The use of intravenous bisphosphonate therapy to treat vertebral fractures due to osteoporosis among boys with Duchenne muscular dystrophy von Sbrocchi, A. M., Rauch, F., Jacob, P., McCormick, A., McMillan, H. J., Matzinger, M. A., Ward, L. M.

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Life expectancy at birth in Duchenne muscular dystrophy: a systematic review and meta-analysis von Landfeldt, Erik, Thompson, Rachel, Sejersen, Thomas, McMillan, Hugh J., Kirschner, Janbernd, Lochmüller, Hanns

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P.042 Anti-HMG Coenzyme A reductase antibody (anti-HMGCR) myopathy: case review of two pediatric patients from a single center von Toupin, A, Jurencak, R, McMillan, HJ, Yaworski, A

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Caregiver Burden of Spinal Muscular Atrophy: A Systematic Review von Landfeldt, Erik, Abner, Sophia, Pechmann, Astrid, Sejersen, Thomas, McMillan, Hugh J., Lochmüller, Hanns, Kirschner, Janbernd

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Debunking Occam's razor: Diagnosing multiple genetic diseases in families by whole‐exome sequencing von Balci, T.B., Hartley, T., Xi, Y., Dyment, D.A., Beaulieu, C.L., Bernier, F.P., Dupuis, L., Horvath, G.A., Mendoza‐Londono, R., Prasad, C., Richer, J., Yang, X.‐R., Armour, C.M., Bareke, E., Fernandez, B.A., McMillan, H.J., Lamont, R.E., Majewski, J., Parboosingh, J.S., Prasad, A.N., Rupar, C.A., Schwartzentruber, J., Smith, A.C., Tétreault, M., Innes, A.M., Boycott, K.M.

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The time to and determinants of first fractures in boys with Duchenne muscular dystrophy von Ma, J., McMillan, H. J., Karagüzel, G., Goodin, C., Wasson, J., Matzinger, M. A., DesClouds, P., Cram, D., Page, M., Konji, V. N., Lentle, B., Ward, L. M.

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Costs of Illness of Spinal Muscular Atrophy: A Systematic Review von Landfeldt, Erik, Pechmann, Astrid, McMillan, Hugh J., Lochmüller, Hanns, Sejersen, Thomas

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P.040 Decreased incidence of neuro-autoimmune disorders during COVID-19 pandemic restrictions von Jaremek, A, Chisvin, R, Kutcher, SA, Webster, RJ, Kazoun, F, Goldbloom, EB, McMillan, HJ, Pohl, D

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P.129 Worster-Drought syndrome caused by LINS mutations von McMillan, HJ, Holahan, A, Richer, J

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Burden of Spinal Muscular Atrophy (SMA) on Patients and Caregivers in Canada von McMillan, H.J., Gerber, B., Cowling, T., Khuu, W., Mayer, M., Wu, J.W., Maturi, B., Klein-Panneton, K., Cabalteja, C., Lochmüller, H.

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Developing standardized corticosteroid treatment for Duchenne muscular dystrophy von Guglieri, Michela, Bushby, Kate, McDermott, Michael P, Hart, Kimberly A, Tawil, Rabi, Martens, William B, Herr, Barbara E, McColl, Elaine, Wilkinson, Jennifer, Kirschner, Janbernd, King, Wendy M, Eagle, Michele, Brown, Mary W, Willis, Tracey, Hirtz, Deborah, Shieh, Perry B, Straub, Volker, Childs, Anne-Marie, Ciafaloni, Emma, Butterfield, Russell J, Horrocks, Iain, Spinty, Stefan, Flanigan, Kevin M, Kuntz, Nancy L, Baranello, Giovanni, Roper, Helen, Morrison, Leslie, Mah, Jean K, Manzur, Adnan Y, McDonald, Craig M, Schara, Ulrike, von der Hagen, Maja, Barohn, Richard J, Campbell, Craig, Darras, Basil T, Finkel, Richard S, Vita, Giuseppe, Hughes, Imelda, Mongini, Tiziana, Pegoraro, Elena, Wicklund, Matthew, Wilichowski, Ekkehard, Bryan Burnette, W, Howard, James F, McMillan, Hugh J, Thangarajh, Mathula, Griggs, Robert C

