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         Creutzfeldt Jakob Disease:     more books (97)
  1. Preclinical lesions and their progression in the experimental spongiform encephalopathies (Kuru and Creutzfeldt-Jakob disease) in primates by Colin L Masters, 1976
  2. Will Creutzfeldt-Jakob Disease
  3. Subacute spongiform encephalopathy (Creutzfeldt-Jakob disease): The nature and progression of spongiform change by Colin L Masters, 1979
  4. Creutzfeldt-Jakob disease in France by Paul Brown, 1979
  5. Pituitary human growth hormone and Creutzfeldt-Jakob disease by KabiVitrum AB (Firm), 1986
  6. Creutzfeldt-Jakob disease surveillance in the United Kingdom: Annual report
  7. Creutzfeldt-Jakob disease (SuDoc HE 20.3520:C 86) by U.S. Dept of Health and Human Services, 1998
  8. Nursing patients with Creutzfeldt-Jakob disease. Are you at risk?(127 CLINICAL UPDATE)(Case study): An article from: Australian Nursing Journal by Peter Stride, Jonathan Hunter, et all 2009-07-01
  9. Chronic neurological diseases: Subacute Sclerosing Panencephalitis, progressive multifocal Leukoencephalopathy, Kuru, Creutzfeldt-Jakob Disease by Jacob A Brody, 1976
  10. Bovine Spongiform Encephalopathy and Creutzfeldt-Jakob Disease: Recent Developments - Minutes of Evidence, March-April 1996 (House of Commons Papers) by Agriculture and Health Committees, 1996-05
  11. Unusual resistance to ionizing radiation of the viruses of kuru, Creutzfeldt-Jakob disease, and scrapie by Clarence J Gibbs, 1979
  12. Prions: Novel Infectious Pathogens Causing Scrapie and Creutzfeldt-Jakob Disease by Thomas A. And Donald W. Stansloski Gossel, 1981-01-01
  13. Transmission of Creutzfeldt-Jakob Disease to the Patas monkey (Erythrocebus patas) with cytopathological changes in in vitro cultivated brain cells by Carlos Espana, 1976
  14. Bibliography of Creutzfeldt-Jakob disease (NIH publication) by Clarence J Gibbs, 1979

61. Mad Cow Disease - Prions - CJD, Creutzfeldt-Jakob Disease - The Doctors Lounge(T
The Doctors Lounge Mad Cow disease, Prions disease, CJD, creutzfeldtjakob disease. Click Here. Kuru; creutzfeldt-jakob disease (sCJD).
http://www.thedoctorslounge.net/studlounge/articles/prions/

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Back to Student Articles Sunday, 30 March 2003 05:30 PM GMT T he protein only hypothesis of Prions diseases (Mad cow disease) won a Nobel prize in 1997. send to a friend printer friendly version Related Infectious disease review
Knowledge begins with a hypothesis or theory that should be subjected to and verified by experimentation. In this article we will highlight on one of these hypothesis that was for a long time not credible and almost not palatable to many.
The protein only hypothesis or prions hypothesis is a novel discovery that earned the scientist Stanley Ben Prusiner the Nobel prize for medicine in 1997. Prion diseases are a group of diseases that share common clinical and neuropathological characteristics. They are also called spongiform encephalopathies because of the post mortem appearance of the brain with large vacuoles in the cortex and cerebellum a change that is caused by prion protein. Worth noting that 2 nobel prizes were given for research related to this scientific field.

