| scholarly article | Q13442814 |
| P356 | DOI | 10.1111/J.1750-3639.1995.TB00596.X |
| P8608 | Fatcat ID | release_xvcjrcsbofaqxp2liym67ul3eu |
| P698 | PubMed publication ID | 8520719 |
| P50 | author | Paweł P. Liberski | Q11814316 |
| P2093 | author name string | Tateishi J | |
| Regele H | |||
| Brown P | |||
| Kitamoto T | |||
| Diringer H | |||
| Hainfellner JA | |||
| Feucht M | |||
| Cervenáková L | |||
| Brantner-Inthaler S | |||
| P2860 | cites work | Ballooned neurons in select neurodegenerative diseases contain phosphorylated neurofilament epitopes | Q48423443 |
| Spongiform encephalopathy transmitted experimentally from Creutzfeldt-Jakob and familial Gerstmann-Sträussler-Scheinker diseases | Q48842211 | ||
| Neurofibrillary tangles of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease share antigenic determinants with those of Alzheimer disease | Q48877614 | ||
| Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism | Q48882672 | ||
| Molecular cloning of a human prion protein cDNA | Q24299790 | ||
| Dystrophic neurites around amyloid plaques of human patients with Gerstmann-Sträussler-Scheinker disease contain ubiquitinated inclusions | Q33262715 | ||
| Molecular biology of prion diseases | Q34534878 | ||
| Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles | Q34539307 | ||
| Proteinase-resistant prion protein accumulation in Syrian hamster brain correlates with regional pathology and scrapie infectivity | Q34541769 | ||
| Pro----leu change at position 102 of prion protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndrome | Q34679642 | ||
| Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gerstmann-Sträussler syndrome | Q34730862 | ||
| Inherited human prion diseases | Q37999562 | ||
| Familial dementia with PrP-positive amyloid plaques: a variant of Gerstmann-Sträussler syndrome | Q39102740 | ||
| A prion protein variant in a family with the telencephalic form of Gerstmann-Straussler-Scheinker syndrome | Q41134144 | ||
| Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease | Q41134643 | ||
| An amber mutation of prion protein in Gerstmann-Sträussler syndrome with mutant PrP plaques | Q42601576 | ||
| An insert mutation in the chromosome 20 amyloid precursor gene in a Gerstmann-Sträussler-Scheinker family | Q42605007 | ||
| Prion dementia without characteristic pathology | Q44108041 | ||
| Gerstmann-Sträussler-Scheinker's disease | Q44497215 | ||
| Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease | Q44697981 | ||
| Creutzfeldt-Jakob disease virus isolations from the Gerstmann-Sträussler syndrome with an analysis of the various forms of amyloid plaque deposition in the virus-induced spongiform encephalopathies | Q45794286 | ||
| Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome | Q46931937 | ||
| Characterisation of antisera raised against species-specific peptide sequences from scrapie-associated fibril protein and their application for post-mortem immunodiagnosis of spongiform encephalopathies | Q48225098 | ||
| Microglia is a component of the prion protein amyloid plaque in the Gerstmann-Sträussler-Scheinker syndrome. | Q48374047 | ||
| P433 | issue | 3 | |
| P921 | main subject | Austria | Q40 |
| P304 | page(s) | 201-211 | |
| P577 | publication date | 1995-07-01 | |
| P1433 | published in | Brain Pathology | Q4955776 |
| P1476 | title | The original Gerstmann-Sträussler-Scheinker family of Austria: divergent clinicopathological phenotypes but constant PrP genotype | |
| P478 | volume | 5 |
| Q35103451 | A case of Gerstmann-Sträussler-Scheinker disease with a novel six octapeptide repeat insertion |
| Q35122345 | A gene-targeted mouse model of P102L Gerstmann-Sträussler-Scheinker syndrome. |
| Q33910752 | Absence of spontaneous disease and comparative prion susceptibility of transgenic mice expressing mutant human prion proteins |
| Q34182647 | Allelic origin of protease-sensitive and protease-resistant prion protein isoforms in Gerstmann-Sträussler-Scheinker disease with the P102L mutation |
| Q36177322 | An overview of transmissible spongiform encephalopathies |
