Page last updated: 2024-10-16

carnitine and Limb-Girdle Muscular Dystrophies

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

Research Excerpts

ExcerptRelevanceReference
"Type 2 familial partial lipodystrophy (FPLD) is an autosomal-dominant lamin A/C-related disease associated with exercise intolerance, muscular pain, and insulin resistance."1.36LMNA 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)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Boschmann, M1
Engeli, S1
Moro, C1
Luedtke, A1
Adams, F1
Gorzelniak, K1
Rahn, G1
Mähler, A1
Dobberstein, K1
Krüger, A1
Schmidt, S1
Spuler, S1
Luft, FC1
Smith, SR1
Schmidt, HH1
Jordan, J1

Other Studies

1 other study available for carnitine and Limb-Girdle Muscular Dystrophies

ArticleYear
LMNA mutations, skeletal muscle lipid metabolism, and insulin resistance.
    The Journal of clinical endocrinology and metabolism, 2010, Volume: 95, Issue:4

    Topics: Adult; Blood Glucose; Carnitine; Cells, Cultured; Energy Metabolism; Female; Glycogen; Humans; Insul

2010