asparagine and Creutzfeldt-Jakob Syndrome
asparagine has been researched along with Creutzfeldt-Jakob Syndrome in 3 studies
Research
Studies (3)
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 2 (66.67) | 18.2507 |
2000's | 1 (33.33) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors
Authors | Studies |
---|---|
Abbamondi, AL; Bugiani, O; Giaccone, G; Macchi, G; Mancia, D; Rossi, G; Tagliavini, F | 1 |
Abelskov, K; Bojsen-Møller, M; Holm, IE; Jørgensen, AL; Nielsen, AL | 1 |
Brown, P; Cortelli, P; Goldfarb, LG; Julien, J; LeBlanc, AC; Montagna, P; Pendelbury, WW; Petersen, RB; Tabaton, M; Vital, C | 1 |
Other Studies
3 other study(ies) available for asparagine and Creutzfeldt-Jakob Syndrome
Article | Year |
---|---|
Diffuse thalamic degeneration in fatal familial insomnia. A morphometric study.
Topics: Adult; Asparagine; Aspartic Acid; Codon; Creutzfeldt-Jakob Syndrome; Fatal Outcome; Female; Humans; Male; Middle Aged; Nerve Degeneration; Neurons; Point Mutation; Prions; Reference Values; Sleep Initiation and Maintenance Disorders; Thalamic Nuclei | 1997 |
Creutzfeldt-Jakob disease segregating in a three generation Danish family.
Topics: Adult; Age of Onset; Aged; Aged, 80 and over; Alleles; Asparagine; Aspartic Acid; Creutzfeldt-Jakob Syndrome; Disease Progression; Electroencephalography; Female; Hippocampus; Humans; Immunohistochemistry; Magnetic Resonance Imaging; Male; Middle Aged; Pedigree; Phenotype; Point Mutation; Polymorphism, Genetic; Prions | 2001 |
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism.
Topics: Adult; Asparagine; Chromosomes, Human, Pair 20; Codon; Creutzfeldt-Jakob Syndrome; DNA; Genotype; Humans; Middle Aged; Mutation; Phenotype; Polymorphism, Genetic; Prion Diseases; Prions; Valine | 1992 |