pteridines has been researched along with Leukodystrophy, Globoid Cell in 1 studies
Leukodystrophy, Globoid Cell: An autosomal recessive metabolic disorder caused by a deficiency of GALACTOSYLCERAMIDASE leading to intralysosomal accumulation of galactolipids such as GALACTOSYLCERAMIDES and PSYCHOSINE. It is characterized by demyelination associated with large multinucleated globoid cells, predominantly involving the white matter of the central nervous system. The loss of MYELIN disrupts normal conduction of nerve impulses.
| 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 |
|---|---|
| Kang, PB | 1 |
| Hunter, JV | 1 |
| Kaye, EM | 1 |
1 other study available for pteridines and Leukodystrophy, Globoid Cell
| Article | Year |
|---|---|
Lactic acid elevation in extramitochondrial childhood neurodegenerative diseases.
Topics: Acidosis, Lactic; Brain; Coenzymes; Female; Genetic Carrier Screening; Heredodegenerative Disorders, | 2001 |