cystine and Malabsorption Syndromes

cystine has been researched along with Malabsorption Syndromes in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19905 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
BLAIR, A; FOX, M; ROSENBERG, LE; SEGAL, S; THIER, SO1
Clifton, JA1
Fujimoto, A; Higami, S; Matsuoka, O; Omura, K; Yamanaka, N1
Boisse, J; Moatti, N1
Miura, R; Oyanagi, K; Yamanouchi, T1

Reviews

1 review(s) available for cystine and Malabsorption Syndromes

ArticleYear
[Amino acid transfer systems and their importance in pathology. II. Specific abnormalities in renal and intestinal amino acid transfer].
    Annales de biologie clinique, 1973, Volume: 31, Issue:4

    Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Child, Preschool; Cystine; Female; Glycine; Hartnup Disease; Humans; Infant; Lysine; Malabsorption Syndromes; Male; Methionine; Renal Tubular Transport, Inborn Errors; Tryptophan

1973

Other Studies

4 other study(ies) available for cystine and Malabsorption Syndromes

ArticleYear
CYSTINURIA: DEFECTIVE INTESTINAL TRANSPORT OF DIBASIC AMINO ACIDS AND CYSTINE.
    The Journal of clinical investigation, 1965, Volume: 44

    Topics: Amino Acids, Diamino; Arginine; Biological Transport; Carbon Isotopes; Cystine; Cystinuria; Genetics, Medical; Humans; Jejunum; Kidney; Lysine; Malabsorption Syndromes; Sulfur Isotopes

1965
[Some hereditary disorders of intestinal resorption with renal dysfunction].
    Der Internist, 1976, Volume: 17, Issue:7

    Topics: Arginine; Child; Chlorides; Cystine; Cystinuria; Diarrhea; Female; Galactose; Glucose; Hartnup Disease; Humans; Infant, Newborn; Intestinal Absorption; Kidney Diseases; Lysine; Malabsorption Syndromes; Male; Pedigree; Tryptophan

1976
Lysine malabsorption syndrome: a new type of transport defect.
    Pediatrics, 1976, Volume: 57, Issue:1

    Topics: Amino Acids; Arginine; Cystine; Female; Humans; Infant; Infant, Newborn; Intestinal Absorption; Lysine; Malabsorption Syndromes; Ornithine

1976
Congenital lysinuria: a new inherited transport disorder of dibasic amino acids.
    The Journal of pediatrics, 1970, Volume: 77, Issue:2

    Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Arginine; Biological Transport; Child; Chromatography, Thin Layer; Consanguinity; Cystine; Cystinuria; Diarrhea; Female; Growth; Humans; Intellectual Disability; Lysine; Malabsorption Syndromes; Ornithine; Renal Aminoacidurias; Vomiting

1970