Muskeldystrophien
Author:
Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/978-3-642-59371-0_33.pdf
Reference109 articles.
1. Amato A A, Shebert R T (1998) Inclusion body myositis in twins (see comments). Neurology 51: 598–600
2. Askanas V, Engel W K (1998) Sporadic inclusion-body myositis and hereditary inclusion-body myopathies: current concepts of diagnosis and pathogenesis. Curr Opin Rheumatol 10: 530–542
3. Banker B Q (1994) Congenital deformities. In: Engel A G, Franzini-Armstrong C (eds) Myology, vol 2. McGraw-Hill, New York, pp 1905–1937
4. Banwell B L, Rüssel J, Fukudome T, Shen XM, Stilling G, Engel AG (1999) Myopathy, myasthenic syndrome, and epidermolysis bullosa simplex due to plectin deficiency. J Neuropathol Exp Neurol 58: 832–846
5. Bashir R, Britton S, Strachan T et al. (1998) A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B. Nat Genet 20: 37–42
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Muskeldystrophien;Der Pathologe;2009-08-09
2. Fazioskapulohumerale Muskeldystrophie mit Herzbeteiligung;Zeitschrift für Kardiologie;2005-05
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