Page last updated: 2024-08-22

molybdenum and Amino Acid Metabolism Disorders, Inborn

molybdenum has been researched along with Amino Acid Metabolism Disorders, Inborn in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19902 (33.33)18.7374
1990's1 (16.67)18.2507
2000's0 (0.00)29.6817
2010's2 (33.33)24.3611
2020's1 (16.67)2.80

Authors

AuthorsStudies
Bender, D; Burlina, AB; Kaczmarek, AT; Kuester, S; Schwarz, G1
Elsea, SH; Jiang, Y; Mistretta, B; Sun, Q1
Janssen, H; Kashyap, A; Natalio, F; Ragg, R; Strand, D; Strand, S; Tahir, MN; Tremel, W1
Beemer, FA; Delleman, JW1
Bakker, HD1
Monnet, JP; Nogues, C; Ogier, H; Roth, A; Saudubray, JM1

Other Studies

6 other study(ies) available for molybdenum and Amino Acid Metabolism Disorders, Inborn

ArticleYear
Oxygen and nitrite reduction by heme-deficient sulphite oxidase in a patient with mild sulphite oxidase deficiency.
    Journal of inherited metabolic disease, 2020, Volume: 43, Issue:4

    Topics: Amino Acid Metabolism, Inborn Errors; Catalytic Domain; Coenzymes; Electron Transport; Heme; Humans; Infant; Mitochondria; Molybdenum; Nitrites; Oxidation-Reduction; Oxidoreductases Acting on Sulfur Group Donors; Oxygen; Sulfite Oxidase

2020
Development of a rapid UPLC-MS/MS determination of urine sulfocysteine for diagnosis of sulfocysteinuria and molybdenum co-factor deficiencies.
    Bioanalysis, 2018, May-01, Volume: 10, Issue:10

    Topics: Amino Acid Metabolism, Inborn Errors; Chromatography, High Pressure Liquid; Coenzymes; Cysteine; Humans; Limit of Detection; Linear Models; Molybdenum; Sulfite Oxidase; Tandem Mass Spectrometry; Time Factors; Urinalysis

2018
Molybdenum trioxide nanoparticles with intrinsic sulfite oxidase activity.
    ACS nano, 2014, May-27, Volume: 8, Issue:5

    Topics: Amino Acid Metabolism, Inborn Errors; Binding Sites; Electrochemistry; Electrodes; Electronics; Kinetics; Light; Metal Nanoparticles; Molybdenum; Nanoparticles; Nanotechnology; Nanowires; Oxidation-Reduction; Oxides; Photochemistry; Photons; Sulfite Oxidase; Zinc Oxide

2014
Combined deficiency of xanthine oxidase and sulfite oxidase; ophthalmological findings in a 3-week-old girl.
    Metabolic and pediatric ophthalmology, 1980, Volume: 4, Issue:1

    Topics: Amino Acid Metabolism, Inborn Errors; Female; Humans; Infant, Newborn; Infant, Newborn, Diseases; Lens Subluxation; Metabolism, Inborn Errors; Molybdenum; Oxidoreductases; Oxidoreductases Acting on Sulfur Group Donors; Xanthine Oxidase; Xanthines

1980
[Remember hereditary metabolic diseases in children in which no satisfactory diagnosis can be established].
    Nederlands tijdschrift voor geneeskunde, 1993, May-08, Volume: 137, Issue:19

    Topics: Amidohydrolases; Amino Acid Metabolism, Inborn Errors; Biotinidase; Child; Child, Preschool; Coenzymes; Female; Humans; Infant, Newborn; Lysine; Male; Metabolism, Inborn Errors; Metalloproteins; Molybdenum; Molybdenum Cofactors; Multiple Carboxylase Deficiency; Pteridines

1993
Anatomo-pathological findings in a case of combined deficiency of sulphite oxidase and xanthine oxidase with a defect of molybdenum cofactor.
    Virchows Archiv. A, Pathological anatomy and histopathology, 1985, Volume: 405, Issue:3

    Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids, Sulfur; Brain; Child, Preschool; Coenzymes; Female; Humans; Liver; Metalloproteins; Microcephaly; Molybdenum; Molybdenum Cofactors; Oxidoreductases; Oxidoreductases Acting on Sulfur Group Donors; Pteridines; Purine-Pyrimidine Metabolism, Inborn Errors; Sulfates; Syndrome; Xanthine Oxidase; Xanthines

1985