Heredofamilial Brain Calcinosis Syndrome von Baba, Yasuhiko, Broderick, Daniel F., Uitti, Ryan J., Hutton, Michael L., Wszolek, Zbigniew K.

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Comparative Adherence Trajectories of Oral Fingolimod and Injectable Disease Modifying Agents in Multiple Sclerosis von Earla, Jagadeswara R, Hutton, George J, Thornton, J Douglas, Chen, Hua, Johnson, Michael L, Aparasu, Rajender R

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Case-control study of the extended tau gene haplotype in Parkinson's disease von Maraganore, Demetrius M., Hernandez, Dena G., Singleton, Andrew B., Farrer, Matthew J., McDonnell, Shannon K., Hutton, Michael L., Hardy, John A., Rocca, Walter A.

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Imbalance in the response of pre- and post-synaptic components to amyloidopathy von Stephen, T, Tamagnin, F, Piegsa, J, Sung, K, Harvey, J, Oliver-Evans, A, Murray, TK, Ahmed, Z, Hutton, ML, Randall, A, O’Neill, MJ, Jackson, J

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Neuropathologic Features of Frontotemporal Lobar Degeneration With Ubiquitin-Positive Inclusions With Progranulin Gene (PGRN) Mutations von Josephs, Keith A, Ahmed, Zeshan, Katsuse, Omi, Parisi, Joseph F, Boeve, Bradley F, Knopman, David S, Petersen, Ronald C, Davies, Peter, Duara, Ranjan, Graff-Radford, Neill R, Uitti, Ryan J, Rademakers, Rosa, Adamson, Jennifer, Baker, Matthew, Hutton, Michael L, Dickson, Dennis W

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Increase in tau tyrosine phosphorylation correlates with the formation of tau aggregates von Vega, Irving E., Cui, Li, Propst, Josh A., Hutton, Michael L., Lee, Gloria, Yen, Shu-Hui

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Hereditary diffuse leukoencephalopathy with spheroids: clinical, pathologic and genetic studies of a new kindred von Baba, Yasuhiko, Ghetti, Bernardino, Baker, Matthew C, Uitti, Ryan J, Hutton, Michael L, Yamaguchi, Keiji, Bird, Thomas, Lin, Wenlang, DeLucia, Michael W, Dickson, Dennis W, Wszolek, Zbigniew K

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Altered synapse stability in the early stages of tauopathy von Jackson, JS, Witton, J, Johnson, JD, Ahmed, Z, Ward, M, Randall, AD, Hutton, ML, Isaac, JT, O'Neill, MJ, Ashby, MC

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High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsy von Rademakers, Rosa, Melquist, Stacey, Cruts, Marc, Theuns, Jessie, Del-Favero, Jurgen, Poorkaj, Parvoneh, Baker, Matt, Sleegers, Kristel, Crook, Richard, De Pooter, Tim, Kacem, Samira Bel, Adamson, Jennifer, Van den Bossche, Dirk, Van den Broeck, Marleen, Gass, Jennifer, Corsmit, Ellen, De Rijk, Peter, Thomas, Natalie, Engelborghs, Sebastiaan, Heckman, Michael, Litvan, Irene, Crook, Julia, De Deyn, Peter P., Dickson, Dennis, Schellenberg, Gerard D., Van Broeckhoven, Christine, Hutton, Michael L.

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Frontal Lobe Dementia With Novel Tauopathy: Sporadic Multiple System Tauopathy With Dementia von BIGIO, EILEEN H, LIPTON, ANNE M, YEN, SHU-HUI, HUTTON, MIKE L, BAKER, MATT, NACHARAJU, PARIMALA, WHITE, CHARLES L, DAVIES, PETER, LIN, WENLANG, DICKSON, DENNIS W

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Clinical and genetic studies of families with the tau N279K mutation (FTDP-17) von TSUBOI, Y, BAKER, M, KOMURE, O, KUNO, S, ARIMA, K, SUNOHARA, N, KOBAYASHI, T, MIZUNO, Y, WSZOLEK, Z. K, HUTTON, M. L, UITTI, R. J, RASCOL, O, DELISLE, M.-B, SOULAGES, X, MURRELL, J. R, GHETTI, B, YASUDA, M

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The Effect of tau genotype on clinical features in FTDP-17 von Baba, Yasuhiko, Tsuboi, Yoshio, Baker, Matthew C., Uitti, Ryan J., Hutton, Michael L., Dickson, Dennis W., Farrer, Matthew, Putzke, John D., Woodruff, Bryan K., Ghetti, Bernardino, Murrell, Jill R., Boeve, Bradley F., Petersen, Ronald C., Verpillat, Patrice, Brice, Alexis, Delisle, Marie-Bernadette, Rascol, Oliver, Arima, Kunimasa, Dysken, Maurice W., Yasuda, Minoru, Kobayashi, Tomonori, Sunohara, Nobuhiko, Komure, Osamu, Kuno, Sadako, Sperfeld, Anne D., Stoppe, Gabriela, Kohlhase, Jürgen, Pickering-Brown, Stuart, Neary, David, Bugiani, Orso, Wszolek, Zbigniew K.

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Cloning of a cDNA that encodes an invertebrate glutamate receptor subunit von Hutton, Michael L., Harvey, Robert J., Barnard, Eric A., Darlison, Mark G.

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A novel invertebrate GABA A receptor-like polypeptide Sequence and pattern of gene expression von Hutton, Michael L., Harvey, Robert J., Earley, Fergus G.P., Barnard, Eric A., Darlison, Mark G.

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Progressive supranuclear palsy as a disease phenotype caused by the S305S tau gene mutation von Wszolek, Zbigniew K., Tsuboi, Yoshio, Uitti, Ryan J., Reed, Lee, Hutton, Michael L., Dickson, Dennis W., Stanford, Prudence M., Halliday, Glenda M., Brooks, William S., Kwok, John B.J., Schofield, Peter R.

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Clinical features of frontotemporal dementia due to the intronic tau 10(+16) mutation von Tsuboi, Y, Uitti, R J, Baker, M, Hutton, M L, Wszolek, Z K

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Self-assembly: its use in at-the-surface imaging schemes for microstructure fabrication in resist films von Taylor, G.N., Hutton, R.S., Stein, S.M., Katz, H.E., Schilling, M.L., Putvinski, T.M.

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Effects of [3H]‐BIDN, a novel bicyclic dinitrile radioligand for GABA‐gated chloride channels of insects and vertebrates von Rauh, James J, Benner, Eric, Schnee, Michael E, Cordova, Daniel, Holyoke, Caleb W, Howard, Michael H, Bai, Donglin, Buckingham, Steven D, Hutton, Michael L, Hamon, Alain, Roush, Richard T, Sattelle, David B

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274 ADA deficiency due to deletion of the ADA gene promoter and first exon by homologous recombination between two alu elements von Markert, ML, Hutton, JJ, Wiginton, DA, States, JC, Kaufman, RE

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Quaterthiophenediphosphonic acid (QDP): a rigid, electron-rich building block for zirconium-based multilayers von Katz, Howard E, Schilling, M. L, Chidsey, C. E. D, Putvinski, T. M, Hutton, R. S

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