316VP What you see is what it is: the tales of two brothers with rare intronic dystrophin gene duplication by Khries, M., Gowda, V.

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241P Long term follow-up of CHRNE congenital myasthenic syndrome (CMS) – a retrospective multi-centre cohort study by Henehan, L., Khries, M., Ramjattan, H., Dong, Y., Everett, R., Munot, P., Jungbluth, H., Beeson, D., Ramdas, S., Palace, J.

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27P Muscle ultrasound findings in paediatric patients with TTN gene related congenital myopathy by Sarkozy, A., Perry, L., Cicala, G., Manzur, A., Vanegas, M., Khries, M., Sudhakar, S., Clark, C., Muntoni, F., Jungbluth, H., Baranello, G.

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33P Description of natural history baseline characteristics of a paediatric cohort of recessive TTN myopathy patients in the UK – a prospective study by Wolfe, A., Cicala, G., Joefield, T., Sheehan, J., Main, M., Vanegas, M., Khries, M., Clark, C., Sudhakar, S., Perry, L., Bilby, J., Jungbluth, H., Muntoni, F., Baranello, G., Sarkozy, A.

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Alle Origini Degli Arabi: Un viaggio nell'Archeologia dell'Arabia Saudita [To the Origins of the Arabs: A Journey into the Archaeology of Saudi Arabia]: ROMOLO LORETO, (Milan: Mond... by Khries, Hashem M.

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