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Au, CG, Butler, TL, Egan, JR, Cooper, ST, Lo, HP, Compton, AG, North, KN, Winlaw, DS.
Changes in skeletal muscle expression of AQP1 and AQP4 in dystrophinopathy and dysferlinopathy patients.
Acta Neuropathologica
116(3)
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235 -246
2008
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Peat, RA, Smith, JM, Compton, AG, Baker, NL, Pace, RA, Burkin, DJ, Kaufman, SJ, Lamandé, SR, North, KN.
Diagnosis and etiology of congenital muscular dystrophySYMBOL.
Neurology
71(5)
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312 -321
2008
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Lo, HP, Cooper, ST, Evesson, FJ, Seto, JT, Chiotis, M, Tay, V, Compton, AG, Cairns, AG, Corbett, A, MacArthur, DG, et al.
Limb–girdle muscular dystrophy: Diagnostic evaluation, frequency and clues to pathogenesis.
Neuromuscular Disorders
18(1)
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34 -44
2008
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Compton, AG, Cooper, ST, Hill, PM, Yang, N, Froehner, SC, North, KN.
The Syntrophin-Dystrobrevin Subcomplex in Human Neuromuscular Disorders.
Journal of Neuropathology & Experimental Neurology
64(4)
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350 -361
2005
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Au, CG, Cooper, ST, Lo, HP, Compton, AG, Yang, N, Wintour, EM, North, KN, Winlaw, DS.
Expression of aquaporin 1 in human cardiac and skeletal muscle.
Journal of Molecular and Cellular Cardiology
36(5)
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655 -662
2004
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