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Huntingtons Disease:     more books (100)

The Official Patient's Sourcebook on Huntington's Disease: A Revised and Updated Directory for the Internet Age by Icon Health Publications, 2002-09-25 Living With Huntington's Disease: A Book for Patients and Families by Dennis Phillips, 1982-05 Huntington's Disease by Thomas N.;Barbeau, Andre;Wexler, Nancy S. Chase, 1979 Huntington's Disease - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References by Health Publica Icon Health Publications, 2004-01-05 Heading for Better Care: Commissioning and Providing Mental Health Services for People with Huntington's Disease, Acquired Brain Injury and Early Onset ... Health Advisory Service Thematic Reviews) by Dept.of Health, 1997-02 Cell Transplantation for Huntington's Disease (Medical Intelligence Unit) by Paul R. Sanberg, Klas Wictorin, et all 1994-08 Huntington's disease (Advances in neurology) Juvenile Huntington's Disease: and other trinucleotide repeat disorders Huntington Disease - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References by ICON Health Publications, 2004-03-31 LIVING WITH HUNTINGTON'S DISEASE! : A BOOK FOR PATIENTS AND FAMILIES by DENIS H PHILIPS, 1982-01-01 Early Warning: Cases and Ethical Guidance for Presymptomatic Testing in Genetic Diseases (Medical Ethics) by David H. Smith, Kimberly A. Quaid, et all 1998-11-01 A New Promise by Julie Eller, 2007-09-11 A Manual of Diseases of the Throat and Nose by Francke Huntington Bosworth, 2010-02-09 Molecular and Cell Biology of Neuropsychiatric Diseases (BT Telecommunications Series)

lists with details

21. Huntingtons Disease Information Page
    These are Links to very helpful resources on Internet Huntington s disease huntingtons disease Menu Huntington s Disease Society of America Support Groups and  
    http://www.euronet.nl/users/ragman/huntingtons.html

22. Encyclopaedia Topic : Huntingtons Disease, Section : Introduction
    huntingtons disease. Search. Now called Huntington’s disease, it affects about 1 person in 20,000 and occurs all over the world. It is an inherited condition.  
    http://www.nhsdirect.nhs.uk/en.asp?TopicID=249

23. Huntingtons Disease
    huntingtons disease. Home Page. Aging_7 Allergies_2 Ankylosing huntingtons disease Association Online HDA Online provides news of  
    http://www.artritis.net/links/huntingtonsdisease.html
    
    Extractions: These web site links are listed as a convenience to our visitors. If you use these links, we take no responsibility and give no guarantees, warranties or representations, implied or otherwise, for the content or accuracy of these third-party sites. Arthritis Problems? The Ideal Cancer Clinic Rejuvenate!! Top of page

24. HUNTINGTONS DISEASE RESEARCH ROSTER
    huntingtons disease RESEARCH ROSTER. What is the Huntington s Disease Research Roster? A research roster of huntingtons disease patients  
    http://www.hdfoundation.org/hdroster.html
    
    Extractions: What is the Huntington's Disease Research Roster? A research roster of Huntingtons Disease patients and families was established in 1979 at Indiana University in response to a recommendation from the Commission for the Control of Huntingtons Disease and its Consequences. The Roster is sponsored by the National Institute of Neurological and Communicative Disorders and Stroke. Because the cooperation and assistance of HD patients and families is vital to research, we are asking your help. The HD Research Roster computerizes the names of families, including information about the history of HD in the family (family trees) and other related data. This information identifies HD patients and families who are interested in participating in research projects. What does the Roster do? Many investigators are intrigued by Huntingtons Disease and are eager to work on the problem but need access to HD families. It is important to have a system whereby scientists and HD families can get in touch with each other. The Roster makes this happen by matching the scientist with the right research volunteers listed in the Roster. Some researchers only need statistical information while other special projects may require a sample of blood, urine or skin from HD family members. The people on the staff explain the particular research study to each individual or family. Then, if they are willing to participate and give written permission, the individual's family name and address are given to the investigator.

