glycine has been researched along with Ganglioside Storage Diseases in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 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 |
|---|---|
| Aicardi, J | 1 |
| Brady, RO | 1 |
| Paw, BH | 1 |
| Kaback, MM | 1 |
| Neufeld, EF | 1 |
| Raghavan, S | 1 |
| Lyerla, TA | 1 |
| Krusell, A | 1 |
| Kolodny, EH | 1 |
1 review available for glycine and Ganglioside Storage Diseases
| Article | Year |
|---|---|
[Myoclonias as a manifestation of degenerative disorders of the central nervous system in childhood].
Topics: Adolescent; Age Factors; Brain Diseases; Cerebellar Diseases; Ceroid; Child; Child, Preschool; Diagn | 1982 |
3 other studies available for glycine and Ganglioside Storage Diseases
| Article | Year |
|---|---|
Inherited metabolic diseases of the nervous system.
Topics: Amino Acid Metabolism, Inborn Errors; Aspartylglucosaminuria; Carbohydrate Metabolism, Inborn Errors | 1976 |
Molecular basis of adult-onset and chronic GM2 gangliosidoses in patients of Ashkenazi Jewish origin: substitution of serine for glycine at position 269 of the alpha-subunit of beta-hexosaminidase.
Topics: Adult; Base Sequence; beta-N-Acetylhexosaminidases; Cells, Cultured; Europe; Fibroblasts; G(M2) Gang | 1989 |
Metabolic activities in human skin fibroblasts preloaded with labeled GM2-ganglioside.
Topics: Fibroblasts; G(M1) Ganglioside; Gangliosidoses; Glycine; Humans; Kinetics; Protein Biosynthesis; Ref | 1987 |