choline has been researched along with Abnormalities, Sex Chromosome in 3 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "Despite regional variability of demyelination, proton magnetic resonance spectroscopy revealed a specific metabolic pattern in all patients, with only moderate reduction of N-acetylaspartate, normal or reduced choline-containing compounds, normal or enhanced myo-inositol and no detectable lactate, which differs from findings in progressive cerebral adrenoleukodystrophy which usually exhibits a severe reduction of N-acetylaspartate and marked increases of choline-containing compounds, myo-inositol, and lactate." | 1.29 | Arrested cerebral adrenoleukodystrophy: a clinical and proton magnetic resonance spectroscopy study in three patients. ( Frahm, J; Hanefeld, F; Hunneman, DH; Jost, W; Korenke, GC; Krasemann, E; Pouwels, PJ; Stoeckler, S, 1996) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (66.67) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Tonduti, D | 1 |
| Vanderver, A | 1 |
| Berardinelli, A | 1 |
| Schmidt, JL | 1 |
| Collins, CD | 1 |
| Novara, F | 1 |
| Genni, AD | 1 |
| Mita, A | 1 |
| Triulzi, F | 1 |
| Brunstrom-Hernandez, JE | 1 |
| Zuffardi, O | 1 |
| Balottin, U | 1 |
| Orcesi, S | 1 |
| Korenke, GC | 1 |
| Pouwels, PJ | 1 |
| Frahm, J | 1 |
| Hunneman, DH | 1 |
| Stoeckler, S | 1 |
| Krasemann, E | 1 |
| Jost, W | 1 |
| Hanefeld, F | 1 |
| Logan, HE | 1 |
| Byers, DM | 1 |
| Ridgway, ND | 1 |
| Cook, HW | 1 |
3 other studies available for choline and Abnormalities, Sex Chromosome
| Article | Year |
|---|---|
MCT8 deficiency: extrapyramidal symptoms and delayed myelination as prominent features.
Topics: Aspartic Acid; Basal Ganglia Diseases; Brain; Child, Preschool; Choline; Chromosomes, Human, X; Codo | 2013 |
Arrested cerebral adrenoleukodystrophy: a clinical and proton magnetic resonance spectroscopy study in three patients.
Topics: Aspartic Acid; Brain; Brain Diseases, Metabolic; Child; Choline; Demyelinating Diseases; Female; Hum | 1996 |
Phospholipase D activity is altered in X-linked adrenoleukodystrophy heterozygous carriers, but not in hemizygous patients.
Topics: Carrier State; Cells, Cultured; Choline; Enzyme Activation; Female; Fibroblasts; Genetic Linkage; Hu | 1998 |