References
1 Carter JC, Sheehan DW, Prochoroff A, et al. Muscular dystrophies[J]. Clin Chest Med, 2018, 39(2): 377-389. PMID: 29779596. DOI: 10.1016/j.ccm.2018.01.004.
2 Day JA, Bajic N, Gentili S, et al. Radiographic patterns of muscle involvement in the idiopathic inflammatory myopathies[J]. Muscle Nerve, 2019, 60(5): 549-557. PMID: 31397909. DOI: 10.1002/mus.26660.
3 梁颖茵, 黎规典, 何荣兴, 等. Duchenne型肌营养不良症肌肉磁共振成像脂肪浸润和水肿特点分析[J]. 中国现代神经疾病杂志, 2018, 18(7): 501-505. DOI: 10.3969/j.issn.1672-6731.2018.07.006.
4 Barp A, Bello L, Caumo L, et al. Muscle MRI and functional outcome measures in Becker muscular dystrophy[J]. Sci Rep, 2017, 7(1): 16060. PMID: 29167533. PMCID: PMC5700122. DOI: 10.1038/s41598-017-16170-2.
5 Barnard AM, Willcocks RJ, Finanger EL, et al. Skeletal muscle magnetic resonance biomarkers correlate with function and sentinel events in Duchenne muscular dystrophy[J]. PLoS One, 2018, 13(3): e0194283. PMID: 29554116. PMCID: PMC5858773. DOI: 10.1371/journal.pone.0194283.
6 Yin L, Xie ZY, Xu HY, et al. T2 mapping and fat quantification of thigh muscles in children with Duchenne muscular dystrophy[J]. Curr Med Sci, 2019, 39(1): 138-145. PMID: 30868504. DOI: 10.1007/s11596-019-2012-8.
7 Brooke MH, Griggs RC, Mendell JR, et al. Clinical trial in Duchenne dystrophy. I. The design of the protocol[J]. Muscle Nerve, 1981, 4(3): 186-197. PMID: 7017401. DOI: 10.1002/mus.880040304.
8 Florence JM, Pandya S, King WM, et al. Intrarater reliability of manual muscle test (Medical Research Council Scale) grades in Duchenne's muscular dystrophy[J]. Phys Ther, 1992, 72(2): 115-122. PMID: 1549632. DOI: 10.1093/ptj/72.2.115.
9 Bushby K, Finkel R, Birnkrant DJ, et al. Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management[J]. Lancet Neurol, 2010, 9(1): 77-93. PMID: 19945913. DOI: 10.1016/S1474-4422(09)70271-6.
10 Monaco AP, Bertelson CJ, Liechti-Gallati S, et al. An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus[J]. Genomics, 1988, 2(1): 90-95. PMID: 3384440. DOI: 10.1016/0888-7543(88)90113-9.
11 中华医学会神经病学分会, 中华医学会神经病学分会神经肌肉病学组, 中华医学会神经病学分会肌电图与临床神经生理学组. 中国假肥大型肌营养不良症诊治指南[J]. 中华神经科杂志, 2016, 49(1): 17-20. DOI: 10.3760/cma.j.issn.1006-7876.2016.01.004.
12 Kim HK, Laor T, Horn PS, et al. T2 mapping in Duchenne muscular dystrophy: distribution of disease activity and correlation with clinical assessments[J]. Radiology, 2010, 255(3): 899-908. PMID: 20501727. DOI: 10.1148/radiol.10091547.
13 卜姗姗, 肖江喜, 朱颖, 等. 杜氏肌营养不良与贝氏肌营养不良常规MRI的对比研究[J]. 中国医学影像技术, 2019, 35(11): 1717-1721. DOI: 10.13929/j.1003-3289.201903166.
14 Lin HT, Liu X, Zhang W, et al. Muscle magnetic resonance imaging in patients with various clinical subtypes of LMNA-related muscular dystrophy[J]. Chin Med J (Engl), 2018, 131(12): 1472-1479. PMID: 29893365. PMCID: PMC6006825. DOI: 10.4103/0366-6999.233957.
15 牛焕红, 陶东英, 成胜权. Becker/Duchenne肌营养不良患儿临床表型与基因关联性预测分析[J]. 中国当代儿科杂志, 2020, 22(6): 602-607. PMID: 32571459. PMCID: PMC7390220. DOI: 10.7499/j.issn.1008-8830.1912133.
16 钟京梓. 肌营养不良基因诊断及新突变致病性研究[D]. 南宁: 广西医科大学, 2018.
17 王霞, 王鹏娟, 熊婷, 等. MRI对进行性肌营养不良大腿肌肉脂肪浸润评估的应用研究[J]. 实用放射学杂志, 2019, 35(1): 81-84. DOI: 10.3969/j.issn.1002-1671.2019.01.020.
18 Schmidt S, Hafner P, Klein A, et al. Timed function tests, motor function measure, and quantitative thigh muscle MRI in ambulant children with Duchenne muscular dystrophy: a cross-sectional analysis[J]. Neuromuscul Disord, 2018, 28(1): 16-23. PMID: 29174526. DOI: 10.1016/j.nmd.2017.10.003.
19 Peng F, Xu H, Song Y, et al. Utilization of T1-mapping for the pelvic and thigh muscles in Duchenne muscular dystrophy: a quantitative biomarker for disease involvement and correlation with clinical assessments[J]. BMC Musculoskelet Disord, 2022, 23(1): 681. PMID: 35842609. PMCID: PMC9288085. DOI: 10.1186/s12891-022-05640-y.
20 汪昌, 周洁, 石永光, 等. Duchenne型肌营养不良酶学与肌肉脂肪浸润度的研究[J]. 中国实用神经疾病杂志, 2021, 24(11): 954-960. DOI: 10.12083/SYSJ.2021.16.008.