phosphorylcholine has been researched along with Autosomal Dominant Juvenile Parkinson Disease in 1 studies
Phosphorylcholine: Calcium and magnesium salts used therapeutically in hepatobiliary dysfunction.
phosphocholine : The phosphate of choline; and the parent compound of the phosphocholine family.
| 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 | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Shi, CH | 1 |
| Tang, BS | 1 |
| Wang, L | 1 |
| Lv, ZY | 1 |
| Wang, J | 1 |
| Luo, LZ | 1 |
| Shen, L | 1 |
| Jiang, H | 1 |
| Yan, XX | 1 |
| Pan, Q | 1 |
| Xia, K | 1 |
| Guo, JF | 1 |
| Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
|---|---|---|---|---|---|---|---|
| Phenotypic Description of Patients With Atypical Clinical Forms of PLA2G6 Mutations[NCT05440994] | 20 participants (Anticipated) | Observational | 2022-06-01 | Enrolling by invitation | |||
| [information is prepared from clinicaltrials.gov, extracted Sep-2024] | |||||||
1 other study available for phosphorylcholine and Autosomal Dominant Juvenile Parkinson Disease
| Article | Year |
|---|---|
PLA2G6 gene mutation in autosomal recessive early-onset parkinsonism in a Chinese cohort.
Topics: Adult; Animals; Asian People; Cell Line, Transformed; Cohort Studies; DNA Mutational Analysis; Famil | 2011 |