aminosalicylic acid has been researched along with Spinal Muscular Atrophies of Childhood 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.
Spinal Muscular Atrophies of Childhood: A group of recessive inherited diseases that feature progressive muscular atrophy and hypotonia. They are classified as type I (Werdnig-Hoffman disease), type II (intermediate form), and type III (Kugelberg-Welander disease). Type I is fatal in infancy, type II has a late infantile onset and is associated with survival into the second or third decade. Type III has its onset in childhood, and is slowly progressive. (J Med Genet 1996 Apr:33(4):281-3)
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 Spinal Muscular Atrophies of Childhood
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 |