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  1. Prion
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    CJD is caused by a prion, a type of infectious protein. Prions trigger normal proteins in the body to misfold, leading to CJD. CJD causes dementia and other neurologic problems. Once symptoms begin, it can lead to death in months to a year.
    TSEs are thought to be caused by the buildup of an abnormal, transmissible protein called 'prion' in the brain.
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    See more... Creutzfeldt-Jakob disease (CJD) is a rapidly progressive, rare, transmissible, and universally fatal neurodegenerative condition caused by prion proteins. The condition has a long incubation period. CJD was first described in 1920 by Hans Creutzfeldt and later in 1921 and 1923 by Alfons Jakob.
    Creutzfeldt-Jakob disease (CJD) is caused by an abnormal infectious protein in the brain called a prion. Proteins are molecules made up of amino acids that help the cells in our body function. They begin as a string of amino acids that then fold themselves into a 3-dimensional shape.
    Creutzfeldt-Jakob disease and related conditions appear to be caused by changes to a type of protein called a prion. These proteins are typically produced in the body. But when they encounter infectious prions, they fold and become another shape that's not typical. They can spread and affect processes in the body.
    The name Creutzfeldt–Jakob disease was introduced by Walther Spielmeyer in 1922, after the German neurologists Hans Gerhard Creutzfeldt and Alfons Maria Jakob. CJD is caused by a type of abnormal shaping of a protein known as a prion.
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    Creutzfeldt–Jakob disease - Wikipedia

    About 70% of people die within a year of diagnosis. [4] The name "Creutzfeldt–Jakob disease" was introduced by Walther Spielmeyer in 1922, after the German neurologists Hans Gerhard Creutzfeldt and Alfons Maria Jakob. [6] CJD is caused by a type of abnormal shaping of a protein known as a prion. [7] Se mere

    Creutzfeldt–Jakob disease (CJD), also known as subacute spongiform encephalopathy or neurocognitive disorder due to prion disease, is a fatal degenerative Se mere

    The first symptom of CJD is usually rapidly progressive dementia, leading to memory loss, personality changes, and hallucinations Se mere

    Testing for CJD has historically been problematic, due to nonspecific nature of early symptoms and difficulty in safely obtaining brain tissue … Se mere

    The condition is universally fatal. As of 1981, no one was known to have lived longer than 2.5 years after the onset of CJD symptoms. In 2011, Se mere

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    CJD is a type of transmissible spongiform encephalopathy (TSE), which are caused by prions. Prions are misfolded proteins that occur in the … Se mere

    As of 2023, there is no cure or effective treatment for CJD. Some of the symptoms like twitching can be managed, but otherwise treatment is palliative care. Psychiatric … Se mere

    CDC monitors the occurrence of CJD in the United States through periodic reviews of national mortality data. According to the CDC:
    • CJD … Se mere

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  4. Creutzfeldt-Jakob disease - Symptoms & causes

    WEBden 28. jan. 2023 · Creutzfeldt-Jakob disease and related conditions appear to be caused by changes to a type of protein called a prion. These proteins are typically produced in the body. But when they encounter …

  5. Creutzfeldt-Jakobs sygdom - Patienthåndbogen på sundhed.dk

  6. Creutzfeldt Jakob Disease - StatPearls - NCBI Bookshelf

    WEBden 30. jan. 2024 · Creutzfeldt-Jakob disease (CJD) is a rapidly progressive, rare, transmissible, and universally fatal neurodegenerative …

    • Forfatter: Kranthi K. Sitammagari, Wajeed Masood
    • Udgivet: 2024/01/30
    • Publish Year: 2019
  7. Creutzfeldt-Jakob disease - Causes - NHS

  8. Clinical Overview of Creutzfeldt-Jakob Disease (CJD)

  9. Creutzfeldt-Jakob Disease (CJD) - Neurologic Disorders - Merck …

  10. Creutzfeldt Jakob Disease Agent - an overview - ScienceDirect

  11. Creutzfeldt-Jakob Disease | National Institute of Neurological ...

  12. Creutzfeldt-Jakob Disease | SpringerLink