glycine has been researched along with Myositis, Inclusion Body in 1 studies
Myositis, Inclusion Body: Progressive myopathies characterized by the presence of inclusion bodies on muscle biopsy. Sporadic and hereditary forms have been described. The sporadic form is an acquired, adult-onset inflammatory vacuolar myopathy affecting proximal and distal muscles. Familial forms usually begin in childhood and lack inflammatory changes. Both forms feature intracytoplasmic and intranuclear inclusions in muscle tissue. (Adams et al., Principles of Neurology, 6th ed, pp1409-10)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Djamshidian, A | 1 |
| Schaefer, J | 1 |
| Haubenberger, D | 1 |
| Stogmann, E | 1 |
| Zimprich, F | 1 |
| Auff, E | 1 |
| Zimprich, A | 1 |
1 other study available for glycine and Myositis, Inclusion Body
| Article | Year |
|---|---|
A novel mutation in the VCP gene (G157R) in a German family with inclusion-body myopathy with Paget disease of bone and frontotemporal dementia.
Topics: Adenosine Triphosphatases; Adult; Arginine; Cell Cycle Proteins; Dementia; DNA Mutational Analysis; | 2009 |