proline has been researched along with Aminoaciduria, Renal in 24 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 23 (95.83) | 18.7374 |
1990's | 1 (4.17) | 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; SCHAFER, IA; SCRIVER, CR | 1 |
DUBOVSKA, E; DUBOVSKY, J; FORMANKOVA, J | 1 |
EFRON, ML; MACCREADY, RA; MOSER, HW; YOUNG, D | 1 |
DAMBORENEA, RG; PINTO, B; VAZQUEZ, J | 1 |
ANYON, CP | 1 |
EFRON, ML | 1 |
Scriver, CR; Wilson, OH | 1 |
Kucharska, D; Michalowski, R; Urban, J | 1 |
Law, EA; Sardharwalla, IB | 1 |
Dabbagh, S; Diven, W; Ellis, D; Epley, M | 1 |
Greene, ML; Lietman, PS; Rosenberg, LE; Seegmiller, JE | 1 |
Maniscalco, RM; Powell, GF; Rasco, MA | 1 |
Buravina, TA; Iur'eva, EA; Koroleva, IA; Lebedev, VP; Mukhina, IuG | 1 |
Auricchio, S; Guazzi, G; Tancredi, F | 1 |
Bell, NH; Del Greco, F; Simon, NM | 1 |
Galin, MA; Gitter, KA; Harris, LS; Plechaty, GP | 1 |
Eickenbusch, W; Langness, U; Zimmermann, J | 1 |
Procopis, PG; Turner, B | 1 |
Scriver, CR | 1 |
Scriver, CR; Whelan, DT | 1 |
Goyer, RA; Leonard, DL; Mitchell, BJ | 1 |
Ando, T; Minagawa, A; Morikawa, T; Tada, K; Yoshida, T | 1 |
Ando, T; Arakawa, T; Morikawa, T; Tada, K; Yokoyama, Y; Yoshida, T | 1 |
Arakawa, T; Morikawa, T; Tada, K | 1 |
2 review(s) available for proline and Aminoaciduria, Renal
Article | Year |
---|---|
AMINOACIDURIA.
Topics: Amino Acid Metabolism, Inborn Errors; Biological Transport; Cystinuria; Histidine; Homocysteine; Humans; Hydroxyproline; Kidney; Methionine; Proline; Renal Aminoacidurias | 1965 |
[Primary and secondary hyperaminoaciduria in children (review of the literature)].
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Biological Transport, Active; Cystinuria; Fanconi Syndrome; Glycine; Glycosuria, Renal; Hartnup Disease; Histidine; Humans; Infant, Newborn; Kidney Diseases; Kidney Tubules; Maple Syrup Urine Disease; Phenylketonurias; Proline; Renal Aminoacidurias; Renal Tubular Transport, Inborn Errors; Sodium | 1970 |
22 other study(ies) available for proline and Aminoaciduria, Renal
Article | Year |
---|---|
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, Medical; Glycine; Humans; Hydroxyproline; Kidney; Kidney Tubules; Proline; Proline Oxidase; Proteins; Renal Aminoacidurias | 1964 |
[HYDROXYLYSINES IN THE URINE IN OSTEOPATHIES WITH MARKED CHANGES IN THE BONE MATRIX].
Topics: Bone Diseases; Bone Matrix; Glycosaminoglycans; Humans; Hydroxylysine; Hydroxyproline; Kidney; Lysine; Ossification, Heterotopic; Osteitis Deformans; Osteomalacia; Osteoporosis; Proline; Renal Aminoacidurias | 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; Citrulline; Glycine; Histidine; Homocysteine; Humans; Hydroxyproline; Intellectual Disability; Maple Syrup Urine Disease; Metabolic Diseases; Phenylketonurias; Proline; Proteins; Renal Aminoacidurias; Urine | 1964 |
[ACQUIRED RENAL GLYCINURIA (REPORT OF 2 CASES WITH ARTERIAL HYPERTENSION)].
Topics: Arginine; Glycine; Humans; Hypertension; Kidney; Kidney Calculi; Kidney Diseases; Pathology; Proline; Renal Aminoacidurias | 1964 |
MENTAL RETARDATION AND ABNORMAL AMINOACIDURIAS OCCURRING IN A FAMILY.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Amino Alcohols; Aminobutyrates; Chromatography; Genetics, Medical; Humans; Infant; Infant, Newborn; Intellectual Disability; Kidney; Phosphates; Physiognomy; Proline; Renal Aminoacidurias; Urine | 1965 |
Amino acid transport: evidence for genetic control of two types in human kidney.
Topics: Absorption; Adult; Biological Transport; Glycine; Humans; Hydroxyproline; Kidney Tubules; Male; Models, Theoretical; Molecular Biology; Mutation; Proline; Renal Aminoacidurias | 1967 |
[The Netherton syndrome with alopecia and prolinuria].
