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Creutzfeldt Jakob Disease:     more books (97)

The fundamentals of variant Creutzfeldt-Jakob disease.: An article from: Journal of Neuroscience Nursing by Anna Budd Fontenot, 2003-12-01 Rare brain disorder suspected in death.(Health)(Fatal illness: Doctors say Creutzfeldt-Jakob Disease may have killed Jerry Ray Collins.): An article from: The Register-Guard (Eugene, OR) Update: Creutzfeldt-Jakob disease associated with cadaveric dura mater grafts--Japan, 1978-2008.: An article from: Morbidity and Mortality Weekly Report by Y. Nakamura, R. Uehara, et all 2008-10-24 UK blood service warns vCJD test could cut donations.(Creutzfeldt-Jakob disease)(Brief Article): An article from: Transplant News vCJD risk from plasma very small.(NEWS FROM THE FDA)(variant Creutzfeldt-Jakob disease)(Brief article): An article from: Internal Medicine News by Unavailable, 2009-08-01 Overall Blood Supply Strategy With Regard to Variant Creutzfeldt-jakob Disease (Vcjd): Report of the Working Group Commissioned by the German Federal Ministry ... (Transfusion Medicine and Hemotherapy 2006) 2004 Essential Guide to Mad Cow Disease and Bovine Spongiform Encephalopathy (BSE), Creutzfeldt-Jakob disease (CJD), and Prions - Authoritative Federal ... (USDA), CDC, FDA, and NIH (CD-ROM) by U.S. Government, 2003-12-29 CREUTZFELDT-JAKOB DISEASE: An entry from Macmillan Reference USA's <i>Encyclopedia of Aging</i> by CHRIS MACKNIGHT, 2002 Diagnostic challenges in Creutzfeldt-Jakob disease: case report.(Case Report): An article from: Southern Medical Journal by Lal K. Tanwani, Christian D. Furman, et all 2003-08-01 Protease-resistant prion protein in lymphoreticular tumors of variant Creutzfeldt-Jakob disease mice.(DISPATCHES): An article from: Emerging Infectious Diseases by Larisa Cervenakova, Oksana Yakovleva, et all 2006-03-01 WHO Manual for Strengthening Diagnosis and Surveillance of Creutzfeldt-Jakob Disease by World Health Organization, 1999-11 CREUTZFELDT-JAKOB DISEASE: An entry from UXL's <i>UXL Complete Health Resource</i> Gale Encyclopedia of Medicine: Creutzfeldt-Jakob disease by Larry I. Lutwick MD, 2002-01-01 Deaths From Amyloidosis: Transmissible Spongiform Encephalopathies, Prion, Fatal Familial Insomnia, Creutzfeldt-jakob Disease, Robert Jordan

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21. Document Redirect Link
    Article and links about Japanese research findings.  
    http://aepo-xdv-www.epo.cdc.gov/wonder/PrevGuid/m0049829/m0049829.htm

22. CJD Voice.org - Awareness - Support - Latest News
    Find help, support, understanding and information concerning all variant forms of creutzfeldt jakob disease, CJD.  
    http://members.aol.com/larmstr853/cjdvoice/cjdvoice.htm

23. HBSEF Home
    Aims to help relatives friends and carers of victims of creutzfeldt jakob disease by providing support.  
    http://www.hbsef.org

24. Monthly Creutzfeldt Jakob Disease Statistics The Department Of
    The Department of Health is today issuing the latest information about the numbers of known cases of creutzfeldt jakob disease.  
    http://www.dh.gov.uk/PublicationsAndStatistics/PressReleases/PressReleasesNotice

25. Creutzfeldt Jakob Disease
    creutzfeldt jakob disease. Links to Australian resources relating to creutzfeldt jakob disease (CJD), variant CJD (vCJD), the human form of Mad Cow  
    http://www.healthinsite.gov.au/topics/Creutzfeldt_Jakob_Disease
    
    Extractions: Advanced Search About Health Insite A-Z Health Topics ... Conditions and Diseases Topics such as asthma, diabetes, cancer, arthritis, depression Health and Wellbeing Topics such as fitness, nutrition, drugs, preventing suicide, health insurance, women's health, living with a disability Life Stages and Events Topics such as menopause, pregnancy, ageing, going into hospital Health Services Includes links to State/Territory Health Services and other services News Health Insite Newsletter ... Home Follow the links below to information on Creutzfeldt Jakob Disease (CJD) and variant CJD (vCJD). Printer friendly page Description: Creutzfeldt-Jakob disease (CJD) is a rapidly progressive disease that causes deterioration of the brain. It is one of a group of rare diseases that affects humans and animals. There is no cure and death usually results within two years of the symptoms first appearing. Variant CJD is sometimes referred to as `mad cow disease'.