25. BrainTalk Communities - Huntingtons Disease
    Post New Thread. Threads in Forum huntingtons disease, Forum Tools, Search this Forum. Views 3,653 Announcement Donations to BrainTalk  
    http://brain.hastypastry.net/forums/forumdisplay.php?f=150

26. Coenzyme Q10 Info On Huntingtons Disease, Co Q10 Coenyzme
    Information on Coenzyme Q10 Supplements and Huntington s Disease. CoenzymeQ10 Huntington s Disease Huntington’s is an inherited  
    http://www.coenzymeq10supplement.com/Huntingtons-disease-coq10.htm
    
    Extractions: Huntington’s is an inherited genetic disease that destroys neurons in brain regions governing movement. Symptoms include involuntary movements, lack of coordination and cognitive difficulties. Huntington’s disease is thought to involve a bioenergetic defect. A pilot study conducted by Beal and associates showed that energy production in the central nervous system and muscle of Huntington’s disease patients is impaired. After two or more months of Coenzyme Q10 supplementation (360 mg per day), 83% of patients showed significant improvements in biochemical markers of energy production. See References back to top

27. Huntington's Disease
    huntingtons disease. huntingtons chorea. huntington chorea. huntingtons disease treatment. huntingtons disease society of america. disease house huntingtons light.  
    http://www.icongrouponline.com/health/Huntington's_Disease.html
    
    Extractions: (Artificial insemination; Chronic Progressive Chorea; Chronic progressive hereditary chorea; Degenerative Chorea; Hereditary Chorea; Hereditary Chronic Progressive Chorea; Huntington chorea; Huntington's chorea; Huntington's disease; Very Early Onset Huntington's Disease; Woody Guthrie's Disease) Revised and Updated for the Internet Age P A P E R B A C K Paperback Book Paperback Book Order by phone: 800-843-2665 (within USA) 1-201-272-3651 (from outside USA) Paperback Book Shipped in 3 to 5 business days E B O O K Electronic File * E-Book version sent via e-mail in 2 business days Electronic File *E-Book version sent via e-mail in 2 business days Pages Price $28.95(USD) ISBN Published Synopsis A comprehensive manual for anyone interested in self-directed research on Huntington's Disease. Fully referenced with ample Internet listings and glossary. Related Conditions/Synonyms Artificial insemination; Chronic Progressive Chorea; Chronic progressive hereditary chorea; Degenerative Chorea; Hereditary Chorea; Hereditary Chronic Progressive Chorea; Huntington chorea; Huntington's chorea; Huntington's disease; Very Early Onset Huntington's Disease; Woody Guthrie's Disease Description Table of Contents Introduction Overview Organization Scope Moving Forward PART I: THE ESSENTIALS Chapter 1. The Essentials on Huntington’s Disease: Guidelines

28. Huntingtons Disease
    Spot Health huntingtons disease - part of spot wot websites directory, 25 May. Health - huntingtons disease. Search huntingtons disease. Search. Help  
    http://www.spot-health.co.uk/diseases/huntingtons-disease.html

29. Huntington Disease
    Huntington disease. FATAL AUTOSOMAL DOMINANT DISORDER GENE IN CHROMO 4p16.3. Return to table of contents *see glossary. What Causes huntingtons disease?  
    http://www.angelfire.com/md/danil/hutington.html
    
    Extractions: DEGENERATION OF CHOLINERGIC AND GABAergic and ENKEPHALIN NEURONS IN THE BASAL GANGLIA AND THE CEREBRAL CORTEX [STRIATUM].Leading to increased activity of the inhibitory [GABAergic ] NEURONS FROM EXTERNAL GLOBUS PALLIDUS TO THE SUBTHALAMUS, WHICH CAUSES DECREASE IN THE GLUTAMATERGIC [EXCITATORY] NEURONAL ACTIVITY ON THE INTERNAL GLOBUS PALLIDUS. Result ia decreased inhibition on the thalamus, and the thalamus increases its excitatory [glutaminergic] effect on the cerebral cortex. Cause of the hyperkinesis. PROGRESSIVE SELECTIVE NEURAL CELL DEATH ASSOCIATED WITH:

30. Huntingtons Disease, Huntingtons Disease Picture, Disease Huntingtons Symptom
    Topics to inquire for huntingtons disease, huntingtons disease picture, disease huntingtons symptom, disease huntingtons information.  
    http://www.healthinquire.com/huntingtons-disease.html

31. HCMC - Huntingtons Disease
    Group home for Huntington s disease has HCMC connection huntingtons disease Society of America www.hdsa.org huntingtons disease Society of Minnesota Chapter www  
    http://www.hcmc.org/depts/hd/hdhome.htm
    
    Extractions: Hennepin County Medical Center is committed to finding a cure for Huntingtion's Disease (HD) while providing education and services to those affected by the disease and their families. We provide services and referrals to families trying to cope with the devastating effects of the disease, and educate the public and health care professionals about Huntington's Disease. We provide the vital link between the laboratory bench and the patient's bedside.

