dapi has been researched along with Myositis, Inclusion Body in 1 studies
DAPI: RN given refers to parent cpd.
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 |
|---|---|
| Salajegheh, M | 1 |
| Pinkus, JL | 1 |
| Taylor, JP | 1 |
| Amato, AA | 1 |
| Nazareno, R | 1 |
| Baloh, RH | 1 |
| Greenberg, SA | 1 |
1 other study available for dapi and Myositis, Inclusion Body
| Article | Year |
|---|---|
Sarcoplasmic redistribution of nuclear TDP-43 in inclusion body myositis.
Topics: Amyloid beta-Peptides; Congo Red; DNA-Binding Proteins; Humans; Indoles; Muscle Fibers, Skeletal; My | 2009 |