2.33 Prazosin for Nightmares in Children and Adolescents von Park, Siin, Young, Keith, Oruebor, Jennifer, Toth, Shannon W., Morrow, Kyle

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Effect of neuromuscular electrical stimulation on skeletal muscle size and function in patients with breast cancer receiving chemotherapy von Toth, Michael J, Voigt, Thomas B, Tourville, Timothy W, Prior, Shannon M, Guigni, Blas A, Schlosberg, Axel V, Smith, Isaac B, Forest, Taylor J, Kaufman, Peter A, Wood, Marie E, Rehman, Hibba, Dittus, Kim

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Multifluid MHD study of the solar wind interaction with Mars' upper atmosphere during the 2015 March 8th ICME event von Dong, Chuanfei, Ma, Yingjuan, Bougher, Stephen W., Toth, Gabor, Nagy, Andrew F., Halekas, Jasper S., Dong, Yaxue, Curry, Shannon M., Luhmann, Janet G., Brain, David, Connerney, Jack E. P., Espley, Jared, Mahaffy, Paul, Benna, Mehdi, McFadden, James P., Mitchell, David L., DiBraccio, Gina A., Lillis, Robert J., Jakosky, Bruce M., Grebowsky, Joseph M.

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Meta-analysis of Parkinson's Disease: Identification of a novel locus, RIT2 von Pankratz, Nathan, Beecham, Gary W., DeStefano, Anita L., Dawson, Ted M., Doheny, Kimberly F., Factor, Stewart A., Hamza, Taye H., Hung, Albert Y., Hyman, Bradley T., Ivinson, Adrian J., Krainc, Dmitri, Latourelle, Jeanne C., Clark, Lorraine N., Marder, Karen, Martin, Eden R., Mayeux, Richard, Ross, Owen A., Scherzer, Clemens R., Simon, David K., Tanner, Caroline, Vance, Jeffery M., Wszolek, Zbigniew K., Zabetian, Cyrus P., Myers, Richard H., Payami, Haydeh, Scott, William K., Foroud, Tatiana

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Genomewide association study for susceptibility genes contributing to familial Parkinson disease von Pankratz, Nathan, Wilk, Jemma B, Latourelle, Jeanne C, DeStefano, Anita L, Halter, Cheryl, Pugh, Elizabeth W, Doheny, Kimberly F, Gusella, James F, Nichols, William C, Foroud, Tatiana, Myers, Richard H

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Mutations in GBA are associated with familial Parkinson disease susceptibility and age at onset von NICHOLS, W. C, PANKRATZ, N, MAREK, D. K, PAUCIULO, M. W, ELSAESSER, V. E, HALTER, C. A, RUDOLPH, A, WOJCIESZEK, J, PFEIFFER, R. F, FOROUD, T

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Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations von PANKRATZ, N, KISSELL, D. K, PAUCIULO, M. W, HALTER, C. A, RUDOLPH, A, PFEIFFER, R. F, MARDER, K. S, FOROUD, T, NICHOLS, W. C

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Copy number variation in familial Parkinson disease von Pankratz, Nathan, Dumitriu, Alexandra, Hetrick, Kurt N, Sun, Mei, Latourelle, Jeanne C, Wilk, Jemma B, Halter, Cheryl, Doheny, Kimberly F, Gusella, James F, Nichols, William C, Myers, Richard H, Foroud, Tatiana, DeStefano, Anita L

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Variation in GIGYF2 is not associated with Parkinson disease von NICHOLS, W. C, KISSELL, D. K, FOROUD, T, PANKRATZ, N, PAUCIULO, M. W, ELSAESSER, V. E, CLARK, K. A, HALTER, C. A, RUDOLPH, A, WOJCIESZEK, J, PFEIFFER, R. F

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Genomewide association study for onset age in Parkinson disease von Latourelle, Jeanne C, Pankratz, Nathan, Dumitriu, Alexandra, Wilk, Jemma B, Goldwurm, Stefano, Pezzoli, Gianni, Mariani, Claudio B, DeStefano, Anita L, Halter, Cheryl, Gusella, James F, Nichols, William C, Myers, Richard H, Foroud, Tatiana

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R1514Q substitution in Lrrk2 is not a pathogenic Parkinson's disease mutation von Nichols, William C., Marek, Diane K., Pauciulo, Michael W., Pankratz, Nathan, Halter, Cheryl A., Rudolph, Alice, Shults, Clifford W., Wojcieszek, Joanne, Foroud, Tatiana

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