Outcome measures for Duchenne muscular dystrophy from ambulant to non-ambulant: Implications for clinical trials

被引:0
|
作者
Ricotti, V. [1 ]
Eagle, M. [2 ]
Butler, J. [1 ]
Decostre, V. [3 ]
Deborah, R. [4 ]
Moraux, A. [3 ]
Anthony, K. [1 ]
Sleby, V. [1 ]
Guglieri, M. [2 ]
van der Holst, M. [5 ]
Jansen, M. [6 ]
Morgan, J. [1 ]
de Groot, I. [6 ]
Niks, E. [5 ]
Verschuuren, J. [5 ]
Servais, L. [3 ]
Hogrel, J. Y. [3 ]
Voit, T. [3 ]
Straub, V. [2 ]
Muntoni, F. [1 ]
机构
[1] UCL Inst Child Hlth, Dubowitz Neuromuscular Ctr, London, England
[2] Newcastle Univ, John Walton Muscular Dystrophy Res Ctr, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[3] Grp Hosp Pitie Salpetriere, Inst Myol, F-75634 Paris, France
[4] UCL Inst Child Hlth, Populat Policy & Practice Programme, London, England
[5] Leids Univ, Med Ctr, Leiden, Netherlands
[6] Radboud Univ Nijmegen, Med Ctr, NL-6525 ED Nijmegen, Netherlands
关键词
D O I
10.1016/j.nmd.2015.06.162
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
G.P.147
引用
收藏
页码:S229 / S229
页数:1
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