: Support VoyForums Main index Post a new message Next Thread Previous Thread ... Previous Message
Date Posted:
18:33:33 12/03/02 Tue
Author: Shelly Wendt
Subject: Re: come join our new huntingtons disease group
In reply to: Lisa 's message, come join our new huntingtons disease group on 18:33:33 12/03/02 Tue
>Hi my name is Shelly and my dad has Huntingtons.
I hava an appointment December 12th 2002 to get tested.
I am not doing to well with all this.
I am 27 and I have 2 brothers 22 and 30.
my dad is 48 and already has signs. He knows he has it and is just waiting. He has attempted suicide severel times and he is a bad alcholic.
Well I would like to talk to somebody that is going through this like me. I think it would HELP!!! Next Thread Previous Thread Next Message Previous Message Replies: Post a reply to this message: Go post a new message HTML allowed in marked fields.

44. Come Join Our New Huntingtons Disease Group HD Folks
Thread Next Message Previous Message Date Posted 190421 09/05/02 Thu AuthorLisa Subject come join our new huntingtons disease group hi there my
http://www.voy.com/24875/8.html

45. Mourning Huntingtons Disease
Mourning HD. I'm sitting here now, with your words in my head; Echoingand screaming and glowing with pain. I feel alone and miserable
http://www.slayingthehddragon.com/mourn.html
Mourning HD I'm sitting here now, with your words in my head;
Echoing and screaming and glowing with pain.
I feel alone and miserable, nothing more than nothing.
I think that you should share my hurting,
Because it was you, after all, who caused it.
Outside it is raining. I don't know why.
How can it rain when I am feeling as I am?
Nothing should happen, nothing should change,
Because I see nothing; because I am nothing.
The earth is cleansed, but why? Butterflies should stop flying and squirrels should stop climbing.
Since you are gone, my life before. And all its components. But still, without you there is rain. I don't know why. The "how" of it eludes me; the where is lost. Flowers seem to be growing, even though it is winter. But then, maybe it isn't winter. It could be spring, and flowers could be dead. Without you, Or baffled; I know nothing, now. You see, you are gone, but it's still raining. Tomorrow it may be sunning, And the day after it may be fogging. I don't know. But even though you still crouch in my heart, saying "This was me,"

46. Huntingtons Disease Memorial Quilt

http://www.slayingthehddragon.com/37.html

47. 2003 Hoop-A-Thon For Huntingtons Disease

http://users.aol.com/hoopathon
You need a browser that can read frames. Try or Microsoft's IE Download page to download a more recent browser.

48. CheatHouse.dk - This Is Essay On Huntingtons Disease, An Essay
point for besvret. This is essay on huntingtons disease, an essaythat critically analyzes an argument about huntingtons disease,
http://www.cheathouse.dk/essay/essay_view.php/p_essay_id/12081

49. Huntington And Disease
Updated 200206-20 huntingtons disease Society of America 158 West29th Street, 7th A home page for huntingtons disease
http://www.bostoncommunitychoir.com/older-woman-free-anal-sex-gallery.htm

50. HUNTINGTONS DISEASE
What is huntingtons disease? huntingtons disease, HD is a devastating degenerativebrain disorder for which there is NO effective treatment or cure.
http://hss.fullerton.edu/womens/bredin/320f02/320f02webs/ms/ms1.html
What is Huntingtons disease? Huntingtons Disease, H.D. is a devastating degenerative brain disorder for which there is NO effective treatment or cure. JENNIFER JONES Dr. George Huntington first described this hereditary disorder in 1872, now H. D. is one of the more common genetic disorders. More than a quarter of a million Americans either have H.D. or are "at risk" of inheriting the disease from an infected parent. Some of the early synptoms may affect cognitive ability or mobility and include
  • mood swings
  • forgetfullness
  • clumsiness
  • involuntarytwitching asnd lack of coordination
As the disease progresses concentration and short term memory weaken and involuntary movement of the head and limbs will increase. The ability to walk, speak, and talk deteriorate. Eventually the person is no longer able to take care of themselves. Death is followed resulting from complications such as choking, infection and heart failure. click here for more info

