Utilisation of goals of care discussions and palliative care prior to image-guided procedures near the end of life by Rockwell, H.D., Beeson, S.A., Keller, E.J., Harman, S.M., Newton, I.G., Kothary, N.

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

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Congenital Myasthenic Syndromes in childhood: Diagnostic and management challenges by Kinali, M, Beeson, D, Pitt, M.C, Jungbluth, H, Simonds, A.K, Aloysius, A, Cockerill, H, Davis, T, Palace, J, Manzur, A.Y, Jimenez-Mallebrera, C, Sewry, C, Muntoni, F, Robb, S.A

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Congenital fibre type disproportion associated with mutations in the tropomyosin 3 ( TPM3 ) gene mimicking congenital myasthenia by Munot, P, Lashley, D, Jungbluth, H, Feng, L, Pitt, M, Robb, S.A, Palace, J, Jayawant, S, Kennet, R, Beeson, D, Cullup, T, Abbs, S, Laing, N, Sewry, C, Muntoni, F

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P16.5 Diagnostic accuracy of stimulation single fibre EMG findings in children with DOK7 congenital myasthenie syndrome by McHugh, J.C., Robb, S.A., Manzur, A.Y., Beeson, D., Muntoni, F., Pitt, M.C.

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2FC2.3 Salbutamol treatment in children with DOK7 congenital myasthenic syndrome by Burke, G., Hiscock, A., Klein, A., Ng, J., Manzur, A.Y., DeVile, C., Beeson, D., Muntoni, F., Robb, S.A.

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P096 Congenital stridor and bilateral vocal cord palsy as a presenting feature of DOK7 congenital myasthenic syndrome by Robb, S.A, Jephson, C, Mills, N, Pitt, M.C, Beeson, D, Aloysius, A, Muntoni, F, Bailey, C.M

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1FC2.6 DOK7 congenital myasthenic syndrome in childhood: early diagnostic clues by Robb, S.A., McHugh, J.C., Pitt, M.C., Sewry, C.A., Finlayson, S., Manzur, A.Y., De Vile, C., Jayawant, S., Palace, J., Beeson, D., Muntoni, F.

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