Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease
Sidransky, E, Nalls, M.A, Aasly, J.O, Aharon-Peretz, J, Annesi, G, Barbosa, E.R, Bar-Shira, A, Berg, D, Bras, J, Brice, A, Chen, C.-M, Clark, L.N, Condroyer, C, De Marco, E.V, Dürr, A, Eblan, M.J, Fahn, S, Farrer, M.J, Fung, H.-C, Gan-Or, Z, Gasser, T, Gershoni-Baruch, R, Giladi, N, Griffith, A, Gurevich, T, Januario, C, Kropp, P, Lang, A.E, Lee-Chen, G.-J, Lesage, S, Marder, K, Mata, I.F, Mirelman, A, Mitsui, J, Mizuta, I, Nicoletti, G, Oliveira, C, Ottman, R, Orr-Urtreger, A, Pereira, L.V, Quattrone, A, Rogaeva, E, Rolfs, A, Rosenbaum, H, Rozenberg, R, Samii, A, Samaddar, T, Schulte, C, Sharma, M, Singleton, A, Spitz, M, Tan, E.-K, Tayebi, N, Toda, T, Troiano, A.R, Tsuji, S, Wittstock, M, Wolfsberg, T.G, Wu, Y.-R, Zabetian, C.P, Zhao, Y, Ziegler, S.G
Published in The New England journal of medicine (22.10.2009)
Published in The New England journal of medicine (22.10.2009)
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Journal Article
Diagnostic criteria for adult‐onset leukoencephalopathy with axonal spheroids and pigmented glia due to CSF1R mutation
Konno, T., Yoshida, K., Mizuta, I., Mizuno, T., Kawarai, T., Tada, M., Nozaki, H., Ikeda, S.‐I., Onodera, O., Wszolek, Z. K., Ikeuchi, T.
Published in European journal of neurology (01.01.2018)
Published in European journal of neurology (01.01.2018)
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Journal Article
Glial fibrillary acidic protein mutations in adult-onset Alexander disease: clinical features observed in 12 Japanese patients
Yoshida, T., Sasayama, H., Mizuta, I., Okamoto, Y., Yoshida, M., Riku, Y., Hayashi, Y., Yonezu, T., Takata, Y., Ohnari, K., Okuda, S., Aiba, I., Nakagawa, M.
Published in Acta neurologica Scandinavica (01.08.2011)
Published in Acta neurologica Scandinavica (01.08.2011)
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Journal Article
A Japanese CADASIL kindred with a novel two-base NOTCH3 mutation
Suda, S., Okubo, S., Ueda, M., Sowa, K., Abe, A., Aoki, J., Muraga, K., Suzuki, K., Sakamoto, Y., Mizuta, I., Mizuno, T., Kimura, K.
Published in European journal of neurology (01.05.2016)
Published in European journal of neurology (01.05.2016)
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Journal Article
Meta-analysis of α synuclein/ NACP polymorphism in Parkinson's disease in Japan
Mizuta, I, Nishimura, M, Mizuta, E, Yamasaki, S, Ohta, M, Kuno, S
Published in Journal of neurology, neurosurgery and psychiatry (01.09.2002)
Published in Journal of neurology, neurosurgery and psychiatry (01.09.2002)
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Journal Article
Developmental expression of NMDA receptor subunits and the emergence of glutamate neurotoxicity in primary cultures of murine cerebral cortical neurons
Mizuta, I, Katayama, M, Watanabe, M, Mishina, M, Ishii, K
Published in Cellular and molecular life sciences : CMLS (01.07.1998)
Published in Cellular and molecular life sciences : CMLS (01.07.1998)
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Journal Article
Conflict of intentions due to callosal disconnection
Nishikawa, T, Okuda, J, Mizuta, I, Ohno, K, Jamshidi, J, Tokunaga, H, Ikejiri, Y, Nakagawa, Y, Yoshimine, T, Tanabe, H, Takeda, M
Published in Journal of neurology, neurosurgery and psychiatry (01.10.2001)
Published in Journal of neurology, neurosurgery and psychiatry (01.10.2001)
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Journal Article
Infarct tolerance accompanied enhanced BDNF-like immunoreactivity in neuronal nuclei
Yanamoto, H., Mizuta, I., Nagata, I., Xue, J.-H., Zhang, Z., Kikuchi, H.
