Epilepsia Partialis Continua as an Early Sign of Anti-Myelin Oligodendrocyte Glycoprotein Antibody-positive Encephalitis von Katsuse, Kazuto, Shimizu, Genki, Sato, Naoko Saito, Hatano, Keiko, Yagi, Shintaro, Kimura, Toshikazu, Irie, Koreaki, Ichi, Shunsuke, Takahashi, Toshiyuki, Hashida, Hideji

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Randomized, double‐blind, placebo‐controlled phase 1 study to evaluate the safety and pharmacokinetics of high doses of ubiquinol in healthy adults von Mitsui, Jun, Matsukawa, Takashi, Tanaka, Masaki, Saito‐Sato, Naoko, Nakamoto, Fumiko Kusunoki, Yasuda, Tsutomu, Naruse, Hiroya, Matsukawa, Miho Kawabe, Ishiura, Hiroyuki, Nagase, Midori, Yamamoto, Yorihiro, Kuzuyama, Haruko, Wada, Ikue, Ga, Toshio, Yamazaki, Tsutomu, Moritoyo, Takashi, Tsuji, Shoji

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Case report: Adult case of A20 haploinsufficiency suspected as neuro-Behçet disease von Shirai, Harumi, Saito-Sato, Naoko, Horiuchi, Emiko, Kikuchi, Hirotoshi, Kadowaki, Saori, Ohnishi, Hidenori, Suzuki, Takeshi

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Myocardial ultrastructure can augment genetic testing for sporadic dilated cardiomyopathy with initial heart failure von Saito, Tsunenori, Sato, Naoko Saito, Mozawa, Kosuke, Adachi, Akiko, Sasaki, Yoshihiro, Nakamura, Kotoka, Oka, Eiichiro, Otsuka, Toshiaki, Kodani, Eitaro, Asai, Kuniya, Mizuno, Kyoichi, Shimizu, Wataru, Gottlieb, Roberta A.

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Partial duplication of DHH causes minifascicular neuropathy von Sato, Naoko Saito, Maekawa, Risa, Ishiura, Hiroyuki, Mitsui, Jun, Naruse, Hiroya, Tokushige, Shin‐ichi, Sugie, Kazuma, Tate, Genshu, Shimizu, Jun, Goto, Jun, Tsuji, Shoji, Shiio, Yasushi

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Spinal Cord Infarction in a Patient with Immune Thrombocytopenic Purpura von Orimo, Kenta, Ogura, Mizuki, Hatano, Keiko, Saito-Sato, Naoko, Nakayama, Hideki, Ishida, Tadao, Hashida, Hideji

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Epilepsia Partialis Continua as an Early Sign of Anti-Myelin Oligodendrocyte Glycoprotein Antibody-positive Encephalitis von Katsuse, Kazuto, Shimizu, Genki, Sato, Naoko Saito, Hatano, Keiko, Yagi, Shintaro, Kimura, Toshikazu, Irie, Koreaki, Ichi, Shunsuke, Takahashi, Toshiyuki, Hashida, Hideji

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Abstract 15050: Dilated Cardiomyopathy Includes Arrhythmogenic Cardiomyopathy as a Type With Severe Myocardial Degeneration von Mozawa, Kosuke, Saito, Tsunenori, Oka, Eiichiro, Saito-Sato, Naoko, Kodani, Eitaro, Iwasaki, Yu-ki, Asai, Kuniya, Shimizu, Wataru

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Abstract 10660: Comparison Between Ultrastructural Features and Causative Genes of Dilated Cardiomyopathy Detected by Whole Exome Sequencing von Saito, Tsunenori, Asai, Kuniya, Saito-Sato, Naoko, Mozawa, Kosuke, Oka, Eiichiro, Sato, Shigeru, Mizuno, Kyoichi, Gottlieb, Roberta A, Shimizu, Wataru

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Partial duplication of DHH causes minifascicular neuropathy: A novel mutation detection of DHH von Sato, Naoko Saito, Maekawa, Risa, Ishiura, Hiroyuki, Mitsui, Jun, Naruse, Hiroya, Tokushige, Shin-Ichi, Sugie, Kazuma, Tate, Genshu, Shimizu, Jun, Goto, Jun, Tsuji, Shoji, Shiio, Yasushi

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Partial duplication of DHH causes minifascicular neuropathy: A novel mutation detection of von Sato, Naoko Saito, Maekawa, Risa, Ishiura, Hiroyuki, Mitsui, Jun, Naruse, Hiroya, Tokushige, Shin‐ichi, Sugie, Kazuma, Tate, Genshu, Shimizu, Jun, Goto, Jun, Tsuji, Shoji, Shiio, Yasushi

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Atypical parkinsonism caused by Pro105Leu mutation of prion protein: A broad clinical spectrum von Mano, Kagari Koshi, Matsukawa, Takashi, Mitsui, Jun, Ishiura, Hiroyuki, Tokushige, Shin-Ichi, Takahashi, Yuji, Sato, Naoko Saito, Nakamoto, Fumiko Kusunoki, Ichikawa, Yaeko, Nagashima, Yu, Terao, Yasuo, Shimizu, Jun, Hamada, Masashi, Uesaka, Yoshikazu, Oyama, Genko, Ogawa, Go, Yoshimura, Jun, Doi, Koichiro, Morishita, Shinichi, Tsuji, Shoji, Goto, Jun

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Spinal Cord Infarction in a Patient with Immune Thrombocytopenic Purpura von Orimo, Kenta, Ogura, Mizuki, Hatano, Keiko, Saito-Sato, Naoko, Nakayama, Hideki, Ishida, Tadao, Hashida, Hideji

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