Quantitative muscle MRI and ultrasound for facioscapulohumeral muscular dystrophy: complementary imaging biomarkers
Author:
Funder
Prinses Beatrix Spierfonds
Stichting Spieren voor Spieren
Publisher
Springer Science and Business Media LLC
Subject
Clinical Neurology,Neurology
Link
http://link.springer.com/article/10.1007/s00415-018-9037-y/fulltext.html
Reference37 articles.
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2. Mul K, Lassche S, Voermans NC, Padberg GW, Horlings CG, van Engelen BG (2016) What’s in a name? The clinical features of facioscapulohumeral muscular dystrophy. Pract Neurol 16(3):201–207
3. Marsollier AC, Ciszewski L, Mariot V, Popplewell L, Voit T, Dickson G, Dumonceaux J (2016) Antisense targeting of 3′ end elements involved in DUX4 mRNA processing is an efficient therapeutic strategy for facioscapulohumeral dystrophy: a new gene-silencing approach. Hum Mol Genet 25(8):1468–1478
4. Himeda CL, Jones TI, Jones PL (2016) CRISPR/dCas9-mediated transcriptional inhibition ameliorates the epigenetic dysregulation at D4Z4 and represses DUX4-fl in FSH muscular dystrophy. Mol Ther 24(3):527–535
5. Tawil R, Padberg GW, Shaw DW, van der Maarel SM, Tapscott SJ, Participants FW ( 2016) Clinical trial preparedness in facioscapulohumeral muscular dystrophy: clinical, tissue, and imaging outcome measures 29–30 May 2015, Rochester, New York. Neuromuscul Disord 26(2):181–186
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