glycine has been researched along with Alkaptonuria in 5 studies
Alkaptonuria: An inborn error of amino acid metabolism resulting from a defect in the enzyme HOMOGENTISATE 1,2-DIOXYGENASE, an enzyme involved in the breakdown of PHENYLALANINE and TYROSINE. It is characterized by accumulation of HOMOGENTISIC ACID in the urine, OCHRONOSIS in various tissues, and ARTHRITIS.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 5 (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 |
|---|---|
| SKARZYNSKI, B | 1 |
| SARNECKA-KELLER, M | 1 |
| FRENDO, J | 1 |
| Greco, GM | 1 |
| Magli, A | 1 |
| Krízek, V | 1 |
| Kroll, S | 2 |
| Zebisch, P | 2 |
| Toussaint, W | 2 |
2 reviews available for glycine and Alkaptonuria
| Article | Year |
|---|---|
[Eye manifestations of amino acid disorders].
Topics: Alanine; Albinism; Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Child; Cystinosis; Cystinuria | 1978 |
[Inborn errors of metabolism and their significance in urology and nephrology].
Topics: Acidosis, Renal Tubular; Alkaptonuria; Cystinuria; Diabetes Insipidus; Female; Glycine; Gout; Humans | 1976 |
3 other studies available for glycine and Alkaptonuria
| Article | Year |
|---|---|
The bound form of homogentisic acid in alkaptonuric urine.
Topics: Alkaptonuria; Body Fluids; Chromatography; Glycine; Homogentisic Acid; Humans; Phenylacetates | 1962 |
[Hereditary amino acid metabolism disorders. Indications for early diagnosis].
Topics: Albinism; Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Amino Acids; Arginine; Cystathionine; | 1972 |
[Diagnosis of inborn amino acid metabolism errors. Important symptoms and laboratory methods].
Topics: Albinism; Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Amino Acids; Arginine; Clinical Labora | 1972 |