glycine has been researched along with Adrenoleukodystrophy in 3 studies
Adrenoleukodystrophy: An X-linked recessive disorder characterized by the accumulation of saturated very long chain fatty acids in the LYSOSOMES of ADRENAL CORTEX and the white matter of CENTRAL NERVOUS SYSTEM. This disease occurs almost exclusively in the males. Clinical features include the childhood onset of ATAXIA; NEUROBEHAVIORAL MANIFESTATIONS; HYPERPIGMENTATION; ADRENAL INSUFFICIENCY; SEIZURES; MUSCLE SPASTICITY; and DEMENTIA. The slowly progressive adult form is called adrenomyeloneuropathy. The defective gene ABCD1 is located at Xq28, and encodes the adrenoleukodystrophy protein (ATP-BINDING CASSETTE TRANSPORTERS).
| Excerpt | Relevance | Reference |
|---|---|---|
| "Neonatal seizures, as distinguished from nonconvulsive abnormal movements, are a significant problem in neonatal intensive care units." | 2.37 | Neonatal seizures. ( Bergman, I; Crumrine, P; Painter, MJ, 1986) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 2 (66.67) | 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 |
|---|---|
| Tzika, AA | 1 |
| Ball, WS | 1 |
| Vigneron, DB | 1 |
| Dunn, RS | 1 |
| Nelson, SJ | 1 |
| Kirks, DR | 1 |
| Libert, R | 1 |
| Hermans, D | 1 |
| Draye, JP | 1 |
| Van Hoof, F | 1 |
| Sokal, E | 1 |
| de Hoffmann, E | 1 |
| Painter, MJ | 1 |
| Bergman, I | 1 |
| Crumrine, P | 1 |
1 review available for glycine and Adrenoleukodystrophy
| Article | Year |
|---|---|
Neonatal seizures.
Topics: Adrenoleukodystrophy; Amino Acid Metabolism, Inborn Errors; Ammonia; Anesthetics, Local; Anticonvuls | 1986 |
2 other studies available for glycine and Adrenoleukodystrophy
| Article | Year |
|---|---|
Childhood adrenoleukodystrophy: assessment with proton MR spectroscopy.
Topics: Adolescent; Adrenoleukodystrophy; Aspartic Acid; Child; Child, Preschool; Choline; Creatine; gamma-A | 1993 |
Bile acids and conjugates identified in metabolic disorders by fast atom bombardment and tandem mass spectrometry.
Topics: Adrenoleukodystrophy; Bile Acids and Salts; Glycine; Humans; Hydroxylation; Mass Spectrometry; Metab | 1991 |