Uveitis and optic perineuritis in the context of myelin oligodendrocyte glycoprotein antibody seropositivity von Ramanathan, S., Fraser, C., Curnow, S. R., Ghaly, M., Leventer, R. J., Lechner‐Scott, J., Henderson, A., Reddel, S., Dale, R. C., Brilot, F.

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Characterizing White Matter Tract Organization in Polymicrogyria and Lissencephaly: A Multifiber Diffusion MRI Modeling and Tractography Study von Arrigoni, F, Peruzzo, D, Mandelstam, S, Amorosino, G, Redaelli, D, Romaniello, R, Leventer, R, Borgatti, R, Seal, M, Yang, J Y-M

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Acute flaccid myelitis in childhood: a retrospective cohort study von Andersen, E. W., Kornberg, A. J., Freeman, J. L., Leventer, R. J., Ryan, M. M.

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Distinctive Brain Malformations in Zhu-Tokita-Takenouchi-Kim Syndrome von Halliday, B J, Baynam, G, Ewans, L, Greenhalgh, L, Leventer, R J, Pilz, D T, Sachdev, R, Scheffer, I E, Markie, D M, McGillivray, G, Robertson, S P, Mandelstam, S

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ACTA2 -Related Dysgyria: An Under-Recognized Malformation of Cortical Development von Subramanian, S, Biswas, A, Alves, C A P F, Sudhakar, S V, Shekdar, K V, Krishnan, P, Shroff, M, Taranath, A, Arrigoni, F, Aldinger, K A, Leventer, R J, Dobyns, W B, Mankad, K

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Neural correlates of working memory in children and adolescents with agenesis of the corpus callosum: An fMRI study von Siffredi, V., Spencer-Smith, M.M., Barrouillet, P., Vaessen, M.J., Leventer, R.J., Anderson, V., Vuilleumier, P.

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Prenatal diagnosis of rhombencephalosynapsis: neuroimaging features and severity of vermian anomaly von Krajden Haratz, K., Oliveira Szejnfeld, P., Govindaswamy, M., Leibovitz, Z., Gindes, L., Severino, M., Rossi, A., Paladini, D., Garcia Rodriguez, R., Ben‐Sira, L., Borkowski Tillman, T., Gupta, R., Lotem, G., Raz, N., Hamamoto, T. E. N. K., Kidron, D., Arad, A., Birnbaum, R., Brussilov, M., Pomar, L., Vial, Y., Leventer, R. J., McGillivray, G., Fink, M., Krzeszowski, W., Fernandes Moron, A., Lev, D., Tamarkin, M., Shalev, J., Har Toov, J., Lerman‐Sagie, T., Malinger, G.

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Unclassified white matter disorders: A diagnostic journey requiring close collaboration between clinical and laboratory services von Stutterd, C.A., Vanderver, A., Lockhart, P.J., Helman, G., Pope, K., Uebergang, E., Love, C., Delatycki, M.B., Thorburn, D., Mackay, M.T., Peters, H., Kornberg, A.J., Patel, C., Rodriguez-Casero, V., Waak, M., Silberstein, J., Sinclair, A., Nolan, M., Field, M., Davis, M.R., Fahey, M., Scheffer, I.E., Freeman, J.L., Wolf, N.I., Taft, R.J., van der Knaap, M.S., Simons, C., Leventer, R.J.

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VP25.20: Molar tooth dysplasias in the fetus: differential diagnosis with vermian anomalies from distinct origin von Haratz, K.K., Leibovitz, Z., Oliveira, P.S., Rodriguez, R. Garcia, Severino, M., Fink, A., McGillivray, G., Leventer, R., ViÑals, F., Krzeszowski, W., Dafna, L., Gindes, L., Dorit, L., Ben‐Sira, L., Kidron, D., Arad, A., Birnbaum, R., Brusilov, M., Har‐Toov, J., Tamarkin, M., Shalev, Y., Lerman‐Sagie, T., Malinger, G.