Published in Brain research (22.09.2000)
Published in Brain research (22.09.2000)
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Journal Article
Effects of GFAP promoter polymorphism on age at onset of Alexander disease
Yasuda, R., Yoshida, T., Mizuta, I., Mizuno, T.
Published in Journal of the neurological sciences (15.10.2017)
Published in Journal of the neurological sciences (15.10.2017)
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Journal Article
Intracranial artery stenosis in Japanese CADASIL patients
Watanabe, A., Koizumi, T., Mukai, M., Mizuta, I., Ohara, T., Mizuno, T.
Published in Journal of the neurological sciences (15.10.2017)
Published in Journal of the neurological sciences (15.10.2017)
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Journal Article
Cysteine-sparing variations of NOTCH3 found on genetic test for CADASIL
Mizuta, I., Koizumi, T., Mukai, M., Watanabe-Hosomi, A., Mizuno, T.
Published in Journal of the neurological sciences (15.10.2017)
Published in Journal of the neurological sciences (15.10.2017)
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Journal Article
Clinical variety of two cases of hereditary sensory and autonomic neuropathy type 1E with cognitive disorders
Watanabe, M., Ninomiya, S., Kondo, S., Matsumoto, Y., Kamogawa, K., Tomita, H., Okamoto, K., Okuda, B., Mizuta, I., Mizuno, T.
Published in Journal of the neurological sciences (15.10.2017)
Published in Journal of the neurological sciences (15.10.2017)
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Journal Article
Diagnostic criteria for adult‐onset leukoencephalopathy with axonal spheroids and pigmented glia due to CSF 1R mutation
Konno, T., Yoshida, K., Mizuta, I., Mizuno, T., Kawarai, T., Tada, M., Nozaki, H., Ikeda, S.‐I., Onodera, O., Wszolek, Z. K., Ikeuchi, T.
Published in European journal of neurology (01.01.2018)
Published in European journal of neurology (01.01.2018)
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Journal Article
Loss of function mutant of ter94, Drosophila VCP, partially enhanced motor neuron degeneration induced by knockdown of TBPH, Drosophila TDP-43
Kushimura, Y., Tokuda, T., Azuma, Y., Yamamoto, I., Yoshida, H., Mizuta, I., Ueyama, M., Nagai, Y., Nakagawa, M., Mizuno, T., Yamaguchi, M.
Published in Journal of the neurological sciences (15.10.2017)
Published in Journal of the neurological sciences (15.10.2017)
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Journal Article
The search for genes that modulate FUS-mediated phenotypes by Drosophila amyotrophic lateral sclerosis model
Azuma, Y., Tokuda, T., Kushimura, Y., Yamamoto, I., Yoshida, H., Mizuta, I., Ueyama, M., Nagai, Y., Nakagawa, M., Mizuno, T., Yamaguchi, M.
Published in Journal of the neurological sciences (15.10.2017)
Published in Journal of the neurological sciences (15.10.2017)
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Journal Article
New diagnostic criteria for cerebral autosomal dominant arteriopathy with subcortical infarcts and leukocencephalopathy in Japan
Mizuno, T., Mizuta, I., Watanabe-Hosomi, A., Koizumi, T., Mukai, M., Hamano, A., Tomii, Y., Kondo, M., Nakagawa, M., Hirano, T., Uchino, M., Onodera, O., Tomimoto, H.
Published in Journal of the neurological sciences (15.10.2017)
Published in Journal of the neurological sciences (15.10.2017)
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Journal Article
Early-onset Parkinsonism in a pedigree with phosphoglycerate kinase deficiency and a heterozygous carrier: Do PGK-1 mutations contribute to vulnerability to Parkinsonism?
Kasai, T., Sakaue, S., Mizuta, I., Suematsu, M., Osone, S., Azuma, Y., Imamura, T., Tokuda, T., Kanno, H., El-Agnaf, O., Morimoto, M., Nakagawa, M., Hosoi, H., Mizuno, T.
Published in Journal of the neurological sciences (15.10.2017)
Published in Journal of the neurological sciences (15.10.2017)
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Journal Article
Revised guidelines for diagnosing Alexander disease and their validity
Yoshida, T., Mizuta, I., Rei, Y., Jun, M., Mieno, M., Kubota, M., Sasaki, M., Matsui, M., Saitsu, H., Takanashi, J., Kurosawa, K., Yamamoto, T., Inoue, K., Mizuno, T., Osaka, H.
Published in Journal of the neurological sciences (15.10.2017)
Published in Journal of the neurological sciences (15.10.2017)
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Journal Article