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Waddell, LB, Kreissl, M, Kornberg, A, Kennedy, P, McLean, C, Labarre-Vila, A, Monnier, N, North, KN, Clarke, NF.
Evidence for a dominant negative disease mechanism in cap myopathy due to TPM3..
Neuromuscul Disord
20(7)
:
464 -466
2010
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Clarke, NF, Waddell, LB, Cooper, ST, Perry, M, Smith, RLL, Kornberg, AJ, Muntoni, F, Lillis, S, Straub, V, Bushby, K, et al.
Recessive mutations in RYR1 are a common cause of congenital fiber type disproportion..
Hum Mutat
31(7)
:
E1544 -E1550
2010
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Pride, N, Payne, JM, Webster, R, Shores, EA, Rae, C, North, KN.
Corpus callosum morphology and its relationship to cognitive function in neurofibromatosis type 1..
J Child Neurol
25(7)
:
834 -841
2010
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Moharir, M, London, K, Howman-Giles, R, North, K.
Utility of positron emission tomography for tumour surveillance in children with neurofibromatosis type 1..
Eur J Nucl Med Mol Imaging
37(7)
:
1309 -1317
2010
view publication
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Vandebrouck, A, Domazetovska, A, Mokbel, N, Cooper, ST, Ilkovski, B, North, KN.
In vitro analysis of rod composition and actin dynamics in inherited myopathies..
J Neuropathol Exp Neurol
69(5)
:
429 -441
2010
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