62. Introduction: Creutzfeldt-Jakob Disease - WrongDiagnosis.com
Introduction to creutzfeldtjakob disease as a medical condition including symptoms, diagnosis, misdiagnosis, treatment, prevention, and prognosis.
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Current chapter: Creutzfeldt-Jakob Disease Next sections Basic Summary for Creutzfeldt-Jakob Disease Prevalence and Incidence of Creutzfeldt-Jakob Disease Prognosis of Creutzfeldt-Jakob Disease Types of Creutzfeldt-Jakob Disease ... Causes of Creutzfeldt-Jakob Disease Next chapters: Variant CJD Kuru Fatal familial insomnia Feline spongiform encephalopathy ... Feedback
Introduction: Creutzfeldt-Jakob Disease
Creutzfeldt-Jakob Disease: Creutzfeldt-Jakob Disease (CJD) is a rare 1-in-a-million disease that occurs spontaneously, with 10-15% inheritance, and unrelated to animal diseases. It usually leads to dementia. CJD is a rare brain disease in humans caused by abnormal brain proteins ( prions ). It is similar to the various transmissible spongiform encephalopathies that afflict animals including " mad cow disease ". Unfortunately, prognosis for CJD is poor as there are no effective treatments against prions. CJD is not usually contagious, except rarely by direct exposure to the brain (such as brain surgery).

63. Article: Creutzfeldt-Jakob Disease Fact Sheet: NINDS - WrongDiagnosis.com
Medical article creutzfeldtjakob disease Fact Sheet NINDS including all symptom, diagnosis, misdiagnosis, treatment and prevention information.
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Creutzfeldt-Jakob Disease Fact Sheet: NINDS
Article title: Creutzfeldt-Jakob Disease Fact Sheet: NINDS Main condition: CJD Conditions: CJD
Table of Contents
  • What is Creutzfeldt-Jakob Disease?
  • What are the Symptoms of the Disease?
  • How is CJD Diagnosed?
  • How is the Disease Treated? ...
  • Where Can I Get Help?
    What is Creutzfeldt-Jakob Disease?
    Creutzfeldt-Jakob disease (CJD) is a rare, degenerative, invariably fatal brain disorder. It affects about one person in every one million people per year worldwide; in the United States there are about 200 cases per year. CJD usually appears in later life and runs a rapid course. Typically, onset of symptoms occurs about age 60, and about 90 percent of patients die within 1 year. In the early stages of disease, patients may have failing memory, behavioral changes, lack of coordination and visual disturbances. As the illness progresses, mental deterioration becomes pronounced and involuntary movements, blindness, weakness of extremities, and coma may occur.
  • 64. Creutzfeldt-Jakob Disease
    creutzfeldtjakob disease jakob-creutzfeldt disease. Mad Cow disease. Scrapie. Causes Sporadic creutzfeldt-jakob disease Growth hormone injections; Corneal grafts;
    http://www.fpnotebook.com/ID187.htm
    Home About Links Index ... Editor's Choice document.write(code); Advertisement Infectious Disease Prion Assorted Pages Creutzfeldt-Jakob Disease Creutzfeldt-Jakob Disease Jakob-Creutzfeldt Disease Mad Cow Disease Scrapie Chronic Wasting Disease New Variant CJD Book Home Page Cardiovascular Medicine Dentistry Dermatology Emergency Medicine Endocrinology Gastroenterology General Medicine Geriatric Medicine Gynecology Hematology and Oncology HIV Infectious Disease Jokes Laboratory Neonatology Nephrology Neurology Obstetrics Ophthalmology Orthopedics Otolaryngology Pediatrics Pharmacology Prevention Psychiatry Pulmonology Radiology Rheumatology Sports Medicine Surgery Urology Chapter Infectious Disease Index Bacteria Dermatology Emerging Examination Ophthalmology Fever Fungus Gastroenterology Helminth HIV Immune Immunization Laboratory General Neurology Obstetrics Parasite Pediatrics Pharmacology Prevention Prion Procedure Rheumatology Sexually Transmitted Disease Travel Medicine Vector Virus Page Prion Index CJD
  • Epidemiology Incidence of sporadic CJD: One case per million Age of onset CJD Mean age of onset: 68 (range: 55-75 years old) nvCJD: Young age of onset Causes Sporadic Creutzfeldt-Jakob Disease Growth hormone injections Cornea l grafts Dural grafts Neurosurgical equipment nvCJD Eating contaminated beef (cattle fed sheep brain) Sheep CJD (Scrapie) Only transmitted to humans if passed via cattle Chronic Wasting Disease (passed by deer and elk) Broad range of positive cases in United States Identified in deer and elk in 1967 Identified in Mt Horeb area: 14 per 500 deer
  • 65. CNEWS - Canada: Creutzfeldt-Jakob Disease Suspected In N.S.
    creutzfeldtjakob disease suspected in NS. By SUSAN AITKEN. The neurosurgery patient had been diagnosed as a suspected carrier of creutzfeldt-jakob disease.
    http://cnews.canoe.ca/CNEWS/Canada/2004/05/01/443779-cp.html
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    Creutzfeldt-Jakob disease suspected in N.S. By SUSAN AITKEN
    HALIFAX (CP) - Another group of hospital patients in Nova Scotia may have been exposed to a fatal brain-wasting disease through contaminated medical instruments, health officials said Saturday. For the second time in less than a week, health officials are putting patients on notice after medical instruments were used on a patient now suspected of having Creutzfeldt-Jakob disease. The new incident is completely unrelated to a similar warning that was issued just days ago in Halifax, officials say.
  • 66. Encyclopaedia Topic : Creutzfeldt-Jakob Disease, Section : Introduction
    NHS Direct Online Health Encyclopaedia. creutzfeldtjakob disease. Search. Help.
    http://www.nhsdirect.nhs.uk/en.asp?TopicID=139

