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Suitability of external controls for drug evaluation in Duchenne muscular dystrophy.
Neurology. 2020 Sep 8;95(10):e1381-e1391. doi: 10.1212/WNL.0000000000010170. Epub 2020 Jul 1.
Neurology. 2020.
PMID: 32611643
Free PMC article.
Evidence for ACTN3 as a genetic modifier of Duchenne muscular dystrophy.
Hogarth MW, Houweling PJ, Thomas KC, Gordish-Dressman H, Bello L; Cooperative International Neuromuscular Research Group (CINRG); Pegoraro E, Hoffman EP, Head SI, North KN.
Hogarth MW, et al.
Nat Commun. 2017 Jan 31;8:14143. doi: 10.1038/ncomms14143.
Nat Commun. 2017.
PMID: 28139640
Free PMC article.
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Towards regulatory endorsement of drug development tools to promote the application of model-informed drug development in Duchenne muscular dystrophy.
Conrado DJ, Larkindale J, Berg A, Hill M, Burton J, Abrams KR, Abresch RT, Bronson A, Chapman D, Crowther M, Duong T, Gordish-Dressman H, Harnisch L, Henricson E, Kim S, McDonald CM, Schmidt S, Vong C, Wang X, Wong BL, Yong F, Romero K; Duchenne Muscular Dystrophy Regulatory Science Consortium (D-RSC).
Conrado DJ, et al.
J Pharmacokinet Pharmacodyn. 2019 Oct;46(5):441-455. doi: 10.1007/s10928-019-09642-7. Epub 2019 May 24.
J Pharmacokinet Pharmacodyn. 2019.
PMID: 31127458
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Fat Embolism Syndrome following minor trauma in Duchenne muscular dystrophy.
McAdam LC, Rastogi A, Macleod K, Douglas Biggar W.
McAdam LC, et al. Among authors: douglas biggar w.
Neuromuscul Disord. 2012 Dec;22(12):1035-9. doi: 10.1016/j.nmd.2012.07.010. Epub 2012 Aug 21.
Neuromuscul Disord. 2012.
PMID: 22920089
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