Clinical and genetic characterization of adult‐onset leukoencephalopathy with axonal spheroids and pigmented glia associated with CSF1R mutation von Konno, T., Yoshida, K., Mizuno, T., Kawarai, T., Tada, M., Nozaki, H., Ikeda, S.‐I., Nishizawa, M., Onodera, O., Wszolek, Z. K., Ikeuchi, T.

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Diagnostic criteria for adult‐onset leukoencephalopathy with axonal spheroids and pigmented glia due to CSF1R mutation von Konno, T., Yoshida, K., Mizuta, I., Mizuno, T., Kawarai, T., Tada, M., Nozaki, H., Ikeda, S.‐I., Onodera, O., Wszolek, Z. K., Ikeuchi, T.

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Presenilin-dependent gamma-secretase-mediated control of p53-associated cell death in Alzheimer's disease von Alves da Costa, Cristine, Sunyach, Claire, Pardossi-Piquard, Raphaelle, Sévalle, Jean, Vincent, Bruno, Boyer, Nicole, Kawarai, Toshitaka, Girardot, Nadège, St George-Hyslop, Peter, Checler, Frédéric

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LRRK2 gene in parkinson disease : Mutation analysis and case control association study von PAISAN-RUIZ, C, LANG, A. E, KAWARAI, T, SATO, C, SALEHI-RAD, S, FISMAN, G. K, AL-KHAIRALLAH, T, ST GEORGE-HYSLOP, P, SINGLETON, A, ROGAEVA, E

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Effects of short-chain fatty acids on Actinomyces naeslundii biofilm formation von Yoneda, S., Kawarai, T., Narisawa, N., Tuna, E.B., Sato, N., Tsugane, T., Saeki, Y., Ochiai, K., Senpuku, H.

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Autopsy-proven coexistence of amyotrophic lateral sclerosis with parkinson’s disease von Izumi, Y, Sumikura, H, Fujita, K, Shimatani, Y, Miyamoto, R, Nodera, H, Kawarai, T, Nishida, Y, Murayama, S, Kaji, R

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Silver syndrome variant of hereditary spastic paraplegia : A locus to 4p and allelism with SPG4 von ORLACCHIO, A, PATRONO, C, GAUDIELLO, F, ROCCHI, C, MOSCHELLA, V, FLORIS, R, BERNARDI, G, KAWARAI, T

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Familial Alzheimer disease : Decreases in CSF Aβ42 levels precede cognitive decline von MOONIS, M, SWEARER, J. M, DAYAW, M. P. E, GEORGE-HYSLOP, P. St, ROGAEVA, E, KAWARAI, T, POLLEN, D. A

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The effects of APOE and tau gene variability on risk of frontotemporal dementia von Bernardi, L., Maletta, R.G., Tomaino, C., Smirne, N., Di Natale, M., Perri, M., Longo, T., Colao, R., Curcio, S.A.M., Puccio, G., Mirabelli, M., Kawarai, T., Rogaeva, E., St. George Hyslop, P.H., Passarino, G., De Benedictis, G., Bruni, A.C.

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Heterogeneity within a large kindred with frontotemporal dementia : A novel progranulin mutation von BRUNI, A. C, MOMENI, P, ANFOSSI, M, GALLO, M, GERACITANO, S, COSTANZO, A, SMIRNE, N, CURCIO, S. A. M, MIRABELLI, M, PUCCIO, G, COLAO, R, MALETTA, R. G, BERNARDI, L, KERTESZ, A, GEORGE-HYSLOP, P. St, HARDY, J, ROGAEVA, E, TOMAINO, C, FRANGIPANE, F, ELDER, J, KAWARAI, T, SATO, C, PRADELLA, S, WAKUTANI, Y

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Spastic paraplegia in Romania: high prevalence of SPG4 mutations von Orlacchio, A, Patrono, C, Borreca, A, Babalini, C, Bernardi, G, Kawarai, T

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SulA-independent filamentation of Escherichia coli during growth after release from high hydrostatic pressure treatment von Kawarai, T, Wachi, M, Ogino, H, Furukawa, S, Suzuki, K, Ogihara, H, Yamasaki, M

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Familial frontotemporal dementia with ubiquitin-positive, tau-negative inclusions von KERTESZ, A, KAWARAI, T, ROGAEVA, E, GEORGE-HYSLOP, P. S, POORKAJ, P, BIRD, T. D, MUNOZ, D. G

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Effect of high pressure gaseous carbon dioxide on the germination of bacterial spores von Furukawa, S., Watanabe, T., Tai, T., Hirata, J., Narisawa, N., Kawarai, T., Ogihara, H., Yamasaki, M.

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Presenilin mutations associated with Alzheimer disease cause defective intracellular trafficking of β-catenin ,a component of the presenilin protein complex von St George-Hyslop, P, Nishimura, M, Yu, G, Levesque, G, Zhang, D.M, Ruel, L, Chen, F, Milman, P, Holmes, E, Liang, Y, Kawarai, T, Jo, E, Supala, A, Rogaeva, E, Xu, D -M, Janus, C, Levesque, L, Bi, Q, Duthie, M, Rozmahel, R, Mattila, K, Lannfelt, L, Westaway, D, Mount, H.T.J, Woodgett, J, Fraser, P.E

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Autosomal recessive hereditary spastic paraplegia with thin corpus callosum: a novel mutation in the SPG11 gene and further evidence for genetic heterogeneity von Pippucci, T., Panza, E., Pompilii, E., Donadio, V., Borreca, A., Babalini, C., Patrono, C., Zuntini, R., Kawarai, T., Bernardi, G., Liguori, R., Romeo, G., Montagna, P., Orlacchio, A., Seri, M.

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Pleasant feeling from watching a comical video enhances free radical-scavenging capacity in human whole saliva von Atsumi, T, Fujisawa, S, Nakabayashi, Y, Kawarai, T, Yasui, T, Tonosaki, K

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A new SPG4 mutation in a variant form of spastic paraplegia with congenital arachnoid cysts von ORLACCHIO, A, GAUDIELLO, F, TOTARO, A, FLORIS, R, ST GEORGE-HYSLOP, P. H, BERNARDI, G, KAWARAI, T

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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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Fine mapping of 10q and 18q for familial Alzheimer's disease in Caribbean Hispanics von LEE, J. H, MAYEUX, R, LANTIGUA, R, KAWARAI, T, TOULINA, A, MEDRANO, M, TORRES, M, STERN, Y, TYCKO, B, ROGAEVA, E, ST. GEORGE-HYSLOP, P, KNOWLES, J. A, MAYO, D, MO, J, SANTANA, V, WILLIAMSON, J, FLAQUER, A, CIAPPA, A, RONDON, H, ESTEVEZ, P

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