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sulfites and Inborn Errors of Metabolism

sulfites has been researched along with Inborn Errors of Metabolism in 11 studies

Sulfites: Inorganic salts of sulfurous acid.
sulfites : Any sulfurous acid derivative that is a salt or an ester of sulfurous acid.
organosulfonate oxoanion : An organic anion obtained by deprotonation of the sufonate group(s) of any organosulfonic acid.
sulfite : A sulfur oxoanion that is the conjugate base of hydrogen sulfite (H2SO3).

Research Excerpts

ExcerptRelevanceReference
"Study of a 4 1/2-year-old boy with the unusual combination of acute infantile hemiplegia, ectopia lentis and the absence of homocystinuria showed large amounts of abnormal sulfur-containing metabolites (sulfite, thiosulfate and S-sulfocysteine) in the urine."3.65Sulfite oxidase deficiency. Biochemical and clinical investigations of a hereditary metabolic disorder in sulfur metabolism. ( Abroms, IF; Carney, M; Cloherty, JP; Johnson, JL; Mandell, R; Rajagopalan, KV; Robb, RM; Shih, VE, 1977)

Research

Studies (11)

TimeframeStudies, this research(%)All Research%
pre-19908 (72.73)18.7374
1990's1 (9.09)18.2507
2000's0 (0.00)29.6817
2010's1 (9.09)24.3611
2020's1 (9.09)2.80

Authors

AuthorsStudies
Kožich, V1
Stabler, S1
Footitt, EJ1
Heales, SJ1
Mills, PB1
Allen, GF1
Oppenheim, M1
Clayton, PT1
JAFFE, ER1
NEURMANN, G1
Mudd, SH1
Irreverre, F1
Laster, L1
Shih, VE1
Abroms, IF1
Johnson, JL1
Carney, M1
Mandell, R1
Robb, RM1
Cloherty, JP1
Rajagopalan, KV1
van der Klei-van Moorsel, JM1
Smit, LM1
Brockstedt, M1
Jakobs, C1
Dorche, C1
Duran, M1
Tardy, P1
Parvy, P1
Charpentier, C1
Bonnefont, JP1
Saudubray, JM1
Kamoun, P1
Roesel, RA1
Bowyer, F1
Blankenship, PR1
Hommes, FA1
Lagier, P1
Tessonnier, JM1
Collet, S1
Lando, A1
Divry, P1
Vianet-Liaud, C1
Desjacques, P1
Bimar, J1
Hervé, F1
Berger, JP1
Soulier, J1
Kutter, D1
Humbel, R1

Reviews

1 review available for sulfites and Inborn Errors of Metabolism

ArticleYear
Lessons Learned from Inherited Metabolic Disorders of Sulfur-Containing Amino Acids Metabolism.
    The Journal of nutrition, 2020, 10-01, Volume: 150, Issue:Suppl 1

    Topics: Amino Acids, Sulfur; Animals; Brain Diseases; Cysteine; Glutathione; Homocysteine; Homocystinuria; H

2020

Other Studies

10 other studies available for sulfites and Inborn Errors of Metabolism

ArticleYear
Pyridoxal 5'-phosphate in cerebrospinal fluid; factors affecting concentration.
    Journal of inherited metabolic disease, 2011, Volume: 34, Issue:2

    Topics: Adolescent; Adult; Biopterins; Child; Child, Preschool; Cysteine; Epilepsy; False Positive Reactions

2011
A COMPARISION OF THE EFFECT OF MENADIONE, METHYLENE BLUE AND ASCORBIC ACID ON THE REDUCTION OF METHEMOGLOBIN IN VIVO.
    Nature, 1964, May-09, Volume: 202

    Topics: Ascorbic Acid; Dihydrolipoamide Dehydrogenase; Drug Therapy; Erythrocytes; Humans; Metabolism, Inbor

1964
Sulfite oxidase deficiency in man: demonstration of the enzymatic defect.
    Science (New York, N.Y.), 1967, Jun-23, Volume: 156, Issue:3782

    Topics: Brain; Cysteine; Cytochromes; Humans; Hydro-Lyases; In Vitro Techniques; Infant; Intellectual Disabi

1967
Sulfite oxidase deficiency. Biochemical and clinical investigations of a hereditary metabolic disorder in sulfur metabolism.
    The New England journal of medicine, 1977, Nov-10, Volume: 297, Issue:19

    Topics: Amino Acids, Sulfur; Child, Preschool; Cysteine; Hemiplegia; Humans; Lens Subluxation; Male; Metabol

1977
Infantile isolated sulphite oxidase deficiency: report of a case with negative sulphite test and normal sulphate excretion.
    European journal of pediatrics, 1991, Volume: 150, Issue:3

    Topics: Humans; Infant; Male; Metabolism, Inborn Errors; Oxidoreductases Acting on Sulfur Group Donors; Sulf

1991
Attempt at therapy in sulphite oxidase deficiency.
    Journal of inherited metabolic disease, 1989, Volume: 12, Issue:1

    Topics: Cysteine; Female; Humans; Infant, Newborn; Metabolism, Inborn Errors; Oxidoreductases; Oxidoreductas

1989
Combined xanthine and sulphite oxidase defect due to a deficiency of molybdenum cofactor.
    Journal of inherited metabolic disease, 1986, Volume: 9, Issue:4

    Topics: Coenzymes; Humans; Infant, Newborn; Liver; Male; Metabolism, Inborn Errors; Metalloproteins; Molybde

1986
[Combined sulfite and xanthine oxidase deficiency due to an anomaly in the metabolism of molybdenum cofactor].
    Annales de pediatrie, 1986, Volume: 33, Issue:9

    Topics: Coenzymes; Humans; Infant, Newborn; Male; Metabolism, Inborn Errors; Metalloproteins; Molybdenum; Mo

1986
[Sulfite and xanthine oxidase deficiency: a diagnosis based on 2 simple tests].
    Annales de pediatrie, 1986, Volume: 33, Issue:9

    Topics: Coenzymes; Female; Humans; Infant; Metabolism, Inborn Errors; Metalloproteins; Methods; Molybdenum;

1986
Screening for sulfite oxidase deficiency.
    Clinica chimica acta; international journal of clinical chemistry, 1969, Volume: 24, Issue:2

    Topics: Amino Acids; Chromatography, Thin Layer; Cysteine; Drug Stability; Humans; Intellectual Disability;

1969