hydroxyproline has been researched along with Aminoaciduria, Renal in 20 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.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 20 (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 |
|---|---|
| JONES, CR | 1 |
| BERGMAN, MW | 1 |
| KITTNER, PJ | 1 |
| PIGMAN, WW | 1 |
| KIVIRIKKO, KI | 1 |
| KOIVUSALO, M | 1 |
| LAITINEN, O | 1 |
| LAMBERG, BA | 1 |
| SCRIVER, CR | 5 |
| EFRON, ML | 3 |
| SCHAFER, IA | 1 |
| DUBOVSKY, J | 1 |
| FORMANKOVA, J | 1 |
| DUBOVSKA, E | 1 |
| YOUNG, D | 1 |
| MOSER, HW | 1 |
| MACCREADY, RA | 1 |
| KIBRICK, AC | 1 |
| HASHIRO, C | 1 |
| WALTERS, M | 1 |
| MILHORAT, AT | 1 |
| GOLDBLOOM, RB | 1 |
| ROY, CC | 1 |
| Wilson, OH | 1 |
| Law, EA | 1 |
| Sardharwalla, IB | 1 |
| Greene, ML | 1 |
| Lietman, PS | 1 |
| Rosenberg, LE | 1 |
| Seegmiller, JE | 1 |
| Tancredi, F | 1 |
| Guazzi, G | 1 |
| Auricchio, S | 1 |
| Simon, NM | 1 |
| Bell, NH | 1 |
| Del Greco, F | 1 |
| Harris, LS | 1 |
| Gitter, KA | 1 |
| Galin, MA | 1 |
| Plechaty, GP | 1 |
| Zimmermann, J | 1 |
| Langness, U | 1 |
| Eickenbusch, W | 1 |
| Procopis, PG | 1 |
| Turner, B | 1 |
| Whelan, DT | 1 |
| Brown, H | 1 |
| Milner, A | 1 |
| Kennedy, J | 1 |
| Delena, S | 1 |
| Morikawa, T | 1 |
| Tada, K | 1 |
| Ando, T | 1 |
| Yoshida, T | 1 |
| Yokoyama, Y | 1 |
| Arakawa, T | 1 |
1 review available for hydroxyproline and Aminoaciduria, Renal
| Article | Year |
|---|---|
AMINOACIDURIA.
Topics: Amino Acid Metabolism, Inborn Errors; Biological Transport; Cystinuria; Histidine; Homocysteine; Hum | 1965 |
19 other studies available for hydroxyproline and Aminoaciduria, Renal
| Article | Year |
|---|---|
URINARY HYDROXYPROLINE EXCRETION IN NORMAL CHILDREN AND ADOLESCENTS.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Body Fluids; Child; Humans; Hydroxyproline; Kidney | 1964 |
HYDROXYPROLINE IN THE SERUM AND URINE OF PATIENTS WITH HYPERTHYROIDISM.
Topics: Amino Acid Metabolism, Inborn Errors; Blood Chemical Analysis; Humans; Hydroxyproline; Hyperthyroidi | 1964 |
RENAL TUBULAR TRANSPORT OF PROLINE, HYDROXYPROLINE, AND GLYCINE IN HEALTH AND IN FAMILIAL HYPERPROLINEMIA.
Topics: 1-Pyrroline-5-Carboxylate Dehydrogenase; Amino Acid Metabolism, Inborn Errors; Child; Genetics, Medi | 1964 |
[HYDROXYLYSINES IN THE URINE IN OSTEOPATHIES WITH MARKED CHANGES IN THE BONE MATRIX].
Topics: Bone Diseases; Bone Matrix; Glycosaminoglycans; Humans; Hydroxylysine; Hydroxyproline; Kidney; Lysin | 1964 |
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 |
HYDROXYPROLINE EXCRETION IN URINE OF PATIENTS WITH MUSCULAR DYSTROPHY AND OTHER MUSCLE DISEASES.
Topics: Adolescent; Amyotrophic Lateral Sclerosis; Child; Creatine; Creatinine; Dermatomyositis; Humans; Hyd | 1964 |
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 |
Amino acid transport: evidence for genetic control of two types in human kidney.
Topics: Absorption; Adult; Biological Transport; Glycine; Humans; Hydroxyproline; Kidney Tubules; Male; Mode | 1967 |
A new type of heterozygote of familial renal iminoglycinuria.
Topics: Female; Genetic Carrier Screening; Glycine; Humans; Hydroxyproline; Intellectual Disability; Male; M | 1978 |
Familial hyperglycinuria. New defect in renal tubular transport of glycine and imino acids.
Topics: Adolescent; Adult; Biological Transport; Glycine; Humans; Hydroxyproline; Intestinal Absorption; Kid | 1973 |
Renal iminoglycinuria without intestinal malabsorption of glycine and imino acids.
Topics: Amblyopia; Child; Color Vision Defects; Female; Glycine; Heterozygote; Homozygote; Humans; Hydroxypr | 1970 |
Iminoacidopathy in renal failure.
Topics: Calcium; Glycine; Humans; Hydroxyproline; Hyperparathyroidism, Secondary; Kidney Diseases; Kidney Fa | 1970 |
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 |
[Determination of amino acids in plasma and urine for the functional diagnosis of the thyroid gland].
Topics: Amino Acids; Diagnosis, Differential; Humans; Hydroxyproline; Hyperthyroidism; Hypothyroidism; Iodin | 1971 |
Iminoaciduria: a benign renal tubular defect.
Topics: Australia; Female; Glomerular Filtration Rate; Glycine; Heterozygote; Humans; Hydroxyproline; Infant | 1971 |
Renal tubular transport of proline, hydroxyproline, and glycine. 3. Genetic basis for more than one mode of transport in human kidney.
Topics: Adolescent; Adult; Alleles; Biological Transport, Active; Child; Child, Preschool; Female; Glycine; | 1968 |
Cystathioninuria and renal iminoglycinuria in a pedigree.
Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Child; Chromatography, Ion Exchange; Chroma | 1968 |
Hydroxyproline excretion during starvation of obese subjects.
Topics: Adult; Bone and Bones; Calcium; Calorimetry; Collagen; Creatinine; Diet Therapy; Fats; Female; Growt | 1968 |
Prolinuria: defect in intestinal absorption of imino acids and glycine.
Topics: Chromatography, Thin Layer; Feces; Female; Glycine; Humans; Hydroxyproline; Infant; Kidney Function | 1966 |