Proteomic Profiling of Exosomal Proteins for Blood-based Biomarkers in Parkinson's Disease von Kitamura, Yuki, Kojima, Midori, Kurosawa, Toshihito, Sasaki, Ryogen, Ichihara, Sahoko, Hiraku, Yusuke, Tomimoto, Hidekazu, Murata, Mariko, Oikawa, Shinji

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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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Expression of Mutant Ubiquitin and Proteostasis Impairment in Kii Amyotrophic Lateral Sclerosis/Parkinsonism-Dementia Complex Brains von Verheijen, Bert M, Morimoto, Satoru, Sasaki, Ryogen, Oyanagi, Kiyomitsu, Kokubo, Yasumasa, Kuzuhara, Shigeki, van Leeuwen, Fred W

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EF hand‐like motif mutations of Nav1.4 C‐terminus cause myotonic syndrome by impairing fast inactivation von Horie, Riho, Kubota, Tomoya, Koh, Jinsoo, Tanaka, Rieko, Nakamura, Yuichiro, Sasaki, Ryogen, Ito, Hidefumi, Takahashi, Masanori P.

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An immigrant family with Kii amyotrophic lateral sclerosis/parkinsonism–dementia complex von Kokubo, Yasumasa, Morimoto, Satoru, Sasaki, Ryogen, Hasegawa, Masato, Ishiura, Hiroyuki, Tsuji, Shoji, Yoshida, Mari, Yamazoe, Naohisa, Miyazaki, Mitsukazu, Kuzuhara, Shigeki

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Chronic cerebral hypoperfusion upregulates leptin receptor expression in astrocytes and tau phosphorylation in tau transgenic mice von Shimada, Takuya, Shindo, Akihiro, Matsuyama, Hirofumi, Yata, Kenichiro, Niwa, Atsushi, Sasaki, Ryogen, Ayaki, Takashi, Maki, Takakuni, Wakita, Hideaki, Tomimoto, Hidekazu

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Chronic cerebral ischemia induces redistribution and abnormal phosphorylation of transactivation-responsive DNA-binding protein-43 in mice von Shindo, Akihiro, Yata, Kenichiro, Sasaki, Ryogen, Tomimoto, Hidekazu

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Initial Result of Stroke Care at the Stroke Center in a New Hospital Opened by the Merger of Three Facilities with Different Management Bases: Effect of Stroke Center on Mechanical... von Sakaida, Hiroshi, Goto, Fuki, Yamamoto, Atsushi, Hamada, Kazuhide, Kuroki, Katsura, Furuta, Tomoyuki, Odachi, Kiyomi, Sasaki, Ryogen, Furukawa, Kazuhiro, Nakajima, Yuki, Arikawa, Shigeo

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Comparison of Premortem Magnetic Resonance Imaging and Postmortem Autopsy Findings of a Cortical Microinfarct von Ishikawa, Hidehiro, Ii, Yuichiro, Niwa, Atsushi, Shindo, Akihiro, Ito, Ai, Matsuura, Keita, Sasaki, Ryogen, Uno, Kenichiro, Maeda, Masayuki, Tomimoto, Hidekazu

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Ustekinumab improves psoriasis without altering T cell cytokine production, differentiation, and T cell receptor repertoire diversity von Tsuda, Kenshiro, Yamanaka, Keiichi, Kondo, Makoto, Matsubara, Kimiko, Sasaki, Ryogen, Tomimoto, Hidekazu, Gabazza, Esteban C, Mizutani, Hitoshi

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Astrocytic neuroprotection through induction of cytoprotective molecules; a proteomic analysis of mutant P301S tau-transgenic mouse von Yata, Kenichiro, Oikawa, Shinji, Sasaki, Ryogen, Shindo, Akihiro, Yang, Rong, Murata, Mariko, Kanamaru, Kenji, Tomimoto, Hidekazu

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Induction of IL-10–producing regulatory T cells with TCR diversity by epitope-specific immunotherapy in pollinosis von Yamanaka, Kei-ichi, MD, Yuta, Atsushi, MD, Kakeda, Masato, MD, Sasaki, Ryogen, MD, Kitagawa, Hiroshi, MD, Gabazza, Esteban C., MD, Okubo, Kimihiro, MD, Kurokawa, Ichiro, MD, Mizutani, Hitoshi, MD

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New mutation of the Na channel in the severe form of potassium-aggravated myotonia von Kubota, Tomoya, Kinoshita, Masanobu, Sasaki, Ryogen, Aoike, Futoshi, Takahashi, Masanori P., Sakoda, Saburo, Hirose, Kazuhiko

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Teaching Video NeuroImage: Carbamazepine Improves Gait Initiation in Autosomal Recessive Myotonia Congenita von Fuseya, Yasuhiro, Ishikawa, Nana, Sasaki, Ryogen, Yamashita, Hirofumi

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Familial amyotrophic lateral sclerosis and parkinsonism-dementia complex of the Kii peninsula of Japan: Clinical and neuropathological study and tau analysis von Kuzuhara, Shigeki, Kokubo, Yasumasa, Sasaki, Ryogen, Narita, Yugo, Yabana, Tadashi, Hasegawa, Masato, Iwatsubo, Takeshi

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APOE Alleles With Tau and Aβ Pathology in Patients With Amyotrophic Lateral Sclerosis and Parkinsonism-Dementia Complex in the Kii Peninsula von Sasaki, Ryogen, Morimoto, Satoru, Ozawa, Fumiko, Okano, Hideyuki, Yoshida, Mari, Ishiura, Hiroyuki, Tsuji, Shoji, Kuzuhara, Shigeki, Kokubo, Yasumasa

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APOE Alleles With Tau and Aβ Pathology In Patients With Amyotrophic Lateral Sclerosis and Parkinsonism-Dementia Complex in the Kii Peninsula von Sasaki, Ryogen, Morimoto, Satoru, Ozawa, Fumiko, Okano, Hideyuki, Yoshida, Mari, Ishiura, Hiroyuki, Tsuji, Shoji, Kuzuhara, Shigeki, Kokubo, Yasumasa

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Mutation spectrum and health status in skeletal muscle channelopathies in Japan von Sasaki, Ryogen, Nakaza, Maki, Furuta, Mitsuru, Fujino, Haruo, Kubota, Tomoya, Takahashi, Masanori P.

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Analysis of the genetic background associated with sporadic periodic paralysis in Japanese patients von Nakaza, Maki, Kitamura, Yuri, Furuta, Mitsuru, Kubota, Tomoya, Sasaki, Ryogen, Takahashi, Masanori P.

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PLA2G6 variant in Parkinson's disease von Tomiyama, Hiroyuki, Yoshino, Hiroyo, Ogaki, Kotaro, Li, Lin, Yamashita, Chikara, Li, Yuanzhe, Funayama, Manabu, Sasaki, Ryogen, Kokubo, Yasumasa, Kuzuhara, Shigeki, Hattori, Nobutaka

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