molybdenum has been researched along with Lens Dislocation in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (60.00) | 18.7374 |
| 1990's | 2 (40.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Beemer, FA; Delleman, JW | 1 |
| Beemer, FA; Duran, M; Johnson, JL; Rajagopalan, KV; Wadman, SK; Waud, WR | 1 |
| Artigas, M; Coll, MJ; Johnson, JL; Naranjo, MA; Pintos-Morell, G; Rajagopalan, KV; Rodes, M; Roge, M | 1 |
| Fairbanks, L; Hughes, EF; Robinson, RO; Simmonds, HA | 1 |
| Beemer, FA; Cats, BP; Duran, M; Wadman, SK | 1 |
5 other study(ies) available for molybdenum and Lens Dislocation
| Article | Year |
|---|---|
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 |
Inborn errors of molybdenum metabolism: combined deficiencies of sulfite oxidase and xanthine dehydrogenase in a patient lacking the molybdenum cofactor.
Topics: Child, Preschool; Coenzymes; Female; Fibroblasts; Humans; Immunologic Techniques; Intellectual Disability; Ketone Oxidoreductases; Lens Subluxation; Liver; Metal Metabolism, Inborn Errors; Metalloproteins; Molybdenum; Molybdenum Cofactors; Nervous System Diseases; Oxidoreductases; Oxidoreductases Acting on Sulfur Group Donors; Pteridines; Xanthine Dehydrogenase | 1980 |
Molybdenum cofactor deficiency associated with Dandy-Walker malformation.
Topics: Coenzymes; Dandy-Walker Syndrome; Humans; Infant, Newborn; Kidney Calculi; Lens Subluxation; Male; Metalloproteins; Molybdenum; Molybdenum Cofactors; Nervous System Diseases; Pteridines; Ultrasonography | 1995 |
Molybdenum cofactor deficiency-phenotypic variability in a family with a late-onset variant.
Topics: Age of Onset; Behavioral Symptoms; Brain; Child; Diagnosis, Differential; Family Relations; Female; Humans; Hypoxanthine; Infant; Lens Subluxation; Magnetic Resonance Imaging; Molybdenum; Oxidoreductases Acting on Sulfur Group Donors; Phenotype; Purine-Pyrimidine Metabolism, Inborn Errors; Uric Acid; Xanthine | 1998 |
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 |