The muscular dystrophies.
作者信息
Emery A E
机构信息
Research Unit, Department of Neurology, Royal Devon and Exeter Hospital, Exeter EX2 5DW.
出版信息
BMJ. 1998 Oct 10;317(7164):991-5. doi: 10.1136/bmj.317.7164.991.
Abstract
摘要
相似文献
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The muscular dystrophies.肌营养不良症
BMJ. 1998 Oct 10;317(7164):991-5. doi: 10.1136/bmj.317.7164.991.
2
Muscular dystrophies.肌营养不良症
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Prenatal diagnosis of congenital myopathies and muscular dystrophies.先天性肌病和肌营养不良症的产前诊断。
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Sleep apnoea and hypoventilation in patients with five major types of muscular dystrophy.五种主要类型肌营养不良症患者的睡眠呼吸暂停和通气不足。
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本文引用的文献
1
Myopathia distalis tarda hereditaria; 249 examined cases in 72 pedigrees.迟发性遗传性远端肌病；72个家系中的249例受检病例。
Acta Med Scand Suppl. 1951;265:1-124.
2
MUSCULAR DYSTROPHY: SOME RECENT ADVANCES IN KNOWLEDGE.肌肉萎缩症：知识领域的一些最新进展
Br Med J. 1964 May 23;1(5394):1344-8 CONCL. doi: 10.1136/bmj.1.5394.1336-a.
3
MUSCULAR DYSTROPHY: SOME RECENT ADVANCES IN KNOWLEDGE.肌肉萎缩症：知识领域的一些最新进展
Br Med J. 1964 May 16;1(5393):1271-4 CONTD. doi: 10.1136/bmj.1.5393.1271.
4
On the classification, natural history and treatment of the myopathies.关于肌病的分类、自然史及治疗
Brain. 1954;77(2):169-231. doi: 10.1093/brain/77.2.169.
5
6
Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy.聚腺苷酸结合蛋白2（PABP2）基因中短的GCG重复序列扩增导致眼咽型肌营养不良。
Nat Genet. 1998 Feb;18(2):164-7. doi: 10.1038/ng0298-164.
7
Proceedings of the First International Symposium on Oculopharyngeal muscular dystrophy. Québec, 22-23 September 1995.第一届眼咽型肌营养不良国际研讨会会议记录。魁北克，1995年9月22 - 23日。
Neuromuscul Disord. 1997 Oct;7 Suppl 1:S1-104.
8
Heart-specific localization of emerin: new insights into Emery-Dreifuss muscular dystrophy.Emerin在心脏中的特异性定位：对Emery-Dreifuss型肌营养不良症的新见解。
Hum Mol Genet. 1997 Dec;6(13):2257-64. doi: 10.1093/hmg/6.13.2257.
9
Utrophin-dystrophin-deficient mice as a model for Duchenne muscular dystrophy.缺乏抗肌萎缩蛋白相关蛋白和抗肌萎缩蛋白的小鼠作为杜氏肌营养不良症的模型。
Cell. 1997 Aug 22;90(4):717-27. doi: 10.1016/s0092-8674(00)80532-2.
10
Problems and potential for gene therapy in Duchenne muscular dystrophy.杜氏肌营养不良症基因治疗的问题与潜力
Neuromuscul Disord. 1997 Jul;7(5):319-24. doi: 10.1016/s0960-8966(97)00056-4.
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