26. NORD - National Organization For Rare Disorders, Inc.
    CreutzfeldtJakob Disease (CJD) is an extremely rare degenerative brain disorder Individuals with Creutzfeldt-Jakob Disease may then experience rapidly  
    http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Creutzfeldt J

27. Bovine Spongiform Encephalopathy (BSE) And Variant Creutzfeldt-Jakob Disease
    TSE s found in humans include creutzfeldt jakob disease (CJD) and variantcreutzfeldt jakob disease (vCJD). What causes BSE?  
    http://www.eufic.org/gb/safe/safe05.htm
    
    Extractions: Bovine Spongiform Encephalopathy (BSE), commonly known as "mad cow disease", is a fatal brain disease that affects cattle. The disease is named after the characteristic sponge-like changes to the brain that it causes. BSE usually has an incubation period of 4-5 years from the time that the animal is exposed. The condition is fatal within weeks or months of its onset. The first signs are weight loss and nervousness. BSE is one type of a group of prion diseases referred to as Transmissible Spongiform Encephalopathies (TSEs). TSEs are fatal diseases that cause spongy degeneration of the brain and severe neurological symptoms. Another example of a TSE is scrapie, a disease found in sheep and goats. TSEs have also been found in other animals including mink, North American mule deer, elk and cats. TSE's found in humans include Creutzfeldt Jakob Disease (CJD) and variant-Creutzfeldt Jakob Disease (vCJD). What causes BSE?

28. Conditions And Diseases/Creutzfeldt Jakob And Mad Cow- Health Care
    Offers resources on creutzfeldt jakob disease or Bovine Spongiform Encephalopathy (BSE), commonly know as Mad Cow disease, including signs and symptoms,  
    http://chp-pcs.gc.ca/CHP/index_e.jsp/pageid/4005/odp/Top/Health/Conditions_and_D

29. Creutzfeldt-Jakob Disease News And Headlines By Microbes.info
    creutzfeldt jakob disease news, headlines, information resources and links on microorganisms, microbes, and microbiology by microbes.info.  
    http://www.microbes.info/news/creutzfeldt_jakob.php

30. CJD Foundation Inc.
    Information about CJD, interactive pages, profiles, polls and details of conferences.  
    http://www.cjdfoundation.org/
    
    Extractions: CLICK HERE FOR INFO Welcome to the Creutzfeldt-Jakob Disease Foundation Website. We hope you will find the information you need. If it is not here, please call us and we will work with you to find needed information. We will respond to all calls and e-mails promptly. Please call us at 1-800-659-1991 or e-mail us at help@cjdfoundation.org

31. MedlinePlus: Creutzfeldt-Jakob Disease
    From the National Institutes of Health; creutzfeldtjakob disease (National Prevention/Screening; creutzfeldt-jakob disease Fact Sheet for Healthcare  
    http://www.nlm.nih.gov/medlineplus/creutzfeldtjakobdisease.html
    
    Extractions: Latest News Mad Cow Detected in Blood (08/28/2005, United Press International) Idaho Probes Outbreak of Creutzfeldt-Jakob Disease (08/12/2005, Reuters Health) From the National Institutes of Health Creutzfeldt-Jakob Disease (National Institute of Neurological Disorders and Stroke) - Short Summary Creutzfeldt-Jakob Disease (National Institute of Neurological Disorders and Stroke) Also available in: Spanish Overviews Commonly Asked Questions about BSE (Center for Food Safety and Applied Nutrition) Creutzfeldt-Jakob Disease (Mayo Foundation for Medical Education and Research) Questions and Answers Regarding Bovine Spongiform Encephalopathy (BSE) and Creutzfeldt-Jakob Disease (CJD) (National Center for Infectious Diseases) Prevention/Screening Creutzfeldt-Jakob Disease Fact Sheet for Healthcare Workers and Morticians (National Institute of Neurological Disorders and Stroke) Specific Conditions Mad Cow Disease Frequently Asked Questions: Don't Panic Get the Facts (Mayo Foundation for Medical Education and Research) Questions and Answers on Bovine Spongiform Encephalopathy (Center for Biologics Evaluation and Research)

