carnitine has been researched along with Mucopolysaccharidoses in 2 studies
Mucopolysaccharidoses: Group of lysosomal storage diseases each caused by an inherited deficiency of an enzyme involved in the degradation of glycosaminoglycans (mucopolysaccharides). The diseases are progressive and often display a wide spectrum of clinical severity within one enzyme deficiency.
| Excerpt | Relevance | Reference |
|---|---|---|
| "glycogenosis type II and III), lysosomal storage diseases (e." | 2.41 | Metabolic cardiomyopathies. ( Guertl, B; Hoefler, G; Noehammer, C, 2000) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (50.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Kachaner, J | 1 |
| Batisse, A | 1 |
| Fermont, L | 1 |
| Piechaud, JF | 1 |
| Ribierre, M | 1 |
| Guertl, B | 1 |
| Noehammer, C | 1 |
| Hoefler, G | 1 |
1 review available for carnitine and Mucopolysaccharidoses
| Article | Year |
|---|---|
Metabolic cardiomyopathies.
Topics: Adult; Animals; Calcium; Cardiomegaly; Cardiomyopathies; Cardiomyopathy, Alcoholic; Carnitine; Diabe | 2000 |
1 other study available for carnitine and Mucopolysaccharidoses
| Article | Year |
|---|---|
["Metabolic" myocardiopathies in childhood (author's transl)].
Topics: Cardiomyopathies; Carnitine; Diabetes Mellitus; Echocardiography; Glycogen Storage Disease; Humans; | 1981 |