nordefrin has been researched along with Glycogen Storage Disease Type II in 1 studies
Nordefrin: A norepinephrine derivative used as a vasoconstrictor agent.
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)
| Excerpt | Relevance | Reference |
|---|---|---|
| "Pompe's disease is an autosomal recessive and often fatal condition, caused by mutations in the acid alpha-glucosidase gene, leading to lysosomal glycogen storage in heart and skeletal muscle." | 1.31 | Cardiac remodeling and contractile function in acid alpha-glucosidase knockout mice. ( Duncker, DJ; Kamphoven, JH; Reuser, AJ; Stubenitsky, R; Van Der Ploeg, AT; Verdouw, PD, 2001) |
| 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 |
|---|---|
| Kamphoven, JH | 1 |
| Stubenitsky, R | 1 |
| Reuser, AJ | 1 |
| Van Der Ploeg, AT | 1 |
| Verdouw, PD | 1 |
| Duncker, DJ | 1 |
1 other study available for nordefrin and Glycogen Storage Disease Type II
| Article | Year |
|---|---|
Cardiac remodeling and contractile function in acid alpha-glucosidase knockout mice.
Topics: alpha-Glucosidases; Anesthetics, Inhalation; Animals; Cardiomyopathy, Hypertrophic; Dobutamine; Gluc | 2001 |