molybdenum has been researched along with Inborn Errors of Metabolism in 17 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 6 (35.29) | 18.7374 |
| 1990's | 9 (52.94) | 18.2507 |
| 2000's | 1 (5.88) | 29.6817 |
| 2010's | 1 (5.88) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Belaidi, AA; Schwarz, G | 1 |
| Beemer, FA; Duran, M; Johnson, JL; Rajagopalan, KV; Wadman, SK | 1 |
| Beemer, FA; Delleman, JW | 1 |
| Johnson, JL; Rajagopalan, KV | 2 |
| Mandel, H; Stroomer, LE; van Cruchten, AG; van Gennip, AH | 1 |
| Sardesai, VM | 1 |
| Johnson, JL; Rajagopalan, KV; Wadman, SK | 1 |
| Arnold, GL; Goodman, SI; Greene, CL; Stout, JP | 1 |
| Bakker, HD | 1 |
| Bellini, C; Bertola, A; Bonioli, E; Caruso, U; DiStefano, A; Dorche, C; Fantasia, AR; Minniti, G; Palmieri, A | 1 |
| Christensen, E; Dorche, C; Kurlemann, G; Reiss, J; Zabot, MT | 1 |
| Kishikawa, M; Nakanishi, T; Shimizu, A; Yoshino, M | 1 |
| Bimar, J; Collet, S; Desjacques, P; Divry, P; Lagier, P; Lando, A; Tessonnier, JM; Vianet-Liaud, C | 1 |
| Berger, JP; Hervé, F; Soulier, J | 1 |
| Beemer, FA; Cats, BP; Duran, M; Wadman, SK | 1 |
| Danks, DM | 1 |
2 review(s) available for molybdenum and Inborn Errors of Metabolism
| Article | Year |
|---|---|
Molybdenum in human health and disease.
Topics: Coenzymes; Humans; Metabolism, Inborn Errors; Molybdenum; Sulfite Oxidase; Trace Elements; Xanthine Dehydrogenase | 2013 |
Inborn errors of trace element metabolism.
Topics: Acrodermatitis; Animals; Breast Feeding; Copper; Cutis Laxa; Disease Models, Animal; Female; Hepatolenticular Degeneration; Humans; Infant, Newborn; Infant, Premature, Diseases; Liver; Manganese; Menkes Kinky Hair Syndrome; Metabolism, Inborn Errors; Molybdenum; Pregnancy; Prenatal Diagnosis; Trace Elements; Zinc | 1985 |
15 other study(ies) available for molybdenum and Inborn Errors of Metabolism
| Article | Year |
|---|---|
Molybdenum metabolism.
Topics: Humans; Infant; Metabolism, Inborn Errors; Molybdenum; Oxidoreductases Acting on Sulfur Group Donors; Trace Elements; Xanthine Dehydrogenase | 1980 |
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 |
An HPLC assay for detection of elevated urinary S-sulphocysteine, a metabolic marker of sulphite oxidase deficiency.
Topics: Amino Acids; Biomarkers; Chromatography, High Pressure Liquid; Coenzymes; Cysteine; Humans; Metabolism, Inborn Errors; Metalloproteins; Molybdenum; Molybdenum Cofactors; Oxidoreductases Acting on Sulfur Group Donors; Pteridines; Taurine | 1995 |
Effect of allopurinol on the xanthinuria in a patient with molybdenum cofactor deficiency.
Topics: Allopurinol; Coenzymes; Female; Humans; Male; Metabolism, Inborn Errors; Metalloproteins; Molybdenum; Molybdenum Cofactors; Pteridines; Purine-Pyrimidine Metabolism, Inborn Errors; Xanthine; Xanthine Dehydrogenase; Xanthines | 1994 |
Molybdenum: an essential trace element.
Topics: Deficiency Diseases; Food Analysis; Humans; Metabolism, Inborn Errors; Molybdenum; Neoplasms; Trace Elements | 1993 |
Human molybdenum cofactor deficiency.
Topics: Biomarkers; Coenzymes; Humans; Metabolism, Inborn Errors; Metalloproteins; Molybdenum; Molybdenum Cofactors; Pteridines; Pterins | 1993 |
Molybdopterin biosynthesis in man. Properties of the converting factor in liver tissue from a molybdenum cofactor deficient patient.
Topics: Coenzymes; Escherichia coli; Humans; Liver; Metabolism, Inborn Errors; Metalloproteins; Molybdenum; Molybdenum Cofactors; Neurospora crassa; Pteridines; Sulfurtransferases | 1993 |
Molybdenum cofactor deficiency.
Topics: Coenzymes; Female; Genes, Recessive; Humans; Infant, Newborn; Metabolism, Inborn Errors; Metalloproteins; Molybdenum; Molybdenum Cofactors; Pteridines; Seizures | 1993 |
[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 |
Combined deficiency of xanthine oxidase and sulphite oxidase due to a deficiency of molybdenum cofactor.
Topics: Coenzymes; Female; Fibroblasts; Humans; Hypoxanthine; Infant; Metabolism, Inborn Errors; Metalloproteins; Molybdenum; Molybdenum Cofactors; Nervous System Diseases; Oxidoreductases Acting on Sulfur Group Donors; Pteridines; Uric Acid; Xanthine; Xanthine Oxidase; Xanthines | 1996 |
Genomic structure and mutational spectrum of the bicistronic MOCS1 gene defective in molybdenum cofactor deficiency type A.
Topics: Amino Acid Sequence; Carbon-Carbon Lyases; Coenzymes; Europe; Exons; Genes, Recessive; Genetic Complementation Test; Genetic Testing; Heterozygote; Homozygote; Humans; Israel; Metabolism, Inborn Errors; Metalloproteins; Molecular Sequence Data; Molybdenum; Molybdenum Cofactors; Mutation; Nuclear Proteins; Pteridines; RNA Splicing | 1998 |
Detection by mass spectrometry of highly increased amount of S-sulfonated transthyretin in serum from a patient with molybdenum cofactor deficiency.
Topics: Child, Preschool; Coenzymes; Humans; Infant; Male; Metabolism, Inborn Errors; Metalloproteins; Molybdenum; Molybdenum Cofactors; Prealbumin; Pteridines; Spectrometry, Mass, Secondary Ion; Sulfonic Acids | 2000 |
[Combined sulfite and xanthine oxidase deficiency due to an anomaly in the metabolism of molybdenum cofactor].
Topics: Coenzymes; Humans; Infant, Newborn; Male; Metabolism, Inborn Errors; Metalloproteins; Molybdenum; Molybdenum Cofactors; Oxidoreductases; Oxidoreductases Acting on Sulfur Group Donors; Pteridines; Sulfites; Uric Acid; Xanthine Oxidase | 1986 |
[Sulfite and xanthine oxidase deficiency: a diagnosis based on 2 simple tests].
Topics: Coenzymes; Female; Humans; Infant; Metabolism, Inborn Errors; Metalloproteins; Methods; Molybdenum; Molybdenum Cofactors; Oxidoreductases; Oxidoreductases Acting on Sulfur Group Donors; Pteridines; Sulfites; Uric Acid; Xanthine Oxidase | 1986 |
Absence of hepatic molybdenum cofactor. An inborn error of metabolism associated with lens dislocation.
Topics: Coenzymes; Female; Humans; Infant; Infant, Newborn; Lens Subluxation; Liver; Male; Metabolism, Inborn Errors; Metalloproteins; Molybdenum; Molybdenum Cofactors; Pregnancy; Prenatal Diagnosis; Pteridines | 1985 |