Search Results - Yamamoto-Watanabe, Yukiko

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  1. 1
    Factors responsible for neurofibrillary tangles and neuronal cell losses in tauopathy

    Factors responsible for neurofibrillary tangles and neuronal cell losses in tauopathy by Wakasaya, Yasuhito, Kawarabayashi, Takeshi, Watanabe, Mitsunori, Yamamoto-Watanabe, Yukiko, Takamura, Ayumi, Kurata, Tomoko, Murakami, Tetsuro, Abe, Koji, Yamada, Kiyofumi, Wakabayashi, Koichi, Sasaki, Atsushi, Westaway, David, Hyslop, Peter St. George, Matsubara, Etsuro, Shoji, Mikio

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  2. 2
    Amyloid β accelerates phosphorylation of tau and neurofibrillary tangle formation in an amyloid precursor protein and tau double-transgenic mouse model

    Amyloid β accelerates phosphorylation of tau and neurofibrillary tangle formation in an amyloid precursor protein and tau double-transgenic mouse model by Seino, Yusuke, Kawarabayashi, Takeshi, Wakasaya, Yasuhito, Watanabe, Mitsunori, Takamura, Ayumi, Yamamoto-Watanabe, Yukiko, Kurata, Tomoko, Abe, Koji, Ikeda, Masaki, Westaway, David, Murakami, Tetsuro, Hyslop, Peter St. George, Matsubara, Etsuro, Shoji, Mikio

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  3. 3
    An Unusual Case of Elderly-Onset Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL) With Multiple Cerebrovascular Risk Factors

    An Unusual Case of Elderly-Onset Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL) With Multiple Cerebrovascular Risk Factors by Watanabe, Mitsunori, MD, PhD, Adachi, Yoshiki, MD, PhD, Jackson, Mandy, DPhil, Yamamoto-Watanabe, Yukiko, MD, Wakasaya, Yasuhito, MD, Shirahama, Ikumi, Takamura, Ayumi, PhD, Matsubara, Etsuro, MD, PhD, Kawarabayashi, Takeshi, MD, PhD, Shoji, Mikio, MD, PhD

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  4. 4
    A Japanese ALS6 family with mutation R521C in the FUS/TLS gene: A clinical, pathological and genetic report

    A Japanese ALS6 family with mutation R521C in the FUS/TLS gene: A clinical, pathological and genetic report by Yamamoto-Watanabe, Yukiko, Watanabe, Mitsunori, Okamoto, Koichi, Fujita, Yukio, Jackson, Mandy, Ikeda, Masaki, Nakazato, Yoichi, Ikeda, Yoshio, Matsubara, Etsuro, Kawarabayashi, Takeshi, Shoji, Mikio

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  5. 5
    Quantification of cystatin C in cerebrospinal fluid from various neurological disorders and correlation with G73A polymorphism in CST3

    Quantification of cystatin C in cerebrospinal fluid from various neurological disorders and correlation with G73A polymorphism in CST3 by Yamamoto-Watanabe, Yukiko, Watanabe, Mitsunori, Jackson, Mandy, Akimoto, Hiroyuki, Sugimoto, Kazuhiro, Yasujima, Minoru, Wakasaya, Yasuhito, Matsubara, Etsuro, Kawarabayashi, Takeshi, Harigaya, Yasuo, Lyndon, Alastair R, Shoji, Mikio

    Published in Brain research
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  6. 6
    A Japanese ALS6 family with mutation R521 C in the FUS/TLS gene: A clinical, pathological and genetic report

    A Japanese ALS6 family with mutation R521 C in the FUS/TLS gene: A clinical, pathological and genetic report by YAMAMOTO-WATANABE, Yukiko, WATANABE, Mitsunori, SHOJI, Mikio, OKAMOTO, Koichi, FUJITA, Yukio, JACKSON, Mandy, IKEDA, Masaki, NAKAZATO, Yoichi, IKEDA, Yoshio, MATSUBARA, Etsuro, KAWARABAYASHI, Takeshi

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