Genetic PrP Prion Diseases

Kim, Mee-Ohk, Takada, Leonel T., Wong, Katherine, Forner, Sven A., Geschwind, Michael D.·2018·Cold Spring Harbor Perspectives in Biology
DOI 10.1101/cshperspect.a033134

Cited by (130)

Items 101–130 of 130

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  2. DOENÇA CAUSADA POR PRÍON ASSOCIADA COM DIARRÉIA E NEUROPATIA AUTÔNOMA
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  4. RELATO DE CASO: INSÔNIA FATAL
    Clara Souza Oliveira, Letícia Edviges Nascimento, Maria Fernanda Santa Rosa Santos, Ray Braga Romero · 2023
  5. PRIONOPATIA VARIAVELMENTE SENSÍVEL À PROTEASE
    Bruna Gonzatti Batista, Gabriel Henrique Ferracioli Alvarenga, Luana Marcondes Emergente Caproni, Fiorita Gonzáles Lopes Mundim · 2023
  6. RELATO DE CASO: CREUTZFELDT-JAKOB VARIANTE
    Annita Maria de Oliveira Fagundes, Anna Clara Fachetti Carvalho, Gustavo Oliveira Silva, Fiorita Gonzáles Lopes Mundim · 2023
  7. RELATO DE CASO: INSÔNIA FAMILIAR FATAL
    Renata Silva Diniz, Luiza D’Ottaviano Cobos, Ana Elisa Molina David, Gérsika Bitencourt Santos · 2023
  8. RELATOS DE CASOS: KURU
    Luiza D’Ottaviano Cobos, Laiane Silva Pires, Lais Bruzadelli Franco De Carvalho, Ray Braga Romero · 2023
  9. RELATOS DE CASOS: DOENÇA DE CREUTZFELDT-JAKOB
    Victória Toledo Silva, Marcela Eduarda de Andrade Sartori Simões, Maria Eduarda Siqueira de Oliveira, Ray Braga Romero · 2023
  10. RELATO DE CASO: DOENÇA DE CREUTZFELDT-JAKOB FAMILIAR
    Marcela Eduarda de Andrade Sartori Simões, Lara de Brito Carneiro, Amanda Santana de Medeiros Dalla Pria, Fiorita Gonzáles Lopes Mundim · 2023
  11. DOENÇA DE GERSTMANN-STRÄUSSLER-SCHEINKER
    Eduarda de Melo Morando Amaral, Letícia Alves Madeira, Letícia Benevenutti, Gérsika Bitencourt Santos · 2023
  12. RELATOS DE CASOS: DOENÇA CAUSADA POR PRÍON ASSOCIADA COM DIARREIA E NEUROPATIA AUTÔNOMA
    Gabriel Henrique Carneiro Junqueira, Karen dos Reis Bracci, Yasmin Teixeira Nunes, Ray Braga Romero · 2023
  13. RELATO DE CASO: DOENÇA DE GERSTMANN-STRÄUSSLER-SCHEINKER
    Carolina Rodrigues Leal, Isabella Miranda Esteves Orsi, Nicole Elamos Rezende Vasconcelos, Gérsika Bitencourt Santos · 2023
  14. Two Chinese patients of sporadic Creutzfeldt–Jacob disease with a S97N mutation in PRNP gene
    Dong-Lin Liang, Qi Shi, Kang Xiao, A Ruhan, Wei Zhou, Xiao‐Ping Dong · 2023 · Prion
  15. Familial Creutzfeld-Jakob disease, compatible with PRNP c.532G>A (p.Asp178sn) gene mutation
    Yeiscimin Sánchez-Escobedo, María del Rosario López-Zapata, Julio César López-Valdés, Rafael Sánchez-Mata, Laura Mestre-Orozco, Ulises García-González · 2023 · Archivos de Neurociencias
  16. An Overview of Prion Diseases: Protein Transformation, Effects on Animals, and Current Treatments
    Neha Katakamshetty, Jothsna Kethar, Rajagopal Appavu · 2023 · Journal of Student Research
  17. Prion protein E219K polymorphism: from the discovery of the KANNO blood group to interventions for human prion disease
    Si-Si Wang, Zhaoli Meng, Yi-Wen Zhang, Yi-Shuang Yan, Ling-Bo Li · 2024 · Frontiers in Neurology
  18. Prion Diseases
    2024 · American Registry of PathologyArlington, Virginia eBooks
  19. Role of Enzymes in Prion Disease: A Molecular Mechanism
    Sayed Mohammed Firdous, Sourav Pal, Subhajit Mandal · 2024 · Springer eBooks
  20. Creutzfeldt-Jakob Disease With Double Mutations at Codon 180 and Codon 232 of PRNP
    Sumin Kim, Yong-Sun Kim, Kee Duk Park, Seung‐Ah Lee · 2025 · Journal of Clinical Neurology
  21. Novel insight into genetic impacts on neurodegenerative dementia
    Xuewen Xiao, Shilin Luo, Jinchen Li, Bin Jiao, Lu Shen · 2025 · Ageing and Neurodegenerative Diseases
  22. Creutzfeldt–Jakob Disease and Other Prion Diseases
    Igor Prufer Araujo, Michael D. Geschwind · 2025 · Cambridge University Press eBooks
  23. Neuropathology of Dementia
    Eunjoo Kim, Sarat C. Vatsavayai, William W. Seeley · 2025 · Cambridge University Press eBooks
  24. Gerstmann–Sträussler–Scheinker syndrome neuropathology in a Creutzfeldt–Jakob disease-like phenotype patient caused by a novel 6-OPRI sequence in the PRNP gene
    Matyáš Sýkora, S. Baranová, Eva Parobková, Tibor Moško, J. Keller, Karel Holada, Robert Rusina, Radoslav Matěj · 2025 · Revue Neurologique
  25. Rare and Rapidly Progressive Syndromes
    Emily N. Vanderbleek, Daniel S. Weitzner, Joseph J. Boscarino · 2026 · Springer eBooks
  26. The octapeptide repeats of prion protein play critical roles in the pathogenesis of prion diseases
    Xiangyi Zhang, Jingjing Zhang, Yan Zhang, Dan Wang, Gaixiu Liu, Mengfei Wang, Chaoyang Li, Qi Shi, Xiaoping Dong, Chonggang Yuan et al. · 2026 · Acta Neuropathologica Communications
  27. Gerstmann—Sträussler—Scheinker disease
    Е А Катунина, I.A. Putyatin, Mikhail B. Dolgushin, Наделяев Ростислав Валерьевич · 2026 · S S Korsakov Journal of Neurology and Psychiatry
  28. Genetic Creutzfeldt–Jakob disease associated with 5-octapeptide repeat insertion in the PRNP gene: case and pedigree report and literature review
    Qiang Geng, Rui Liu, Jianing Xia, Yinglei Lv, Zhongyun Chen, Yan Lu · 2026 · Neurological Sciences
  29. Metal Ions and Protein Aggregation: Unraveling Molecular Interactions and Theranostic Prospects in Proteinopathies
    Danilo Milardi, Jiyeon Han, Hyuck Jin Lee, Feng Ding, Yifat Miller, Peter Faller, Ashley Ian Bush, Peter John Crouch, David Isaac Finkelstein, Kay L. Double et al. · 2026 · Chemical Reviews
  30. Therapeutic strategies in prion disease: current evidence, translational challenges, and emerging directions
    Yi-Xin Zhu, Barry M. Bradford, N. Mabbott · 2026 · Frontiers in Neuroscience