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Laing, NG, Clarke, NF, Dye, DE, Liyanage, K, Walker, KR, Kobayashi, Y, Shimakawa, S, Hagiwara, T, Ouvrier, R, Sparrow, JC, et al. Actin mutations are one cause of congenital fibre type disproportion.
Annals of Neurology
56(5)
:
689 -694
2004
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Minkler, PE, Kerner, J, North, KN, Hoppel, CL. Quantitation of long-chain acylcarnitines by HPLC/fluorescence detection: application to plasma and tissue specimens from patients with carnitine palmitoyltransferase-II deficiency.
Clinica Chimica Acta
352(1-2)
:
81 -92
2005
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North, KN, Laing, NG, Wallgren-Pettersson, C. Nemaline myopathy: current concepts. The ENMC International Consortium and Nemaline Myopathy..
Journal of Medical Genetics
34(9)
:
705
1997
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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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Schindeler, A, Liu, R, Ginn, SL, Lek, M, North, KN, Alexander, IE, Little, DG. Bmpr1a expression correlates with the osteogenic sensitivity of muscle progenitors.
Bone
44:
s156
2009
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