Progressive Muskeldystrophien und kongenitale Myopathien
Author:
Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/978-3-662-60676-6_34
Reference54 articles.
1. Blumen SC, Bouchard JP, Brais B et al (2009) Cognitive impairment and reduced life span of oculopharyngeal muscular dystrophy homozygotes. Neurology 73:596–601
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3. Brais B, Bouchard JP, Xie YG et al (1998) Short GCG expansion in the PABP2 gene cause oculopharyngeal muscular dystrophy. Nat Genet 18:164–167
4. Bushby K, Finkel R, Birnkrant DJ et al (2010a) Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management. Lancet Neurol 9:77–93
5. Bushby K, Finkel R, Birnkrant DJ et al (2010b) Diagnosis and management of Duchenne muscular dystrophy, part 2: implementation of multidisciplinary care. Lancet Neurol 9:177–189
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