asparagine and Creutzfeldt-Jakob Syndrome

asparagine has been researched along with Creutzfeldt-Jakob Syndrome in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (66.67)18.2507
2000's1 (33.33)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Abbamondi, AL; Bugiani, O; Giaccone, G; Macchi, G; Mancia, D; Rossi, G; Tagliavini, F1
Abelskov, K; Bojsen-Møller, M; Holm, IE; Jørgensen, AL; Nielsen, AL1
Brown, P; Cortelli, P; Goldfarb, LG; Julien, J; LeBlanc, AC; Montagna, P; Pendelbury, WW; Petersen, RB; Tabaton, M; Vital, C1

Other Studies

3 other study(ies) available for asparagine and Creutzfeldt-Jakob Syndrome

ArticleYear
Diffuse thalamic degeneration in fatal familial insomnia. A morphometric study.
    Brain research, 1997, Oct-10, Volume: 771, Issue:1

    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.
    Acta neurologica Scandinavica, 2001, Volume: 103, Issue:3

    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.
    Science (New York, N.Y.), 1992, Oct-30, Volume: 258, Issue:5083

    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
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