Oates, EC, Clarke, NF, Reddel, SW, North, KN. G.P.9.08 Insights into the pathological basis of autosomal dominant distal spinal muscular atrophy from a large Australian family. Neuromuscular Disorders 19(8-9) : 596 -597 2009
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Quinlan, KGR, Seto, JT, Turner, N, Floetenmeyer, M, Macarthur, DG, Raftery, JM, Yang, N, Parton, RG, Cooney, GJ, North, KN. G.O.4 α-Actinin-3 regulates muscle glycogen phosphorylase: A potential mechanism for the metabolic consequences of the common human null allele of ACTN3. Neuromuscular Disorders 19(8-9) : 545 -546 2009
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Clarke, NF, Monnier, N, Smith, RLL, Kornberg, AJ, Farrell, MA, Waddell, L, Cooper, S, Lunardi, J, North, KN. G.P.1.05 RYR1 is a common cause of congenital fibre type disproportion with ptosis, ophthalmoplegia, scoliosis and pronounced axial muscle weakness. Neuromuscular Disorders 19(8-9) : 557 2009
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Butler, TL, Egan, JR, Graf, FG, Au, CG, McMahon, AC, North, KN, Winlaw, DS. Dysfunction induced by ischemia versus edema: Does edema matter?. Journal of Thoracic and Cardiovascular Surgery 138(1) : 141 -147.e1 2009
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Boyd, KP, Korf, BR, Theos, A. Neurofibromatosis type 1. 61: 1 -14 2009
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