SEPN1-related myopathies: Clinical course in a large cohort of patients von SCOTO, M, CIRAK, S, LONGMAN, C, CHOW, G, PANE, M, MAIN, M, HANNA, M. G, BUSHBY, K, SEWRY, C, ABBS, S, MERCURI, E, MUNTONI, F, MEIN, R, FENG, L, MANZUR, A. Y, ROBB, S, CHILDS, A.-M, QUINLIVAN, R. M, ROPER, H, JONES, D. H

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Reporting of paediatric osteoporotic vertebral fractures in Duchenne muscular dystrophy and potential impact on clinical management: the need for standardised and structured report... von Martin, H., Henderson, A., Allen, R., Childs, A. M., Dunne, J., Horrocks, I., Joseph, S., Kraft, J. K., Ward, K., Mushtaq, T., Mason, A., Kyriakou, A., Wong, S. C.

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Intralabyrinthine Schwannomas: Imaging Diagnosis and Classification von SALZMAN, K. L, CHILDS, A. M, DAVIDSON, H. C, KENNEDY, R. J, SHELTON, C, HARNSBERGER, H. R

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Subdural haematoma and effusion in infancy: an epidemiological study von Hobbs, C, Childs, A-M, Wynne, J, Livingston, J, Seal, A

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Severe childhood SMA and axonal CMT due to anticodon binding domain mutations in the GARS gene von JAMES, P. A, CADER, M. Z, MUNTONI, F, CHILDS, A.-M, CROW, Y. J, TALBOT, K

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Assessment of face validity of a disease model of nonsense mutation Duchenne muscular dystrophy: a multi-national Delphi panel study von Landfeldt, Erik, Zhang, Rongrong, Childs, Anne-Marie, Johannsen, Jessika, O'Rourke, Declan, Sejersen, Thomas, Strautmanis, Jurgis, Schara-Schmidt, Ulrike, Tulinius, Mar, Walter, Maggie C., Willis, Tracey, Buesch, Katharina

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Variable Phenotype Including Leigh Syndrome with a 9185T>C Mutation in the MTATP6 Gene von Childs, A.-M., Hutchin, T., Pysden, K., Highet, L., Bamford, J., Livingston, J., Crow, Y. J.

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Magnetic resonance imaging of the infant brain: anatomical characteristics and clinical significance of punctate lesions von Cornette, L G, Tanner, S F, Ramenghi, L A, Miall, L S, Childs, A M, Arthur, R J, Martinez, D, Levene, M I

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On the receiving end V: Patient perceptions of the side effects of cancer chemotherapy in 1993 von Griffin, A. M., Butow, P. N., Coates, A. S., Childs, A. M., Ellis, P. M., Dunn, S. M., Tattersall, M. H. N.

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PLA2G6-associated neurodegeneration (PLAN): Further expansion of the clinical, radiological and mutation spectrum associated with infantile and atypical childhood-onset disease von Illingworth, M.A., Meyer, E., Chong, W.K., Manzur, A.Y., Carr, L.J., Younis, R., Hardy, C., McDonald, F., Childs, A.M., Stewart, B., Warren, D., Kneen, R., King, M.D., Hayflick, S.J., Kurian, M.A.

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Differential induction of PPAR-gamma by luminal glutamine and iNOS by luminal arginine in the rodent postischemic small bowel von Sato, N, Moore, F A, Kone, B C, Zou, L, Smith, M A, Childs, M A, Moore-Olufemi, S, Schultz, S G, Kozar, R A

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Neurovascular compression of the trigeminal and glossopharyngeal nerve: three case reports von Childs, A-M, Meaney, J F, Ferrie, C D, Holland, P C

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Surface Morphology of Poly(caprolactone)-b-poly(dimethylsiloxane)-b-poly(caprolactone) Copolymers: Effects on Protein Adsorption von Childs, M. A, Matlock, D. D, Dorgan, J. R, Ohno, T. R

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Endocrine and Bone Monitoring in Boys with Duchenne Muscular Dystrophy; Do we adhere to the standards of care? von Henderson, A., Harley, G., Horrocks, I., Joseph, S., Dunne, J., Pysden, K., Mushtaq, T., Wong, S.C., Childs, A.M.

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Cerebral Maturation in Premature Infants: Quantitative Assessment Using MR Imaging von Childs, Anne-Marie, Ramenghi, Luca A, Cornette, Luc, Tanner, Steven F, Arthur, Rosemary J, Martinez, Delia, Levene, Malcolm I

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Small particle growth in silane radio-frequency discharges von Childs, M. A., Gallagher, Alan

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MANNA: Just Enough for the Day von Childs, Jeanne

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MR features of developing periventricular white matter in preterm infants: evidence of glial cell migration von Childs, AM, Ramenghi, LA, Evans, DJ, Ridgeway, J, Saysell, M, Martinez, D, Arthur, R, Tanner, S, Levene, MI

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Hospice provision and usage amongst young people with neuromuscular disease in the United Kingdom von Fraser, L.K, Aldridge, J, Manning, S, O’Leary, S, Miller, M, McCulloch, R, Childs, A.M

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P24 Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signalling von Sharpe, J.A, Logan, C.V, Szabadkai, G, Parry, D.A, Torelli, S, Childs, A.-M, Kriek, M, Phadke, R, Johnson, C.A, Roberts, N.Y, Bonthron, D.T, Pysden, K.A, Whyte, T, Munteanu, I, Foley, A.R, Wheway, G, Szymanska, K, Natarajan, S, Abdelhamed, Z.A, Morgan, J.E, Roper, H, Santen, G.W.E, Niks, E.H, van der Pol, W.L, Lindhout, D, Raffaello, A, De Stefani, D, den Dunnen, J.T, Sun, Y, Ginjaar, I, Sewry, C.A, Hurles, M, Rizzuto, R, Duchen, M.R, Muntoni, F, Sheridan, E

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