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Pontine Tegmental Cap Dysplasia : MR Imaging and Diffusion Tensor Imaging Features of Impaired Axonal Navigation von JISSENDI-TCHOFO, P, DOHERTY, D, MCGILLIVRAY, G, HEVNER, R, SHAW, D, ISHAK, G, LEVENTER, R, BARKOVICH, A. J

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Bilateral posterior periventricular nodular heterotopia: a recognizable cortical malformation with a spectrum of associated brain abnormalities von Mandelstam, S A, Leventer, R J, Sandow, A, McGillivray, G, van Kogelenberg, M, Guerrini, R, Robertson, S, Berkovic, S F, Jackson, G D, Scheffer, I E

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OC03.07: Prenatal diagnosis of malformations of cortical development associated to midbrain‐hindbrain anomalies von Haratz, K.K., Leibovitz, Z., Oliveira, P.S., Moron, A.F., Fink, A., McGillivray, G., Viñals, F., Farajov, A.T., Leventer, R., Gindes, L., Lev, D., Tamarkin, M., Shalev, Y., Ben‐Sira, L., Kidron, D., Arad, A., Dafna, L., Malinger, G., Sagie, T.

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OC03.01: Prenatal diagnosis of rhombencephalosynapsis: beyond the fusion of the cerebellar hemispheres von Haratz, K.K., Govindaswamy, M., Oliveira, P.S., Leibovitz, Z., Dafna, L., Hamamoto, T.E., Gindes, L., Lev, D., Tamarkin, M., Shalev, Y., Ben‐Sira, L., Kidron, D., Arad, A., Fink, A., McGillivray, G., Leventer, R., Borkowski, T., Gupta, R.R., Sagie, T., Malinger, G.

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Clinical and imaging features of cortical malformations in childhood von LEVENTER, R. J, PHELAN, E. M, COLEMAN, L. T, KEAN, M. J, JACKSON, G. D, HARVEY, A. S

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Water column sediment fluxes in the Ross Sea, Antarctica: Atmospheric and sea ice forcing von Dunbar, Robert B., Leventer, Amy R., Mucciarone, David A.

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Physical control of chlorophyll a, POC, and TPN distributions in the pack ice of the Ross Sea, Antarctica von Arrigo, Kevin R., Robinson, Dale H., Dunbar, Robert B., Leventer, Amy R., Lizotte, Michael P.

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Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndrome von SHEEN, V. L, JANSEN, A, VAID, R. R, RUIZ, D. E, HUTCHINS, G. M, MENASHA, J, WILLNER, J, GENG, Y, GRIPP, K. W, NICHOLSON, L, BERRY-KRAVIS, E, BODELL, A, CHEN, M. H, APSE, K, HILL, R. S, DUBEAU, F, ANDERMANN, F, BARKOVICH, J, ANDERMANN, E, SHUGART, Y. Y, THOMAS, P, VIRI, M, VEGGIOTTI, P, PARRINI, E, ROBERTSON, S, GUERRINI, R, WALSH, C. A, MORGAN, T, RAVENSCROFT, R, GANESH, V, UNDERWOOD, T, WILEY, J, LEVENTER, R

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Refinement of a 400-kb Critical Region Allows Genotypic Differentiation between Isolated Lissencephaly, Miller-Dieker Syndrome, and Other Phenotypes Secondary to Deletions of 17p13... von Cardoso, Carlos, Leventer, Richard J., Ward, Heather L., Toyo-oka, Kazuhito, Chung, June, Gross, Alyssa, Martin, Christa L., Allanson, Judith, Pilz, Daniela T., Olney, Ann H., Mutchinick, Osvaldo M., Hirotsune, Shinji, Wynshaw-Boris, Anthony, Dobyns, William B., Ledbetter, David H.

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OC06.02: Prenatal diagnosis of brainstem anomalies: phenotypic spectrum and neuroimaging features von Haratz, K.K., Leibovitz, Z., Oliveira, P.S., Gindes, L., Raz, N., Dafna, L., Tamarkin, M., Shalev, Y., Malinger, G., Schreiber, L., Kidron, D., Arad, A., Egenburg, S., Lev, D., Ben‐Sira, L., Moron, A.F., Kasprian, G., Prayer, D., Viñals, F., Fink, A., McGillivray, G., Leventer, R., Garel, C., Poretti, A., Lerman‐Sagie, T.

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Bilateral generalized polymicrogyria (BGP): A distinct syndrome of cortical malformation von CHANG, B. S, PIAO, X, BARKOVICH, A. J, GRANT, P. E, WALSH, C. A, GIANNINI, C, CASCINO, G. D, SCHEFFER, I, WOODS, C. G, TOPCU, M, TEZCAN, K, BODELL, A, LEVENTER, R. J

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