glycine has been researched along with Hematuria in 6 studies
Hematuria: Presence of blood in the urine.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Alport syndrome is the commonest inherited kidney disease and nearly half the pathogenic variants in the COL4A3-COL4A5 genes that cause Alport syndrome result in Gly substitutions." | 1.72 | Genotype-phenotype correlations for COL4A3-COL4A5 variants resulting in Gly substitutions in Alport syndrome. ( Cerkauskaite, A; Chan, MMY; Deltas, C; Gale, DP; Gibson, JT; Hilbert, P; Huang, M; Lipska-Ziętkiewicz, BS; Rothe, H; Sadeghi-Alavijeh, O; Savige, J; Shenelli Croos Dabrera, M; Shukla, K; Storey, H, 2022) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (50.00) | 18.7374 |
| 1990's | 1 (16.67) | 18.2507 |
| 2000's | 1 (16.67) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (16.67) | 2.80 |
| Authors | Studies |
|---|---|
| Gibson, JT | 1 |
| Huang, M | 1 |
| Shenelli Croos Dabrera, M | 1 |
| Shukla, K | 1 |
| Rothe, H | 1 |
| Hilbert, P | 1 |
| Deltas, C | 1 |
| Storey, H | 1 |
| Lipska-Ziętkiewicz, BS | 1 |
| Chan, MMY | 1 |
| Sadeghi-Alavijeh, O | 1 |
| Gale, DP | 1 |
| Cerkauskaite, A | 1 |
| Savige, J | 2 |
| Buzza, M | 1 |
| Dagher, H | 1 |
| Wang, YY | 1 |
| Wilson, D | 1 |
| Babon, JJ | 1 |
| Cotton, RG | 1 |
| KUSUNOKI, T | 1 |
| IKOMA, F | 1 |
| Suzuki, S | 1 |
| Gejyo, F | 1 |
| Kuroda, T | 1 |
| Kazama, JJ | 1 |
| Imai, N | 1 |
| Kimura, H | 1 |
| Arakawa, M | 1 |
| Breckenridge, RT | 1 |
| Ratnoff, OD | 1 |
| Minder, FC | 1 |
| Dubach, UC | 1 |
| Antener, I | 1 |
1 review available for glycine and Hematuria
| Article | Year |
|---|---|
Therapy of hereditary disorders of blood coagulation.
Topics: Abdomen, Acute; Afibrinogenemia; Blood Coagulation Disorders; Blood Transfusion; Cerebral Hemorrhage | 1968 |
5 other studies available for glycine and Hematuria
| Article | Year |
|---|---|
Genotype-phenotype correlations for COL4A3-COL4A5 variants resulting in Gly substitutions in Alport syndrome.
Topics: Adult; Amino Acid Substitution; Autoantigens; Collagen Type IV; Databases, Genetic; Deafness; Female | 2022 |
Mutations in the COL4A4 gene in thin basement membrane disease.
Topics: Adolescent; Adult; Aged; Amino Acid Substitution; Basement Membrane; Child; Codon, Nonsense; Codon, | 2003 |
[CLINICAL EXPERIENCE OF "STRONG NEO-MINOPHAGEN-C" IN UROLOGY].
Topics: Child; Cysteine; Cystitis; Glycine; Glycyrrhiza; Hematuria; Humans; Injections, Intravenous; Kidney | 1964 |
Effects of a novel elastase inhibitor, ONO-5046, on nephrotoxic serum nephritis in rats.
Topics: Animals; Antibodies, Heterophile; Basement Membrane; Disease Models, Animal; Glycine; Hematuria; Hum | 1998 |
[Hereditary nephropathy and hardness of hearing (with metabolic disorders of amino acids and fats in a family from Switzerland)].
Topics: Adolescent; Adult; Aged; Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Deafness; Dw | 1965 |