Topics: Alopecia; Ectodermal Dysplasia; Hair; Humans; Ichthyosis; Infant; Male; Proline; Renal Aminoacidurias; Scalp Dermatoses; Syndrome | 1978 |
A new type of heterozygote of familial renal iminoglycinuria.
Topics: Female; Genetic Carrier Screening; Glycine; Humans; Hydroxyproline; Intellectual Disability; Male; Mass Screening; Middle Aged; Pedigree; Proline; Renal Aminoacidurias; Scotland | 1978 |
Aminoaciduria of phosphate depletion manifests at the renal brush border membrane.
Topics: Animals; Kidney; Kinetics; Microvilli; Phosphates; Proline; Rats; Rats, Inbred Strains; Renal Aminoacidurias; Sodium; Taurine; Vitamin D Deficiency | 1990 |
Familial hyperglycinuria. New defect in renal tubular transport of glycine and imino acids.
Topics: Adolescent; Adult; Biological Transport; Glycine; Humans; Hydroxyproline; Intestinal Absorption; Kidney Tubules; Male; Middle Aged; Mutation; Pedigree; Proline; Protein Binding; Renal Aminoacidurias; Stimulation, Chemical; Sweat | 1973 |
A prolidase deficiency in man with iminopeptiduria.
Topics: Biological Assay; Child; Chromatography, Thin Layer; Chromosome Aberrations; Chromosome Disorders; Dansyl Compounds; Diagnosis, Differential; Dipeptidases; Erythrocytes; Humans; Lathyrism; Leukocytes; Male; Metabolism, Inborn Errors; Peptides; Proline; Proteinuria; Renal Aminoacidurias; Syndrome; Time Factors | 1974 |
Renal iminoglycinuria without intestinal malabsorption of glycine and imino acids.
Topics: Amblyopia; Child; Color Vision Defects; Female; Glycine; Heterozygote; Homozygote; Humans; Hydroxyproline; Intestinal Absorption; Kidney; Pedigree; Proline; Renal Aminoacidurias | 1970 |
Iminoacidopathy in renal failure.
Topics: Calcium; Glycine; Humans; Hydroxyproline; Hyperparathyroidism, Secondary; Kidney Diseases; Kidney Failure, Chronic; Parathyroid Glands; Proline; Renal Aminoacidurias; Sodium Chloride | 1970 |
Oculo-cerebro-renal syndrome. Report of a case in a baby girl.
Topics: Ammonia; Cataract; Female; Glaucoma; Growth Disorders; Humans; Hydroxyproline; Infant; Infant, Newborn; Infant, Newborn, Diseases; Intellectual Disability; Proline; Renal Aminoacidurias | 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; Iodine Radioisotopes; Proline; Protein Binding; Renal Aminoacidurias; Thyroid Diseases; Thyroid Function Tests; Tyrosine | 1971 |
Iminoaciduria: a benign renal tubular defect.
Topics: Australia; Female; Glomerular Filtration Rate; Glycine; Heterozygote; Humans; Hydroxyproline; Infant; Male; Mass Screening; Proline; Renal Aminoacidurias; Renal Tubular Transport, Inborn Errors | 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; Heterozygote; Homozygote; Humans; Hydroxyproline; Infant; Intestinal Absorption; Kidney Tubules; Male; Middle Aged; Pedigree; Proline; Renal Aminoacidurias | 1968 |
Cystathioninuria and renal iminoglycinuria in a pedigree.
Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Child; Chromatography, Ion Exchange; Chromatography, Paper; Counseling; Female; Glycine; Heterozygote; Humans; Hydroxyproline; Infant; Infant, Newborn; Jaundice; Jews; Male; Metabolic Clearance Rate; Methionine; Middle Aged; Pedigree; Phenotype; Proline; Pyridoxine; Renal Aminoacidurias; Tryptophan | 1968 |
Dietary reduction of hyperprolinemia.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Autoanalysis; Blood Urea Nitrogen; Diet Therapy; Dietary Proteins; Female; Humans; Kidney Failure, Chronic; Proline; Renal Aminoacidurias | 1969 |
Prolinuria: a new renal tubular defect in transport of proline and glycine.
Topics: Child; Female; Glycine; Humans; In Vitro Techniques; Infant; Male; Proline; Renal Aminoacidurias; Renal Tubular Transport, Inborn Errors; Urine | 1965 |
Prolinuria: defect in intestinal absorption of imino acids and glycine.
Topics: Chromatography, Thin Layer; Feces; Female; Glycine; Humans; Hydroxyproline; Infant; Kidney Function Tests; Malabsorption Syndromes; Proline; Renal Aminoacidurias | 1966 |
Prolinuria: transport of proline by leukocytes.
Topics: Carbon Isotopes; Collagen; Glycine; Humans; Leukocytes; Malabsorption Syndromes; Proline; Renal Aminoacidurias; Skin | 1966 |