| scholarly article | Q13442814 |
| P50 | author | Suman Jayadev | Q43407273 |
| Bernardino F. Ghetti | Q56863342 | ||
| Thomas J Montine | Q67207389 | ||
| P2093 | author name string | Thomas D Bird | |
| Gerard D Schellenberg | |||
| James B Leverenz | |||
| Ellen J Steinbart | |||
| David Nochlin | |||
| James A Mastrianni | |||
| Parvoneh Poorkaj | |||
| P2860 | cites work | Neuropathological stageing of Alzheimer-related changes | Q27860862 |
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| A sporadic case of Creutzfeldt-Jakob disease with beta-amyloid deposits and alpha-synuclein inclusions | Q48098461 | ||
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| Gerstmann-Sträussler-Scheinker disease. II. Neurofibrillary tangles and plaques with PrP-amyloid coexist in an affected family | Q69375844 | ||
| Gerstmann-Sträussler-Scheinker disease (PRNP P102L): amyloid deposits are best recognized by antibodies directed to epitopes in PrP region 90-165 | Q71832807 | ||
| Amyloid fibrils in Gerstmann-Sträussler-Scheinker disease (Indiana and Swedish kindreds) express only PrP peptides encoded by the mutant allele | Q93870994 | ||
| P433 | issue | 4 | |
| P921 | main subject | Alzheimer's disease | Q11081 |
| prion protein family | Q24724413 | ||
| P304 | page(s) | 712-720 | |
| P577 | publication date | 2011-03-17 | |
| P1433 | published in | Annals of Neurology | Q564414 |
| P1476 | title | Familial prion disease with Alzheimer disease-like tau pathology and clinical phenotype | |
| P478 | volume | 69 |
| Q33881345 | 11C-PIB PET imaging reveals that amyloid deposition in cases with early-onset Alzheimer's disease in the absence of known mutations retains higher levels of PIB in the basal ganglia |
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| Q84522846 | A novel mutation I215V in the PRNP gene associated with Creutzfeldt-Jakob and Alzheimer's diseases in three patients with divergent clinical phenotypes |
| Q37393739 | A novel prion disease associated with diarrhea and autonomic neuropathy |
| Q37377977 | Activation of the unfolded protein response and granulovacuolar degeneration are not common features of human prion pathology |
| Q60309357 | Amyloid- and tau-PET imaging in a familial prion kindred |
| Q26765999 | Beta-Amyloid and Tau-Protein: Structure, Interaction, and Prion-Like Properties |
| Q42007280 | Burial of the polymorphic residue 129 in amyloid fibrils of prion stop mutants |
| Q48000756 | C-Terminal-Deleted Prion Protein Fragment Is a Major Accumulated Component of Systemic PrP Deposits in Hereditary Prion Disease With a 2-Bp (CT) Deletion in PRNP Codon 178. |
| Q58781975 | Characterization of mutations in (prion) gene and their possible roles in neurodegenerative diseases |
| Q33761828 | Complex proteinopathy with accumulations of prion protein, hyperphosphorylated tau, α-synuclein and ubiquitin in experimental bovine spongiform encephalopathy of monkeys |
| Q41893320 | Conserved amyloid core structure of stop mutants of the human prion protein |
| Q37522591 | Distinct patterns of spread of prion infection in brains of mice expressing anchorless or anchored forms of prion protein |
| Q37053839 | Drivers: A Biologically Contextualized, Cross-Inferential View of the Epidemiology of Neurodegenerative Disorders |
| Q92603855 | Early-onset Alzheimer's disease patient with prion (PRNP) p.Val180Ile mutation |
| Q95933928 | Evaluating drug targets through human loss-of-function genetic variation |
| Q46560834 | Genetic PrP Prion Diseases |
| Q37491711 | Genetic Prion Disease Caused by PRNP Q160X Mutation Presenting with an Orbitofrontal Syndrome, Cyclic Diarrhea, and Peripheral Neuropathy |
| Q53396036 | Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer's Disease Sequencing Project. |
| Q39036368 | Genetic prion disease: Experience of a rapidly progressive dementia center in the United States and a review of the literature. |
| Q56069696 | Genetics of dementia |
| Q38027808 | Genetics of dementia: update and guidelines for the clinician |
| Q38091816 | Genetics of prion diseases |
| Q37596331 | Gerstmann-Sträussler-Scheinker disease and "anchorless prion protein" mice share prion conformational properties diverging from sporadic Creutzfeldt-Jakob disease |
| Q38871224 | Hereditary Human Prion Diseases: an Update |
| Q37969262 | Interaction between pathogenic proteins in neurodegenerative disorders |
| Q38600851 | Lavandula angustifolia extract improves deteriorated synaptic plasticity in an animal model of Alzheimer's disease |
| Q34576746 | Levels of the Mahogunin Ring Finger 1 E3 ubiquitin ligase do not influence prion disease |
| Q26750717 | Molecular genetics of early-onset Alzheimer's disease revisited |
| Q37464666 | Mutational analysis of PRNP in Alzheimer's disease and frontotemporal dementia in China |
| Q36218610 | New approaches to genetic counseling and testing for Alzheimer's disease and frontotemporal degeneration |
| Q34222296 | Next generation sequencing techniques in neurological diseases: redefining clinical and molecular associations |
| Q34244138 | Nonsense mutation in PRNP associated with clinical Alzheimer's disease |
| Q49957320 | Prion Proteins Without the Glycophosphatidylinositol Anchor: Potential Biomarkers in Neurodegenerative Diseases |
| Q34488612 | Proteomics analysis of amyloid and nonamyloid prion disease phenotypes reveals both common and divergent mechanisms of neuropathogenesis |
| Q36639581 | Quantifying prion disease penetrance using large population control cohorts |
| Q38089232 | Review: cerebral amyloid angiopathy, prion angiopathy, CADASIL and the spectrum of protein elimination failure angiopathies (PEFA) in neurodegenerative disease with a focus on therapy |
| Q37058503 | Screening of dementia genes by whole-exome sequencing in early-onset Alzheimer disease: input and lessons |
| Q35784863 | Squirrel monkeys (Saimiri sciureus) infected with the agent of bovine spongiform encephalopathy develop tau pathology |
| Q37989099 | The contribution of different prion protein types and host polymorphisms to clinicopathological variations in Creutzfeldt-Jakob disease |
| Q38623320 | The pathogenesis of soluble PrP fragments containing Aβ binding sites |
| Q55285207 | Two novel PRNP truncating mutations broaden the spectrum of prion amyloidosis. |
| Q37485590 | Unusual cerebral vascular prion protein amyloid distribution in scrapie-infected transgenic mice expressing anchorless prion protein |
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