histidine has been researched along with Creutzfeldt-Jakob Syndrome in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (16.67) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (33.33) | 29.6817 |
| 2010's | 3 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Alboini, PE; Bizzarro, A; Capellari, S; Di Giuda, D; Gangemi, E; Gaudino, S; Masullo, C; Parchi, P; Sauchelli, D; Scaricamazza, E; Vita, MG | 1 |
| Abdi, Z; Adamson, G; Barnes, J; Beck, JA; Blair, M; Campbell, T; Clegg, SL; Collinge, J; Crutch, SJ; Druyeh, R; Fox, NC; Gambetti, P; Guerreiro, RJ; Harper, L; Kenny, J; Kretzschmar, H; Leung, KK; Lowe, J; Mahoney, CJ; Mead, S; Nicholas, JM; Ponto, C; Rohrer, JD; Rossor, MN; Rowe, JB; Schott, JM; Slattery, CF; Uphill, J; Warren, JD; Zerr, I | 1 |
| Johanidesová, S; Keller, J; Keller, O; Kovacs, GG; Matěj, R; Matějčková, M; Nováková, J; Rusina, R; Sigut, V | 1 |
| Grasbon-Frodl, EM; Krebs, B; Kretzschmar, HA; Neumann, M; Roeber, S; Windl, O; Zerr, I | 1 |
| Andreoletti, O; Basset-Leobon, C; Delisle, MB; Haik, S; Hauw, JJ; Peoc'h, K; Rigal, M; Sazdovitch, V; Uro-Coste, E | 1 |
| Harper, PS | 1 |
1 review(s) available for histidine and Creutzfeldt-Jakob Syndrome
| Article | Year |
|---|---|
Mendelian inheritance or transmissible agent? The lesson Kuru and the Australia antigen.
Topics: Alzheimer Disease; Animals; Chromosome Aberrations; Chromosome Disorders; Creutzfeldt-Jakob Syndrome; Erythroblastosis, Fetal; Female; Genes, Dominant; Genetic Diseases, Inborn; Haplorhini; Hepatitis B; Hepatitis B Surface Antigens; Histidine; Humans; Huntington Disease; Infant, Newborn; Kuru; Liver Diseases; Male; Maternal-Fetal Exchange; Mice; Myotonia Congenita; Nephritis, Hereditary; Optic Atrophy; Phenylketonurias; Pregnancy; Scrapie; Sheep; Slow Virus Diseases | 1977 |
5 other study(ies) available for histidine and Creutzfeldt-Jakob Syndrome
| Article | Year |
|---|---|
R208H-129VV haplotype in the prion protein gene: phenotype and neuroimaging of a patient with genetic Creutzfeldt-Jakob disease.
Topics: Arginine; Brain; Creutzfeldt-Jakob Syndrome; Female; Haplotypes; Histidine; Humans; Middle Aged; Neuroimaging; Phenotype; Prions; Radiography; Radionuclide Imaging | 2013 |
R47H TREM2 variant increases risk of typical early-onset Alzheimer's disease but not of prion or frontotemporal dementia.
Topics: Aged; Aged, 80 and over; Alzheimer Disease; Arginine; Brain; Cohort Studies; Creutzfeldt-Jakob Syndrome; Exons; Female; Frontotemporal Dementia; Genetic Predisposition to Disease; Genetic Variation; Genome-Wide Association Study; Genotype; Histidine; Humans; Male; Membrane Glycoproteins; Middle Aged; Phenotype; Receptors, Immunologic; Risk Factors | 2014 |
Genetic Creutzfeldt-Jakob disease with R208H mutation presenting as progressive supranuclear palsy.
Topics: Arginine; Creutzfeldt-Jakob Syndrome; DNA Mutational Analysis; Female; Histidine; Humans; Magnetic Resonance Imaging; Middle Aged; Mutation; Prion Proteins; Prions; Supranuclear Palsy, Progressive | 2012 |
Creutzfeldt-Jakob disease in a patient with an R208H mutation of the prion protein gene (PRNP) and a 17-kDa prion protein fragment.
Topics: Aged; Arginine; Blotting, Western; Brain; Creutzfeldt-Jakob Syndrome; DNA Mutational Analysis; Female; Histidine; Histological Techniques; Humans; Immunohistochemistry; Molecular Weight; Mutation; Prions | 2005 |
Familial Creutzfeldt-Jakob disease with an R208H-129V haplotype and Kuru plaques.
Topics: Amyloid; Arginine; Blotting, Western; Brain; Creutzfeldt-Jakob Syndrome; Haplotypes; Histidine; Humans; Immunohistochemistry; Male; Middle Aged; Mutation; Plaque, Amyloid; Prion Proteins; Prions; Protein Precursors; Valine | 2006 |