Cell Therapy Strategies on Duchenne Muscular Dystrophy: A Systematic Review of Clinical Applications
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s12015-023-10653-8.pdf
Reference92 articles.
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2. Emery, A. E. (2002). The muscular dystrophies. The Lancet, 359(9307), 687–695. https://doi.org/10.1016/s0140-6736(02)07815-7
3. Connuck, D. M., Sleeper, L. A., Colan, S. D., Cox, G. F., Towbin, J. A., Lowe, A. M., Wilkinson, J. D., Orav, E. J., Cuniberti, L., Salbert, B. A., Lipshultz, S. E., Pediatric Cardiomyopathy Registry Study Group. (2008). Characteristics and outcomes of cardiomyopathy in children with Duchenne or Becker muscular dystrophy: a comparative study from the Pediatric Cardiomyopathy Registry. American Heart Journal, 155(6), 998–1005. https://doi.org/10.1016/j.ahj.2008.01.018
4. Freilinger, M., Schmidt, I., Dysek, S., Seidl, R., Schmidt, W. M., & Bittner, R. E. (2013). Muscle-specific discordant skewing of X chromosome inactivation leads to different clinical phenotypes of Duchenne muscular dystrophy in two monozygotic female twins. Neuropediatrics, 44, FV16_04.
5. Ferrier, P., Bamatter, F., & Klein, D. (1965). Muscular dystrophy (Duchenne) in a girl with Turner’s syndrome. Journal of Medical Genetics, 2(1), 38–46. https://doi.org/10.1136/jmg.2.1.38
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