32. NINDS Forwarding Page
    What Causes creutzfeldtjakob disease? How is CJD Transmitted? creutzfeldt-jakob disease (CJD) is a rare, degenerative, invariably fatal brain disorder.  
    http://www.ninds.nih.gov/health_and_medical/pubs/creutzfeldt-jakob_disease_fact_

33. DH Home : The Department Of Health
    Information from the Department of Health (England) on CJD and BSE. Includes monthly statistics, press releases, and details of publications and guidance.  
    http://www.doh.gov.uk/cjd/cjd1.htm
    
    Extractions: @import "/pages/css-p/layout_108.css"; @import "/pages/css/core_standard.css"; @import "/pages/css/core_modules.css"; @import "/pages/css/core_links.css"; @import "/pages/css/core_buttons.css"; @import "/pages/css/core_forms.css"; @import "/pages/css/core_tables.css"; @import "/pages/css/core_corners.css"; @import "/pages/default/css/brnd_buttons.css"; @import "/pages/default/css/brnd_forms.css"; @import "/pages/default/css/brnd_links.css"; @import "/pages/default/css/brnd_modules.css"; @import "/pages/default/css/brnd_standard.css"; @import "/pages/default/css/brnd_tables.css"; @import "/pages/default/css/brnd_corners.css"; @import "/pages/default/css/bspk_standard.css"; @import("/pages/css/standard_fix_ie51mac.css"); Skip Navigation

34. Introduction To CJD
    creutzfeldtjakob disease (CJD) is a rare and fatal neurodegenerative disease of unknown cause. Patients are usually aged between 50 and 75 and typical  
    http://www.cjd.ed.ac.uk/intro.htm
    
    Extractions: Introduction Creutzfeldt-Jakob disease (CJD) is a rare and fatal neurodegenerative disease of unknown cause. Patients are usually aged between 50 and 75 and typical clinical features include a rapidly progressive dementia associated, myoclonus and a characteristic electroencephalographic pattern. Neuropathological examination reveals cortical spongiform change, hence the term `spongiform encephalopathy'. H.G. Creutzfeldt is credited with the first description of the disorder in 1920, although by current diagnostic criteria his case would be highly atypical. A year later another German neurologist, A. Jakob, described four cases, at least two of whom had clinical features suggestive of the entity we recognise as CJD. Aetiology The nature of the transmissible agent is the matter of some controversy. Previously considered a `slow virus' no viral agent has ever been convincingly demonstrated and no evidence of an immunological response seen. Additionally the infectious pathogen shows a remarkable resistance to treatments that would normally be expected to inactivate viruses. The viral hypothesis has been elegantly challenged by the prion (` pro teinaceous in Epidemiology The majority of cases are sporadic (85%), between 10-15% are familial and the remainder are iatrogenic.

35. CDC - Bovine Spongiform Encephalopathy And Variant Creutzfeldt-Jakob Disease: Ba
    Brown P. The clinical epidemiology of creutzfeldtjakob disease in the context of Brown P. Can creutzfeldt-jakob disease be transmitted by transfusion?  
    http://www.cdc.gov/ncidod/EID/vol7no1/brown.htm
    
    Extractions: *National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA; †National Creutzfeldt-Jakob Disease Surveillance Unit, Western General Hospital, Edinburgh, Scotland; ‡Central Veterinary Laboratory, New Haw, Addlestone, UK; §Center for Biologics Evaluation and Research, Food and Drug Administration, Rockville, Maryland, USA; ¶Animal and Plant Health Inspection Service, U.S. Department of Agriculture, Robbinsville, New Jersey, USA The epidemic of bovine spongiform encephalopathy in the United Kingdom, which began in 1986 and has affected nearly 200,000 cattle, is waning to a conclusion, but leaves in its wake an outbreak of human Creutzfeldt-Jakob disease, most probably resulting from the consumption of beef products contaminated by central nervous system tissue. Although averaging only 10-15 cases a year since its first appearance in 1994, its future magnitude and geographic distribution (in countries that have imported infected British cattle or cattle products, or have endogenous BSE) cannot yet be predicted. The possibility that large numbers of apparently healthy persons might be incubating the disease raises concerns about iatrogenic transmissions through instrumentation (surgery and medical diagnostic procedures) and blood and organ donations. Government agencies in many countries continue to implement new measures to minimize this risk.

