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1-anilino-8-naphthalenesulfonate and Metabolism, Inborn Errors

1-anilino-8-naphthalenesulfonate has been researched along with Metabolism, Inborn Errors in 21 studies

1-anilino-8-naphthalenesulfonate: RN given refers to parent cpd
8-anilinonaphthalene-1-sulfonic acid : A naphthalenesulfonic acid that is naphthalene-1-sulfonic acid substituted by a phenylamino group at position 8.

Metabolism, Inborn Errors: Errors in metabolic processes resulting from inborn genetic mutations that are inherited or acquired in utero.

Research

Studies (21)

TimeframeStudies, this research(%)All Research%
pre-199019 (90.48)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (4.76)24.3611
2020's1 (4.76)2.80

Authors

AuthorsStudies
Selen, ES1
Choi, J1
Wolfgang, MJ1
Steiner, C1
Holleboom, AG1
Karuna, R1
Motazacker, MM1
Kuivenhoven, JA1
Frikke-Schmidt, R1
Tybjaerg-Hansen, A1
Rohrer, L1
Rentsch, KM1
Eckardstein, Av1
TOWNES, PL2
Krivit, W1
Goldberg, DM2
Galton, DJ1
Betteridge, DJ1
Taylor, KG1
Holdsworth, G1
Stocks, J1
Hadorn, B2
Haworth, JC1
Gourley, B1
Prasad, A1
Troesch, V1
Brown, WJ1
Warfel, J1
Greenspan, P1
Tarlow, MJ1
Lloyd, JK1
Wolff, OH1
Wormsley, KG1
Poley, JR1
Snook, JT1
Figarella, C1
Negri, GA1
Sarles, H1
Auricchio, S1
Ciccimarra, F1
Moauro, L1
Rey, F1
Jos, J1
Rey, J2
Walker-Smith, JA1
Greten, H1
Maillard, E1
Young, EP1
Patrick, AD1
Bradford, RH1
Furman, RH1
Bass, HB1

Reviews

5 reviews available for 1-anilino-8-naphthalenesulfonate and Metabolism, Inborn Errors

ArticleYear
Correction of inborn errors of metabolism by bone marrow transplant.
    Basic life sciences, 1983, Volume: 25

    Topics: Animals; Bone Marrow Cells; Bone Marrow Transplantation; Brain; Catalase; Glucuronidase; Humans; Kup

1983
Clinical enzymology.
    Progress in medicinal chemistry, 1976, Volume: 13

    Topics: Acid Phosphatase; Alkaline Phosphatase; alpha-Amylases; Biliary Tract Diseases; Clinical Enzyme Test

1976
The interrelationships of the pancreatic enzymes.
    Gut, 1972, Volume: 13, Issue:5

    Topics: Amylases; Animals; Animals, Newborn; Chymotrypsin; Chymotrypsinogen; Diet; Duodenum; Humans; Infant,

1972
Chronic diarrhea in infants and children. I.
    Southern medical journal, 1973, Volume: 66, Issue:9

    Topics: Adolescent; Bile Acids and Salts; Child; Child, Preschool; Chronic Disease; Cystic Fibrosis; Diarrhe

1973
Adaptive and nonadaptive changes in digestive enzyme capacity influencing digestive function.
    Federation proceedings, 1974, Volume: 33, Issue:1

    Topics: Adaptation, Physiological; Amylases; Animals; Chickens; Diet; Dietary Carbohydrates; Dietary Fats; D

1974

Other Studies

16 other studies available for 1-anilino-8-naphthalenesulfonate and Metabolism, Inborn Errors

ArticleYear
Discordant hepatic fatty acid oxidation and triglyceride hydrolysis leads to liver disease.
    JCI insight, 2021, 01-25, Volume: 6, Issue:2

    Topics: Animals; Carnitine O-Palmitoyltransferase; Disease Progression; Fatty Acids; Female; Hydrolysis; Lip

2021
Lipoprotein distribution and serum concentrations of 7α-hydroxy-4-cholesten-3-one and bile acids: effects of monogenic disturbances in high-density lipoprotein metabolism.
    Clinical science (London, England : 1979), 2012, Volume: 122, Issue:8

    Topics: Apolipoprotein A-I; ATP Binding Cassette Transporter 1; ATP-Binding Cassette Transporters; Bile Acid

