Page last updated: 2024-11-08

alanine and Creutzfeldt-Jakob Syndrome

alanine has been researched along with Creutzfeldt-Jakob Syndrome in 2 studies

Alanine: A non-essential amino acid that occurs in high levels in its free state in plasma. It is produced from pyruvate by transamination. It is involved in sugar and acid metabolism, increases IMMUNITY, and provides energy for muscle tissue, BRAIN, and the CENTRAL NERVOUS SYSTEM.
alanine : An alpha-amino acid that consists of propionic acid bearing an amino substituent at position 2.

Creutzfeldt-Jakob Syndrome: A rare transmissible encephalopathy most prevalent between the ages of 50 and 70 years. Affected individuals may present with sleep disturbances, personality changes, ATAXIA; APHASIA, visual loss, weakness, muscle atrophy, MYOCLONUS, progressive dementia, and death within one year of disease onset. A familial form exhibiting autosomal dominant inheritance and a new variant CJD (potentially associated with ENCEPHALOPATHY, BOVINE SPONGIFORM) have been described. Pathological features include prominent cerebellar and cerebral cortical spongiform degeneration and the presence of PRIONS. (From N Engl J Med, 1998 Dec 31;339(27))

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (50.00)18.2507
2000's1 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Dyrbye, H1
Broholm, H1
Dziegiel, MH1
Laursen, H1
Shibuya, S1
Higuchi, J1
Shin, RW1
Tateishi, J1
Kitamoto, T1

Other Studies

2 other studies available for alanine and Creutzfeldt-Jakob Syndrome

ArticleYear
The M129V polymorphism of codon 129 in the prion gene (PRNP) in the Danish population.
    European journal of epidemiology, 2008, Volume: 23, Issue:1

    Topics: Adult; Aged; Alanine; Alleles; Codon; Creutzfeldt-Jakob Syndrome; Denmark; Female; Genotype; Humans;

2008
Codon 219 Lys allele of PRNP is not found in sporadic Creutzfeldt-Jakob disease.
    Annals of neurology, 1998, Volume: 43, Issue:6

    Topics: Alanine; Alleles; Creutzfeldt-Jakob Syndrome; DNA Mutational Analysis; Humans; Lysine; Point Mutatio

1998