| Q64108049 | Analysis of 12 Chinese Patients with Proline-to-Leucine Mutation at Codon 102-Associated Gerstmann-Sträussler-Scheinker Disease |
| Q48192334 | Atypical parkinsonism due to a D202N Gerstmann-Sträussler-Scheinker prion protein mutation: first in vivo diagnosed case |
| Q49076261 | Biology and neuropathology of prion diseases |
| Q48808752 | Clinical and diagnostic findings in a patient with Creutzfeldt-Jakob disease (type Heidenhain). |
| Q42590888 | Codon 219 polymorphism of PRNP in healthy Caucasians and Creutzfeldt-Jakob disease patients |
| Q34057654 | Creutzfeldt-Jakob disease and the eye. I. Background and patient management |
| Q36174780 | Different patterns of truncated prion protein fragments correlate with distinct phenotypes in P102L Gerstmann-Sträussler-Scheinker disease |
| Q37258238 | Discriminant analysis of prion sequences for prediction of susceptibility |
| Q38162179 | From prion diseases to prion-like propagation mechanisms of neurodegenerative diseases. |
| Q46560834 | Genetic PrP Prion Diseases |
| Q39036368 | Genetic prion disease: Experience of a rapidly progressive dementia center in the United States and a review of the literature. |
| Q33457931 | Gerstmann-Sträussler-Scheinker disease subtypes efficiently transmit in bank voles as genuine prion diseases |
| Q47577189 | Gerstmann-Sträussler-Scheinker disease with atypical presentation. |
| Q61799148 | Gerstmann-Sträussler-Scheinker disease: A case report |
| Q47780564 | Gerstmann-Sträussler-Scheinker syndrome with variable phenotype in a new kindred with PRNP-P102L mutation |
| Q35122324 | Hereditary prion protein amyloidoses |
| Q38704461 | High phenotypic variability in Gerstmann-Sträussler-Scheinker disease. |
| Q34146052 | High prevalence of pathogenic mutations in patients with early-onset dementia detected by sequence analyses of four different genes |
| Q33952856 | Intracerebral distribution of the abnormal isoform of the prion protein in sporadic Creutzfeldt-Jakob disease and fatal insomnia |
| Q47149313 | Joint Scientific Opinion on any possible epidemiological or molecular association between TSEs in animals and humans |
| Q47690532 | Methods for Molecular Diagnosis of Human Prion Disease |
| Q34462913 | Molecular pathology of human prion disease |
| Q44572993 | Molecular-imaging probe 2-(1-[6-[(2-fluoroethyl)(methyl) amino]-2-naphthyl]ethylidene) malononitrile labels prion plaques in vitro. |
| Q38476222 | Pathology and immunocytochemistry of a kuru brain |
| Q36944491 | Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international series |
| Q83016325 | Phenotypic heterogeneity and genetic modifiers in prion disease caused by a Pro102Leu mutation in the PRNP gene |
| Q36359872 | Prion disease genetics |
| Q47950242 | Prion encephalopathy with insertion of octapeptide repeats: the number of repeats determines the type of cerebellar deposits. |
| Q35788165 | Prion protein-deficient neurons reveal lower glutathione reductase activity and increased susceptibility to hydrogen peroxide toxicity |
| Q34474868 | Review: contribution of transgenic models to understanding human prion disease. |
| Q35788064 | Selective neuronal vulnerability in human prion diseases. Fatal familial insomnia differs from other types of prion diseases |
| Q48357570 | Severe, early and selective loss of a subpopulation of GABAergic inhibitory neurons in experimental transmissible spongiform encephalopathies |
| Q45004848 | Targeting prion amyloid deposits in vivo. |
| Q85180476 | The Prion Diseases |
| Q48313878 | The prion diseases: Creutzfeldt-Jakob, Gerstmann-Sträussler-Scheinker, and related disorders |
| Q36319802 | The risk of transmission of variant Creutzfeldt-Jakob disease via contact lenses and ophthalmic devices |
| Q41888735 | Transmissibility of Gerstmann-Sträussler-Scheinker syndrome in rodent models: New insights into the molecular underpinnings of prion infectivity. |
| Q35681248 | Transmission Properties of Human PrP 102L Prions Challenge the Relevance of Mouse Models of GSS. |
| Q42821914 | Ultrastructural characteristics (or evaluation) of Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies or prion diseases |
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