A and B utrophin in human muscle and sarcolemmal A-utrophin associated with tumours. by Sewry, C, Nowak, K, Ehmsen, J, Davies, K

Expression of different isoforms of utrophin in human muscle; potentials for therapy of Duchenne muscular dystrophy by Sewry, C, Nowak, K, Ehmsen, J, Davies, K

INCLUSION BODY MYOSITIS: A DIAGNOSTIC CHALLENGE by Brady, S, Squier, W, Hilton-Jones, D, Sewry, C, Holton, J

Inclusion body myositis: A diagnostic challenge by Brady, S, Squier, W, Hilton-Jones, D, Sewry, C, Holton, J

Inclusion body myositis: a diagnostic challenge by Brady, S, Squier, W, Hanna, MG, Hilton-Jones, D, Sewry, C, Holton, J

A histological evaluation of protein accumulation in inflammatory myopathies by Brady, S, Squier, W, Hilton-Jones, D, Sewry, C, Hanna, M, Holton, J

Evaluation of classical and novel histopathological features in the diagnosis of inclusion body myositis by Brady, S, Squier, W, Sewry, C, Hanna, M, Hilton-Jones, D, Holton, J

A retrospective cohort study identifying the principal pathological features useful in the diagnosis of inclusion body myositis by Brady, S, Squier, W, Sewry, C, Hanna, M, Hilton-Jones, D, Holton, J

Inclusion body myositis: MRC Centre for Neuromuscular Diseases, IBM workshop, London, 13 June 2008. by Hilton-Jones, D, Miller, A, Parton, M, Holton, J, Sewry, C, Hanna, MG

Correlation of utrophin levels with the dystrophin protein complex and muscle fibre regeneration in Duchenne and Becker muscular dystrophy muscle biopsies by Janghra, N, Morgan, J, Sewry, C, Wilson, F, Davies, K, Muntoni, F, Tinsley, J

Congenital myopathies with secondary neuromuscular transmission defects; A case report and review of the literature by Rodríguez Cruz, P, Sewry, C, Beeson, D, Jayawant, S, Squier, W, McWilliam, R, Palace, J

Congenital myopathies with secondary neuromuscular transmission defects; A case report and review of the literature. by Rodríguez Cruz, P, Sewry, C, Beeson, D, Jayawant, S, Squier, W, McWilliam, R, Palace, J

Relative frequency of congenital muscular dystrophy subtypes: Analysis of the UK diagnostic service 2001–2008 by Clement, E, Feng, L, Mein, R, Sewry, C, Robb, SA, Manzur, A, Mercuri, E, Godfrey, C, Cullup, T, Abbs, S, Muntoni, F

RYR1-related congenital myopathy with fatigable weakness, responding to pyridostigimine. by Illingworth, M, Main, M, Pitt, M, Feng, L, Sewry, C, Gunny, R, Vorstman, E, Beeson, D, Manzur, A, Muntoni, F, Robb, SA

Muscle X-inactivation patterns and dystrophin expression in Duchenne muscular dystrophy carriers. by Matthews, P, Benjamin, D, Van Bakel, I, Squier, M, Nicholson, L, Sewry, C, Barnes, P, Hopkin, J, Brown, R, Hilton-Jones, D

Tubular aggregates and cylindrical spirals have distinct immunohistochemical signatures by Brady, S, Healy, E, Gang, Q, Parton, M, Quinlivan, R, Jacob, S, Curtis, E, Al-Sarraj, S, Sewry, C, Hanna, M, Houlden, H, Beeson, D, Holton, J

Actin nemaline myopathy mouse reproduces disease, suggests other actin disease phenotypes and provides cautionary note on muscle transgene expression by Ravenscroft, G, Jackaman, C, Sewry, C, McNamara, E, Squire, SE, Potter, A, Papadimitriou, J, Griffiths, L, Bakker, A, Davies, K, Laing, N, Nowak, K

Actin nemaline myopathy mouse reproduces disease, suggests other actin disease phenotypes and provides cautionary note on muscle transgene expression. by Ravenscroft, G, Jackaman, C, Sewry, C, McNamara, E, Squire, SE, Potter, A, Papadimitriou, J, Griffiths, L, Bakker, A, Davies, K, Laing, N, Nowak, K

Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dyst... by Brockington, M, Blake, D, Prandini, P, Brown, S, Torelli, S, Benson, M, Ponting, C, Estournet, B, Romero, N, Mercuri, E, Voit, T, Sewry, C, Guicheney, P, Muntoni, F

gene mutations in steroid-responsive limb girdle muscular dystrophy by Godfrey, C, Escolar, D, Brockington, M, Clement, E, Mein, R, Jimenez-Mallebrera, C, Torelli, S, Feng, L, Brown, S, Sewry, C, Rutherford, M, Shapira, Y, Abbs, S, Muntoni, F