molybdenum has been researched along with Amino Acid Metabolism Disorders, Inborn in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (33.33) | 18.7374 |
| 1990's | 1 (16.67) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (33.33) | 24.3611 |
| 2020's | 1 (16.67) | 2.80 |
| Authors | Studies |
|---|---|
| Bender, D; Burlina, AB; Kaczmarek, AT; Kuester, S; Schwarz, G | 1 |
| Elsea, SH; Jiang, Y; Mistretta, B; Sun, Q | 1 |
| Janssen, H; Kashyap, A; Natalio, F; Ragg, R; Strand, D; Strand, S; Tahir, MN; Tremel, W | 1 |
| Beemer, FA; Delleman, JW | 1 |
| Bakker, HD | 1 |
| Monnet, JP; Nogues, C; Ogier, H; Roth, A; Saudubray, JM | 1 |
6 other study(ies) available for molybdenum and Amino Acid Metabolism Disorders, Inborn
| Article | Year |
|---|---|
Oxygen and nitrite reduction by heme-deficient sulphite oxidase in a patient with mild sulphite oxidase deficiency.
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.
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.
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.
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].
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.
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 |