lysine has been researched along with Creutzfeldt-Jakob Syndrome in 17 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (11.76) | 18.2507 |
| 2000's | 5 (29.41) | 29.6817 |
| 2010's | 9 (52.94) | 24.3611 |
| 2020's | 1 (5.88) | 2.80 |
| Authors | Studies |
|---|---|
| Foliaki, ST; Groveman, BR; Haigh, CL; Walters, RO; Williams, K; Wood, AR; Yuan, J; Zou, WQ | 1 |
| Hirata, K; Kitamoto, T; Nakamura, T; Satoh, K; Suzuki, K; Takayanagi, M | 1 |
| Appel, S; Chapman, J; Cohen, OS; Hoffmann, C; Kahana, E; Korczyn, AD; Lee, H; Nitsan, Z; Rosenmann, H | 1 |
| Clerici, F; Contri, P; Di Fede, G; Elia, A; Girotti, F; Mariani, C; Tagliavini, F | 1 |
| Capellari, S; Di Fede, G; Mancuso, M; Moretti, P; Murri, L; Orsucci, D; Parchi, P; Siciliano, G; Strammiello, R; Suardi, S; Tagliavini, F | 1 |
| Miwa, M; Nagasaka, K; Nagasaka, T; Nakamura, Y; Ohta, E; Shindo, K; Shiozawa, Z; Togashi, S | 1 |
| Biacabe, AG; Budka, H; Höftberger, R; Kapás, I; Kovacs, GG; László, L; Majtenyi, K; Meyronet, D; Perret-Liaudet, A; Quadrio, I; Sciot, R; Seguin, J; Streichenberger, N; Ströbel, T; Vandenberghe, R | 1 |
| Bizzarro, A; Capellari, S; Guglielmi, V; Iannaccone, E; Masullo, C; Minicuci, G; Parchi, P; Servidei, S; Vita, MG | 1 |
| Appel, SA; Blatt, I; Chapman, J; Cohen, OS; Hoffman, C; Prohovnik, I | 1 |
| Binyamin, O; Canello, T; Cohen, E; Frid, K; Friedman-Levi, Y; Gabizon, R; Mizrahi, M | 1 |
| Botond, G; Budka, H; Keller, E; Kovacs, GG; László, L; Molnár, K | 1 |
| Barcs, G; Finta, L; Holló, A; Kamondi, A; Osztie, E; Papp, E; Sólyom, A; Szucs, A; Várallyay, P; Varga, D | 1 |
| Belay, G; Budka, H; Hainfellner, JA; Jarius, C; Kovacs, GG; Mitrova, E | 1 |
| Bindoff, LA; Farbu, E; Krossnes, BK; Mørk, S; Tysnes, OB | 1 |
| Doh-ura, K; Goto, I; Inoue, I; Kitamoto, T; Shii, H; Tateishi, J | 1 |
| Higuchi, J; Kitamoto, T; Shibuya, S; Shin, RW; Tateishi, J | 1 |
| Attane, F; Beaudry, P; Besson, G; Delasnerie-Lauprêtre, N; Hannequin, D; Laplanche, JL; Manivet, P; Peoc'h, K | 1 |
17 other study(ies) available for lysine and Creutzfeldt-Jakob Syndrome
| Article | Year |
|---|---|
Hereditary E200K mutation within the prion protein gene alters human iPSC derived cardiomyocyte function.
Topics: Creutzfeldt-Jakob Syndrome; Humans; Induced Pluripotent Stem Cells; Lysine; Mutation; Myocytes, Cardiac; Prion Proteins; Superoxides | 2022 |
[Genetic Creutzfeldt-Jakob disease with a glutamate-to-lysine substitution at codon 219 (E219K) in the presence of the E200K mutation presenting with rapid progressive dementia following slowly progressive clinical course].
Topics: 14-3-3 Proteins; Alleles; Amino Acid Substitution; Biomarkers; Brain; Codon; Creutzfeldt-Jakob Syndrome; Diffusion Magnetic Resonance Imaging; Disease Progression; Electroencephalography; Frontotemporal Dementia; Glutamates; Humans; Lysine; Male; Middle Aged; Mutation; Polymorphism, Genetic; Prion Proteins; tau Proteins | 2018 |
Familial Creutzfeldt-Jakob disease with the E200K mutation: longitudinal neuroimaging from asymptomatic to symptomatic CJD.
Topics: Adult; Brain; Creutzfeldt-Jakob Syndrome; Electroencephalography; Female; Glutamic Acid; Humans; Image Processing, Computer-Assisted; Longitudinal Studies; Lysine; Magnetic Resonance Imaging; Male; Mental Status Schedule; Middle Aged; Mutation; Neuroimaging; Prion Proteins; Prions | 2015 |
Atypical presentation of Creutzfeldt-Jakob disease: the first Italian case associated with E196K mutation in the PRNP gene.
Topics: Aged; Creutzfeldt-Jakob Syndrome; DNA Mutational Analysis; Female; Glutamic Acid; Humans; Italy; Lysine; Magnetic Resonance Imaging; Prion Proteins; Prions | 2008 |
Creutzfeldt-Jakob disease with E200K PRNP mutation: a case report and revision of the literature.
