phosphorylcholine has been researched along with Parkinsonian Disorders 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.
Parkinsonian Disorders: A group of disorders which feature impaired motor control characterized by bradykinesia, MUSCLE RIGIDITY; TREMOR; and postural instability. Parkinsonian diseases are generally divided into primary parkinsonism (see PARKINSON DISEASE), secondary parkinsonism (see PARKINSON DISEASE, SECONDARY) and inherited forms. These conditions are associated with dysfunction of dopaminergic or closely related motor integration neuronal pathways in the BASAL GANGLIA.
| 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 Parkinsonian Disorders
| 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 |