glycine has been researched along with Myotonic Dystrophy in 4 studies
Myotonic Dystrophy: Neuromuscular disorder characterized by PROGRESSIVE MUSCULAR ATROPHY; MYOTONIA, and various multisystem atrophies. Mild INTELLECTUAL DISABILITY may also occur. Abnormal TRINUCLEOTIDE REPEAT EXPANSION in the 3' UNTRANSLATED REGIONS of DMPK PROTEIN gene is associated with Myotonic Dystrophy 1. DNA REPEAT EXPANSION of zinc finger protein-9 gene intron is associated with Myotonic Dystrophy 2.
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 4 (100.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
BARGY, P | 1 |
Bolton, CE | 2 |
Emery, AE | 3 |
Burt, D | 1 |
4 other studies available for glycine and Myotonic Dystrophy
Article | Year |
---|---|
[Curious modifications of electric reactions during Steinert's disease].
Topics: Atrophy; Electricity; Exploratory Behavior; Fabaceae; Glycine; Humans; Myotonic Dystrophy | 1950 |
Arginine-glycine amidinotransferase activity in myotonic dystrophy.
Topics: Amidinotransferases; Arginine; Glycine; Humans; Kidney; Myotonic Dystrophy; Transferases | 1973 |
Myotonic dystrophy: investigation of the proposed defect in guanidoacetic acid synthesis.
Topics: Acetates; Arginine; Glycine; Guanidines; Humans; Kidney Cortex; Metabolism, Inborn Errors; Myotonic | 1972 |
Amino acid, creatine and creatinine studies in myotonic dystrophy.
Topics: Adult; Age Factors; Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Creatine; Creatin | 1972 |