981 Skeletal Surveys for Non-Accidental Injury von Ali, F, Spendiff, R

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Imaging assessment of renal masses von Spendiff, R, Rockall, A

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The role of ultrasound in the management of nodular thyroid disease von Jones, R, Spendiff, R, Fareedi, S, Richards, P S

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Picture Quiz von MARTIN, A V, SHARMA, B, MUNNEKE, G J, SPENDIFF, R, ROCKALL, A

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Picture quiz von Connor, S E J, Hussain, S, Woo, E, Morley, S, Liyanage, S H, Spencer, S P, Hogarth, K M, Makdissi, J, Bhatia, K S S, Iyngkaran, T, Richards, P S, Chaudhary, N, Micallef, C, Saunders, D E, Siddiqui, A, Jones, R, Spendiff, R, Fareedi, S

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Neuromuscular Junction Changes in a Mouse Model of Charcot-Marie-Tooth Disease Type 4C von Cipriani, Silvia, Phan, Vietxuan, Médard, Jean-Jacques, Horvath, Rita, Lochmüller, Hanns, Chrast, Roman, Roos, Andreas, Spendiff, Sally

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Salbutamol modifies the neuromuscular junction in a mouse model of ColQ myasthenic syndrome von McMacken, Grace M, Spendiff, Sally, Whittaker, Roger G, O’Connor, Emily, Howarth, Rachel M, Boczonadi, Veronika, Horvath, Rita, Slater, Clarke R, Lochmüller, Hanns

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512P Investigating muscle specific kinase agonist antibody treatment for Agrn and ColQ congenital myasthenic syndromes von Ho, K., Adjei-Afriyie, O., Carmona, R., Ray, R., Zeldin, J., O'Neil, D., Vanhauwaert, R., Spendiff, S., Lochmüller, H.

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Advances in the diagnosis of inherited neuromuscular diseases and implications for therapy development von Thompson, Rachel, Spendiff, Sally, Roos, Andreas, Bourque, Pierre R, Warman Chardon, Jodi, Kirschner, Janbernd, Horvath, Rita, Lochmüller, Hanns

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GFPT1 deficiency in muscle leads to myasthenia and myopathy in mice von Issop, Yasmin, Hathazi, Denisa, Khan, Muzamil Majid, Rudolf, Rüdiger, Weis, Joachim, Spendiff, Sally, Slater, Clarke R, Roos, Andreas, Lochmüller, Hanns

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Targeted Therapies for Metabolic Myopathies Related to Glycogen Storage and Lipid Metabolism: a Systematic Review and Steps Towards a ‘Treatabolome’ von Manta, A., Spendiff, S., Lochmüller, H., Thompson, R.

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Discovery and Toxicological Profiling of Aminopyridines as Orally Bioavailable Selective Inhibitors of PI3-Kinase γ von Bellenie, Benjamin R, Hall, Edward, Bruce, Ian, Spendiff, Matthew, Culshaw, Andrew, McDonald, Sarah, Ambarkhane, Ameet, Chinn, Colin, Thomas, Matthew, Rosner, Elisabeth, Bracher, Marguerite, Nicklin, Paul, Marshall, Stephen, Coote, Julie, Cullen, Eva, Tessier, Clemence, Wuersch, Kuno, Lal, Ajay, Wallis, Gillian, Hollingworth, Gregory J, Neef, James

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Characterizing Uncertainty and Variability in Physiologically Based Pharmacokinetic Models: State of the Science and Needs for Research and Implementation von Barton, Hugh A., Chiu, Weihsueh A., Woodrow Setzer, R., Andersen, Melvin E., Bailer, A. John, Bois, Frédéric Y., DeWoskin, Robert S., Hays, Sean, Johanson, Gunnar, Jones, Nancy, Loizou, George, MacPhail, Robert C., Portier, Christopher J., Spendiff, Martin, Tan, Yu-Mei

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Functionality of the Crosswise Model for Assessing Sensitive or Transgressive Behavior: A Systematic Review and Meta-Analysis von Sagoe, D, Cruyff, Maarten, Spendiff, O, Chegeni, R, De Hon, O, van der Heijden, P.G.M, Saugy, M, Petróczi , A

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Anthracycline-containing chemotherapy causes long-term impairment of mitochondrial respiration and increased reactive oxygen species release in skeletal muscle von Gouspillou, Gilles, Scheede-Bergdahl, Celena, Spendiff, Sally, Vuda, Madhusudanarao, Meehan, Brian, Mlynarski, Heather, Archer-Lahlou, Elodie, Sgarioto, Nicolas, Purves-Smith, Fennigje M., Konokhova, Yana, Rak, Janusz, Chevalier, Stéphanie, Taivassalo, Tanja, Hepple, Russell T., Jagoe, R. Thomas

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GFPT1 deficiency in muscle leads to myasthenia and myopathy in mice von Issop, Yasmin, Hathazi, Denisa, Khan, Muzamil Majid, Rudolf, Rüdiger, Weis, Joachim, Spendiff, Sally, Slater, Clarke R, Roos, Andreas, Lochmüller, Hanns

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NMJ&C08 - Strengthening the neuromuscular junction as a concept for the treatment of congenital myasthenic syndromes and motor neuropathies with synaptic dysfunction von Howarth, R., Spendiff, S., McMacken, G., Cipriani, S., Roos, A., Horvath, R., Lochmuller, H.

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Strengthening the neuromuscular junction as a concept for the treatment of congenital myasthenic syndromes and motor neuropathies with synaptic dysfunction von Howarth, R., Spendiff, S., McMacken, G., Cipriani, S., Roos, A., Horvath, R., Lochmuller, H.

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Salbutamol modifies the neuromuscular junction in a mouse model of ColQ myasthenic syndrome von McMacken, Grace M, Spendiff, Sally, Whittaker, Roger G, O'Connor, Emily, Howarth, Rachel M, Boczonadi, Veronika, Horvath, Rita, Slater, Clarke R, Lochmüller, Hanns

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Clinical improvement of DM1 patients reflected by reversal of disease-induced gene expression in blood von van Cruchten, Remco T. P., van As, Daniël, Glennon, Jeffrey C., van Engelen, Baziel G. M., ‘t Hoen, Peter A. C., Okkersen, K, Jimenez-Moreno, C, Wenninger, S, Daidj, F, Cumming, S, Littleford, R, Monckton, D G, Lochmüller, H, Catt, M, Faber, C G, Hapca, A, Donnan, P T, Gorman, G, Bassez, G, Schoser, B, Knoop, H, Treweek, S, Wansink, Derick G., Impens, Francis, Gabriels, Ralf, Claeys, Tine, Ravel-Chapuis, Aymeric, Jasmin, Bernard J., Mahon, Niamh, Nieuwenhuis, Sylvia, Martens, Lennart, Novak, Petr, Furling, Denis, Baak, Arie, Gourdon, Genevieve, MacKenzie, Alex, Martinat, Cecile, Neault, Nafisa, Roos, Andreas, Duchesne, Elise, Salz, Renee, Thompson, Rachel, Baghdoyan, Sandrine, Varghese, Anu Mary, Blom, Paul, Spendiff, Sally, Manta, Alexander

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