    67. HealthlinkUSA Creutzfeldt-jakob Disease (CJD) Links
    Find creutzfeldtjakob disease (CJD) at searchwaves.com. Click here for page 1 of creutzfeldt-jakob disease (CJD) information from the HealthlinkUSA directory.
    http://www.healthlinkusa.com/Creutzfeldt-jakob_Disease_(CJD).htm

    68. Creutzfeldt-Jakob Disease
    creutzfeldtjakob disease. It is clear that creutzfeldt-jakob disease is caused by an infectious agent, but it is not yet clear what type of agent that is.
    http://www.ehendrick.org/healthy/000383.htm
    MAIN SEARCH INDEX
    Creutzfeldt-Jakob disease
    Definition
    Creutzfeldt-Jakob disease (CJD) is a transmissible, rapidly progressing, fatal neurodegenerative disorder called a spongioform degeneration that seems to be related to "mad cow disease."
    Description
    Before 1995, Creutzfeldt-Jakob disease was little-known outside of the medical profession; even within it, many practitioners did not know much about it. Most doctors had never seen a case. With the recognition of a so-called "new variant" or simply variant form of CJD with the strong possibility that those with it became infected simply by eating contaminated beef, CJD has become one of the most talked-about diseases in the world. Additionally, the radical theory that the infectious agent is a normal protein that has been changed in its form has also sparked much interest. First described in the first part of the twentieth century independently by Cretzfeldt and Jakob, CJD is a neurodegenerative disease causing a rapidly progressing dementia ending in death , usually within eight months of the onset of symptoms. It is also a very rare disease, affecting only about one in every million in the population through out the world. In the United States, CJD is thought to affect about 250 people each year. CJD affects adults primarily between ages 50 and 75.

    69. Creutzfeldt-Jakob Syndrome
    which aims to investigate the emergence and identification of Bovine Spongiform Encephalopathy (BSE) and the new variant CJD (creutzfeldtjakob disease) in the
    http://omni.ac.uk/browse/mesh/detail/C0022336L0022336.html
    low graphics
    Creutzfeldt-Jakob Syndrome
    Creutzfeldt-Jakob Syndrome Creutzfeldt-Jakob Syndrome / transmission broader: Dementia Prion Diseases other: AIDS Dementia Complex Alzheimer Disease Dementia, Vascular Encephalopathy, Bovine Spongiform ... Pick Disease of the Brain
    Creutzfeldt-Jakob Syndrome
    DEFRA BSE information A collection of imformation on BSE in cattle provided by DEFRA (Department for Environment, Food and Rural Affairs), formerly MAFF. Included are press releases and a bibliography of mainly government publications in this area. Encephalopathy, Bovine Spongiform Creutzfeldt-Jakob Syndrome UK Creutzfeldt-Jakob Surveillance Unit The incidence of CJD is monitored in the UK by the CJD Surveillance Unit at the Western General Hospital in Edinburgh. This site summarises the research in progress at the Unit and provides some background information on CJD and other human spongiform encephalopathies, also providing links to other resources. Features include statistics on CJD in the UK and Europe, the Annual Report and list of publications of the Unit. Encephalopathy, Bovine Spongiform