2012
TRYPSINOGEN DEFICIENCY DISEASE.
    The Journal of pediatrics, 1965, Volume: 66

    Topics: Amylases; Carbamoyl-Phosphate Synthase I Deficiency Disease; Carboxypeptidases; Chymotrypsin; Clinic

1965
Defects of enzyme regulation in metabolic disease.
    Clinical science and molecular medicine, 1977, Volume: 53, Issue:3

    Topics: Allosteric Regulation; Glycogen Storage Disease; Gout; Humans; Hydroxymethylglutaryl CoA Reductases;

1977
Intestinal enterokinase deficiency. Occurrence in two sibs and age dependency of clinical expression.
    Archives of disease in childhood, 1975, Volume: 50, Issue:4

    Topics: Amylases; Body Weight; Carboxypeptidases; Child; Child, Preschool; Chymotrypsin; Duodenum; Endopepti

1975
Use of Nile red stain in the detection of cholesteryl ester accumulation in acid lipase-deficient fibroblasts.
    Archives of pathology & laboratory medicine, 1988, Volume: 112, Issue:3

    Topics: Cholesterol Esters; Chromatography, Thin Layer; Fibroblasts; Fluorescent Dyes; Humans; Lipase; Metab

1988
Intestinal enterokinase deficiency.
    Lancet (London, England), 1969, Apr-19, Volume: 1, Issue:7599

    Topics: Amylases; Carboxypeptidases; Chromatography; Chromatography, Gel; Chymotrypsin; Diarrhea, Infantile;

1969
Presence of colipase in a congenital pancreatic lipase deficiency.
    Biochimica et biophysica acta, 1972, Sep-07, Volume: 280, Issue:1

    Topics: Child; Duodenum; Female; Humans; Immunodiffusion; Lipase; Metabolism, Inborn Errors; Pancreatic Dise

1972
Intraluminal and mucosal starch digestion in congenital deficiency of intestinal sucrase and isomaltase activities.
    Pediatric research, 1972, Volume: 6, Issue:11

    Topics: Age Factors; Amylases; Blood Glucose; Carbohydrates; Child, Preschool; Feces; Glucosidases; Glycosid

1972
Exocrine pancreatic disease in childhood.
    The Medical journal of Australia, 1973, Apr-07, Volume: 1, Issue:14

    Topics: Amylases; Autopsy; Bone Marrow Diseases; Child, Preschool; Clinical Enzyme Tests; Copper; Endopeptid

1973
Post-heparin plasma phospholipases in normals and patients with hyperlipoproteinemia.
    Klinische Wochenschrift, 1972, Jan-01, Volume: 50, Issue:1

    Topics: Blood Protein Disorders; Carbon Isotopes; Heparin; Humans; Hydrolysis; Lipase; Lipoproteins; Metabol

1972
[Hereditary abnormalities of digestive enzymes].
    Revue medico-chirurgicale des maladies du foie, 1971, Volume: 46, Issue:4

    Topics: Cystic Fibrosis; Endopeptidases; Humans; Lipase; Malabsorption Syndromes; Metabolism, Inborn Errors;

1971
[Hereditary pancreatic deficiencies].
    Lille medical : journal de la Faculte de medecine et de pharmacie de l'Universite de Lille, 1971, Volume: 16, Issue:10

    Topics: Adolescent; Amylases; Child; Child, Preschool; Female; Humans; Infant; Infant, Newborn; Lipase; Lipo

1971
Deficiency of acid esterase activity in Wolman's disease.
    Archives of disease in childhood, 1970, Volume: 45, Issue:243

    Topics: Esterases; Esters; Fatty Acids; Female; Heterozygote; Humans; Hydrolases; Infant; Leukocytes; Lipase

1970
Plasma post-heparin lipolytic activity in hyperchylomi-cronemia (fat-induced lipemia).
    Biochimica et biophysica acta, 1968, Oct-22, Volume: 164, Issue:2

    Topics: Adolescent; Adult; Cholesterol; Chylomicrons; Esterases; Fats, Unsaturated; Fatty Acids, Nonesterifi

1968
Proteolytic and lipolytic deficiency of the exocrine pancreas.
    The Journal of pediatrics, 1969, Volume: 75, Issue:2

    Topics: Amylases; Anemia; Body Weight; Carboxypeptidases; Child, Preschool; Chronic Disease; Chymotrypsin; D

1969