51. Huntingtons Disease
To apply the knowledge that you have learned, you will be researching the geneticcondition know as huntingtons disease. How is huntingtons disease treated?
http://www.orcsd.org/staff/jmartel/Huntingtons Disease.htm
OVERVIEW As part of our unit on genetics we have studied how recessive, dominant and sex-linked traits are inherited. We have also looked at how a condition know as trisomy can occur during meiosis. To apply the knowledge that you have learned, you will be researching the genetic condition know as huntingtons disease. Using the internet , you will search for answers to a given list of research questions. PRODUCT The requirements of this project include: Completing note sheets that answers the list of research questions below. An informational booklet that conveys the information on the note sheets. RESEARCH QUESTIONS
  • Is huntingtons disease caused by a dominant, recessive or sex-linked gene? What are the chances of someone with huntingtons disease having a child with huntingtons disease? What is the only possible way to inherit huntingtons disease? What are the symptoms of huntingtons disease (include the age that these symptoms usually occur)? What causes these symptoms? How is huntingtons disease treated?
  • 52. Huntingtons Disease Informational Booklet
    disease has a child. The chances of a person with huntingtons diseasehaving a child with huntington's disease. A pedigree that shows
    http://www.orcsd.org/staff/jmartel/Huntington's Disease Informational Booklet.ht
    You will create an informational booklet to present the information that you have researched on a genetic condition. The booklet should contain the following: Cover The cover should include the following: The name of the genetic condition The student’s name The student’s section The date Illustration and text that give an overview of the contents of the booklet. Cover should be done on white paper that has been mounted on colored oak tag. Table of Contents Each page of the booklet should have a title and a page number. The table of contents should list these titles and page numbers. Pedigree and Explanation This section should include the following: An explanation of how the condition is inherited (dominant, recessive or sex-linked) A pedigree that shows the possible outcomes that could occur if a person with huntington's disease has a child. The chances of a person with huntingtons disease having a child with huntington's disease. A pedigree that shows the possible outcomes if a person with huntington's disease has a child with a person who has huntington's disease. The chances of 2 persons with huntington's disease having a child with huntington's disease.

    53. HACKERSONS HD LINKS
    Laycock was probably the first to realise the need for internet communication andinformation regarding huntingtons disease and set up his web page in 1995.
    http://www.hackers.demon.co.uk/links/hd.html

    HD.COM

    THE LIFT

    MAIN PAGE

    HELP!

    HD LINKS HD HOMEPAGES HD INFO (UK) Robert Laycock was probably the first to realise the need for internet communication and information regarding Huntingtons Disease and set up his web page in 1995. He is a member of the Huntingtons society of Canada's national internet commitee. He is very friendly and makes a mean cup of coffee! This is a very good place to start. Renette Davis is a librarian from Chicago and another pioneering web site owner. This site contains a huge library of resourses on Huntingtons Disease and is also a good place to start. The HD Lighthouse is owned by Jerry Lampson who lives in northern California. His 'lighthouse' contains an extensive database and search facilities for Huntingtons Disease and is a great place to conduct research for the latest news. Carmen Leal-Pock is an author, singer, speaker and caregiver for her husband David. She has written a... NEW ...book called 'Faces of Huntingtons'. Visit her homepage to order your copy. Julie's Homepage has been set up in the hope that young carers or people at risk have a chance to talk with others who understand and to help them find out more. Lou's Web Shana's Web Kym's Web Shirley's Web ... Growing Wild
    Deb's Web HDA North West Lancashire is a support group comprising of sufferers, carers, professionals, those at risk and supporters. They have close links to the 'Frank Gardham House' and a very good section for young carers.

    54. HACKERSONS HD.COM SPLASH
    HACKERSONS HD.COM huntingtons disease 'THE WORST CONDITION NOW KNOWN TO BEFALLA HUMAN BEING' Netscape 3/Explorer 3 or Higher. All Other Browsers.
    http://www.hackers.demon.co.uk/hd.html
    HACKERSONS HD.COM
    HUNTINGTONS DISEASE
    'THE WORST CONDITION NOW KNOWN TO BEFALL A HUMAN BEING' All Other Browsers. Latest: Hackersons are proud to anounce
    that they are now British agents for a new book
    called 'Faces of Huntingtons' by Carmen Leal Pock.
    Visit the 'Faces of Huntingtons' web site to order your copy NOW at:
    http://ddi.digital.net/~promo/faces.html
    Latest: Hackersons are pleased to anounce
    a new HD discussion forum made possible by MEDSITE
    For more information, click one of the links bellow.
    All Other Browsers.

