338P Very late-onset Becker muscular dystrophy caused by a new DMD variant von Soltanzadeh, P., Boutros, N.

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Unilateral tensor fascia lata muscle mass as a presentation of lumbosacral radiculopathy von Soltanzadeh, P, Pierce, B, Lietman, S, Ilaslan, H

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Hereditary inclusion body myopathy in Persian Jews: a case report from Iran von Miryounesi, M., Soltanzadeh, P., Modarressi, M.H.

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O18 Topline safety and efficacy data analysis of phase 1/2 clinical trial evaluating AOC 1001 in adults with myotonic dystrophy type 1: MARINA TM von Johnson, N., Day, J., Hamel, J., Thornton, C., Subramony, S., Soltanzadeh, P., Statland, J., Wicklund, M., Arnold, W., Freimer, M., DiTrapani, K., Heusner, C., Chen, C., McEvoy, B., Zhu, Y., Tai, L., Ackermann, E.

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VP55 Topline data analysis of the phase 1/2 clinical trial evaluating AOC 1001 in adult patients with myotonic dystrophy type 1: MARINA von Johnson, N., Day, J., Hamel, J., Thornton, C., Subramony, S., Soltanzadeh, P., Statland, J., Wicklund, M., Arnold, W., Freimer, M., DiTrapani, K., Heusner, C., Chen, C., Cho, H., McEvoy, B., Zhu, Y., Tai, L., Ackermann, E.

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HeterozygousCAPN3missense variants causing autosomal-dominant calpainopathy in seven unrelated families von Gonzalez-Mera, L., Ravenscroft, G., Cabrera-Serrano, M., Ermolova, N., Dominguez-Gonzalez, C., Arteche-Lopez, A., Soltanzadeh, P., Evesson, F., Navas, C., Mavillard, F., Clayton, J., Rodrigo, P., Servian-Morilla, E., Cooper, S. T., Waddell, L., Reardon, K., Corbett, A., Hernandez-Lain, A., Sanchez, A., Esteban Perez, J., Paradas-Lopez, C., Rivas-Infante, E., Spencer, M., Laing, N., Olive, M.

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P.210 A phase 1/2 clinical trial evaluating the safety and pharmacokinetics of AOC 1001 in adults with myotonic dystrophy type 1: MARINA study design von Johnson, N., Day, J., Hamel, J., Statland, J., Subramony, S., Arnold, W., Thornton, C., Wicklund, M., Soltanzadeh, P., Knisely, B., Goel, V., DiTrapani, K., Chen, C., Clark, K., Peters, A., Heusner, C., Younis, H., Tai, L., Ackermann, E.

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G.P.195 - Unilateral tensor fascia lata muscle mass as a presentation of lumbosacral radiculopathy von Soltanzadeh, P., Pierce, B., Lietman, S., Ilaslan, H.

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Heterozygous CAPN3 missense variants causing autosomal‐dominant calpainopathy in seven unrelated families von González‐Mera, L., Ravenscroft, G., Cabrera‐Serrano, M., Ermolova, N., Domínguez‐González, C., Arteche‐López, A., Soltanzadeh, P., Evesson, F., Navas, C., Mavillard, F., Clayton, J., Rodrigo, P., Servián‐Morilla, E., Cooper, S. T, Waddell, L., Reardon, K., Corbett, A., Hernandez‐Laín, A., Sanchez, A., Esteban Perez, J., Paradas‐Lopez, C., Rivas‐Infante, E., Spencer, M., Laing, N., Olivé, M.

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An Iranian family with congenital myasthenic syndrome caused by a novel acetylcholine receptor mutation (CHRNE K171X) von Soltanzadeh, P, Müller, J S, Ghorbani, A, Abicht, A, Lochmüller, H, Soltanzadeh, A

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Criteria Assessment of a Expect Teacher for Effective Teaching von H Dargahi, P Hamouzadeh, J Sadeghifar, M Raadabadi, M Roshani, M Salimi, P Soltanzadeh

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Criteria Assessment of a Expect Teacher for Effective Teaching von H Dargahi, P Hamouzadeh, J Sadeghifar, M Raadabadi, M Roshani, M Salimi, P Soltanzadeh

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Zilucoplan in immune-mediated necrotising myopathy: a phase 2, randomised, double-blind, placebo-controlled, multicentre trial von Mammen, AL, Amato, AA, Dimachkie, MM, Chinoy, H, Hussain, Y, Lilleker, JB, Pinal-Fernandez, I, Allenbach, Y, Boroojerdi, B, Vanderkelen, M, Delicha, EM, Koendgen, H, Farzaneh-Far, R, Duda, PW, Sayegh, C, Benveniste, O, Biliciler, S, Edmundson, C, Freimer, M, Geraci, A, Machado, P, Mozaffar, T, Soltanzadeh, P, Suresh, N, van der Kooi, A, Appleby, M, Barohn, RJ, Champtiaux, N, Doughty, C, Farias, J, Farmakidis, C, Habib, AA, Karam, C, Lilleker, J, Lorusso, S, Pasnoor, M, Querin, G, Raaphorst, J, Ransley, G, Saba, S, Sheikh, K, Snedden, A, Statland, J, Vu, T

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Supplementary Material for: Wilson’s Disease: A Great Masquerader von Soltanzadeh, P., Nafissi, S., Ghorbani, A., Sikaroodi, H., Lotfi, J., Soltanzadeh, A.

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Hereditary inclusion body myopathy in Persian Jews: a case report from Iran von Miryounesi, M, Soltanzadeh, P, Modarressi, M H

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ASSOCIATION OF SPORADIC AMYOTROPHIC LATERAL SCLEROSIS WITH HUMAN T LYMPHO-TROPIC VIRUS 1, HUMAN IMMUNODEFICIENCY VIRUS AND HUMAN HERPES VIRUS 8 von A. Tarazi, S. Nafissi, A. A. Amirzargar, P. Ayatollahi A. Soltanzadeh

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ASSOCIATION OF SPORADIC AMYOTROPHIC LATERAL SCLEROSIS WITH HUMAN T LYMPHO-TROPIC VIRUS 1, HUMAN IMMUNODEFICIENCY VIRUS AND HUMAN HERPES VIRUS 8 von A. Tarazi, S. Nafissi, A. A. Amirzargar, P. Ayatollahi A. Soltanzadeh

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An Iranian family with congenital myasthenic syndrome caused by a novel acetylcholine receptor mutation (CHRNE K171X) von Soltanzadeh, P, Müller, J S, Ghorbani, A, Abicht, A, Lochmüller, H, Soltanzadeh, A

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Psychedelics Promote Structural and Functional Neural Plasticity von Ly, Calvin, Greb, Alexandra C., Cameron, Lindsay P., Wong, Jonathan M., Barragan, Eden V., Wilson, Paige C., Burbach, Kyle F., Soltanzadeh Zarandi, Sina, Sood, Alexander, Paddy, Michael R., Duim, Whitney C., Dennis, Megan Y., McAllister, A. Kimberley, Ori-McKenney, Kassandra M., Gray, John A., Olson, David E.

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Assessment of climate variations in temperature and precipitation extreme events over Iran von Soltani, M., Laux, P., Kunstmann, H., Stan, K., Sohrabi, M. M., Molanejad, M., Sabziparvar, A. A., Ranjbar SaadatAbadi, A., Ranjbar, F., Rousta, I., Zawar-Reza, P., Khoshakhlagh, F., Soltanzadeh, I., Babu, C. A., Azizi, G. H., Martin, M. V.

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