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North, KN.
Clinical Approach to the Diagnosis of Congenital Myopathies.
Seminars in Pediatric Neurology
18(4)
:
216 -220
2011
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Waddell, LB, Tran, J, Zheng, XF, Bönnemann, CG, Hu, Y, Evesson, FJ, Lek, M, Arbuckle, S, Wang, M-X, Smith, RL, et al.
A study of FHL1, BAG3, MATR3, PTRF and TCAP in Australian muscular dystrophy patients.
Neuromuscular Disorders
21(11)
:
776 -781
2011
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Yang, N, Schindeler, A, McDonald, MM, Seto, JT, Houweling, PJ, Lek, M, Hogarth, M, Morse, AR, Raftery, JM, Balasuriya, D, et al.
α-Actinin-3 deficiency is associated with reduced bone mass in human and mouse.
Bone
49(4)
:
790 -798
2011
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Menezes, MP, Ryan, MM, Thorburn, D, Christodoulou, JC, North, KN, Ouvrier, RA.
P3.27 Childhood mitochondrial neuropathies: Clinical, electrophysiological and histopathological characteristics.
Neuromuscular Disorders
21(9-10)
:
690
2011
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Foley, AR, Quijano-Roy, S, Collins, J, Straub, V, Deconinck, N, Mercuri, E, D’Amico, A, Bertini, E, North, K, Ryan, M, et al.
P2.5 The identification of a viable outcome measure in the collagen VI myopathies promotes progress toward clinical trials.
Neuromuscular Disorders
21(9-10)
:
662
2011
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