Open Access
| Issue |
Cah. Myol.
Number 25, juillet 2022
|
|
|---|---|---|
| Page(s) | 10 - 15 | |
| Section | Mise au point / Focus | |
| DOI | https://doi.org/10.1051/myolog/202225004 | |
| Published online | 11 août 2022 | |
- McDonagh MJ, Hayward CM, Davies CT. Isometric training in human elbow flexor muscles. The effects on voluntary and electrically evoked forces. J Bone Joint Surg Br 1983 ; 65 : 355–8. [CrossRef] [Google Scholar]
- Krzysztofik M, Wilk M, Wojdala G, et al. Maximizing Muscle Hypertrophy: A Systematic Review of Advanced Resistance Training Techniques and Methods. Int J Environ Res Public Health 2019 ; 16 : 4897. [CrossRef] [Google Scholar]
- Grobet L, Royo Martin LJ, Poncelet D, et al. A deletion in the bovine myostatin gene causes the double-muscled phenotype in cattle. Nat Genet 1997 ; 17 : 71–4. [CrossRef] [PubMed] [Google Scholar]
- Schuelke M, Wagner KR, Stolz LE, et al. Myostatin mutation associated with gross muscle hypertrophy in a child. NEJM 2004 ; 350 : 2682–8. [CrossRef] [PubMed] [Google Scholar]
- Mendel JR, Sahenk Z, Malik V, et al. A phase 1/2a follistatin gene therapy trial for Becker muscular dystrophy. Mol Ther 2015 ; 23 : 192–201. [CrossRef] [PubMed] [Google Scholar]
- Schakman O, Gilson H, Thissen JP. Mechanisms of glucocorticoid-induced myopathy. J Endocrinol 2008 ; 197 : 1–10. [CrossRef] [PubMed] [Google Scholar]
- Walters J. Muscle hypertrophy and pseudohypertrophy. J Pract Neurol 2017 ; 17 : 369–79. [CrossRef] [PubMed] [Google Scholar]
- Molenaar JP, Verhoeven JI, Rodenburg RJ, et al. Clinical, morphological and genetic characterization of Brody disease: an international study of 40 patients. Brain 2020 ; 143 : 452–66. [CrossRef] [PubMed] [Google Scholar]
- Conte TC. The Strongman trait: Clinical and molecular characterization of a dominant Herculean myalgic disorder. Department of Human Genetics McGill University, Montreal May, 2019 (thesis). [Google Scholar]
- Witting N, Laforet P, Voermans NC, et al. Phenotype and genotype of muscle ryanodine receptor rhabdomyolysis-myalgia syndrome. Acta Neurol Scand 2018 ; 137 : 452–61. [CrossRef] [PubMed] [Google Scholar]
- Hayashi YK, Matsuda C, Ogawa M, et al. Human PTRF mutations cause secondary deficiency of caveolins resulting in muscular dystrophy with generalized lipodystrophy. J Clin Invest 2009 ; 119 : 2623–33. [CrossRef] [PubMed] [Google Scholar]
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