Development and initial validation of a screening tool for Parkinson disease surgical candidates von OKUN, M. S, FERNANDEZ, H. H, GRACE, J, ROMRELL, J, FOOTE, K. D, PEDRAZA, O, MISRA, M, LYONS, K. E, PAHWA, R, TARSY, D, SCOLLINS, L, CORAPI, K, FRIEHS, G. 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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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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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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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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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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Clinical correlates of depressive symptoms in familial Parkinson's disease von Pankratz, Nathan, Marder, Karen S., Halter, Cheryl A., Rudolph, Alice, Shults, Cliff W., Nichols, William C., Foroud, Tatiana

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Maternal inheritance and mitochondrial DNA variants in familial Parkinson's disease von Simon, David K, Pankratz, Nathan, Kissell, Diane K, Pauciulo, Michael W, Halter, Cheryl A, Rudolph, Alice, Pfeiffer, Ronald F, Nichols, William C, Foroud, Tatiana

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Progression of Parkinson’s Disease following Thalamic Deep Brain Stimulation for Tremor von Tarsy, Daniel, Scollins, Lisa, Corapi, Kristin, O’Herron, Siobhan, Apetauerova, Diana, Norregaard, Thorkild

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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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Steering system for ship pod drive von J. C. SCOLLINS, B. L. DANA

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Fetal lung to liver reflectivity ratio and lung maturity von Feingold, Michael, Scollins, James, Cetrulo, Curtis L., Koza, Douglas

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