chimyl alcohol has been researched along with Barth Syndrome in 1 studies
*Barth Syndrome: Rare congenital X-linked disorder of lipid metabolism. Barth syndrome is transmitted in an X-linked recessive pattern. The syndrome is characterized by muscular weakness, growth retardation, DILATED CARDIOMYOPATHY, variable NEUTROPENIA, 3-methylglutaconic aciduria (type II) and decreases in mitochondrial CARDIOLIPIN level. Other biochemical and morphological mitochondrial abnormalities also exist. [MeSH]
| 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 | 0 (0.00) | 24.3611 |
| 2020's | 1 (100.00) | 2.80 |
| Authors | Studies |
|---|---|
| Atilla-Gokcumen, GE; Bozelli, JC; Epand, RM; Lu, D | 1 |
1 other study(ies) available for chimyl alcohol and Barth Syndrome
| Article | Year |
|---|---|
Promotion of plasmalogen biosynthesis reverse lipid changes in a Barth Syndrome cell model.
Topics: Acyltransferases; Barth Syndrome; Cardiolipins; Cell Survival; Cells, Cultured; Child; Child, Preschool; Dietary Fats; Dietary Supplements; Glyceryl Ethers; Humans; Infant; Loss of Function Mutation; Lymphocytes; Lysophospholipids; Male; Membrane Potential, Mitochondrial; Mitochondria; Organelle Biogenesis; Plasmalogens; Primary Cell Culture; Transcription Factors | 2020 |