hydroxyproline has been researched along with BCKD Deficiency in 7 studies
Hydroxyproline: A hydroxylated form of the imino acid proline. A deficiency in ASCORBIC ACID can result in impaired hydroxyproline formation.
hydroxyproline : A proline derivative that is proline substituted by at least one hydroxy group.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Hydroxyprolinemia is an inborn error of amino acid degradation that is considered a non-disease." | 1.43 | Genetic cause and prevalence of hydroxyprolinemia. ( Fang-Hoffmann, J; Feyh, P; Gramer, G; Haack, TB; Hoffmann, GF; Kölker, S; Mayatepek, E; Okun, JG; Prokisch, H; Raga, DE; Sauer, S; Staufner, C; Terrile, C, 2016) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 5 (71.43) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (14.29) | 29.6817 |
| 2010's | 1 (14.29) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Staufner, C | 1 |
| Haack, TB | 1 |
| Feyh, P | 1 |
| Gramer, G | 1 |
| Raga, DE | 1 |
| Terrile, C | 1 |
| Sauer, S | 1 |
| Okun, JG | 1 |
| Fang-Hoffmann, J | 1 |
| Mayatepek, E | 1 |
| Prokisch, H | 1 |
| Hoffmann, GF | 1 |
| Kölker, S | 1 |
| Fingerhut, R | 1 |
| EFRON, ML | 2 |
| YOUNG, D | 1 |
| MOSER, HW | 1 |
| MACCREADY, RA | 1 |
| Wellner, D | 1 |
| Meister, A | 1 |
| Frimpter, GW | 1 |
| Ampola, MG | 1 |
| Menne, F | 1 |
4 reviews available for hydroxyproline and BCKD Deficiency
| Article | Year |
|---|---|
A survey of inborn errors of amino acid metabolism and transport in man.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Amino Acids, Branched-Chain; Biological Transport | 1981 |
Aminoacidurias due to inherited disorders of metabolism. 2.
Topics: Acidosis; Alanine; Amino Acid Metabolism, Inborn Errors; Arginase; Arginine; Carbamates; Citrulline; | 1973 |
The aminoacidurias.
Topics: Amino Acid Metabolism, Inborn Errors; Glycine; Hartnup Disease; Histidine; Homocystinuria; Humans; H | 1967 |
[Feeble mindedness caused by genetic disorders of amino acid metabolism].
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Arginine; Citrulline; Glycine; Hartnup Disease; Histi | 1968 |
3 other studies available for hydroxyproline and BCKD Deficiency
| Article | Year |
|---|---|
Genetic cause and prevalence of hydroxyprolinemia.
Topics: Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Female; Germany; Heterozygote; Homozy | 2016 |
Recall rate and positive predictive value of MSUD screening is not influenced by hydroxyproline.
Topics: Humans; Hydroxyproline; Infant, Newborn; Isoleucine; Maple Syrup Urine Disease; Neonatal Screening; | 2009 |
A SIMPLE CHROMATOGRAPHIC SCREENING TEST FOR THE DETECTION OF DISORDERS OF AMINO ACID METABOLISM. A TECHNIC USING WHOLE BLOOD OR URINE COLLECTED ON FILTER PAPER.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Blood Chemical Analysis; Chromatography; Citrulli | 1964 |