32. HCMC - Huntingtons Disease
    HD CLINIC SERVICES PROVIDED · Recruit, enroll coordinate HD studies · Member of HSG (Huntingtons Study Group) · Current Studies PHAROS, PREDICTHD, HD  
    http://www.hcmc.org/depts/hd/hdteam.htm

33. Huntingtons Disease Association
    Medical Helpsites. +, huntingtons disease Association, Address, Tel, Fax, Hernia Information, huntingtons disease Association, International Spinal Research Trust,  
    http://www.4ni.co.uk/listing.asp?cat=39&style=0&company=96567&level1=18

34. SupportPath.com: Huntington's Disease
    Braintalk Communities huntingtons disease Website http//neuromancer.mgh.harvard.edu/cgi-bin/forumdisplay.cgi?action=topics forum=Huntingtons+Disease number  
    http://www.supportpath.com/sl_h/huntingtons_disease.htm

35. Huntington's Disease - 28 Of The Best Sites Selected By Humans
    Huntington s Disease. CBEL Health ( 28 links, last update 12 April 2004 ) * = new links Find on this page Australian huntingtons disease Association  
    http://www.cbel.com/huntington's_disease/

36. Chance Of Having Huntingtons Disease
    Health topic area and articles about huntingtons disease. ); . Med Help International I just recently had got tested for Huntington s disease.  
    http://www.medhelp.org/perl6/neuro/messages/30084a.html
    
    Extractions: I just recently had got tested for Huntington's disease. I'm waiting for blood work to come back now. What are the chances of me actually having this disease if there is to my knowledge no family history of it? I've read a few things about it, wouldn't a parent know they have it? How long does it take for test results to come back? Answer Posted By: CCF neuro MD MM on Thursday, September 02, 1999

37. Huntingtons Disease At MedVolumes.com
    huntingtons disease Shop for 11 huntingtons disease items available with reviews, descriptions, and more information. huntingtons disease  
    http://www.medvolumes.com/h/Huntingtons_Disease/
    
    Extractions: Diet and Fitness ... Help Huntingtons Disease Purchase the most popular and in-stock Huntingtons Disease and related Discount Medical Books here! Choose from 11 Huntingtons Disease items available as of 6-8-2004. Get product descriptions, prices, reviews, and more information by clicking on any item. Thank you for shopping at MedVolumes.com.

38. Caring For People With Huntington's Disease
    Information about caring for people with Huntington's disease, for patients, families and professionals.  
    http://www.kumc.edu/hospital/huntingtons/
    
    Extractions: Huntington's Disease is an inherited degenerative neuropsychiatric disorder which affects both body and mind. Symptoms most commonly begin between the ages of 35 and 50, although onset may occur any time from childhood to old age. Research is progressing rapidly, but there is currently no cure. Huntington's disease is inherited in an autosommal dominant fashion. Each child of an affected parent has a 50 % chance of inheriting the disease and is said to be at risk . The discovery of the HD gene in 1993 has made it possible to test at-risk individuals for Huntington's disease before symptoms occur. In the absence of a cure, however, the decision to be tested or not remains a difficult one, and there are many important legal, financial and personal considerations. For more information about the genetic basis of Huntington's disease, you may wish to visit the Online Mendellian Inheritance in Man (OMIN) to learn about the genetic basis or the DNA library at the National Library of Medicine to see the actual gene sequence. The clinical features of Huntington's disease can be thought of as a triad of emotional, cognitive and motor disturbances. Symptoms include chorea (dance-like involuntary movements), clumsiness, slurred speech, depression, irritability and apathy. Cognitive losses include intellectual speed, attention and short-term memory.

39. Huntington's Disease - Neurologychannel
    Introduction to Huntington's disease, and an ask a doctor forum.  
    http://www.neurologychannel.com/huntingtons/
    
    Extractions: Overview Huntington’s disease (HD) is a fatal hereditary disease that destroys neurons in areas of the brain involved in the emotions, intellect, and movement. The course of Huntington’s is characterized by jerking uncontrollable movement of the limbs, trunk, and face (chorea); progressive loss of mental abilities; and the development of psychiatric problems. Huntington’s disease progresses without remission over 10 to 25 years and patients ultimately are unable to care for themselves. Huntington’s disease usually appears in middle age (30-50 years), but can develop in younger and older people.

40. Auto-forward To Hungtington's Disease Page
    Services of the Huntington's disease program of the University of Connecticut Health Center.  
    http://huntingtons.uchc.edu

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