Molecular genetics of Parkinson's disease: Contributions and global trends von Funayama, Manabu, Nishioka, Kenya, Li, Yuanzhe, Hattori, Nobutaka

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Erratum to: Homozygous alpha-synuclein p.A53V in familial Parkinson’s disease von Nishioka, Kenya

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Radiation-induced Brain Calcification Leads to L-dopa-resistant Parkinsonism and Cerebellar Ataxia von Shimada, Tomoyo, Kamo, Ryota, Daida, Kensuke, Nishioka, Kenya, Hattori, Nobutaka, Tsunemi, Taiji

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Music Intervention Reduces Persistent Fibromyalgia Pain and Alters Functional Connectivity Between the Insula and Default Mode Network von Usui, Chie, Kirino, Eiji, Tanaka, Shoji, Inami, Rie, Nishioka, Kenya, Hatta, Kotaro, Nakajima, Toshihiro, Nishioka, Kusuki, Inoue, Reiichi

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Parkinsonism Relating to Intoxication with Glyphosate von Eriguchi, Makoto, Iida, Kotaro, Ikeda, Shuhei, Osoegawa, Manabu, Nishioka, Kenya, Hattori, Nobutaka, Nagayama, Hiroshi, Hara, Hideo

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Motor neuron TDP-43 proteinopathy in progressive supranuclear palsy and corticobasal degeneration von Riku, Yuichi, Iwasaki, Yasushi, Ishigaki, Shinsuke, Akagi, Akio, Hasegawa, Masato, Nishioka, Kenya, Li, Yuanzhe, Riku, Miho, Ikeuchi, Takeshi, Fujioka, Yusuke, Miyahara, Hiroaki, Sone, Jun, Hattori, Nobutaka, Yoshida, Mari, Katsuno, Masahisa, Sobue, Gen

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CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study von Funayama, Manabu, PhD, Ohe, Kenji, MD, Amo, Taku, PhD, Furuya, Norihiko, PhD, Yamaguchi, Junji, MSc, Saiki, Shinji, MD, Li, Yuanzhe, MD, Ogaki, Kotaro, MD, Ando, Maya, MD, Yoshino, Hiroyo, PhD, Tomiyama, Hiroyuki, MD, Nishioka, Kenya, MD, Hasegawa, Kazuko, MD, Saiki, Hidemoto, MD, Satake, Wataru, MD, Mogushi, Kaoru, PhD, Sasaki, Ryogen, MD, Kokubo, Yasumasa, Prof, Kuzuhara, Shigeki, Prof, Toda, Tatsushi, Prof, Mizuno, Yoshikuni, Prof, Uchiyama, Yasuo, Prof, Ohno, Kinji, Prof, Hattori, Nobutaka, Prof

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Homozygous alpha-synuclein p.A53V in familial Parkinson’s disease von Yoshino, Hiroyo, PhD, Hirano, Makito, MD, PhD, Stoessl, A. Jon, MD, Imamichi, Yoko, BS, Ikeda, Aya, MD, Li, Yuanzhe, MD, PhD, Funayama, Manabu, PhD, Yamada, Ikuko, MD, PhD, Nakamura, Yusaku, MD, PhD, Sossi, Vesna, PhD, Farrer, Matthew J., PhD, Nishioka, Kenya, MD, PhD, Hattori, Nobutaka, MD, PhD

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Variants in saposin D domain of prosaposin gene linked to Parkinson's disease von Oji, Yutaka, Hatano, Taku, Ueno, Shin-Ichi, Funayama, Manabu, Ishikawa, Kei-Ichi, Okuzumi, Ayami, Noda, Sachiko, Sato, Shigeto, Satake, Wataru, Toda, Tatsushi, Li, Yuanzhe, Hino-Takai, Tomoko, Kakuta, Soichiro, Tsunemi, Taiji, Yoshino, Hiroyo, Nishioka, Kenya, Hattori, Tatsuya, Mizutani, Yasuaki, Mutoh, Tatsuro, Yokochi, Fusako, Ichinose, Yuta, Koh, Kishin, Shindo, Kazumasa, Takiyama, Yoshihisa, Hamaguchi, Tsuyoshi, Yamada, Masahito, Farrer, Matthew J, Uchiyama, Yasuo, Akamatsu, Wado, Wu, Yih-Ru, Matsuda, Junko, Hattori, Nobutaka

