carnitine has been researched along with Muscular Dystrophies, Limb-Girdle in 1 studies
Muscular Dystrophies, Limb-Girdle: A heterogenous group of inherited muscular dystrophy that can be autosomal dominant or autosomal recessive. There are many forms (called LGMDs) involving genes encoding muscle membrane proteins such as the sarcoglycan (SARCOGLYCANS) complex that interacts with DYSTROPHIN. The disease is characterized by progressing wasting and weakness of the proximal muscles of arms and legs around the HIPS and SHOULDERS (the pelvic and shoulder girdles).
| Excerpt | Relevance | Reference |
|---|---|---|
| "Type 2 familial partial lipodystrophy (FPLD) is an autosomal-dominant lamin A/C-related disease associated with exercise intolerance, muscular pain, and insulin resistance." | 1.36 | LMNA mutations, skeletal muscle lipid metabolism, and insulin resistance. ( Adams, F; Boschmann, M; Dobberstein, K; Engeli, S; Gorzelniak, K; Jordan, J; Krüger, A; Luedtke, A; Luft, FC; Mähler, A; Moro, C; Rahn, G; Schmidt, HH; Schmidt, S; Smith, SR; Spuler, S, 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 | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Boschmann, M | 1 |
| Engeli, S | 1 |
| Moro, C | 1 |
| Luedtke, A | 1 |
| Adams, F | 1 |
| Gorzelniak, K | 1 |
| Rahn, G | 1 |
| Mähler, A | 1 |
| Dobberstein, K | 1 |
| Krüger, A | 1 |
| Schmidt, S | 1 |
| Spuler, S | 1 |
| Luft, FC | 1 |
| Smith, SR | 1 |
| Schmidt, HH | 1 |
| Jordan, J | 1 |
1 other study available for carnitine and Muscular Dystrophies, Limb-Girdle
| Article | Year |
|---|---|
LMNA mutations, skeletal muscle lipid metabolism, and insulin resistance.
Topics: Adult; Blood Glucose; Carnitine; Cells, Cultured; Energy Metabolism; Female; Glycogen; Humans; Insul | 2010 |