Randomized, blinded trial of weekend vs daily prednisone in Duchenne muscular dystrophy von ESCOLAR, D. M, HACHE, L. P, PESTRONK, A, RYAN, M. M, MONASTERIO, E, DAY, J. W, ZIMMERMAN, A, ARRIETA, A, HENRICSON, E, MAYHEW, J, FLORENCE, J, HU, F, CLEMENS, P. R, CONNOLLY, A. M, CNAAN, A, MCDONALD, C. M, VISWANATHAN, V, KORNBERG, A. J, BERTORINI, T. E, NEVO, Y, LOTZE, T

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Pentoxifylline as a rescue treatment for DMD: A randomized double-blind clinical trial von ESCOLAR, D. M, ZIMMERMAN, A, NEVO, Y, TESI-ROCHA, C, NAGARAJU, K, RAYAVARAPU, S, HACHE, L. P, MAYHEW, J. E, FLORENCE, J, HU, F, ARRIETA, A, HENRICSON, E, BERTORINI, T, LESHNER, R. T, MAH, J. K, CLEMENS, P. R, CONNOLLY, A. M, MESA, L, GORNI, K, KORNBERG, A, KOLSKI, H, KUNTZ, N

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111. Limb edema and anasarca associated with severe dermatomyositis: Four case reports von Li, Y, Mitchell, C, Bertorini, T

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P.10.21 Next-generation sequencing meets genetic diagnostics: Development of a comprehensive workflow for neuromuscular disorders von Kesari, A, Punetha, J, Uapinyoying, P, Clarke, N, Waddell, L, North, K, Plotz, P, Tesi-Rocha, C, Bonnemann, C, Grosmann, C, Bertorini, T, Hoffman, E

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Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: A study of 56 patients von Santorelli, F. M., Sciacco, M., Tanji, K., Shanske, S., Vu, T. H., Golzi, V., Griggs, R. C., Mendell, J. R., Hays, A. P., Bertorini, T. E., Pestronk, A., Bonilla, E., Dimauro, S.

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DMD genotypes and loss of ambulation in the CINRG Duchenne Natural History Study von Bello, Luca, Morgenroth, Lauren P, Gordish-Dressman, Heather, Hoffman, Eric P, McDonald, Craig M, Cirak, Sebahattin

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Neurologic and neuropsychiatric complications of Crohn's disease von ELSEHETY, A, BERTORINI, T. E

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Longitudinal pulmonary function testing outcome measures in Duchenne muscular dystrophy: Long-term natural history with and without glucocorticoids von McDonald, Craig M., Gordish-Dressman, Heather, Henricson, Erik K., Duong, Tina, Joyce, Nanette C., Jhawar, Sanjay, Leinonen, Mika, Hsu, Fengming, Connolly, Anne M., Cnaan, Avital, Abresch, Richard T., Dubrovsky, A., Kornberg, A., Ryan, M., Webster, R., Biggar, W.D., McAdam, L.C., Mah, J.K., Kolski, H., Vishwanathan, V., Chidambaranathan, S., Nevo, Y., Gorni, K., Carlo, J., Tulinius, M., Lotze, T., Bertorini, T.E., Day, J.W., Karachunski, P., Clemens, P.R., Abdel-Hamid, H., Teasley, J., Kuntz, N., Driscoll, S., Bodensteiner, J.B., Connolly, A.M., Pestronk, A., Abresch, R.T., Henricson, E.K., Joyce, N.C., McDonald, C.M., Cnaan, A., Morgenroth, L.P., Leshner, R., Tesi-Rocha, C., Thangarajh, M., Duong, T.

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Laminin α2 muscular dystrophy: Genotype/phenotype studies of 22 patients von PEGORARO, E, MARKS, H, STELLA, A, SCAVINA, M, MUNK, R. L, SERVIDEI, S, BÖNNEMANN, C. C, BERTORINI, T, ACSADI, G, THOMPSON, C. E, GAGNON, D, HOGANSON, G, GARCIA, C. A, CARVER, V, ZIMMERMAN, R. A, HOFFMAN, E. P, CRAWFORD, T, MANCIAS, P, CONNOLLY, A. M, FANIN, M, MARTINELLO, F, TREVISAN, C. P, ANGELINI, C

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Complications of intravenous gammaglobulin in neuromuscular and other diseases von Bertorini, Tulio E., Nance, Adriana M., Horner, Linda H., Greene, William, Gelfand, Michael S., Jaster, J. Howard

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P.14 Analysis of the longitudinal CINRG Becker natural history study dataset von Clemens, P., Gordish-Dressman, H., Niizawa, G., Gorni, K., Guglieri, M., Connolly, A., Wicklund, M., Bertorini, T., Mah, J., Thangarajh, M., Smith, E., Kuntz, N., McDonald, C., Henricson, E., Upadhyayula, S., Byrne, B., Manousakis, G., Harper, A., Iannaccone, S., Dang, U.

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T.P.5.02 Pentoxifylline treatment fails to rescue muscle strength and function deterioration in prednisone-treated Duchenne muscular dystrophy (DMD) von Escolar, D.M, Gorni, K, Tesi-Rocha, A.C, Mah, J, Nevo, Y, Korengberg, A, Kolski, H, Bertorini, T, Connolly, A, Kuntz, N, Zimmerman, A, Morgenroth, L, Arrieta, A, Mayhew, J, Florence, J, Nei, L, Hu, F, Henricson, E, Leshner, R, Dubrovsky, A

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T.P.5.04 Randomized, double-blind, controlled study to compare efficacy and tolerability of standard daily prednisone regime with a novel intermittent high dose regime in ambulant... von Escolar, D, McDonald, C, Korengberg, A, Bertorini, T, Lotze, T, Ryan, M, Clemens, P, Leshner, R, Pestronk, A, Morgenroth, L, A. Arrieta, Henricson, E, Mayhew, J, Florence, J, Duong, T, Nei, L, Hu, F, Tesi-Rocha, A.C, Connolly, A

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Bilateral ophthalmoplegia and exophthalmos complicating central hemodialysis catheter placement von Varelas, Panayiotis N., Bertorini, Tulio E., Halford, Hollis

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HTLV-1 and Its Neurological Complications von Khan, Raja B., Bertorini, Tulio E., Levin, Michael C.

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Single-fiber electromyography of the laryngeal muscles von Schweizer, Valerie, Woodson, Gayle E., Bertorini, Tulio E.

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Focal myositis presenting with radial nerve palsy von Alzagatiti, Bassam I., Bertorini, Tulio E., Horner, Linda H., Maccarino, Virginia S., O'brien, Thomas

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Assessment of whole body composition with dual energy X-ray absorptiometry in Duchenne muscular dystrophy: Correlation of lean body mass with muscle function von Palmieri, Genaro M.A., Bertorini, Tulio E., Griffin, Judy W., Igarashi, Masanori, Karas, James G.

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Hypophosphatemia-induced neuropathy: Clinical and electrophysiologic findings von Siddiqui, Muhammad F., Bertorini, Tulio E.

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Selective paraspinal muscle amyotrophy von Narayanaswami, Pushpa, Bertorini, Tulio E, Halford, Hollis

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