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There is a page named "Familial Alzheimer-like prion disease" on Wikipedia
- Transmissible spongiform encephalopathy (redirect from Prion disease)(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
- 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
- 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
- Fatal insomnia (redirect from Fatal Familial 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
- 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
- Proteinopathy (redirect from Protein misfolding disease)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
- 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
- Amyloid (redirect from Amyloidosis, familial)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
- ALS (redirect from Familial amyotrophic lateral sclerosis)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
- 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
- Camel spongiform encephalopathy (redirect from Mad camel disease)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
- 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
- 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
- Dementia with Lewy bodies (redirect from Diffuse Lewy body disease)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
- 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
- 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
- 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
- animals to human. This disease causes by the misfolding of prions. The process of misfolding is the self-replicating of the prions. Prions are protein particles