36. Guardian Unlimited | Special Reports | Special Report: BSE And CJD
    Ongoing collection of news, commentary, audio, graphics and interactive guides about Bovine Spongiform Encephalopathy (BSE) and variant creutzfeldtjakob disease (CJD).  
    http://www.guardian.co.uk/bse/0,8250,388290,00.html
    
    Extractions: Read today's paper Sign in Register Go to: Guardian Unlimited home UK news World news Newsblog Archive search Arts Books Business EducationGuardian.co.uk Film Football The Guide Jobs Life MediaGuardian.co.uk Money The Observer Online Politics Shopping SocietyGuardian.co.uk Sport Talk Travel Audio Email services Special reports The Guardian The northerner The wrap Advertising guide Crossword Soulmates dating Headline service Syndication services Events / offers Help / contacts Feedback Information GNL press office Living our values Newsroom Reader Offers Style guide Travel offers TV listings Weather Web guides Working at GNL Guardian Weekly Money Observer Public Home UK Business Online ... Quiz

37. WHO | Variant Creutzfeldt-Jakob Disease
    Variant creutzfeldtjakob disease (vCJD) is a rare and fatal human neurodegenerative condition. As with creutzfeldt-jakob disease, vCJD is classified as a  
    http://www.who.int/mediacentre/factsheets/fs180/en/
    
    Extractions: Variant Creutzfeldt-Jakob disease Variant Creutzfeldt-Jakob disease (vCJD) is a rare and fatal human neurodegenerative condition. As with Creutzfeldt-Jakob disease, vCJD is classified as a Transmissible Spongiform Encephalopathy (TSE) because of characteristic spongy degeneration of the brain and its ability to be transmitted. vCJD is a new disease that was first described in March 1996. Before the identification of vCJD, CJD was recognized to exist in only three forms. Sporadic cases, which have an unknown cause and occur throughout the world at the rate of about one per million people, account for 85–90% of CJD cases. Familial cases are associated with a gene mutation and make up 5–10% of all CJD cases. Iatrogenic cases result from the accidental transmission of the causative agent via contaminated surgical equipment or as a result of cornea or dura mater transplants or the administration of human-derived pituitary growth hormones. Less than 5% of CJD cases are iatrogenic. In contrast to the traditional forms of CJD, vCJD has affected younger patients (average age 29 years, as opposed to 65 years), has a relatively longer duration of illness (median of 14 months as opposed to 4.5 months) and is strongly linked to exposure, probably through food, to a TSE of cattle called Bovine Spongiform Encephalopathy (BSE).

38. WHO Fact Sheets
    Variant creutzfeldtjakob disease Video display units (VDUs) and human health Violence against women. Back to top  
    http://www.who.int/mediacentre/factsheets/

39. MedlinePlus Medical Encyclopedia: Creutzfeldt-Jakob Disease
    creutzfeldtjakob disease is a disorder involving rapid decrease of mental creutzfeldt-jakob disease may be related to several other diseases also  
    http://www.nlm.nih.gov/medlineplus/ency/article/000788.htm
    
    Extractions: @import url(/medlineplus/images/advanced.css); Skip navigation Other encyclopedia topics: A-Ag Ah-Ap Aq-Az B-Bk ... Z Contents of this page: Creutzfeldt-Jakob disease Central nervous system Alternative names Return to top Transmissible Spongiform Encephalopathy; Mad Cow - new variant CJD Definition Return to top Creutzfeldt-Jakob disease is a disorder involving rapid decrease of mental function and movement. These are abnormalities believed to be caused by damage done to the brain by a protein called a prion. This protein folds abnormally, and seems to encourage other proteins to become similarly misshapen, affecting their ability to function. Causes, incidence, and risk factors Return to top Creutzfeldt-Jakob disease can occur sporadically (for no known reason), as a result of exposure to contaminated products. Rarely, it can be genetically inherited. The disorder itself is rare, occurring in about 1 out of 1 million people. It usually first appears in midlife, beginning between ages 20 and 70, with average age at onset of symptoms in the late 50s. However, some cases have occurred in adolescents who have received

40. CJD Foundation, Inc. On The World Wide Web
    creutzfeldtjakob disease Foundation, Inc. The Foundation has moved. Our new website address is. cjdfoundation.org. Please update your bookmarks!  
    http://members.aol.com/crjakob/

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