Topics: Creutzfeldt-Jakob Syndrome; DNA Mutational Analysis; Female; Glutamic Acid; Humans; Lysine; Middle Aged; Mutation; Prion Proteins; Prions | 2009 |
Rhythmic pupillary oscillation in Creutzfeldt-Jakob disease associated with the Glu/Lys mutation of prion protein codon 200.
Topics: Aged; Creutzfeldt-Jakob Syndrome; Female; Glutamic Acid; Humans; Lysine; Magnetic Resonance Imaging; Male; Mutation; Periodicity; Prions; Pupil Disorders | 2010 |
Genetic Creutzfeldt-Jakob disease associated with the E200K mutation: characterization of a complex proteinopathy.
Topics: Amino Acid Substitution; Creutzfeldt-Jakob Syndrome; Female; Genetic Predisposition to Disease; Glutamic Acid; Humans; Lysine; Male; Middle Aged; Prion Proteins; Prions | 2011 |
An atypical phenotype of CJD associated with the E200K mutation in the prion protein gene.
Topics: Amino Acid Substitution; Creutzfeldt-Jakob Syndrome; Female; Genetic Heterogeneity; Glutamic Acid; Humans; Lysine; Middle Aged; Phenotype; Point Mutation; Prion Proteins; Prions | 2010 |
The EEG in E200K familial CJD: relation to MRI patterns.
Topics: Aged; Brain; Brain Mapping; Creutzfeldt-Jakob Syndrome; Diffusion Magnetic Resonance Imaging; Electroencephalography; Female; Glutamic Acid; Humans; Lysine; Magnetic Resonance Imaging; Male; Middle Aged; Prions; Retrospective Studies | 2012 |
Copper is toxic to PrP-ablated mice and exacerbates disease in a mouse model of E200K genetic prion disease.
Topics: Age Factors; Animals; Cells, Cultured; Cerebellum; Chromatography, Affinity; Copper; Copper Sulfate; Creutzfeldt-Jakob Syndrome; Disease Models, Animal; Dose-Response Relationship, Drug; Embryo, Mammalian; Enzyme Inhibitors; Fibroblasts; Gene Expression Regulation; Glutamic Acid; Humans; Imidazoles; Lysine; Mice; Mice, Inbred C57BL; Mice, Transgenic; Prions; Protein Binding | 2012 |
Intraneuronal immunoreactivity for the prion protein distinguishes a subset of E200K genetic from sporadic Creutzfeldt-Jakob Disease.
Topics: Adaptor Proteins, Signal Transducing; Aged; Amyloid beta-Peptides; Chi-Square Distribution; Creutzfeldt-Jakob Syndrome; DNA-Binding Proteins; Female; Glutamic Acid; Humans; Intranuclear Inclusion Bodies; Lysine; Male; Microscopy, Electron, Transmission; Middle Aged; Mutation; Nerve Tissue Proteins; Neurons; Prions; rab5 GTP-Binding Proteins; Sequestosome-1 Protein; Synucleins; Tubulin | 2012 |
Clinical experiences with Creutzfeldt-Jakob disease: three case studies.
Topics: Aged; Autopsy; Brain; Cerebellar Ataxia; Creutzfeldt-Jakob Syndrome; Diagnosis, Differential; Electroencephalography; Fatal Outcome; Female; Glutamic Acid; Humans; Lysine; Magnetic Resonance Imaging; Male; Middle Aged; Mutation; Prion Proteins; Prions; Seizures; Speech Disorders | 2012 |
Distinctive cerebellar immunoreactivity for the prion protein in familial (E200K) Creutzfeldt-Jakob disease.
Topics: Cerebellum; Creutzfeldt-Jakob Syndrome; Genetic Variation; Glutamic Acid; Humans; Immunohistochemistry; Lysine; Methionine; Mutation; Prions; Valine | 2003 |
Two Norwegian sisters with late onset Creutzfeldt-Jakob disease caused by the E200K mutation.
Topics: Aged, 80 and over; Creutzfeldt-Jakob Syndrome; Female; Glutamic Acid; Humans; Lysine; Mutation; Norway; Prions; Siblings | 2007 |
Japanese family with Creutzfeldt-Jakob disease with codon 200 point mutation of the prion protein gene.
Topics: Adolescent; Adult; Cerebellum; Codon; Creutzfeldt-Jakob Syndrome; Deoxyribonucleases, Type II Site-Specific; DNA; Female; Genetic Variation; Humans; Immunohistochemistry; Japan; Lymphocytes; Lysine; Male; Middle Aged; Pedigree; Point Mutation; Polymerase Chain Reaction; Prions; PrPSc Proteins | 1994 |
Codon 219 Lys allele of PRNP is not found in sporadic Creutzfeldt-Jakob disease.
Topics: Alanine; Alleles; Creutzfeldt-Jakob Syndrome; DNA Mutational Analysis; Humans; Lysine; Point Mutation; Polymorphism, Genetic; Prions | 1998 |
Identification of three novel mutations (E196K, V203I, E211Q) in the prion protein gene (PRNP) in inherited prion diseases with Creutzfeldt-Jakob disease phenotype.
Topics: Aged; Amino Acid Substitution; Amyloid; Creutzfeldt-Jakob Syndrome; Female; Glutamic Acid; Glutamine; Humans; Isoleucine; Lysine; Male; Middle Aged; Mutation, Missense; Phenotype; Prion Proteins; Prions; Protein Precursors; Valine | 2000 |