Facioscapulohumeral muscular dystrophy
Author:
Publisher
Springer Science and Business Media LLC
Subject
Clinical Neurology,General Neuroscience
Link
http://link.springer.com/content/pdf/10.1007/s11910-004-0012-x.pdf
Reference27 articles.
1. Padberg GW: Facioscapulohumeral disease [PhD thesis]. Leiden, The Netherlands: University of Leiden; 1982.
2. Felice KJ, Moore SA: Unusual clinical presentations in patients harboring the facioscapulohumeral dystrophy 4q35 deletion. Muscle Nerve 2001, 24:352–356. Describes the widening clinical spectrum of FSHD since the widespread availability of molecular genetic testing.
3. Tawil R, Forrester J, Griggs RC, et al.: Evidence for anticipation and association of deletion size with severity of facioscapulohumeral muscular dystrophy. Ann Neurol 1996, 39:744–748.
4. Padberg G, Brouwer OF, de Keizer RJ, et al.: On the significance of retinal vascular disease and hearing loss in facioscapulohumeral muscular dystrophy. Muscle Nerve 1995, 2(suppl):S73-S80.
5. Laforet P, de Toma C, Eymard B, et al.: Cardiac involvement in genetically confirmed facioscapulohumeral muscular dystrophy. Neurology 1998, 51:1454–1456.
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