toluene has been researched along with Homocystinuria in 1 studies
methylbenzene : Any alkylbenzene that is benzene substituted with one or more methyl groups.
Homocystinuria: Autosomal recessive inborn error of methionine metabolism usually caused by a deficiency of CYSTATHIONINE BETA-SYNTHASE and associated with elevations of homocysteine in plasma and urine. Clinical features include a tall slender habitus, SCOLIOSIS, arachnodactyly, MUSCLE WEAKNESS, genu varus, thin blond hair, malar flush, lens dislocations, an increased incidence of MENTAL RETARDATION, and a tendency to develop fibrosis of arteries, frequently complicated by CEREBROVASCULAR ACCIDENTS and MYOCARDIAL INFARCTION. (From Adams et al., Principles of Neurology, 6th ed, p979)
| Excerpt | Relevance | Reference |
|---|---|---|
| "Three circumstances prompted us to reexamine the relationship between abnormal cystathionine accumulation and possible homocystinuria resulting from this condition: (a) discovery of an infant girl with apparently alternating massive cystathioninuria and homocystinuria; (b) the presence of homocystinuria in some, but not all, previously reported cases of cystathioninuria probably due to gamma-cystathionine deficiency; and (c) the recent demonstration that mammalian cystathionine beta-synthase can cleave cystathionine to homocysteine." | 3.65 | Cystathioninuria and homocystinuria. ( Levy, HL; Madigan, PM; Mudd, SH; Uhlendorf, BW, 1975) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (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 |
|---|---|
| Levy, HL | 1 |
| Mudd, SH | 1 |
| Uhlendorf, BW | 1 |
| Madigan, PM | 1 |
1 other study available for toluene and Homocystinuria
| Article | Year |
|---|---|
Cystathioninuria and homocystinuria.
Topics: Amino Acid Metabolism, Inborn Errors; Bacteria; Cystathionine; Female; Homocystinuria; Humans; Infan | 1975 |