Compounds > galactose
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galactose and Amino Acid Transport Disorder, Neutral

galactose has been researched along with Amino Acid Transport Disorder, Neutral in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19904 (80.00)18.7374
1990's0 (0.00)18.2507
2000's1 (20.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Clifton, JA1
Schreier, K1
Bartsocas, CS; Crawford, JD1
Linneweh, F1
Hasegawa, H; Mitarai, T; Takayanagi, K1

Reviews

1 review(s) available for galactose and Amino Acid Transport Disorder, Neutral

ArticleYear
[Disorders of renal tubular transport of amino acids, hexose and phosphate].
    Nihon rinsho. Japanese journal of clinical medicine, 2006, Volume: 64 Suppl 2

    Topics: Amino Acids; Biological Transport; Cystinuria; Glycosuria, Renal; Hartnup Disease; Hexoses; Humans; Hypophosphatemia, Familial; Kidney Tubules; Osteomalacia; Phosphates; Renal Tubular Transport, Inborn Errors

2006

Other Studies

4 other study(ies) available for galactose and Amino Acid Transport Disorder, Neutral

ArticleYear
[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
[Intestinal enzymopathies of children (author's transl)].
    MMW, Munchener medizinische Wochenschrift, 1976, Dec-24, Volume: 118, Issue:52-53

    Topics: Abetalipoproteinemia; Adolescent; Adult; Blood Protein Disorders; Child; Child, Preschool; Cholesterol; Cystinuria; Disaccharidases; Enteritis; Galactose; Glucose; Glycoside Hydrolases; Hartnup Disease; Humans; Infant; Infant, Newborn; Intestinal Absorption; Intestinal Mucosa; Lactose Intolerance; Metabolism, Inborn Errors; Sucrose

1976
Clinical phenotypes in kidney transport disorders.
    Birth defects original article series, 1974, Volume: 10, Issue:4

    Topics: Abnormalities, Multiple; Acidosis, Renal Tubular; Cerebrospinal Fluid Proteins; Chronic Kidney Disease-Mineral and Bone Disorder; Cystinuria; Diabetes Insipidus; Galactose; Glucose; Glycosuria, Renal; Growth Disorders; Hartnup Disease; Humans; Hypophosphatemia, Familial; Kidney Tubules; Malabsorption Syndromes; Methionine; Phenotype; Pseudohypoparathyroidism; Pulmonary Heart Disease; Renal Aminoacidurias; Renal Tubular Transport, Inborn Errors; Seizures; Syndrome

1974
[Malabsorption in hereditary disorders of the carbohydrate and amino acid metabolism].
    Acta paediatrica Academiae Scientiarum Hungaricae, 1969, Volume: 10, Issue:1

    Topics: Amino Acid Metabolism, Inborn Errors; Animals; Carbohydrate Metabolism, Inborn Errors; Cystinuria; Galactose; Glucose; Hartnup Disease; Humans; Malabsorption Syndromes; Phenylketonurias; Rats

1969