    70. MD Travel Health - Variant Creutzfeldt - Jakob Disease
    Variant creutzfeldtjakob disease and bovine spongiform encephalopathy ( mad cow disease ). ©2004 MDtravelhealth.com. Variant creutzfeldt-jakob disease.
    http://www.mdtravelhealth.com/infectious/mad_cow_disease.html
    Variant Creutzfeldt-Jakob disease and bovine spongiform encephalopathy ("mad cow disease") Variant Creutzfeldt-Jakob disease (CJD) is a degenerative neurologic disease acquired by eating beef from cows with a related illness known as bovine spongiform encephalopathy (BSE) ("mad cow disease"). The disorder was initially described in the United Kingdom. As of February 2003, there were 129 definite or probable cases of variant CJD reported from the United Kingdom, six from France, and two from the Republic of Ireland. "Mad cow disease" has also been identified in Austria, Belgium, Czech Republic, Denmark, Finland, Germany, Greece, Italy, Liechtenstein, Luxembourg, the Netherlands, Portugal, Slovak Republic, Slovenia, Spain, Switzerland, Israel, and Japan, but human cases have not been reported from these countries to date. Bovine spongiform encephalopathy appears to be caused by abnormal proteins called prions, which do not resemble bacteria, viruses, or other conventional causes of human and animal disease. The agent that causes BSE is transmitted when meat and bone meal feed prepared from the carcasses of infected animals is fed back to other cattle. (This practice has been banned within the European Union and many other countries). The infection is not transmitted directly from animal to animal within herds. A new case of BSE arising within a country is therefore much more significant than an imported case, because it implies that recycled ruminant protein is still being used within that country as animal feed, against all current recommendations.

    71. Creutzfeldt-Jakob Disease (www.whonamedit.com)
    creutzfeldtjakob disease A very rare, progressive syndrome of motor, sensory, and mental disturbances, involving the cerebral cortex, basal ganglia and
    http://www.whonamedit.com/synd.cfm/696.html

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    Creutzfeldt-Jakob disease Also known as:
    Creutzfeldt-Jakob syndrome
    Jakob’s pseudosclerosis Jakob-Creutzfeldt disease Jakob-Creutzfeldt pseudosclerosis Synonyms: Spastic pseudosclerosis; abiotrophic dementia; corticopallidospinal degeneration; corticostriatal-spinal degeneration syndrome; spongioform cerebral atrophy; subacute, presenile spongious atrophy with terminal dyskinesy; progressive encephalopathy with spongioform degeneration of the brain. Associated persons: Hans Gerhard Creutzfeldt Alfons Maria Jakob Description: A very rare, progressive syndrome of motor, sensory, and mental disturbances, involving the cerebral cortex, basal ganglia and spinal cord. Presents with rapidly progressive dementia, stiffness and weakness of the limbs, convulsive seizures, and various pyramidal and extrapyramidal symptoms. The clinical diagnosis is substantiated by a peculiar electroencephalogram and at autopsy by widespread degeneration and atrophy of the cerebral cortex, basal ganglia, and thalamus, with the presence of coarse and fine vacuoles in all cortical layers (status spongiosus).