    55. Huntingtons Disease
    huntingtons disease. Follow Ups Post Followup FAQ . Postedby Mary Boze on August 17, 19102 at 150042 Husband is terminally
    http://www.snowcrest.net/writers/help/3308.html
    huntingtons disease
    Follow Ups Post Followup FAQ
    Posted by Mary Boze on August 17, 19102 at 15:00:42: Husband is terminally ill w/huntingtons, need financial help for house/bills.
    Follow Ups:
    Post a Followup Name:
    E-Mail: Subject: Comments:
    : Husband is terminally ill w/huntingtons, need financial help for house/bills. Optional Link URL:
    Link Title:
    Optional Image URL: Follow Ups Post Followup FAQ

    56. Huntingtons Disease Assn - Rayleigh Support Group: Home Page
    huntingtons disease Assn Rayleigh Support Group. What Is Huntington’sDisease? It is a degenerative neurological disorder caused
    http://beehive.thisisessex.co.uk/default.asp?WCI=SiteHome&ID=185

    57. Huntingtons Disease Association
    huntingtons disease Association Merseyside Support Group 13 Croston AvenueRainhill L35 8QA Contact Margaret Moxon. Tel 0151 426 8858.
    http://www.knowsley.gov.uk/community/groups/huyton/sgsc/support42.html
    Huntingtons Disease Association
    Merseyside Support Group
    13 Croston Avenue
    Rainhill
    Contact: Margaret Moxon
    Tel:
    We exist to further the aims of Huntingtons Disease Association and to provide a local contact point for all sufferers, carers and those at risk to Huntingtons Disease who live in and around the Merseyside area.
    We meet at Jospice International, Ince Road, Thornton on the last Wednesday of each month between 7.30pm-10.00pm. For further information, please call the above number

    58. The Official Newsletter Of The HD Foundation
    To Receive Information From Us About The huntingtons disease. Either DealingWith The huntingtons disease Or Just Wants To Learn About The Disease.
    http://www.thdf.org/newsletter.html
    The Official Newsletter Of The HD Foundation Save The Future Of Tomorrow Today
    2002 Edition Cure Updates A preliminary study published on THE LANCET’s website today www.thelancet.com - outlines a surgical technique involving transplantation of fetal brain cells which could be of future benefit to people with Huntington’s disease. TAMPA Researchers at the University of South Florida have found that fetal tissue can survive being transplanted into the brains of patients with Huntington's disease, and that the transplanted tissue remains disease-free. The cover article of the March 31, 2000 issue of Cell, titled "Reversal of Neuropathology and Motor Dysfunction in a Conditional Model of Huntington's Disease," raised for the first time the possibility that HD might be reversible! While this work is still far from being applicable to humans, the basic discoveries are very exciting. To Receive Information From Us About The Huntingtons Disease. Either Email Us At

    59. Cowboys & Cowgirls - Informative Sites - United States & World Resources - Hunti
    huntingtons disease . huntingtons disease - Courtesy of SNAP. huntingtons disease- South Africa - Welcome to the South African Pages on Huntington's Disease.
    http://cyberrodeo.com/guysgals/riding4kk44.htm
    Huntingtons Disease -
    Facing Huntington's Disease -
    Huntingtons Disease -
    Courtesy of SNAP.
    Huntingtons Disease - South Africa -
    Welcome to the South African Pages on Huntington's Disease. Many interesting and helpful links.
    Return to United States and World Resources
    Return to Informative Sites

    Return to Riding for the Disabled

    Return to Cowboys and Cowgirls
    ... Return Home
    This site is being developed and maintained for CyberRodeo by
    ... when it's time to establish an Internet presence.

    60. Free-TermPapers.com - Huntingtons Disease
    huntingtons disease huntingtons disease is caused by the geneticallyprogrammed degeneration of brain cells, called neurons. Symptoms
    http://www.free-termpapers.com/tp/39/skx161.shtml
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