serine has been researched along with Cerebral Palsy in 2 studies
Serine: A non-essential amino acid occurring in natural form as the L-isomer. It is synthesized from GLYCINE or THREONINE. It is involved in the biosynthesis of PURINES; PYRIMIDINES; and other amino acids.
serine : An alpha-amino acid that is alanine substituted at position 3 by a hydroxy group.
Cerebral Palsy: A heterogeneous group of nonprogressive motor disorders caused by chronic brain injuries that originate in the prenatal period, perinatal period, or first few years of life. The four major subtypes are spastic, athetoid, ataxic, and mixed cerebral palsy, with spastic forms being the most common. The motor disorder may range from difficulties with fine motor control to severe spasticity (see MUSCLE SPASTICITY) in all limbs. Spastic diplegia (Little disease) is the most common subtype, and is characterized by spasticity that is more prominent in the legs than in the arms. Pathologically, this condition may be associated with LEUKOMALACIA, PERIVENTRICULAR. (From Dev Med Child Neurol 1998 Aug;40(8):520-7)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (50.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (50.00) | 2.80 |
| Authors | Studies |
|---|---|
| Tang, H | 1 |
| Peng, T | 1 |
| Yang, X | 1 |
| Liu, L | 1 |
| Xu, Y | 1 |
| Zhao, Y | 1 |
| Huang, S | 1 |
| Fu, C | 1 |
| Huang, Y | 1 |
| Zhou, H | 1 |
| Li, J | 1 |
| He, L | 1 |
| Wang, W | 1 |
| Niu, H | 1 |
| Xu, K | 1 |
| Hodes, ME | 1 |
| Hadjisavvas, A | 1 |
| Butler, IJ | 1 |
| Aydanian, A | 1 |
| Dlouhy, SR | 1 |
2 other studies available for serine and Cerebral Palsy
| Article | Year |
|---|---|
Plasma Metabolomic Changes in Children with Cerebral Palsy Exposed to Botulinum Neurotoxin.
Topics: Botulinum Toxins, Type A; Cerebral Palsy; Child; Cysteine; Glycine; Humans; Injections, Intramuscula | 2022 |
X-linked spastic paraplegia due to a mutation (C506T; Ser169Phe) in exon 4 of the proteolipid protein gene (PLP).
Topics: Amino Acid Substitution; Cerebral Palsy; Child; Exons; Genetic Linkage; Humans; Male; Myelin Proteol | 1998 |