The Persistence of Duchenne vs Becker Muscular Dystrophies: ?
作者信息
Hoffman Eric P
机构信息
Department of Pharmaceutical Sciences, School of Pharmacy and Pharmaceutical Sciences, Binghamton, NY.
出版信息
Neurol Genet. 2024 Dec 17;11(1):e200230. doi: 10.1212/NXG.0000000000200230. eCollection 2025 Feb.
Abstract
摘要
相似文献
1
The Persistence of Duchenne vs Becker Muscular Dystrophies: ?杜兴氏与贝克氏肌肉萎缩症的持续性：？
Neurol Genet. 2024 Dec 17;11(1):e200230. doi: 10.1212/NXG.0000000000200230. eCollection 2025 Feb.
2
Giovanni Nigro and the Naples's school: historical contribution to the knowledge of heart involvement in Duchenne/Becker muscular dystrophies.乔瓦尼·尼格鲁和那不勒斯学派：对杜兴氏肌营养不良症/贝克肌营养不良症心脏受累知识的历史贡献。
Acta Myol. 2020 Dec 1;39(4):187-190. doi: 10.36185/2532-1900-021. eCollection 2020 Dec.
3
Epilepsy in Duchenne and Becker muscular dystrophies.杜氏和贝克型肌营养不良症中的癫痫
Eur J Paediatr Neurol. 1997;1(4):115-9. doi: 10.1016/s1090-3798(97)80042-6.
4
Complementary and alternative medicine for Duchenne and Becker muscular dystrophies: characteristics of users and caregivers.杜兴氏和贝克氏肌营养不良症的补充和替代医学：使用者及护理者的特征
Pediatr Neurol. 2014 Jul;51(1):71-7. doi: 10.1016/j.pediatrneurol.2014.02.003. Epub 2014 Feb 15.
5
Cardiac assessment in duchenne and becker muscular dystrophies.杜兴氏和贝克氏肌营养不良症的心脏评估
Curr Heart Fail Rep. 2010 Dec;7(4):212-8. doi: 10.1007/s11897-010-0028-2.
6
[Dystrophin in the differentiation between Duchenne and Becker muscular dystrophies: an immunohistochemical study compared with clinical stage, serum enzymes and muscle biopsy].
Arq Neuropsiquiatr. 1990 Dec;48(4):454-64. doi: 10.1590/s0004-282x1990000400009.
7
Causes of clinical variability in Duchenne and Becker muscular dystrophies and implications for exon skipping therapies.杜氏肌营养不良症和贝克肌营养不良症临床变异性的原因及其对外显子跳跃疗法的影响。
Acta Myol. 2020 Dec 1;39(4):179-186. doi: 10.36185/2532-1900-020. eCollection 2020 Dec.
8
Bone mass development in patients with Duchenne and Becker muscular dystrophies: a 4-year clinical follow-up.杜氏肌营养不良症和贝克肌营养不良症患者的骨量发育：4 年临床随访。
Acta Paediatr. 2012 Apr;101(4):424-32. doi: 10.1111/j.1651-2227.2011.02532.x. Epub 2011 Dec 9.
9
Genetic diagnosis of Duchenne and Becker muscular dystrophy using multiplex ligation-dependent probe amplification in Rwandan patients.使用多重连接依赖性探针扩增技术对卢旺达患者进行 Duchenne 和 Becker 肌营养不良症的基因诊断。
J Trop Pediatr. 2014 Apr;60(2):112-7. doi: 10.1093/tropej/fmt090. Epub 2013 Nov 7.
10
Comparative analysis between Duchenne and Becker types muscular dystrophy.杜兴氏和贝克氏型肌营养不良症的比较分析
Electromyogr Clin Neurophysiol. 1999 Jul-Aug;39(5):315-8.
本文引用的文献
1
Characterization of Phenotypic Variability in Becker Muscular Dystrophy for Clinical Practice and Towards Trial Readiness: A Two-Years Follow up Study.贝氏肌营养不良症临床表型变异性的特征分析及其临床试验准备情况：一项为期两年的随访研究
J Neuromuscul Dis. 2024;11(2):375-387. doi: 10.3233/JND-221513.
2
Findings from the Longitudinal CINRG Becker Natural History Study.纵向 CINRG Becker 自然史研究结果。
J Neuromuscul Dis. 2024;11(1):201-212. doi: 10.3233/JND-230178.
3
Natural history of Becker muscular dystrophy: a multicenter study of 225 patients.贝克型肌营养不良症的自然病史：225 例患者的多中心研究。
Ann Clin Transl Neurol. 2023 Dec;10(12):2360-2372. doi: 10.1002/acn3.51925. Epub 2023 Oct 26.
4
Muscle histological changes in a large cohort of patients affected with Becker muscular dystrophy.患有 Becker 型肌营养不良症的大量患者的肌肉组织学变化。
Acta Neuropathol Commun. 2022 Apr 8;10(1):48. doi: 10.1186/s40478-022-01354-3.
5
Investigating the role of dystrophin isoform deficiency in motor function in Duchenne muscular dystrophy.研究抗肌萎缩蛋白异构体缺乏在杜氏肌营养不良症运动功能中的作用。
J Cachexia Sarcopenia Muscle. 2022 Apr;13(2):1360-1372. doi: 10.1002/jcsm.12914. Epub 2022 Jan 26.
6
Very Low Residual Dystrophin Quantity Is Associated with Milder Dystrophinopathy.极低残余肌营养不良蛋白量与较轻微的肌营养不良症相关。
Ann Neurol. 2021 Feb;89(2):280-292. doi: 10.1002/ana.25951. Epub 2020 Nov 24.
7
Muscle MRI and functional outcome measures in Becker muscular dystrophy.贝克型肌营养不良症的肌肉 MRI 和功能结局测量。
Sci Rep. 2017 Nov 22;7(1):16060. doi: 10.1038/s41598-017-16170-2.
8
Functional changes in Becker muscular dystrophy: implications for clinical trials in dystrophinopathies.贝克型肌营养不良症的功能变化：对肌营养不良症中抗肌萎缩蛋白病临床试验的影响。
Sci Rep. 2016 Sep 1;6:32439. doi: 10.1038/srep32439.
9
[A new x-chromosomal muscular dystrophy].[一种新的X染色体连锁型肌营养不良症]
Arch Psychiatr Nervenkr Z Gesamte Neurol Psychiatr. 1955;193(4):427-48. doi: 10.1007/BF00343141.
10
The clinical, genetic and dystrophin characteristics of Becker muscular dystrophy. I. Natural history.贝克肌营养不良症的临床、遗传及抗肌萎缩蛋白特征。I. 自然病史。
J Neurol. 1993 Feb;240(2):98-104. doi: 10.1007/BF00858725.
Zotero 插件