    72. HPA - Infections | Topics A-Z | CJD | Variant And Sporadic Creutzfeldt-Jakob Dis
    creutzfeldtjakob disease (CJD). creutzfeldt-jakob disease (CJD) is a rare and ultimately fatal progressive degenerative brain disease.
    http://www.hpa.org.uk/infections/topics_az/cjd/menu.htm
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    The CDSC CJD Team CJD Incidents Panel The National Anonymous Tonsil Archive Investigation of geographically associated cases of vCJD ... Laboratory Services, Transmissible Spongiform Encephalopathy Unit, Specialist and Reference Microbiology Division Creutzfeldt-Jakob disease (CJD) is a rare and ultimately fatal progressive degenerative brain disease. It is one of a group of diseases called Transmissible Spongiform Encephalopathies (TSEs) that affect humans and animals. TSEs are thought to be caused by the build up in the brain of an abnormal form of the naturally occuring 'prion' protein.

    73. Creutzfeldt-Jakob Disease - Minnesota Dept. Of Health
    creutzfeldtjakob disease (CJD). •, CJD Home. •, CJD Basics. , Bovine Spongiform Encephalopathy (BSE). creutzfeldt-jakob disease (CJD).
    http://www.health.state.mn.us/divs/idepc/diseases/cjd/
    dqmcodebase = "http://www.health.state.mn.us/script/" Creutzfeldt-Jakob Disease (CJD) CJD Home CJD Basics CJD Information for Health Care Providers BSE and Variant CJD Resources ... CJD Surveillance In Minnesota More from MDH Chronic Wasting Disease (CWD) Bovine Spongiform Encephalopathy (BSE)
    Creutzfeldt-Jakob Disease (CJD)
    Creutzfeldt-Jakob Disease is a rare, 100% fatal, neurodegenerative brain disorder believed to be caused by abnormally folded proteins called "prions" (pree-ons). Other human prion diseases include kuru, Gerstmann-Straussler-Scheinker disease, "variant" CJD, and fatal familial insomnia.
    To view the PDF files, you will need Adobe Acrobat Reader or for screen reader accessibility Adobe Acrobat Access (free downloads from Adobe's web site).
    CJD Basics
    CJD Information for Health Care Providers

    74. THE MERCK MANUALSECOND HOME EDITION, Creutzfeldt-Jakob Disease
    creutzfeldtjakob disease. creutzfeldt creutzfeldt-jakob disease affects 1 of 1 million people each year throughout the world. It
    http://www.merck.com/mrkshared/mmanual_home2/sec06/ch090/ch090b.jsp

    75. BSE (Creutzfeldt-Jakob Disease)
    Title, Apoptosis in relation to neuronal loss in experimental creutzfeldtjakob disease in mice. Title, Chronology of the new variant of creutzfeldt-jakob disease.
    http://www.laboklin.de/l_forsch/for0c11.htm
    Creutzfeldt-Jakob disease CJD
    Apoptosis in relation to neuronal loss in experimental Creutzfeldt-Jakob disease in mice

    BSE as zoonosis

    In search of a cure for CJD

    Creutzfeldt-Jakob Disease (CJD) and other prion diseases: an update
    ...
    Creutzfeldt-Jakob disease, new variant Creutzfeldt-Jakob disease, and BSE

    Authors Title Full source Author Keywords Keywords TGA/Book No. Discipline Document type Language Address ISBN/ISSN Publisher Abstract Authors Title Full source Author Keywords Keywords TGA/Book No. Discipline Document type Language Address ISBN/ISSN Publisher Abstract Authors
    D JesionekKupnicka, R Kordek, J Buczynski, PP Liberski Title Apoptosis in relation to neuronal loss in experimental Creutzfeldt-Jakob disease in mice Full source Acta Neurobiologiae Experimentalis, 2001, Vol 61, Iss 1, pp 13-19 Author Keywords Creutzfeldt-Jakob disease; apoptosis; TUNEL; neuronal loss; PrP-prion diseases Keywords PRION PROTEIN-FRAGMENT; PROGRAMMED CELL-DEATH; SPONGIFORM ENCEPHALOPATHY; ALZHEIMERS-DISEASE; DNA FRAGMENTATION; MURINE SCRAPIE; NEUROTOXICITY; ACTIVATION; CLEAVAGE; ABSENCE TGA/Book No.

