aminosalicylic acid has been researched along with HMN (Hereditary Motor Neuropathy) Proximal Type I in 1 studies
Aminosalicylic Acid: An antitubercular agent often administered in association with ISONIAZID. The sodium salt of the drug is better tolerated than the free acid.
4-aminosalicylic acid : An aminobenzoic acid that is salicylic acid substituted by an amino group at position 4.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Glycogen storage disease type IV or Andersen disease is an autosomal recessive disorder due to deficiency of glycogen branching enzyme." | 1.32 | Fatal infantile neuromuscular presentation of glycogen storage disease type IV. ( Akman, HO; Chung, WK; DiMauro, S; Hays, AP; Mickelson, JR; Muntoni, F; Pike, MG; Shanske, S; Tanji, K; Tay, SK; Valberg, SJ, 2004) |
| 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 |
|---|---|
| Tay, SK | 1 |
| Akman, HO | 1 |
| Chung, WK | 1 |
| Pike, MG | 1 |
| Muntoni, F | 1 |
| Hays, AP | 1 |
| Shanske, S | 1 |
| Valberg, SJ | 1 |
| Mickelson, JR | 1 |
| Tanji, K | 1 |
| DiMauro, S | 1 |
1 other study available for aminosalicylic acid and HMN (Hereditary Motor Neuropathy) Proximal Type I
| Article | Year |
|---|---|
Fatal infantile neuromuscular presentation of glycogen storage disease type IV.
Topics: 1,4-alpha-Glucan Branching Enzyme; Aminosalicylic Acid; Biopsy; Blotting, Western; Brain Stem; DNA M | 2004 |