carnitine has been researched along with Becker Muscular Dystrophy in 7 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "A milder form of the disease, Becker muscular dystrophy (BMD), is characterised by the presence of a semi-functional truncated dystrophin, or the full-length dystrophin at reduced level." | 2.43 | [Pharmacological treatments for Duchenne and Becker dystrophies]. ( de la Porte, S; Voisin, V, 2005) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (42.86) | 29.6817 |
| 2010's | 2 (28.57) | 24.3611 |
| 2020's | 2 (28.57) | 2.80 |
| Authors | Studies |
|---|---|
| Xu, H | 1 |
| Cai, X | 1 |
| Xu, K | 1 |
| Wu, Q | 1 |
| Xu, B | 1 |
| Lamhonwah, AM | 2 |
| Tein, I | 2 |
| Zolkipli, Z | 1 |
| Mai, L | 1 |
| Le Borgne, F | 1 |
| Guyot, S | 1 |
| Logerot, M | 1 |
| Beney, L | 1 |
| Gervais, P | 1 |
| Demarquoy, J | 1 |
| Sharma, U | 1 |
| Atri, S | 1 |
| Sharma, MC | 1 |
| Sarkar, C | 1 |
| Jagannathan, NR | 1 |
| Voisin, V | 1 |
| de la Porte, S | 1 |
| Hnia, K | 1 |
| Hugon, G | 1 |
| Rivier, F | 1 |
| Masmoudi, A | 1 |
| Mercier, J | 1 |
| Mornet, D | 1 |
1 review available for carnitine and Becker Muscular Dystrophy
| Article | Year |
|---|---|
[Pharmacological treatments for Duchenne and Becker dystrophies].
Topics: Adrenal Cortex Hormones; Adult; Aminoglycosides; Animals; Carnitine; Child; Child, Preschool; Creati | 2005 |
6 other studies available for carnitine and Becker Muscular Dystrophy
| Article | Year |
|---|---|
The metabolomic plasma profile of patients with Duchenne muscular dystrophy: providing new evidence for its pathogenesis.
Topics: Amino Acids; Carnitine; Humans; Lipids; Male; Metabolomics; Muscular Dystrophy, Duchenne | 2023 |
Expression of the organic cation/carnitine transporter family (Octn1,-2 and-3) in mdx muscle and heart: Implications for early carnitine therapy in Duchenne muscular dystrophy to improve cellular carnitine homeostasis.
Topics: Animals; Carnitine; Diaphragm; Homeostasis; Male; Mice; Mice, Inbred C57BL; Mice, Inbred mdx; Mitoch | 2020 |
The mdx mouse as a model for carnitine deficiency in the pathogenesis of Duchenne muscular dystrophy.
Topics: Animals; Carnitine; Disease Models, Animal; Male; Mice; Mice, Inbred C3H; Mice, Inbred C57BL; Mice, | 2012 |
Exploration of lipid metabolism in relation with plasma membrane properties of Duchenne muscular dystrophy cells: influence of L-carnitine.
Topics: Adolescent; Carnitine; Cell Membrane; Fatty Acids; Humans; Lipid Metabolism; Male; Mitochondria; Mus | 2012 |
Skeletal muscle metabolism in Duchenne muscular dystrophy (DMD): an in-vitro proton NMR spectroscopy study.
Topics: Adolescent; Adult; Carnitine; Child; Child, Preschool; Humans; Immunohistochemistry; In Vitro Techni | 2003 |
Modulation of p38 mitogen-activated protein kinase cascade and metalloproteinase activity in diaphragm muscle in response to free radical scavenger administration in dystrophin-deficient Mdx mice.
Topics: Animals; Apoptosis; Calcium; Carnitine; Creatine Kinase; Diaphragm; Dystroglycans; Dystrophin; Free | 2007 |