Compounds > glutamic acid

glutamic acid and CJD (Creutzfeldt-Jakob Disease)

glutamic acid has been researched along with CJD (Creutzfeldt-Jakob Disease) in 15 studies

Research

Studies (15)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	6 (40.00)	29.6817
2010's	9 (60.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Akagi, A; Iwasaki, Y; Kitamoto, T; Mimuro, M; Yamada, M; Yoshida, 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
Cordery, RJ; Godbolt, A; MacManus, D; Rossor, MN; Waldman, AD	1
Bindoff, LA; Farbu, E; Krossnes, BK; Mørk, S; Tysnes, OB	1
Attane, F; Beaudry, P; Besson, G; Delasnerie-Lauprêtre, N; Hannequin, D; Laplanche, JL; Manivet, P; Peoc'h, K	1

Other Studies

15 other study(ies) available for glutamic acid and CJD (Creutzfeldt-Jakob Disease)

Article	Year
Pathological progression of genetic Creutzfeldt-Jakob disease with a PrP V180I mutation. Prion, 2018, 01-02, Volume: 12, Issue:1 Topics: Aged; Aged, 80 and over; Brain; Creutzfeldt-Jakob Syndrome; Disease Progression; Gliosis; Glutamic Acid; Humans; Isoleucine; Methionine; Middle Aged; Mutation; Prion Proteins; Vacuoles; Valine	2018
Familial Creutzfeldt-Jakob disease with the E200K mutation: longitudinal neuroimaging from asymptomatic to symptomatic CJD. Journal of neurology, 2015, Volume: 262, Issue:3 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. Journal of the neurological sciences, 2008, Dec-15, Volume: 275, Issue:1-2 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. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2009, Volume: 30, Issue:5 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. Movement disorders : official journal of the Movement Disorder Society, 2010, Jan-15, Volume: 25, Issue:1 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. Acta neuropathologica, 2011, Volume: 121, Issue:1 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. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2010, Volume: 31, Issue:6 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. Journal of neurology, 2012, Volume: 259, Issue:3 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. Neurobiology of disease, 2012, Volume: 45, Issue:3 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. Journal of neuropathology and experimental neurology, 2012, Volume: 71, Issue:3 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. Ideggyogyaszati szemle, 2012, Nov-30, Volume: 65, Issue:11-12 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. Acta neuropathologica, 2003, Volume: 105, Issue:5 Topics: Cerebellum; Creutzfeldt-Jakob Syndrome; Genetic Variation; Glutamic Acid; Humans; Immunohistochemistry; Lysine; Methionine; Mutation; Prions; Valine	2003
Short TE quantitative proton magnetic resonance spectroscopy in variant Creutzfeldt-Jakob disease. European radiology, 2006, Volume: 16, Issue:8 Topics: Adult; Aspartic Acid; Case-Control Studies; Choline; Creatine; Creutzfeldt-Jakob Syndrome; Female; Glutamic Acid; Humans; Inositol; Magnetic Resonance Spectroscopy; Male; Phosphocreatine; Protons; Statistics, Nonparametric	2006
Two Norwegian sisters with late onset Creutzfeldt-Jakob disease caused by the E200K mutation. Journal of neurology, 2007, Volume: 254, Issue:2 Topics: Aged, 80 and over; Creutzfeldt-Jakob Syndrome; Female; Glutamic Acid; Humans; Lysine; Mutation; Norway; Prions; Siblings	2007
Identification of three novel mutations (E196K, V203I, E211Q) in the prion protein gene (PRNP) in inherited prion diseases with Creutzfeldt-Jakob disease phenotype. Human mutation, 2000, Volume: 15, Issue:5 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