    76. CBC News:Variant Creutzfeldt-Jakob Disease Linked To Blood Transfusion
    Variant creutzfeldtjakob disease linked to blood transfusion Last Updated Wed, 17 Dec 2003 190932 LONDON - British health officials
    http://www.cbc.ca/stories/2003/12/17/sci-tech/vcjd_blood031217
    document.write(""); document.write("");
    Variant Creutzfeldt-Jakob disease linked to blood transfusion
    Last Updated Wed, 17 Dec 2003 19:09:32 LONDON - British health officials say they may have come across the world's first case of the human form of BSE transmitted through a blood transfusion. An unidentified patient died earlier this year. In 1996, the patient received blood from a donor who later died of variant Creutzfeldt-Jakob disease (vCJD). Variant CJD is the human form of bovine spongiform encephalopathy, also known as mad cow disease. The original infected donor showed no signs of the brain-wasting illness when giving blood. He developed the disease three years later. It isn't possible to determine whether the recipient contracted the disease from blood or if they were both infected independently by eating BSE-infected meat, Britain's health secretary told Parliament on Wednesday. "This is a possibility, not a proven causal connection," John Reid said. In 1997, Britain began applying safeguards for its blood supply. Most of the world's cases of vCJD have been in Britain.

    77. MSN Encarta - Creutzfeldt-Jakob Disease
    Sign in above. creutzfeldtjakob disease. I. Introduction. , Discovery Health creutzfeldt-jakob disease. -, UK creutzfeldt-jakob disease Surveillance Unit. 2 items.
    http://encarta.msn.com/encyclopedia_761582527/Creutzfeldt-Jakob_Disease.html
    MSN Home My MSN Hotmail Shopping ... Money Web Search: logoImg('http://sc.msn.com'); Encarta Subscriber Sign In Help Home ... Upgrade to Encarta Premium Search Encarta
    Subscription Article MSN Encarta Premium: Get this article, plus 60,000 other articles, an interactive atlas, dictionaries, thesaurus, articles from 100 leading magazines, homework tools, daily math help and more for $4.95/month or $29.95/year (plus applicable taxes.) Learn more. This article is exclusively available for MSN Encarta Premium Subscribers. Already a subscriber? Sign in above. Creutzfeldt-Jakob Disease I. Introduction Creutzfeldt-Jakob Disease (CJD) form of human spongiform encephalopathy caused by an infection of the brain, probably by a particle called a prion.... II. Causes Related Items vCJD variant, caused by eating BSE-contaminated meat link to mad cow disease 18 items Selected Web Links Discovery Health: Creutzfeldt-Jakob Disease UK Creutzfeldt-Jakob Disease Surveillance Unit 2 items Sidebars SCIENTIFIC DISCOVERIES
    Disease Leads to Ban on Beef 2 items Want more Encarta?

    78. US Mad Cow Link Questioned In Creutzfeldt-Jakob Cases
    NEW YORK/SAN FRANCISCO Family and friends of American victims of creutzfeldt-jakob disease, the fatal brain disorder sometimes linked to mad cow disease, on
    http://www.commondreams.org/headlines03/1227-01.htm
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    E-Mail This Article Published on Saturday, December 27, 2003 by Reuters US Mad Cow Link Questioned in Creutzfeldt-Jakob Cases by Jed Seltzer and Elinor Mills Abreu NEW YORK/SAN FRANCISCO - Family and friends of American victims of Creutzfeldt-Jakob Disease, the fatal brain disorder sometimes linked to mad cow disease, on Friday questioned whether the wasting illness that killed their loved ones was actually due to eating contaminated U.S. beef. After federal authorities said on Tuesday that a cow in Washington state was found to have mad cow disease, public health experts have been calling for a review of the U.S. Agriculture Department's screening procedures for cattle. But some victim's families have gone further, saying that the human form of the disease may have already hit the United States and that the government has been lax in its testing possible links and enforcing safety standards. "The most frustrating part of this disease is that there are no answers," said Chris Turnley, whose brother Peter Putnam, who grew up in Washington state, died of the disease last October at age 35. "They need to figure out the cause but also start figuring out treatments." So far, none of the roughly 300 cases of Creutzfeldt-Jakob Disease diagnosed in the United States each year has been linked to U.S.-produced beef, said Pierluigi Gambetti, director of the National Prion Disease Pathology Surveillance Center at Case Western University.

