A gene (ETM) for essential tremor maps to chromosome 2p22-p25 von Higgins, Joseph J., Pho, Lana T., Nee, Linda E.

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Frontotemporal dementia with novel tau pathology and a Glu342Val tau mutation von Lippa, Carol F., Zhukareva, Victoria, Kawarai, T., Uryu, Kunihiro, Shafiq, M., Nee, L. E., Grafman, J., Liang, Yan, St George-Hyslop, Peter H., Trojanowski, John Q., Lee, Virginia M.-Y.

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Progressive supranuclear gaze palsy is in linkage disequilibrium with the τ and not the α-synuclein gene von HIGGINS, J. J, LITVAN, I, PHO, L. T, LI, W, NEE, L. E

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Familial Alzheimer's disease: Site of mutation influences clinical phenotype von Lippa, C. F., Swearer, J. M., Kane, K. J., Nochlin, D., Bird, T. D., Ghetti, B., Nee, L. E., St. George-Hyslop, P., Pollen, D. A., Drachman, D. A.

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Lewy Bodies Contain Altered α-Synuclein in Brains of Many Familial Alzheimer's Disease Patients with Mutations in Presenilin and Amyloid Precursor Protein Genes von Lippa, Carol F., Fujiwara, Hideo, Mann, David M.A., Giasson, Benoit, Baba, Minami, Schmidt, Marie L., Nee, Linda E., O'Connell, Brendan, Pollen, Dan A., St. George-Hyslop, Peter, Ghetti, Bernardino, Nochlin, David, Bird, Thomas D., Cairns, Nigel J., Lee, Virginia M.-Y., Iwatsubo, Takeshi, Trojanowski, John Q.

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Presenilin 1 Suppresses the Function of c-Jun Homodimers via Interaction with QM/Jif-1 von Imafuku, I., Masaki, T., Waragai, M., Takeuchi, S., Kawabata, M., S.-I. Hirai, Ohno, S., Nee, L. E., Lippa, C. F., Kanazawa, I., Imagawa, M., Okazawa, H.

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Aβ −42 deposition precedes other changes in PS-1 Alzheimer's disease von Lippa, CF, Nee, LE, Mori, H, George-Hyslop, PSt

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Alzheimer’s Disease in 22 Twin Pairs – 13-Year Follow-Up: Hormonal, Infectious and Traumatic Factors von Nee, Linda E., Lippa, Carol F.

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An atypical intronic deletion widens the spectrum of mutations in hereditary spastic paraplegia von HIGGINS, J. J, LOVELESS, J. M, GOSWAMI, S, NEE, L. E, COZZO, C, DE BIASE, A, ROSEN, D. R

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Mutations in American families with spinocerebellar ataxia (SCA) type 3 : SCA3 is allelic to Machado-Joseph disease von HIGGINS, J. J, NEE, L. E, VASCONCELOS, O, IDE, S. E, LAVEDAN, C, GOLDFARB, L. G, POLYMEROPOULOS, M. H

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AMY plaques in familial AD : Comparison with sporadic Alzheimer's disease von LIPPA, C. F, SCHMIDT, M. L, NEE, L. E, BIRD, T, NOCHLIN, D, HULETTE, C, MORI, H, LEE, V. M.-Y, TROJANOWSKI, J. Q

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Fluorescent Light-Induced Chromatid Breaks Distinguish Alzheimer Disease Cells from Normal Cells in Tissue Culture von Parshad, Ram, Sanford, Katherine K., Price, Floyd M., Melnick, Lynn K., Nee, Linda E., Schapiro, Mark B., Tarone, Robert E., Robbins, Jay H.

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An autosomal recessive disorder with posterior column ataxia and retinitis pigmentosa von HIGGINS, J. J, MORTON, D. H, PATRONAS, N, NEE, L. E

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Evidence for a new spinocerebellar ataxia locus von Higgins, J. J., Pho, L. T., Ide, S. E., Nee, L. E., Polymeropoulos, M. H.

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A lack of the R406W tau mutation in progressive supranuclear palsy and corticobasal degeneration von HIGGINS, J. J, LITVAN, I, NEE, L. E, LOVELESS, J. M

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Serum- and bradykinin-induced calcium transients in familial Alzheimer's fibroblasts von McCoy, K.R., Mullins, R.D., Newcomb, T.G., Ng, G.M., Pavlínková, G., Polinsky, R.J., Nee, L.E., Sisken, J.E.

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Should spinocerebellar ataxia type 5 be called Lincoln ataxia? von NEE, L. E, HIGGINS, J. J

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Brain MRI, lumbar CSF monoamine concentrations, and clinical descriptors of patients with spinocerebellar ataxia mutations von Higgins, J J, Harvey-White, J D, Nee, L E, Colli, M J, Grossi, T A, Kopin, I J

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Studies of activated microglial cells and macrophages using Alzheimer's disease cerebrospinal fluid in adult rats with experimentally induced lesions von Ling, E.A., Dahlström, A., Polinsky, R.J., Nee, L.E., McRae, A.

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Familial Alzheimer disease: a large, multigeneration German kindred von FROMMELT, P, SCHNABEL, R, KÜHNE, W, NEE, L. E, POLINSKY, R. J

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