cytidine monophosphate n-acetylneuraminic acid has been researched along with Metabolism, Inborn Errors in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (50.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Braga, AC; Ferreira, H; Gahl, WA; Gomes, L; Huizing, M; Krasnewich, DM; Martins, E; Pinto, R; Sa Miranda, MC; Seppala, R | 1 |
| Dacremont, G; De Simpel, H; Gahl, WA; Huizing, M; Krasnewich, DM; Leroy, JG; Orvisky, E; Seppala, R; Van Coster, RN | 1 |
2 other study(ies) available for cytidine monophosphate n-acetylneuraminic acid and Metabolism, Inborn Errors
| Article | Year |
|---|---|
Sialuria in a Portuguese girl: clinical, biochemical, and molecular characteristics.
Topics: Abnormalities, Multiple; Carbohydrate Epimerases; Cells, Cultured; Child; Cytidine Monophosphate N-Acetylneuraminic Acid; Escherichia coli Proteins; Female; Fibroblasts; Humans; Intellectual Disability; Metabolism, Inborn Errors; N-Acetylneuraminic Acid; Point Mutation; Sialic Acids; Subcellular Fractions | 1999 |
Dominant inheritance of sialuria, an inborn error of feedback inhibition.
Topics: Adult; Base Sequence; Carbohydrate Epimerases; Child; Child, Preschool; Cytidine Monophosphate N-Acetylneuraminic Acid; Cytoplasm; Developmental Disabilities; Escherichia coli Proteins; Feedback; Female; Fibroblasts; France; Genes, Dominant; Heterozygote; Humans; Infant; Infant, Newborn; Male; Metabolism, Inborn Errors; Middle Aged; Molecular Sequence Data; Mutation, Missense; Pedigree; Sialic Acids; Uridine Diphosphate N-Acetylglucosamine | 2001 |