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Crossed cerebellar diaschisis in Creutzfeldt-Jakob disease evaluated through single photon emission computed tomography von Nishioka, Kenya, Suzuki, Michimasa, Satoh, Katsuya, Hattori, Nobutaka

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Analysis of LIN28A variants in patients with Parkinson's disease von Peng, Hao, Li, Yuanzhe, Yoshino, Hiroyo, Shimizu, Mai, Nishioka, Kenya, Funayama, Manabu, Hattori, Nobutaka

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An Epidemiologic Internet Survey of Fibromyalgia and Chronic Pain in Japan von Nakamura, Ikuro, Nishioka, Kenya, Usui, Chie, Osada, Kenichi, Ichibayashi, Hisao, Ishida, Mitsuhiro, Turk, Dennis C., Matsumoto, Yoshifuji, Nishioka, Kusuki

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The absence of orthostatic heart rate increase is associated with cognitive impairment in Parkinson's disease von Tanaka, Ryota, Yamashiro, Kazuo, Ogawa, Takashi, Oyama, Genko, Nishioka, Kenya, Umemura, Atsushi, Shimo, Yasushi, Hattori, Nobutaka

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Genetic analysis of ATP10B for Parkinson's disease in Japan von Ishiguro, Mayu, Yoshino, Hiroyo, Li, Yuanzhe, Ikeda, Aya, Funayama, Manabu, Nishioka, Kenya, Hattori, Nobutaka

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DNAJC12 and dopa‐responsive nonprogressive parkinsonism von Straniero, Letizia, Guella, Ilaria, Cilia, Roberto, Parkkinen, Laura, Rimoldi, Valeria, Young, Alexander, Asselta, Rosanna, Soldà, Giulia, Sossi, Vesna, Stoessl, A. Jon, Priori, Alberto, Nishioka, Kenya, Hattori, Nobutaka, Follett, Jordan, Rajput, Alex, Blau, Nenad, Pezzoli, Gianni, Farrer, Matthew J., Goldwurm, Stefano, Rajput, Ali H., Duga, Stefano

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Clinical characterization of patients with leucine-rich repeat kinase 2 genetic variants in Japan von Li, Yuanzhe, Ikeda, Aya, Yoshino, Hiroyo, Oyama, Genko, Kitani, Mitsuhiro, Daida, Kensuke, Hayashida, Arisa, Ogaki, Kotaro, Yoshida, Kousuke, Kimura, Takashi, Nakayama, Yoshiaki, Ito, Hidefumi, Sugeno, Naoto, Aoki, Masashi, Miyajima, Hiroaki, Kimura, Katsuo, Ueda, Naohisa, Watanabe, Masao, Urabe, Takao, Takanashi, Masashi, Funayama, Manabu, Nishioka, Kenya, Hattori, Nobutaka

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Clinical characteristics and pathophysiological properties of newly discovered LRRK2 variants associated with Parkinson's disease von Tezuka, Toshiki, Ishiguro, Mayu, Taniguchi, Daisuke, Osogaguchi, Ehoto, Shiba-Fukushima, Kahori, Ogata, Jun, Ishii, Ryota, Ikeda, Aya, Li, Yuanzhe, Yoshino, Hiroyo, Matsui, Taro, Kaida, Kenichi, Funayama, Manabu, Nishioka, Kenya, Kumazawa, Fumihisa, Matsubara, Tomoyasu, Tsuda, Hitoshi, Saito, Yuko, Murayama, Shigeo, Imai, Yuzuru, Hattori, Nobutaka

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Clinical Manifestations and Molecular Backgrounds of Parkinson's Disease Regarding Genes Identified From Familial and Population Studies von Nishioka, Kenya, Imai, Yuzuru, Yoshino, Hiroyo, Li, Yuanzhe, Funayama, Manabu, Hattori, Nobutaka

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Generation of three clones (JUCGRMi002-A, B, C) of induced pluripotent stem cells from a Parkinson’s disease patient with SNCA duplication von Ishikawa, Kei-ichi, Shiga, Takahiro, Yoshino, Hiroyo, Nishioka, Kenya, Hattori, Nobutaka, Akamatsu, Wado

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A Novel LRRK2 Variant p.G2294R in the WD40 Domain Identified in Familial Parkinson's Disease Affects LRRK2 Protein Levels von Ogata, Jun, Hirao, Kentaro, Nishioka, Kenya, Hayashida, Arisa, Li, Yuanzhe, Yoshino, Hiroyo, Shimizu, Soichiro, Hattori, Nobutaka, Imai, Yuzuru

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