ropinirole has been researched along with Leukodystrophy, Metachromatic in 1 studies
Leukodystrophy, Metachromatic: An autosomal recessive metabolic disease caused by a deficiency of CEREBROSIDE-SULFATASE leading to intralysosomal accumulation of cerebroside sulfate (SULFOGLYCOSPHINGOLIPIDS) in the nervous system and other organs. Pathological features include diffuse demyelination, and metachromatically-staining granules in many cell types such as the GLIAL CELLS. There are several allelic and nonallelic forms with a variety of neurological symptoms.
| 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 |
|---|---|
| Finsterer, J | 1 |
| Reining-Festa, A | 1 |
| Stollbergr, C | 1 |
| Voigtlander, T | 1 |
1 other study available for ropinirole and Leukodystrophy, Metachromatic
| Article | Year |
|---|---|
Dopamine-deficiency-enhanced hyperthermia and rhabdomyolysis during a heat wave in a metachromatic leucodystrophy heterozygote with metabolic myopathy.
Topics: Antiparkinson Agents; Dopamine; Fever; Humans; Indoles; Leukodystrophy, Metachromatic; Male; Middle | 2011 |