    79. Medicine-Worldwide: New Variant Creutzfeldt- Jakob-Disease (nvCJD)
    Translate this page New variant creutzfeldt - jakob-disease (nvCJD).
    http://www.medicine-worldwide.de/krankheiten/prionenkrankheiten/nvcjd.html
    Sie befinden sich hier: startseite krankheiten prionenkrankheiten Prionenkrankheiten ... Über uns
    New variant Creutzfeldt - Jakob-Disease (nvCJD)
    Seite: vor Kapitelübersicht: Zusammenfassung Allgemeines Erreger Symptome ... Ratgeber
    Zusammenfassung
    Allgemeines
    (CJD). Insgesamt sind an dieser Krankheit nachgewiesenermassen bisher 107 Personen in England, 3 in Frankreich und eine in Irland verstorben (Stand: Oktober 2001).
    Erreger
    Es gilt mittlerweile als nahezu sicher, dass Prionen die Erreger dieser Krankheit sind. Sc C ) gebildet werden. Das Gen, welches die Information für dieses Prion-Protein trägt, liegt auf dem Chromosom 20. Der Zusatz "Sc" steht für Scrapie- spezifisch, der von "C" für cellulär, also für körpereigen. Die Prionen (PrP Sc
    Diese Erkrankung war bis vor wenigen Jahren nahezu unbekannt und auch die "normale" Creutzfeldt- Jakob- Erkrankung kam nur extrem selten vor. Dies hat sich in allerletzter Zeit teilweise dramatisch geändert. Im Mutterland von BSE, also in England, sind bis Mai 2001 99 Menschen an der nvCJD verstorben. In Frankreich hat es bisher 3 Todesfälle an nv CJD gegeben, sowie einen in Irland. Der englische Epidemiologe Roy Anderson aus Oxford hält bis zu 500.000 Tote in den nächsten 30 Jahren für nicht unmöglich.
    Symptome
    • Tremor, also Zittern von Armen, Beinen oder dem Kopf

    80. Creutzfeldt-Jakob Disease - National Institutes Of Health (NIH)
    creutzfeldtjakob disease - Health Information from National Institutes of Health (NIH). Skip Over Navigation Links. creutzfeldt-jakob disease. Resources. NINDS.
    http://health.nih.gov/result.asp/172

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    Health Information Browse Health Topics Alphabetically Creutzfeldt-Jakob Disease Resources NINDS NIDDK NIEHS ... Medline Plus NIH Institute and Center Resources National Institute of Neurological Diseases and Stroke
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    Creutzfeldt-Jakob Disease Creutzfeldt-Jakob Disease Fact Sheet ... La Enfermedad de Creutzfeldt-Jakob Spanish Call 301-496-5751 for more information National Institute of Diabetes and Digestive and Kidney Diseases
    NIDDK
    Follow-Up Study of NHPP Growth Hormone Recipients Human Growth Hormone and Creutzfeldt-Jakob Disease ... Mad Cow Disease Related Topics: Brain and Nervous System Up to Top Look up "Creutzfeldt-Jakob Disease" in: MEDLINEplus - health resources from US government agencies and other credible organizations Clinical Trials Database - research studies in which you can participate Creutzfeldt-Jakob Disease Study This page was last reviewed on Tuesday, February 24, 2004. Career Opportunities Visitor Information FOIA
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