carnitine has been researched along with Congenital Ichthyosiform Erythroderma in 2 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "Not surprisingly, a group of muscle disorders due to defects in this system usually leads to the development of acute rhabdomyolysis in conditions such as infection, fasting and prolonged exercise." | 2.46 | State of the art in muscle lipid diseases. ( Liang, WC; Nishino, I, 2010) |
| 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 | 2 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Liang, WC | 2 |
| Nishino, I | 2 |
| Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
|---|---|---|---|---|---|---|---|
| Fat and Sugar Metabolism During Exercise in Patients With Metabolic Myopathy[NCT02635269] | 60 participants (Actual) | Interventional | 2016-01-31 | Active, not recruiting | |||
| [information is prepared from clinicaltrials.gov, extracted Sep-2024] | |||||||
2 reviews available for carnitine and Congenital Ichthyosiform Erythroderma
| Article | Year |
|---|---|
Lipid storage myopathy.
Topics: Acyl-CoA Dehydrogenase; Carnitine; Diagnosis, Differential; Humans; Ichthyosiform Erythroderma, Cong | 2011 |
State of the art in muscle lipid diseases.
Topics: Acyl-CoA Dehydrogenase, Long-Chain; Cardiomyopathies; Carnitine; Carnitine O-Palmitoyltransferase; H | 2010 |