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Evidence for clinical, genetic and biochemical variability in spinal muscular atrophy with progressive myoclonic epilepsy von Dyment, D.A., Sell, E., Vanstone, M.R., Smith, A.C., Garandeau, D., Garcia, V., Carpentier, S., Le Trionnaire, E., Sabourdy, F., Beaulieu, C.L., Schwartzentruber, J.A., McMillan, H.J., Majewski, J., Bulman, D.E., Levade, T., Boycott, K.M.

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P.131 De novo PIK3CB mutation associated with macrocephaly and diffuse polymicrogyria von Kernohan, KD, McMillan, HJ, McBride, A, Hartley, T, Dyment, DA, Boycott, KM

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P.070 Autosomal dominant MARS mutation linked to severe early onset CMT2U von McMillan, HJ, Gillespie, MK, Kernohan, KD, Myer-Schuman, R, Antonellis, A, Boycott, KM

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P.068 Abnormal fatty acid metabolism is a feature of spinal muscular atrophy von Deguise, M, Beauvais, A, Baranello, G, Pileggi, C, Mastella, C, Tierney, A, Chehade, L, Leone, A, De Amicis, R, Battezzati, A, De Repentigny, Y, Warman Chardon, J, McMillan, HJ, Llavero-Hurtado, M, Huang, Y, Courtney, NL, Mole, AJ, Lamont, D, Atrih, A, Kubinski, S, Claus, P, Murray, LM, Wishart, TM, Bowerman, M, Gillingwater, TH, Harper, M, Bertoli, S, Parson, SH, Kothary, R

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B.02 Recessive mutations in ATP8A2 cause severe hypotonia, cognitive impairment, hyperkinetic movement disorders and progressive optic atrophy von McMillan, HJ, Telegrafi, A, Singleton, A, Cho, M, Lelli, D, Lynn, FC, Griffin, J, Asamoah, A, Rinne, T, Erasmus, CE, Koolen, DA, Haaxma, CA, Keren, B, Doummar, D, Mignot, C, Thompson, I, Velsher, L, Dehghani, M, Vahidi Mehrjardi, M, Maroofian, R, Tchan, M, Simons, C, Christodoulou, J, Martín-Hernández, E, Guillen Sacoto, MJ, Henderson, LB, McLaughlin, H, Molday, LL, Molday, RS, Yoon, G

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B.03 The Canadian neurology graduate survey von Murray, BJ, Major, P, Poppe, A, Murphy, C, Jenkins, M, Nicolle, M, Watling, C, McMillan, HJ, Yeung, M, Callen, D, Briemberg, H, Tang-Wai, DF, De Meulemeester, C, Brna, P, Savard, M, Sahlas, D, Yeh, A, Gubitz, G, Moore, F, Khan, K, Squarey, K, Deacon, C, Esser, M, Vosoughi, R, Taylor, S, Weiss, S, Hollenberg, E

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Brachial Plexopathy and Nonaccidental Injury: Role of the Neurologist von McMillan, Hugh J., Yang, Michele, Jones, H. Royden

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P4.9 A phase 2, randomized, placebo-controlled, multiple ascending-dose study of ACE-031 (ActRIIB-IgG1) in Duchenne muscular dystrophy (DMD): Preliminary results von Campbell, C, Attie, K.M, Mah, J.K, Tarnopolsky, M, Selby, K, McMillan, H.J, Yang, Y, Wilson, D, Barger, R, Sherman, M.L, Escolar, D

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Divergent reproductive endocrinology of the estrous cycle and pregnancy in dwarf hamsters ( Phodopus) von McMillan, Hugh J., Wynne-Edwards, Katherine E.

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