Anorexic action of a new potential neuropeptide Y antagonist [ d-Tyr 27,36, d-Thr 32]-NPY (27–36) infused into the hypothalamus of the rat von Myers, R.D., Wooten, M.H., Ames, C.D., Nyce, J.W.

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Fever of unknown origin: due toC. albicans or other fungi acting on the hypothalamus? von Barwick, V.S., Wooten, M.H., Bradfield, J.F., Myers, R.D.

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Fever of unknown origin: due to C. albicans or other fungi acting on the hypothalamus? von Barwick, V.S., Wooten, M.H., Bradfield, J.F., Myers, R.D.

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Interaction between aryl-piperazine and benzodiazepine anxioiytic drugs on mouse intraspecies aggression and monoaminergic function von McMillen, B.A., Wooten, M.H., King, S.W., Williams, H.L.

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Haplotypes and gene expression implicate the MAPT region for Parkinson disease : The GenePD Study von TOBIN, J. E, LATOURELLE, J. C, RACETTE, B. A, PERLMUTTER, J. S, WATTS, R, GUTTMAN, M, BAKER, K. B, GOLDWURM, S, PEZZOLI, G, SINGER, C, SAINT-HILAIRE, M. H, HENDRICKS, A. E, LEW, M. F, WILLIAMSON, S, NAGLE, M. W, WILK, J. B, MASSOOD, T, LARAMIE, J. M, DESTEFANO, A. L, LITVAN, I, NICHOLSON, G, CORBETT, A, ISAACSON, S, KLEIN, C, BURN, D. J, CHINNERY, P. F, PRAMSTALLER, P. P, SHERMAN, S, AL-HINTI, J, DRASBY, E, NANCE, M, MOLLER, A. T, OSTERGAARD, K, ROXBURGH, R, SUCHOWERSKY, O, SNOW, B, SLEVIN, J. T, CAMBI, F, GUSELLA, J. F, MYERS, R. H, SHILL, H. A, GOLBE, Li, MARK, M. H, GROWDON, J. H, WOOTEN, G. F

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Absence of previously reported variants in the SCNA (G88C and G209A), NR4A2 (T291D and T245G) and the DJ-1 (T497C) genes in familial Parkinson's disease from the GenePD study von Karamohamed, Samer, Golbe, L.I., Mark, M.H., Lazzarini, A.M., Suchowersky, O., Labelle, N., Guttman, Mark, Currie, L.J., Wooten, G.F., Stacy, M., Saint-Hilaire, M., Feldman, R.G., Liu, J., Shoemaker, C.M., Wilk, J.B., DeStefano, A.L., Latourelle, J.C., Xu, G., Watts, R., Growdon, J., Lew, M., Waters, C., Vieregge, P., Pramstaller, P.P., Klein, C., Racette, B.A., Perlmutter, J.S., Parsian, A., Singer, Carlos, Montgomery, E., Baker, K., Gusella, J.F., Herbert, A., Myers, R.H.

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Absence of previously reported variants in the SCNA (G88C and G209A), NR4A2 (T291D and T245G) and the DJ ‐ 1 (T497C) genes in familial Parkinson's disease from the Gene PD study von Karamohamed, Samer, Golbe, L.I., Mark, M.H., Lazzarini, A.M., Suchowersky, O., Labelle, N., Guttman, Mark, Currie, L.J., Wooten, G.F., Stacy, M., Saint‐Hilaire, M., Feldman, R.G., Liu, J., Shoemaker, C.M., Wilk, J.B., DeStefano, A.L., Latourelle, J.C., Xu, G., Watts, R., Growdon, J., Lew, M., Waters, C., Vieregge, P., Pramstaller, P.P., Klein, C., Racette, B.A., Perlmutter, J.S., Parsian, A., Singer, Carlos, Montgomery, E., Baker, K., Gusella, J.F., Herbert, A., Myers, R.H.

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Segregation analysis of Parkinson disease revealing evidence for a major causative gene von Maher, N.E., Currie, L.J., Lazzarini, A.M., Wilk, J.B., Taylor, C.A., Saint-Hilaire, M.H., Feldman, R.G., Golbe, L.I., Wooten, G.F., Myers, R.H.

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