phosphorylcholine has been researched along with Hepatolenticular Degeneration 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.
Hepatolenticular Degeneration: A rare autosomal recessive disease characterized by the deposition of copper in the BRAIN; LIVER; CORNEA; and other organs. It is caused by defects in the ATP7B gene encoding copper-transporting ATPase 2 (EC 3.6.3.4), also known as the Wilson disease protein. The overload of copper inevitably leads to progressive liver and neurological dysfunction such as LIVER CIRRHOSIS; TREMOR; ATAXIA and intellectual deterioration. Hepatic dysfunction may precede neurologic dysfunction by several years.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Wilson disease is an autosomal recessive disorder of copper metabolism in which copper is deposited in the brain and liver." | 1.34 | Wilson disease with visceral leishmaniasis: an extremely uncommon presentation. ( Bhattacharya, SK; Bimal, S; Das, P; Das, VN; Kumar, N; Lal, CS; Pandey, K; Singh, D; Sinha, PK; Topno, RK; Verma, N; Verma, RB, 2007) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Pandey, K | 1 |
| Sinha, PK | 1 |
| Das, VN | 1 |
| Kumar, N | 1 |
| Verma, N | 1 |
| Bimal, S | 1 |
| Lal, CS | 1 |
| Topno, RK | 1 |
| Singh, D | 1 |
| Verma, RB | 1 |
| Bhattacharya, SK | 1 |
| Das, P | 1 |
1 other study available for phosphorylcholine and Hepatolenticular Degeneration
| Article | Year |
|---|---|
Wilson disease with visceral leishmaniasis: an extremely uncommon presentation.
Topics: Adolescent; Chelating Agents; Hepatolenticular Degeneration; Humans; Leishmaniasis, Visceral; Male; | 2007 |