glycine has been researched along with Multiple System Atrophy in 4 studies
Multiple System Atrophy: A syndrome complex composed of three conditions which represent clinical variants of the same disease process: STRIATONIGRAL DEGENERATION; SHY-DRAGER SYNDROME; and the sporadic form of OLIVOPONTOCEREBELLAR ATROPHIES. Clinical features include autonomic, cerebellar, and basal ganglia dysfunction. Pathologic examination reveals atrophy of the basal ganglia, cerebellum, pons, and medulla, with prominent loss of autonomic neurons in the brain stem and spinal cord. (From Adams et al., Principles of Neurology, 6th ed, p1076; Baillieres Clin Neurol 1997 Apr;6(1):187-204; Med Clin North Am 1999 Mar;83(2):381-92)
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (50.00) | 29.6817 |
2010's | 2 (50.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Coon, EA | 1 |
Rocca, W | 1 |
Melson, CS | 1 |
Ahlskog, JE | 1 |
Matsumoto, JY | 1 |
Low, PA | 1 |
Singer, W | 1 |
Yamamoto-Watanabe, Y | 1 |
Watanabe, M | 1 |
Jackson, M | 1 |
Akimoto, H | 1 |
Sugimoto, K | 1 |
Yasujima, M | 1 |
Wakasaya, Y | 1 |
Matsubara, E | 1 |
Kawarabayashi, T | 1 |
Harigaya, Y | 1 |
Lyndon, AR | 1 |
Shoji, M | 1 |
Schmitt, I | 1 |
Wüllner, U | 1 |
Healy, DG | 1 |
Wood, NW | 1 |
Kölsch, H | 1 |
Heun, R | 1 |
Lu, CS | 1 |
Chang, HC | 1 |
Weng, YH | 1 |
Chen, RS | 1 |
Bonifati, V | 1 |
Wu-Chou, YH | 1 |
4 other studies available for glycine and Multiple System Atrophy
Article | Year |
---|---|
Conjugal multiple system atrophy: Chance, shared risk factors, or evidence of transmissibility?
Topics: Autonomic Nervous System Diseases; Female; Glycine; Glyphosate; Herbicides; Humans; Male; Middle Age | 2019 |
Quantification of cystatin C in cerebrospinal fluid from various neurological disorders and correlation with G73A polymorphism in CST3.
Topics: Aged; Aged, 80 and over; Alanine; Alzheimer Disease; Amyotrophic Lateral Sclerosis; Biomarkers; Case | 2010 |
The ADH1C stop mutation in multiple system atrophy patients and healthy probands in the United Kingdom and Germany.
Topics: Alcohol Dehydrogenase; Case-Control Studies; Codon, Terminator; DNA Mutational Analysis; Female; Gen | 2006 |
Analysis of the LRRK2 Gly2385Arg variant in primary dystonia and multiple system atrophy in Taiwan.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Arginine; Child; DNA Mutational Analysis; Dystonic Disor | 2008 |