proline has been researched along with Child Development Deviations in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Galvanovskis, J; Hasegawa, S; Horita, S; Kumamoto, K; Maejima, Y; Shimomura, K; Takenoshita, S | 1 |
| Anderson, G; Benatti, M; Brown, R; Chong, K; Clayton, PT; Footitt, E; Gissen, P; Hemingway, C; Holden, S; James, C; Little, D; Mills, PB; Ocaka, L; Parker, A; Rahman, S; Reid, ES; Williams, H | 1 |
2 other study(ies) available for proline and Child Development Deviations
| Article | Year |
|---|---|
Water intake disorder in a DEND syndrome afflicted patient with R50P mutation.
Topics: Amino Acid Substitution; Animals; Arginine; Child; Developmental Disabilities; Drinking; Epilepsy; Humans; Hyperglycemia; Male; Models, Molecular; Mutation, Missense; Potassium Channels, Inwardly Rectifying; Proline; Rats; Rats, Wistar; Syndrome | 2015 |
Mutations in SLC25A22: hyperprolinaemia, vacuolated fibroblasts and presentation with developmental delay.
Topics: Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Developmental Disabilities; Female; Fibroblasts; Glutamic Acid; Humans; Infant; Infant, Newborn; Male; Mitochondria; Mitochondria, Liver; Mitochondrial Membrane Transport Proteins; Muscle Hypotonia; Mutation; Proline; Seizures | 2017 |