A PERIOD3 variant causes a circadian phenotype and is associated with a seasonal mood trait von Zhang, Luoying, Hirano, Arisa, Hsu, Pei-Ken, Jones, Christopher R., Sakai, Noriaki, Okuro, Masashi, McMahon, Thomas, Yamazaki, Maya, Xu, Ying, Saigoh, Noriko, Saigoh, Kazumasa, Lin, Shu-Ting, Kaasik, Krista, Nishino, Seiji, Ptáček, Louis J., Fu, Ying-Hui

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CANVAS-related RFC1 mutations in patients with immune-mediated neuropathy von Hirano, Makito, Kuwahara, Motoi, Yamagishi, Yuko, Samukawa, Makoto, Fujii, Kanako, Yamashita, Shoko, Ando, Masahiro, Oka, Nobuyuki, Nagano, Mamoru, Matsui, Taro, Takeuchi, Toshihide, Saigoh, Kazumasa, Kusunoki, Susumu, Takashima, Hiroshi, Nagai, Yoshitaka

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Phenotypic and molecular diversities of spinocerebellar ataxia type 2 in Japan von Inada, Rino, Hirano, Makito, Oka, Nobuyuki, Samukawa, Makoto, Saigoh, Kazumasa, Suzuki, Hidekazu, Udaka, Fukashi, Hashiguchi, Akihiro, Takashima, Hiroshi, Hamada, Yukihiro, Nakamura, Yusaku, Kusunoki, Susumu

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Longitudinal study of primary progressive aphasia in a patient with pathologically diagnosed Alzheimer's disease: a case report von Takaya, Masahiko, Ishii, Kazunari, Saigoh, Kazumasa, Shirakawa, Osamu

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Hemiplegic migraine type 2 with new mutation of the ATP1A2 gene in Japanese cases von Oda, Ituki, Danno, Daisuke, Saigoh, Kazumasa, Wolf, Johanna, Kawashita, Norihito, Hirano, Makito, Samukawa, Makoto, Kitamura, Shigekazu, Kikui, Shoji, Takeshima, Takao, Mitsui, Yoshiyuki, Kusunoki, Susumu, Nagai, Yoshitaka

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A Guillain-Barré syndrome-associated SIGLEC10 rare variant impairs its recognition of gangliosides von Alborzian Deh Sheikh, Amin, Gomaa, Soha, Li, Xuexin, Routledge, Matthew, Saigoh, Kazumasa, Numoto, Nobutaka, Angata, Takashi, Hitomi, Yuki, Takematsu, Hiromu, Tsuiji, Makoto, Ito, Nobutoshi, Kusunoki, Susumu, Tsubata, Takeshi

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Regional gray matter-dedicated SUVR with 3D-MRI detects positive amyloid deposits in equivocal amyloid PET images von Ishii, Kazunari, Yamada, Takahiro, Hanaoka, Kohei, Kaida, Hayato, Miyazaki, Koichi, Ueda, Masami, Hanada, Kazushi, Saigoh, Kazumasa, Sauerbeck, Julia, Rominger, Axel, Bartenstein, Peter, Kimura, Yuichi

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Memantine administration prevented chorea movement in Huntington’s disease: a case report von Saigoh, Kazumasa, Hirano, Makito, Mitsui, Yoshiyuki, Oda, Itsuki, Ikegawa, Atsuko, Samukawa, Makoto, Yoshikawa, Keisuke, Yamagishi, Yuko, Kusunoki, Susumu, Nagai, Yoshitaka

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Effect of expression alteration in flanking genes on phenotypes of St8sia2-deficient mice von Ikegami, Keisuke, Saigoh, Kazumasa, Fujioka, Atsuko, Nagano, Mamoru, Kitajima, Ken, Sato, Chihiro, Masubuchi, Satoru, Kusunoki, Susumu, Shigeyoshi, Yasufumi

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A comparative study of curated contents by knowledge-based curation system in cancer clinical sequencing von Sakai, Kazuko, Takeda, Masayuki, Shimizu, Shigeki, Takahama, Takayuki, Yoshida, Takeshi, Watanabe, Satomi, Iwasa, Tsutomu, Yonesaka, Kimio, Suzuki, Shinichiro, Hayashi, Hidetoshi, Kawakami, Hisato, Nonagase, Yoshikane, Tanaka, Kaoru, Tsurutani, Junji, Saigoh, Kazumasa, Ito, Akihiko, Mitsudomi, Tetsuya, Nakagawa, Kazuhiko, Nishio, Kazuto

