tyrosine has been researched along with Developmental Disabilities in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (66.67) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| AUERBACH, VH; BRIGHAM, MP; DIGEORGE, AM; DOBBS, JM | 1 |
| Connie Hung, CC; Farooqi, IS; Gray, J; Keogh, J; O'Rahilly, S; Rochford, J; Sivaramakrishnan, S; Yeo, GS | 1 |
| Gilbert, DL; Merhar, SL | 1 |
3 other study(ies) available for tyrosine and Developmental Disabilities
| Article | Year |
|---|---|
Delayed maturation of tyrosine metabolism in a full-term sibling of a child with phenylketonuria.
Topics: Child; Developmental Disabilities; Female; Humans; Metabolism; Phenylketonurias; Siblings; Term Birth; Tyrosine | 1963 |
A de novo mutation affecting human TrkB associated with severe obesity and developmental delay.
Topics: Age Factors; Animals; Blotting, Western; Body Mass Index; Body Weight; Brain-Derived Neurotrophic Factor; Child; COS Cells; Cysteine; Developmental Disabilities; DNA Mutational Analysis; Eating; Fluorescent Antibody Technique; Gene Expression Regulation; Humans; Male; MAP Kinase Signaling System; Memory Disorders; Mutation, Missense; Obesity; PC12 Cells; Phosphorylation; Rats; Receptor, trkB; Transfection; Tyrosine | 2004 |
Clinical (video) findings and cerebrospinal fluid neurotransmitters in 2 children with severe chronic bilirubin encephalopathy, including a former preterm infant without marked hyperbilirubinemia VIDEO.
Topics: Child; Developmental Disabilities; Female; Follow-Up Studies; Globus Pallidus; Homovanillic Acid; Humans; Hydroxyindoleacetic Acid; Hyperbilirubinemia; Infant, Newborn; Infant, Premature; Infant, Premature, Diseases; Kernicterus; Magnetic Resonance Imaging; Neurotransmitter Agents; Tyrosine | 2005 |