potassium chloride has been researched along with Glycogen Storage Disease Type II in 3 studies
Potassium Chloride: A white crystal or crystalline powder used in BUFFERS; FERTILIZERS; and EXPLOSIVES. It can be used to replenish ELECTROLYTES and restore WATER-ELECTROLYTE BALANCE in treating HYPOKALEMIA.
potassium chloride : A metal chloride salt with a K(+) counterion.
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 disease is an autosomal recessive disorder caused by a deficiency of acid α-glucosidase (GAA), an enzyme responsible for hydrolyzing lysosomal glycogen." | 1.46 | Airway smooth muscle dysfunction in Pompe ( ( Bellvé, K; Byrne, BJ; ElMallah, MK; Fuller, DD; Keeler, AM; Liu, D; Salemi, J; Xiong, L; ZhuGe, R; Zieger, M, 2017) |
| "In the patient with the adult form of Pompe's disease the faster band of the Peak I enzyme from heart and muscle was not found and the slower band of the Peak I enzyme from liver was more cathodic." | 1.26 | Properties of the alpha-glucosidase from various human tissues in relation to glycogenosis type II (Pompe's disease). ( Ono, E; Oya, N; Shimada, N; Soyama, K; Tanaka, K, 1977) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (66.67) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Keeler, AM | 1 |
| Liu, D | 1 |
| Zieger, M | 1 |
| Xiong, L | 1 |
| Salemi, J | 1 |
| Bellvé, K | 1 |
| Byrne, BJ | 1 |
| Fuller, DD | 1 |
| ZhuGe, R | 1 |
| ElMallah, MK | 1 |
| Soyama, K | 2 |
| Ono, E | 2 |
| Shimada, N | 2 |
| Tanaka, K | 2 |
| Kusunoki, T | 1 |
| Oya, N | 1 |
3 other studies available for potassium chloride and Glycogen Storage Disease Type II
| Article | Year |
|---|---|
Airway smooth muscle dysfunction in Pompe (
Topics: Albuterol; alpha-Glucosidases; Animals; Bronchi; Calcium Signaling; Extracellular Space; Glycogen; G | 2017 |
Urinary alpha-glucosidase analysis for the detection of the adult form of Pompe's disease.
Topics: Adolescent; Adult; Child; Child, Preschool; Chromatography, Gel; Clinical Enzyme Tests; Female; Gluc | 1977 |
Properties of the alpha-glucosidase from various human tissues in relation to glycogenosis type II (Pompe's disease).
Topics: Copper; Electrophoresis; Glucosidases; Glycogen Storage Disease; Glycogen Storage Disease Type II; H | 1977 |