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Tooley, LD, Zamurs, LK, Beecher, N, Baker, NL, Peat, RA, Adams, NE, Bateman, JF, North, KN, Baldock, C, Lamandé, SR.
Collagen VI microfibril formation is abolished by an {alpha}2(VI) von Willebrand factor type A domain mutation in a patient with Ullrich congenital muscular dystrophy..
J Biol Chem
285(43)
:
33567 -33576
2010
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Bray, P, Bundy, AC, Ryan, MM, North, KN, Everett, A.
Health-related quality of life in boys with Duchenne muscular dystrophy: agreement between parents and their sons..
J Child Neurol
25(10)
:
1188 -1194
2010
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Waddell, LB, Lemckert, F, Tran, J, Zheng, F, Evesson, FJ, Hawkes, J, Lek, A, Street, N, Lin, P, Clarke, NF, et al.
P1.23 Muscle membrane repair proteins are upregulated in muscular dystrophy and localise to t-tubule membranes following mechanical stretch.
Neuromuscular Disorders
20(9-10)
:
607
2010
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Sambuughin, N, Kyle, SY, Olive, M, Duff, RM, Bayarsaikhan, M, Sivadorai, P, Nowak, KJ, Mastaglia, FL, North, K, Ilkovski, B, et al.
O.12 A new member of the BTB/Kelch family of proteins is mutated in nemaline myopathy type 6 (NEM6).
Neuromuscular Disorders
20(9-10)
:
638
2010
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Menezes, MP, Waddell, L, Evesson, F, Cooper, S, North, KN, Clarke, NF.
P1.49 The importance and challenge of diagnosing myopathies due to LMNA.
Neuromuscular Disorders
20(9-10)
:
615
2010
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