WNK1/HSN2 founder mutation in patients with hereditary sensory and autonomic neuropathy: A Japanese cohort study von Yuan, J.‐H., Hashiguchi, A., Yoshimura, A., Sakai, N., Takahashi, M.P., Ueda, T., Taniguchi, A., Okamoto, S., Kanazawa, N., Yamamoto, Y., Saigoh, K., Kusunoki, S., Ando, M., Hiramatsu, Y., Okamoto, Y., Takashima, H.

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Functional consequences of a CKIδ mutation causing familial advanced sleep phase syndrome von Fu, Ying-Hui, Padiath, Quasar S, Saigoh, Noriko, Xu, Ying, Saigoh, Kazumasa, Wu, Susan C, Jones, Christopher R, Shapiro, Robert E, Ptá ek, Louis J

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Clinical differences between a patient with intermediate CTA/CTG repeats and patients with typically expanded CTA/CTG repeats in spinocerebellar ataxia type 8 von Samukawa, M., Hirano, M., Saigoh, K., Kusunoki

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Mutations in the gene encoding p62 in Japanese patients with amyotrophic lateral sclerosis von HIRANO, Makito, NAKAMURA, Yusaku, SAIGOH, Kazumasa, SAKAMOTO, Hikaru, UENO, Shuichi, ISONO, Chiharu, MIYAMOTO, Katsuichi, AKAMATSU, Maiko, MITSUI, Yoshiyuki, KUSUNOKI, Susumu

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COQ2 gene analyses in multiple system atrophy and other neurodegenerative diseases and treatment of patients’ cells with coenzyme Q10 von Hirano, M., Nakamura, Y., Saigoh, K., Samukawa, M., Kusunoki, S.

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Clinical features and progression of dysphagia in bulbar-onset or limb-onset amyotrophic lateral sclerosis between patients with genetic mutations and those without mutations von Isono, C., Hirano, M., Fukuda, K., Samukawa, M., Saigoh, K., Nakamura, Y., Kusunoki, S.

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CTA/CTG repeat sizes in the atxn8os gene afefct age at onset and phenotype in spinocerebellar ATAXIA type8 von Samukawa, M., Hirano, M., Saigoh, K., Kawai, S., Hamada, Y., Takahashi, D., Nakamura, Y., Kusunoki, S.

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Non-coding repeat expansions in the ATXN8OS gene are identified in Japanese patients with amyotrophic lateral sclerosis von Hirano, M., Samukawa, M., Isono, C., Saigoh, K., Nakamura, Y., Kusunoki, S.

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Fremanezumab for Episodic Migraine Prevention in Japanese Patients: Subgroup Analysis from Two International Trials von Saigoh, Kazumasa, Takeshima, Takao, Nakai, Masami, Shibasaki, Yoshiyuki, Ishida, Miki, Ning, Xiaoping, Barash, Steve, Isogai, Yuki, Koga, Nobuyuki

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Fremanezumab for Chronic Migraine Prevention in Japanese Patients: Subgroup Analysis from Two International Trials von Saigoh, Kazumasa, Takeshima, Takao, Nakai, Masami, Shibasaki, Yoshiyuki, Ishida, Miki, Ning, Xiaoping, Barash, Steve, Isogai, Yuki, Koga, Nobuyuki

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Intragenic deletion in the gene encoding ubiquitin carboxy-terminal hydrolase in gad mice von Wada, Keiji, Saigoh, Kazumasa, Wang, Yu-Lai, Suh, Jun-Gyo, Yamanishi, Toshiyuki, Sakai, Yoshihisa, Kiyosawa, Hidenori, Harada, Takayuki, Ichihara, Nobutsune, Wakana, Shigeharu, Kikuchi, Tateki

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The level of oxidized DJ-1 protein in Parkinson’s disease and other parkinsonism syndromes von Yamagishi, Y., Saigoh, K., Saito, Y., Ogawa, I., Mitsui, Y., Hamada, M., Samukawa, M., Suzuki, H., Kuwahara, M., Hirano, M., Noguchi, N., Kusunoki, S.

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Abnormally high levels of oxidized DJ-1 in cases of Parkinson’s disease (PD) and dementia with lewy bodies (DLB) von Saigoh, K., Yamagishi, Y., Saito, Y., Ogawa, I., Mitsui, Y., Hamada, Y., Samukawa, M., Suzuki, H., Kuwahara, M., Hirano, M., Noguchi, N., Kusunoki, S.

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Detection of Hepatitis B Virus x Transcripts in Human Hepatocellular Carcinoma Tissues von Kobayashi, Susumu, Saigoh, Ken-ichi, Urashima, Tetsuroh, Asano, Takehide, Isono, Kaichi

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An in-frame deletion in peripheral myelin protein-22 gene causes hypomyelination and cell death of the schwann cells in the new Trembler mutant mice von Suh, J.-G, Ichihara, N, Saigoh, K, Nakabayashi, O, Yamanishi, T, Tanaka, K, Wada, K, Kikuchi, T

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GaAs homojunction phototransistor with minority carrier transport assisted by photo-generated carrier profile in the base von Ohsawa, J., Yamaguchi, S., Saigoh, K., Migitaka, M.

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The stereo-specific effect of d-serine ethylester and the d-cycloserine in ataxic mutant mice von Saigoh, Kazumasa, Matsui, Kyoko, Takahashi, Katsunobu, Nishikawa, Toru, Wada, Keiji

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Supplementary Material for: Neutral Lipid Storage Disease Associated with the PNPLA2 Gene: Case Report and Literature Review von Samukawa, M., Nakamura, N., Hirano, M., Morikawa, M., Sakata, H., Nishino, I., Izumi, R., Suzuki, N., Kuroda, H., Shiga, K., Saigoh, K., Aoki, M., Kusunoki, S.

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YAC/BAC-Based Physical and Transcript Mapping around the Gracile Axonal Dystrophy (gad) Locus Identifies Uchl1, Pmx2b, Atp3a2, and Hip2 Genes von Wang, Yu-Lai, Saigoh, Kazumasa, Osaka, Hitoshi, Yamanishi, Toshiyuki, Suh, Jun-Gyo, Kiyosawa, Hidenori, Sakai, Yoshihisa, Wakana, Shigeharu, Wada, Keiji

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Asymmetric Photocurrent Characteristics in GaAs/AlGaAs Phototransistors with Very Short Carrier-Diffusion Lengths von Ohsawa, Jun, Saigoh, Kaoru, Yamaguchi, Satoshi, Migitaka, Masatoshi

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