carnitine has been researched along with Limb-Girdle Muscular Dystrophies in 1 studies
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 Limb-Girdle Muscular Dystrophies
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 |