Progression of alpha‐synuclein pathology in multiple system atrophy of the cerebellar type von Brettschneider, J., Irwin, D. J., Boluda, S., Byrne, M. D., Fang, L., Lee, E. B., Robinson, J. L., Suh, E., Van Deerlin, V. M., Toledo, J. B., Grossman, M., Hurtig, H., Dengler, R., Petri, S., Lee, V. M.‐Y., Trojanowski, J. Q.

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CSF biomarkers in frontotemporal lobar degeneration with known pathology von BIAN, H, VAN SWIETEN, J. C, TROJANOWSKI, J, LEE, V. M.-Y, GROSSMAN, M, LEIGHT, S, MASSIMO, L, WOOD, E, FORMAN, M, MOORE, P, DE KONING, I, CLARK, C. M, ROSSO, S

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Novel conformation‐selective alpha‐synuclein antibodies raised against different in vitro fibril forms show distinct patterns of Lewy pathology in Parkinson's disease von Covell, D. J., Robinson, J. L., Akhtar, R. S., Grossman, M., Weintraub, D., Bucklin, H. M., Pitkin, R. M., Riddle, D., Yousef, A., Trojanowski, J. Q., Lee, V. M.‐Y.

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Distinct cerebral perfusion patterns in FTLD and AD von HU, W. T, WANG, Z, LEE, V. M.-Y, TROJANOWSKI, J. Q, DETRE, J. A, GROSSMAN, M

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Glucocerebrosidase mutations are an important risk factor for lewy body disorders von GOKER-ALPAN, O, GIASSON, B. I, EBLAN, M. J, NGUYEN, J, HURTIG, H. I, LEE, V. M.-Y, TROJANOWSKI, J. Q, SIDRANSKY, E

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Comparison of family histories in FTLD subtypes and related tauopathies von GOLDMAN, J. S, FARMER, J. M, MILLER, B. L, WOOD, E. M, JOHNSON, J. K, BOXER, A, NEUHAUS, J, LOMEN-HOERTH, C, WILHELMSEN, K. C, LEE, V. M.-Y, GROSSMAN, M

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Multimodal predictors for Alzheimer disease in nonfluent primary progressive aphasia von HU, W. T, MCMILLAN, C, LIBON, D, LEIGHT, S, FORMAN, M, LEE, V. M.-Y, TROJANOWSKI, J. Q, GROSSMAN, M

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Longitudinal decline in autopsy-defined frontotemporal lobar degeneration von GROSSMAN, M, XIE, S. X, HURTIG, H. I, FORMAN, M. S, LEE, V. M.-Y, TROJANOWSKI, J. Q, LIBON, D. J, WANG, X, MASSIMO, L, MOORE, P, VESELY, L, BERKOWITZ, R, CHATTERJEE, A, COSLETT, H. B

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A novel progranulin mutation associated with variable clinical presentation and tau, TDP43 and alpha-synuclein pathology von Leverenz, J. B., Yu, C. E., Montine, T. J., Steinbart, E., Bekris, L. M., Zabetian, C., Kwong, L. K., Lee, V. M-Y., Schellenberg, G. D., Bird, T. D.

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TDP-43 pathology occurs infrequently in multiple system atrophy von Geser, F., Malunda, J. A., Hurtig, H. I., Duda, J. E., Wenning, G. K., Gilman, S., Low, P. A., Lee, V. M.-Y., Trojanowski, J. Q.

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Cortical biochemistry in MCI and alzheimer disease : Lack of correlation with clinical diagnosis von FORMAN, M. S, MUFSON, E. J, LEURGANS, S, PRATICO, D, JOYCE, S, LEIGHT, S, LEE, V. M.-Y, TROJANOWSKI, J. Q

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Corticobasal syndrome and primary progressive aphasia as manifestations of LRRK2 gene mutations von Chen-Plotkin, A S, Yuan, W, Anderson, C, McCarty Wood, E, Hurtig, H I, Clark, C M, Miller, B L, Lee, V M-Y, Trojanowski, J Q, Grossman, M, Van Deerlin, V M

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Axonopathy and amyotrophy in mice transgenic for human four-repeat tau protein von PROBST, A, GÖTZ, J, JAKES, R, CROWTHER, R. A, SPILLANTINI, M. G, BÜRKI, K, GOEDERT, M, WIEDERHOLD, K. H, TOLNAY, M, MISTL, C, JATON, A. L, HONG, M, ISHIHARA, T, LEE, V. M.-Y, TROJANOWSKI, J. Q

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NTera 2 Cells: A human cell line which displays characteristics expected of a human committed neuronal progenitor cell von Pleasure, S. J., Lee, V. M.-Y.

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Monoclonal antibody PHF-1 recognizes tau protein phosphorylated at serine residues 396 and 404 von Otvos Jr, L., Feiner, L., Lang, E., Szendrei, G. I., Goedert, M., Lee, V. M-Y.

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The North American Multiple System Atrophy Study Group von Gilman, S, May, S J, Shults, C W, Tanner, C M, Kukull, W, Lee, V M-Y, Masliah, E, Low, P, Sandroni, P, Trojanowski, J Q, Ozelius, L, Foroud, T

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Novel CSF biomarkers for frontotemporal lobar degenerations von Hu, W T, Chen-Plotkin, A, Grossman, M, Arnold, S E, Clark, C M, Shaw, L M, McCluskey, L, Elman, L, Hurtig, H I, Siderowf, A, Lee, V M-Y, Soares, H, Trojanowski, J Q

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The Neuropathology of a Chromosome 17-Linked Autosomal Dominant Parkinsonism and Dementia (“Pallido-Ponto-Nigral Degeneration”) von Reed, L A, Schmidt, M L, Wszolek, Z K, Balin, B J, Soontornniyomkij, V, Lee, V M -Y, Trojanowski, J Q, Schelper, R L

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Cognitive and motor assessment in autopsy-proven corticobasal degeneration von Murray, R, Neumann, M, Forman, M S, Farmer, J, Massimo, L, Rice, A, Miller, B L, Johnson, J K, Clark, C M, Hurtig, H I, Gorno-Tempini, M L, Lee, V M-Y, Trojanowski, J Q, Grossman, M

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Mutations in TDP-43 link glycine-rich domain functions to amyotrophic lateral sclerosis von Pesiridis, G. Scott, Lee, Virginia M.-Y., Trojanowski, John Q.

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