glycine has been researched along with Congenital Hyperinsulinism in 1 studies
Congenital Hyperinsulinism: A familial, nontransient HYPOGLYCEMIA with defects in negative feedback of GLUCOSE-regulated INSULIN release. Clinical phenotypes include HYPOGLYCEMIA; HYPERINSULINEMIA; SEIZURES; COMA; and often large BIRTH WEIGHT. Several sub-types exist with the most common, type 1, associated with mutations on an ATP-BINDING CASSETTE TRANSPORTERS (subfamily C, member 8).
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bushman, JD | 1 |
| Gay, JW | 1 |
| Tewson, P | 1 |
| Stanley, CA | 1 |
| Shyng, SL | 1 |
1 other study available for glycine and Congenital Hyperinsulinism
| Article | Year |
|---|---|
Characterization and functional restoration of a potassium channel Kir6.2 pore mutation identified in congenital hyperinsulinism.
Topics: Amino Acids; Animals; Chlorocebus aethiops; Congenital Hyperinsulinism; COS Cells; Electrophysiology | 2010 |