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Lamandé, SR, North, KN. Activating internal ribosome entry to treat Duchenne muscular dystrophy.
Nature Medicine
20(9)
:
987 -988
2014
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Clarke, N, Kolski, H, Dye, D, Lim, E, Smith, R, Patel, R, Fahey, M, Laing, N, North, K. C.P.1.03 TPM3 is a recurrent cause of congenital fibre type disproportion and is associated with a consistent phenotype.
Neuromuscular Disorders
17(9-10)
:
834 -835
2007
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Rose, KJ, Burns, J, North, KN. Relationship between foot strength and motor function in preschool-age children.
Neuromuscular Disorders
19(2)
:
104 -107
2008
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Sullivan, K, El-Hoss, J, Quinlan, KGR, Deo, N, Garton, F, Seto, JTC, Gdalevitch, M, Turner, N, Cooney, GJ, Kolanczyk, M, et al. NF1 is a critical regulator of muscle development and metabolism.
Human Molecular Genetics
23(5)
:
1250 -1259
2013
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Aartsma-Rus, A, Hoffman, E, Bucella, F, Flanigan, K, Kirschner, J, Kole, A, Mercuri, E, Nishino, I, North, K, Alonso, AP, et al. G.P.285 TREAT-NMD (translational research in Europe, assessment and treatment for neuromuscular disorders).
Neuromuscular Disorders
25:
s271
2015
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