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There is a page named "Familial Alzheimer-like prion disease" on Wikipedia

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  • Thumbnail for Transmissible spongiform encephalopathy
    (TSEs), also known as prion diseases, are a group of progressive, incurable, and fatal conditions that are associated with the prion hypothesis and affect...
    39 KB (4,300 words) - 01:33, 21 March 2025
  • Thumbnail for Prion
    neurodegenerative diseases like Alzheimer's disease, Parkinson's disease, and amyotrophic lateral sclerosis (ALS), which are sometimes referred to as prion-like diseases...
    101 KB (11,011 words) - 06:40, 20 March 2025
  • Familial Alzheimer-like prion disease is an exceptionally rare inherited prion disease. Its name comes from its presentation, which is similar to Alzheimer's...
    2 KB (154 words) - 18:23, 24 January 2025
  • Thumbnail for Creutzfeldt–Jakob disease
    disease (CJD), also known as subacute spongiform encephalopathy or neurocognitive disorder due to prion disease, is a fatal neurodegenerative disease...
    72 KB (7,743 words) - 20:22, 16 March 2025
  • Thumbnail for Fatal insomnia
    neurodegenerative prion disease that results in trouble sleeping as its hallmark symptom. The majority of cases are familial (fatal familial insomnia [FFI])...
    26 KB (2,892 words) - 01:26, 14 February 2025
  • Thumbnail for Parkinson's disease
    PMID 20351351. Brundin P, Melki R (October 2017). "Prying into the Prion Hypothesis for Parkinson's Disease". Journal of Neuroscience. 37 (41): 9808–9818. doi:10.1523/JNEUROSCI...
    129 KB (13,833 words) - 01:00, 21 March 2025
  • Thumbnail for Proteinopathy
    include such diseases as Creutzfeldt–Jakob disease (and a variant associated with mad cow disease) and other prion diseases, Alzheimer's disease, Parkinson's...
    62 KB (4,598 words) - 18:40, 29 January 2025
  • Thumbnail for Neurodegenerative disease
    disease, Huntington's disease, multiple system atrophy, tauopathies, and prion diseases. Neurodegeneration can be found in the brain at many different levels...
    61 KB (6,893 words) - 22:47, 2 February 2025
  • Thumbnail for Amyloid
    mainly sporadic and only a few cases are familial. Others are only familial. Some result from medical treatment. Prions are an infectious form of amyloids that...
    60 KB (6,536 words) - 06:58, 4 November 2024
  • Thumbnail for ALS
    family history of the disease, and these are known as familial ALS (hereditary). About half of these genetic cases are due to disease-causing variants in...
    133 KB (14,289 words) - 04:52, 10 March 2025
  • Thumbnail for Huntington's disease
    illnesses with genetic variants such as polycystic kidney disease, familial Alzheimer's disease and breast cancer. The European Molecular Genetics Quality...
    140 KB (14,628 words) - 20:23, 19 March 2025
  • collaboration with Italian researchers. This infection is a form of prion disease (transmissible spongiform encephalopathy, TSE) that affects camels....
    3 KB (248 words) - 22:38, 17 September 2024
  • neurodegenerative diseases, cells of the central nervous system stop working or die via neurodegeneration. An example of this is Alzheimer's disease. The other...
    16 KB (1,642 words) - 17:42, 20 January 2025
  • Thumbnail for Amyloid beta
    Amyloid beta (category Alzheimer's disease)
    prion infection. The oligomers are toxic to nerve cells. The other protein implicated in Alzheimer's disease, tau protein, also forms such prion-like...
    48 KB (5,298 words) - 23:41, 1 February 2025
  • Thumbnail for Variably protease-sensitive prionopathy
    Variably protease-sensitive prionopathy (category Rare diseases)
    Sensitive Prionopathy) is a sporadic prion protein disease first described in an abstract for a conference on prions in 2006, and this study was published...
    9 KB (910 words) - 13:01, 24 January 2024
  • Thumbnail for Dementia with Lewy bodies
    individuals with Alzheimer's disease (AD) are often found on autopsy to also have Lewy bodies, DLB has been characterized as an Alzheimer disease-related dementia;...
    134 KB (14,383 words) - 20:33, 14 February 2025
  • encephalopathies Prion Disease (Kuru, CJD, GSS, BSE) Alzheimer's disease Sickle cell anemia Parkinson's disease Huntington's disease Gibbs, Clarence J...
    6 KB (698 words) - 20:47, 22 June 2024
  • Thumbnail for Alpha-synuclein
    Alpha-synuclein pathology is also found in both sporadic and familial cases with Alzheimer's disease. The aggregation mechanism of alpha-synuclein is uncertain...
    84 KB (9,536 words) - 03:24, 10 March 2025
  • Thumbnail for Humanin
    Humanin (category Alzheimer's disease)
    factor abolishing neuronal cell death by a wide spectrum of familial Alzheimer's disease genes and Abeta". Proceedings of the National Academy of Sciences...
    18 KB (2,141 words) - 16:58, 18 September 2024
  • Thumbnail for NLRP3
    NLRP3 (category NOD-like receptors)
    protein-misfolding diseases, such as Alzheimer's, Parkinson's, and prion diseases. Amelioration of mouse models of many diseases has been shown to occur...
    17 KB (1,736 words) - 07:04, 19 October 2024
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