edaravone has been researched along with Glycogen Storage Disease Type II in 2 studies
Glycogen Storage Disease Type II: An autosomal recessively inherited glycogen storage disease caused by GLUCAN 1,4-ALPHA-GLUCOSIDASE deficiency. Large amounts of GLYCOGEN accumulate in the LYSOSOMES of skeletal muscle (MUSCLE, SKELETAL); HEART; LIVER; SPINAL CORD; and BRAIN. Three forms have been described: infantile, childhood, and adult. The infantile form is fatal in infancy and presents with hypotonia and a hypertrophic cardiomyopathy (CARDIOMYOPATHY, HYPERTROPHIC). The childhood form usually presents in the second year of life with proximal weakness and respiratory symptoms. The adult form consists of a slowly progressive proximal myopathy. (From Muscle Nerve 1995;3:S61-9; Menkes, Textbook of Child Neurology, 5th ed, pp73-4)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Sowell, J | 1 |
| Wood, T | 1 |
| Rozaklis, T | 1 |
| Ramsay, SL | 1 |
| Whitfield, PD | 1 |
| Ranieri, E | 1 |
| Hopwood, JJ | 1 |
| Meikle, PJ | 1 |
2 other studies available for edaravone and Glycogen Storage Disease Type II
| Article | Year |
|---|---|
Towards a selected reaction monitoring mass spectrometry fingerprint approach for the screening of oligosaccharidoses.
Topics: Antipyrine; Chromatography, High Pressure Liquid; Edaravone; Fucosidosis; Glycogen Storage Disease T | 2011 |
Determination of oligosaccharides in Pompe disease by electrospray ionization tandem mass spectrometry.
Topics: Adolescent; Adult; Antipyrine; Child; Child, Preschool; Edaravone; Glycogen Storage Disease Type II; | 2002 |