Therapeutic efforts in Duchenne muscular dystrophy; the need for a common language between basic scientists and clinicians
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health
Cited by 12 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Quantitative T2 Combined with Texture Analysis of Nuclear Magnetic Resonance Images Identify Different Degrees of Muscle Involvement in Three Mouse Models of Muscle Dystrophy: mdx, Largemyd and mdx/Largemyd;PLOS ONE;2015-02-24
2. Myogenic Precursors from iPS Cells for Skeletal Muscle Cell Replacement Therapy;Journal of Clinical Medicine;2015-01-29
3. Heterozygote Testing and Carrier Screening;Emery and Rimoin's Principles and Practice of Medical Genetics;2013
4. Cardiac MRI in Muscular Dystrophy: An Overview and Future Directions;Physical Medicine and Rehabilitation Clinics of North America;2012-02
5. The risks of therapeutic misconception and individual patient (n=1) “trials” in rare diseases such as Duchenne dystrophy;Neuromuscular Disorders;2011-01
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