glycine has been researched along with Wolman Disease in 1 studies
Wolman Disease: The severe infantile form of inherited lysosomal lipid storage diseases due to deficiency of acid lipase (STEROL ESTERASE). It is characterized by the accumulation of neutral lipids, particularly CHOLESTEROL ESTERS in leukocytes, fibroblasts, and hepatocytes. It is also known as Wolman's xanthomatosis and is an allelic variant of CHOLESTEROL ESTER STORAGE DISEASE.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (100.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Kikuchi, M | 1 |
| Igarashi, K | 1 |
| Noro, T | 1 |
| Igarashi, Y | 1 |
| Hirooka, M | 1 |
| Tada, K | 1 |
1 other study available for glycine and Wolman Disease
| Article | Year |
|---|---|
Evaluation of jejunal function in Wolman's disease.
Topics: Disaccharidases; Evoked Potentials; Female; Galactose; Glucose; Glycine; Humans; Infant; Intestinal | 1991 |