Minimal change prion retinopathy: Morphometric comparison of retinal and brain prion deposits in Creutzfeldt-Jakob disease

[1]  Neena Singh,et al.  Upregulation of brain hepcidin in prion diseases , 2021, Prion.

[2]  B. Chesebro,et al.  Prion-induced photoreceptor degeneration begins with misfolded prion protein accumulation in cones at two distinct sites: cilia and ribbon synapses , 2021, Acta neuropathologica communications.

[3]  Neena Singh,et al.  Prions and prion diseases: Insights from the eye. , 2020, Experimental eye research.

[4]  C. Leung,et al.  Adaptive optics two-photon microscopy enables near-diffraction-limited and functional retinal imaging in vivo , 2020, Light: Science & Applications.

[5]  C. Carroll,et al.  Creutzfeldt-Jakob disease: a systematic review of global incidence, prevalence, infectivity, and incubation. , 2020, The Lancet. Infectious diseases.

[6]  B. Caughey,et al.  Prion Seeds Distribute throughout the Eyes of Sporadic Creutzfeldt-Jakob Disease Patients , 2018, mBio.

[7]  S. Sorbi,et al.  Sporadic Fatal Insomnia in Europe: Phenotypic Features and Diagnostic Challenges , 2018, Annals of neurology.

[8]  M. Takao,et al.  PrPres deposition in the retina is a common finding of sporadic, familial and iatrogenic Creutzfeldt-Jakob diseases (CJD) , 2018, Acta Neuropathologica Communications.

[9]  D. Kazis,et al.  Diagnostic challenge of non‐specific visual symptoms: consideration of Heidenhain variant of Creutzfeldt‐Jakob disease , 2018, Clinical & experimental optometry.

[10]  J. Lenk,et al.  Rapid progressive visual decline and visual field defects in two patients with the Heidenhain variant of Creutzfeld-Jakob disease , 2018, Journal of Clinical Neuroscience.

[11]  Keith L Black,et al.  Retinal amyloid pathology and proof-of-concept imaging trial in Alzheimer's disease. , 2017, JCI insight.

[12]  J. Collinge.  Mammalian prions and their wider relevance in neurodegenerative diseases , 2016, Nature.

[13]  Jodi D. Smith,et al.  Temporal Resolution of Misfolded Prion Protein Transport, Accumulation, Glial Activation, and Neuronal Death in the Retinas of Mice Inoculated with Scrapie. , 2016, The American journal of pathology.

[14]  S. Capellari,et al.  Revisiting the Heidenhain Variant of Creutzfeldt-Jakob Disease: Evidence for Prion Type Variability Influencing Clinical Course and Laboratory Findings , 2015, Journal of Alzheimer's disease : JAD.

[15]  H. Danesh-Meyer,et al.  Visual symptoms in the presentation of Creutzfeldt–Jakob disease , 2015, Journal of Clinical Neuroscience.

[16]  C. Haigh,et al.  The Prion Protein N1 and N2 Cleavage Fragments Bind to Phosphatidylserine and Phosphatidic Acid; Relevance to Stress-Protection Responses , 2015, PloS one.

[17]  M. Halliday,et al.  Prions: Generation and Spread Versus Neurotoxicity , 2014, The Journal of Biological Chemistry.

[18]  B. Ghetti,et al.  Incidence and spectrum of sporadic Creutzfeldt–Jakob disease variants with mixed phenotype and co-occurrence of PrPSc types: an updated classification , 2009, Acta Neuropathologica.

[19]  J. Richt,et al.  Retinal Function and Morphology Are Altered in Cattle Infected with the Prion Disease Transmissible Mink Encephalopathy , 2009, Veterinary pathology.

[20]  D. Nicolle,et al.  Creutzfeldt-Jakob disease presenting with visual manifestations. , 2008, Canadian journal of ophthalmology. Journal canadien d'ophtalmologie.

[21]  M. Horiguchi,et al.  Electroretinograms in three cases of Creutzfeldt-Jakob disease with visual disturbances , 2008, Japanese Journal of Ophthalmology.

