Compounds > citrulline

citrulline and Aminoaciduria, Renal

citrulline has been researched along with Aminoaciduria, Renal in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19905 (83.33)18.7374
1990's1 (16.67)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
FREYCON, F; FREYCON, MT1
COFFEY, VP1
EFRON, ML; MACCREADY, RA; MOSER, HW; YOUNG, D1
Perheentupa, J; Rajantie, J; Simell, O1
González-Noriega, A; Prieto, E; Velázquez, A; Verduzco, J1
Golbus, MS; Laframboise, R; Mandell, R; Packman, S; Saudubray, JM; Schmidt, K; Shih, VE; Workman, L1

Reviews

1 review(s) available for citrulline and Aminoaciduria, Renal

ArticleYear
[CITRULLINURIA].
    Pediatrie, 1963, Volume: 18

    Topics: Amino Acid Metabolism, Inborn Errors; Child; Citrulline; Citrullinemia; Humans; Infant; Intellectual Disability; Kidney; Renal Aminoacidurias; Urologic Diseases

1963

Other Studies

5 other study(ies) available for citrulline and Aminoaciduria, Renal

ArticleYear
MENTAL RETARDATION AND THE INBORN ERRORS OF METABOLISM.
    Journal of the Irish Medical Association, 1964, Volume: 54

    Topics: Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Arginine; Citrulline; Fructose; Galactosemias; Histidine; Homocysteine; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Intellectual Disability; Maple Syrup Urine Disease; Metabolic Diseases; Phenylketonurias; Renal Aminoacidurias; Vitamin B 6 Deficiency

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.
    The New England journal of medicine, 1964, Jun-25, Volume: 270

    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
Intestinal absorption in lysinuric protein intolerance: impaired for diamino acids, normal for citrulline.
    Gut, 1980, Volume: 21, Issue:6

    Topics: Adolescent; Adult; Amino Acids, Diamino; Citrulline; Female; Heterozygote; Homozygote; Humans; Infant; Intestinal Absorption; Lysine; Male; Renal Aminoacidurias

1980
Argininosuccinic acid synthetase deficiency in a hamster cell line and its complementation of argininosuccinic aciduria human fibroblasts.
    Journal of inherited metabolic disease, 1980, Volume: 3, Issue:2

    Topics: Animals; Arginine; Argininosuccinate Lyase; Argininosuccinate Synthase; Argininosuccinic Acid; Cell Line; Citrulline; Cricetinae; Female; Fibroblasts; Genes, Recessive; Genetic Complementation Test; HeLa Cells; Humans; Hybrid Cells; Ligases; Liver; Lyases; Male; Renal Aminoacidurias

1980
Use of amniotic fluid amino acids in prenatal testing for argininosuccinic aciduria and citrullinaemia.
    Prenatal diagnosis, 1996, Volume: 16, Issue:5

    Topics: Amino Acid Metabolism, Inborn Errors; Amniocentesis; Amniotic Fluid; Argininosuccinate Lyase; Argininosuccinate Synthase; Argininosuccinic Acid; Argininosuccinic Aciduria; Carbon Radioisotopes; Cells, Cultured; Chorionic Villi; Chorionic Villi Sampling; Citrulline; Female; Fetal Diseases; Fibroblasts; Humans; Infant; Infant, Newborn; Pregnancy; Pregnancy Trimester, Second; Renal Aminoacidurias; Tritium

1996