glycine has been researched along with Glycosuria, Renal in 3 studies
Glycosuria, Renal: An autosomal inherited disorder due to defective reabsorption of GLUCOSE by the PROXIMAL RENAL TUBULES. The urinary loss of glucose can reach beyond 50 g/day. It is attributed to the mutations in the SODIUM-GLUCOSE TRANSPORTER 2 encoded by the SLC5A2 gene.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| SCRIVER, CR | 1 |
| GOLDBLOOM, RB | 1 |
| ROY, CC | 1 |
| GEROK, W | 1 |
| PABST, K | 1 |
| Lebedev, VP | 1 |
| Iur'eva, EA | 1 |
| Mukhina, IuG | 1 |
| Buravina, TA | 1 |
| Koroleva, IA | 1 |
2 reviews available for glycine and Glycosuria, Renal
| Article | Year |
|---|---|
[ON THE PATHOPHYSIOLOGY AND CLINICAL MANIFESTATIONS OF DISORDERS OF RENAL TUBULAR PARTIAL FUNCTION].
Topics: Acidosis; Acidosis, Renal Tubular; Amino Acids; Cystinuria; Diabetes Insipidus; Glycine; Glycosuria; | 1965 |
[Primary and secondary hyperaminoaciduria in children (review of the literature)].
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Biological Transport, Active; Cystinuria; Fanconi | 1970 |
1 other study available for glycine and Glycosuria, Renal
| Article | Year |
|---|---|
HYPOPHOSPHATEMIC RICKETS WITH RENAL HYPER-GLYCINURIA, RENAL GLUCOSURIA, AND GLYCYL-PROLINURIA. A SYNDROME WITH EVIDENCE FOR RENAL TUBULAR SECRETION OF PHOSPHORUS.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Chronic Kidney Disease-Mineral and Bone Disorder; | 1964 |