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Page 1
Caveolinopathy--new mutations and additional symptoms.
Aboumousa A, Hoogendijk J, Charlton R, Barresi R, Herrmann R, Voit T, Hudson J, Roberts M, Hilton-Jones D, Eagle M, Bushby K, Straub V. Aboumousa A, et al. Among authors: eagle m. Neuromuscul Disord. 2008 Jul;18(7):572-8. doi: 10.1016/j.nmd.2008.05.003. Epub 2008 Jun 25. Neuromuscul Disord. 2008. PMID: 18583131
The phenotype of limb-girdle muscular dystrophy type 2I.
Poppe M, Cree L, Bourke J, Eagle M, Anderson LV, Birchall D, Brockington M, Buddles M, Busby M, Muntoni F, Wills A, Bushby K. Poppe M, et al. Among authors: eagle m. Neurology. 2003 Apr 22;60(8):1246-51. doi: 10.1212/01.wnl.0000058902.88181.3d. Neurology. 2003. PMID: 12707425
Cardiac and respiratory failure in limb-girdle muscular dystrophy 2I.
Poppe M, Bourke J, Eagle M, Frosk P, Wrogemann K, Greenberg C, Muntoni F, Voit T, Straub V, Hilton-Jones D, Shirodaria C, Bushby K. Poppe M, et al. Among authors: eagle m. Ann Neurol. 2004 Nov;56(5):738-41. doi: 10.1002/ana.20283. Ann Neurol. 2004. PMID: 15505776
Severe phenotype in infantile facioscapulohumeral muscular dystrophy.
Klinge L, Eagle M, Haggerty ID, Roberts CE, Straub V, Bushby KM. Klinge L, et al. Among authors: eagle m. Neuromuscul Disord. 2006 Oct;16(9-10):553-8. doi: 10.1016/j.nmd.2006.06.008. Epub 2006 Aug 24. Neuromuscul Disord. 2006. PMID: 16934468
189 results