hydroxyproline has been researched along with Deficiency, Mental in 21 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 |
|---|---|---|
| "Hydroxyproline is a major constituent of collagen." | 1.30 | Hydroxyprolinemia: comparison of a patient and her unaffected twin sister. ( Kim, SZ; Levy, HL; Varvogli, L; Waisbren, SE, 1997) |
| "Hydroxyproline metabolism was evaluated in two sisters with hydroxyprolinemia and their mother." | 1.26 | Hydroxyproline metabolism in two sisters with hydroxyprolinemia. ( Blankenship, PR; Coryell, ME; Hall, WK; Lynch, WR; Roesel, RA; Thevaos, TG, 1979) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 18 (85.71) | 18.7374 |
| 1990's | 3 (14.29) | 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 |
|---|---|
| EFRON, ML | 2 |
| YOUNG, D | 1 |
| MOSER, HW | 1 |
| MACCREADY, RA | 1 |
| BIXBY, EM | 1 |
| PRYLES, CV | 1 |
| Iavanainen, M | 1 |
| Laitinen, O | 1 |
| Palo, J | 1 |
| Näntö-Salonen, K | 1 |
| Autio, S | 1 |
| Härö, E | 1 |
| Kivimäki, T | 1 |
| Koskela, SL | 1 |
| Näntö, V | 1 |
| Penttinen, R | 1 |
| Lejeune, J | 1 |
| Takahashi, M | 1 |
| Nagao, H | 1 |
| Matsuda, H | 1 |
| Kim, SZ | 1 |
| Varvogli, L | 1 |
| Waisbren, SE | 1 |
| Levy, HL | 1 |
| Roesel, RA | 1 |
| Blankenship, PR | 1 |
| Lynch, WR | 1 |
| Coryell, ME | 1 |
| Thevaos, TG | 1 |
| Hall, WK | 1 |
| Law, EA | 1 |
| Sardharwalla, IB | 1 |
| Statter, M | 1 |
| Ben-Zvi, A | 1 |
| Shina, A | 1 |
| Schein, R | 1 |
| Russell, A | 1 |
| Foldes, J | 1 |
| Balena, R | 1 |
| Ho, A | 1 |
| Parfitt, AM | 1 |
| Kleerekoper, M | 1 |
| Goodman, SI | 1 |
| Browder, JA | 1 |
| Winick, M | 1 |
| Brasel, JA | 1 |
| Velasco, E | 1 |
| Rosso, P | 1 |
| Krieger, I | 1 |
| Hart, ZH | 1 |
| Menne, F | 1 |
| Emery, FA | 1 |
| Goldie, L | 1 |
| Stern, J | 1 |
| Harris, LS | 1 |
| Gitter, KA | 1 |
| Galin, MA | 1 |
| Plechaty, GP | 1 |
| Prockop, DJ | 1 |
| Rosenberg, LE | 1 |
| Durant, JL | 1 |
| Elsas, LJ | 1 |
| Rokkones, T | 1 |
| Loken, AC | 1 |
| Berger, R | 1 |
| Broyer, M | 1 |
1 review available for hydroxyproline and Deficiency, Mental
| Article | Year |
|---|---|
[Feeble mindedness caused by genetic disorders of amino acid metabolism].
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Arginine; Citrulline; Glycine; Hartnup Disease; Histi | 1968 |
20 other studies available for hydroxyproline and Deficiency, Mental
| Article | Year |
|---|---|
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 |
HYDROXYPROLINEMIA. II. A RARE METABOLIC DISEASE DUE TO A DEFICIENCY OF THE ENZYME "HYDROXYPROLINE OXIDASE".
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Amino Acid Oxidoreductases; Blood; Blood Chemical | 1965 |
Diagnostic criteria in Marfan's disease.
Topics: Adolescent; Adult; Cardiomyopathies; Child; Child, Preschool; Consanguinity; Eye Diseases; Female; H | 1967 |
Metabolism of collagen in aspartylglycosaminuria: urinary excretion of hydroxyproline.
Topics: Acetylglucosamine; Adolescent; Adult; Age Factors; Child; Child, Preschool; Collagen; Connective Tis | 1984 |
[Fragile site Xq27 and metabolism of monocarbons].
Topics: Amino Acids; Aminolevulinic Acid; Female; Formyltetrahydrofolates; Humans; Hydroxyproline; Intellect | 1980 |
Estimating bone change in patients with severe disability.
Topics: Alkaline Phosphatase; Anticonvulsants; Bone Density; Bone Diseases; Calcium; Epilepsy; Glycosaminogl | 1995 |
Hydroxyprolinemia: comparison of a patient and her unaffected twin sister.
Topics: Amino Acid Metabolism, Inborn Errors; Child; Diseases in Twins; Female; Humans; Hydroxyproline; Inte | 1997 |
Hydroxyproline metabolism in two sisters with hydroxyprolinemia.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Female; Glycolates; Humans; Hydroxyproline; Intellectua | 1979 |
A new type of heterozygote of familial renal iminoglycinuria.
Topics: Female; Genetic Carrier Screening; Glycine; Humans; Hydroxyproline; Intellectual Disability; Male; M | 1978 |
Familial iminoglycinuria with normal intestinal absorption of glycine and imino acids in association with profound mental retardation, a possible "cerebral phenotype".
Topics: Amino Acid Metabolism, Inborn Errors; Female; Glycine; Humans; Hydroxyproline; Imino Acids; Infant; | 1976 |
Hypophosphatemic rickets with hypocalciuria following long-term treatment with aluminum-containing antacid.
Topics: Adolescent; Aluminum Hydroxide; Antacids; Calcitriol; Calcium; Drug Administration Schedule; Drug Co | 1991 |
Hydroxylysinuria in association with trisomy 21.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Child, Preschool; Chromatography, Paper; Collagen | 1970 |
Effects of early nutrition on growth of the central nervous system.
Topics: Amino Acid Metabolism, Inborn Errors; Amniotic Fluid; Animals; Brain; Brain Chemistry; Central Nervo | 1974 |
Valine-sensitive nonketotic hyperglycinemia. Case report.
Topics: Administration, Oral; Amino Acid Metabolism, Inborn Errors; Benzoates; Brain Diseases; Brain Stem; C | 1974 |
Hyperprolinaemia type 2.
Topics: Adolescent; Chromatography, Paper; Electroencephalography; Epilepsy, Absence; Female; Glycine; Human | 1968 |
Oculo-cerebro-renal syndrome. Report of a case in a baby girl.
Topics: Ammonia; Cataract; Female; Glaucoma; Growth Disorders; Humans; Hydroxyproline; Infant; Infant, Newbo | 1970 |
Hydroxyprolinemia as an illustration of nonessential enzymes in man.
Topics: Amino Acid Metabolism, Inborn Errors; Collagen; Humans; Hydroxyproline; Intellectual Disability; Pep | 1970 |
Familial iminoglycinuria. An inborn error of renal tubular transport.
Topics: Adult; Child; Chromosome Aberrations; Chromosome Disorders; Deafness; Female; Genotype; Glycine; Het | 1968 |
Congenital renal dysplasia, retinal dysplasia and mental retardation associated with hyperprolinuria and hyper-oh-prolinuria.
Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Child; Female; Genetic Diseases, Inborn; Hu | 1968 |
[Hyperprolinemia and hydroxyprolinemia].
Topics: Amino Acid Metabolism, Inborn Errors; Child; Collagen; Consanguinity; Female; Genes, Recessive; Glyc | 1969 |