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Progressive amnestic cognitive impairment in a middle-aged patient with developmental language disorder: a case report von Takaya, Masahiko, Ishii, Kazunari, Kiguchi, Kaori, Saigoh, Kazumasa, Shirakawa, Osamu

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Diagnosis of Parkinson’s disease and the level of oxidized DJ-1 protein von Yamagishi, Yuko, Saigoh, Kazumasa, Saito, Yoshiro, Ogawa, Ikuko, Mitsui, Yoshiyuki, Hamada, Yukihiro, Samukawa, Makoto, Suzuki, Hidekazu, Kuwahara, Motoi, Hirano, Makito, Noguchi, Noriko, Kusunoki, Susumu

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Lung carcinoma–associated cognitive impairment in a patient with Alzheimer’s disease pathology: A case report von Takigawa, Kiyoto, Takaya, Masahiko, Ishii, Kazunari, Saigoh, Kazumasa, Shirakawa, Osamu

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Chondroitin sulfate β-1,4-N-acetylgalactosaminyltransferase-1 (ChGn-1) polymorphism: Association with progression of multiple sclerosis von Saigoh, Kazumasa, Yoshimura, Satoshi, Izumikawa, Tomomi, Miyata, Shinji, Tabara, Yasuharu, Matsushita, Takuya, Miki, Tetsuro, Miyamoto, Katsuichi, Hirano, Makito, Kitagawa, Hiroshi, Kira, Jun-Ichi, Kusunoki, Susumu

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Chondroitin beta-1,4-N-acetylgalactosaminyltransferase-1 missense mutations are associated with neuropathies von Saigoh, Kazumasa, Izumikawa, Tomomi, Koike, Toshiyasu, Shimizu, Jun, Kitagawa, Hiroshi, Kusunoki, Susumu

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A new mouse allele of glutamate receptor delta 2 with cerebellar atrophy and progressive ataxia von Miyoshi, Yuka, Yoshioka, Yoshichika, Suzuki, Kinuko, Miyazaki, Taisuke, Koura, Minako, Saigoh, Kazumasa, Kajimura, Naoko, Monobe, Yoko, Kusunoki, Susumu, Matsuda, Junichiro, Watanabe, Masahiko, Hayasaka, Naoto

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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 novel de novo mutation of KIF1A gene as the cause for Spastic paraplegia 30 in a Japanese case von Yoshikawa, Keisuke, Kuwahara, Motoi, Saigoh, Kazumasa, Ishiura, Hiroyuki, Yamagishi, Yuko, Hamano, Yuta, Samukawa, Makoto, Suzuki, Hidekazu, Hirano, Makito, Mitsui, Yoshiyuki, Tsuji, Shoji, Kusunoki, Susumu

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Clinical practice guideline for chronic headache 2013 von Araki, Nobuo, Takeshima, Takao, Ando, Naoki, Iizuka, Takahiro, Igarashi, Hisaka, Ikeda, Yukio, Ito, Yasuo, Inagaki, Mieko, Imamura, Keiko, Ohkuma, Hirohisa, Ogawa, Karin, Kato, Yuji, Kikui, Shoji, Kitamura, Takayuki, Kudo, Masako, Kuwabara, Kentaro, Gono, Yukari, Kowa, Hisanori, Saigoh, Kazumasa, Sato, Shinya, Shibata, Koichi, Shibata, Mamoru, Shimazu, Tomokazu, Shimizu, Toshihiko, Suzuki, Michiyasu, Takahashi, Yuji, Takekawa, Hidehiro, Doi, Hikaru, Nagata, Eiichiro, Nakano, Toshiya, Hashizume, Masahiro, Hashimoto, Shiori, Hamada, Junichi, Hirata, Koichi, Fujiki, Naoto, Fujita, Mitsue, Yamane, Kiyomi, Wajima, Koichi, Watanabe, Yuka

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Migraine therapy from the pathogenesis of calcitonin gene–related peptide (CGRP) von Saigoh, Kazumasa

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