[22]  B. Chesebro,et al.  Prion Protein Expression Differences in Microglia and Astroglia Influence Scrapie-Induced Neurodegeneration in the Retina and Brain of Transgenic Mice , 2007, Journal of Virology.

[23]  Hyoung-Gon Lee,et al.  Increased expression of prion protein is associated with changes in dopamine metabolism and MAO activity in PC12 cells , 1999, Journal of Molecular Neuroscience.

[24]  C. Masters,et al.  Correlative studies support lipid peroxidation is linked to PrPres propagation as an early primary pathogenic event in prion disease , 2006, Brain Research Bulletin.

[25]  N. Barbaro,et al.  Trends in acoustic neuroma and cellular phones: Is there a link? , 2006, Neurology.

[26]  R. Armstrong.  Creutzfeldt‐Jakob disease and vision , 1997, Clinical & experimental optometry.

[27]  R. Will,et al.  Isolated visual symptoms at onset in sporadic Creutzfeldt-Jakob disease: the clinical phenotype of the “Heidenhain variant” , 2005, British Journal of Ophthalmology.

[28]  J. Ironside,et al.  Abnormal prion protein in the retina of the most commonly occurring subtype of sporadic Creutzfeldt-Jakob disease , 2005, British Journal of Ophthalmology.

[29]  P. Lantos,et al.  Size frequency distribution of prion protein (PrP) aggregates in variant Creutzfeldt-Jakob disease (vCJD) , 2005, Journal of Neural Transmission.

[30]  Charles Weissmann,et al.  The state of the prion , 2004, Nature Reviews Microbiology.

[31]  T. Shirabe,et al.  Electrophysiological and pathological studies on Creutzfeldt-Jakob disease with retinal involvement , 1986, Documenta Ophthalmologica.

[32]  J. Ironside,et al.  Prion protein accumulation in eyes of patients with sporadic and variant Creutzfeldt-Jakob disease. , 2003, Investigative ophthalmology & visual science.

[33]  H. Budka,et al.  Evidence for Oxidative Stress in Experimental Prion Disease , 2000, Neurobiology of Disease.

[34]  C. Lueck,et al.  Creutzfeldt-Jakob disease and the eye. II. Ophthalmic and neuro-ophthalmic features , 2000, Eye.

[35]  B. Steinhoff,et al.  The Heidenhain variant of Creutzfeldt-Jakob disease. , 1999, Archives of neurology.

[36]  S. Prusiner,et al.  Etiology and pathogenesis of prion diseases. , 1995, The American journal of pathology.

[37]  S. Chiba,et al.  [A case of the panencephalopathic type of Creutzfeldt-Jakob disease with retinal involvement]. , 1992, [Hokkaido igaku zasshi] The Hokkaido journal of medical science.

[38]  N. Cashman,et al.  Nearly ubiquitous tissue distribution of the scrapie agent precursor protein , 1992, Neurology.

[39]  S. Prusiner,et al.  Molecular biology of prion diseases , 1991, Science.

[40]  Stephen J. DeArmond,et al.  Transgenetic studies implicate interactions between homologous PrP isoforms in scrapie prion replication , 1990, Cell.

[41]  C. Sigurdson,et al.  [Prion diseases?]. , 1985, Deutsche medizinische Wochenschrift.

[42]  R. Will,et al.  A retrospective study of Creutzfeldt-Jakob disease in England and Wales 1970-79. I: Clinical features. , 1984, Journal of neurology, neurosurgery, and psychiatry.

[43]  A. Tarkkanen,et al.  Creutzfeld-Jakob disease. , 1980, Transactions of the ophthalmological societies of the United Kingdom.

[44]  A. Roth,et al.  Virus-simulating structures in the optic nerve head in Creutzfeldt-Jakob disease. , 1979, American journal of ophthalmology.

[45]  D. Albert,et al.  Creutzfeldt-Jakob disease and optic atrophy. , 1979, American journal of ophthalmology.