BOTTLED CARBONATED BEVERAGE WITH ENHANCED DEPTH AND COMPLEXITY OF FLAVOR, AND MANUFACTURING METHOD THEREFOR von CHEN NEISHIN, KUMADA NORIKO, NAGAI MAKI

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BUBBLE-CONTAINING BEVERAGE UTILIZING HIGH CO2 CONTENT ICE, AND METHOD FOR PRODUCING SAME von SATO, Ai, KUMADA, Noriko

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SODIUM-CONTAINING PACKED BEVERAGE von KUMADA NORIKO, GOTO TAKETOMO, WATANABE ASUKA, YOTSUMOTO YUKO, KUWAKO KAZUHIRO

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ALCOHOLIC BEVERAGE WITH IMPROVED RICH TASTE AND METHOD FOR PRODUCING THE SAME von KUMADA NORIKO, TABOKU KYOKO, OGAWA KAORI, ARITA ASAMI, KOIZUMI KUMIKO, MASUDA HARUKA, WEI DANDAN, ODAI HIDEHARU

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CITRUS-FLAVORED ALCOHOLIC BEVERAGE CONTAINING FERMENTED FRUIT JUICE von IKEDA SATOSHI, NAKAJIMA KEIKO, KUMADA NORIKO, OGAWA KAORI, WEI DANDAN, CHAGI KAORI, HASEDA KEISUKE, MASUZAKI RURIKO, ODAI HIDEHARU

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FOOD EXPANSION AGENT von KUMADA NORIKO, EGUCHI KEIKO, SATO AI

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Biobank Establishment and Sample Management in the Tohoku Medical Megabank Project von Minegishi, Naoko, Nishijima, Ichiko, Nobukuni, Takahiro, Kudo, Hisaaki, Ishida, Noriko, Terakawa, Takahiro, Kumada, Kazuki, Yamashita, Riu, Katsuoka, Fumiki, Ogishima, Soichi, Suzuki, Kichiya, Sasaki, Makoto, Satoh, Mamoru, Tohoku Medical Megabank Project Study Group, Yamamoto, Masayuki

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De novo mutations in the autophagy gene WDR45 cause static encephalopathy of childhood with neurodegeneration in adulthood von Saitsu, Hirotomo, Nishimura, Taki, Muramatsu, Kazuhiro, Kodera, Hirofumi, Kumada, Satoko, Sugai, Kenji, Kasai-Yoshida, Emi, Sawaura, Noriko, Nishida, Hiroya, Hoshino, Ai, Ryujin, Fukiko, Yoshioka, Seiichiro, Nishiyama, Kiyomi, Kondo, Yukiko, Tsurusaki, Yoshinori, Nakashima, Mitsuko, Miyake, Noriko, Arakawa, Hirokazu, Kato, Mitsuhiro, Mizushima, Noboru, Matsumoto, Naomichi

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Novel EXOSC9 variants cause pontocerebellar hypoplasia type 1D with spinal motor neuronopathy and cerebellar atrophy von Sakamoto, Masamune, Iwama, Kazuhiro, Sekiguchi, Futoshi, Mashimo, Hideaki, Kumada, Satoko, Ishigaki, Keiko, Okamoto, Nobuhiko, Behnam, Mahdiyeh, Ghadami, Mohsen, Koshimizu, Eriko, Miyatake, Satoko, Mitsuhashi, Satomi, Mizuguchi, Takeshi, Takata, Atsushi, Saitsu, Hirotomo, Miyake, Noriko, Matsumoto, Naomichi

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Identification of Dominant Transcripts in Oxidative Stress Response by a Full-Length Transcriptome Analysis von Otsuki, Akihito, Okamura, Yasunobu, Aoki, Yuichi, Ishida, Noriko, Kumada, Kazuki, Minegishi, Naoko, Katsuoka, Fumiki, Kinoshita, Kengo, Yamamoto, Masayuki

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De novo hotspot variants in CYFIP2 cause early‐onset epileptic encephalopathy von Nakashima, Mitsuko, Kato, Mitsuhiro, Aoto, Kazushi, Shiina, Masaaki, Belal, Hazrat, Mukaida, Souichi, Kumada, Satoko, Sato, Atsushi, Zerem, Ayelet, Lerman‐Sagie, Tally, Lev, Dorit, Leong, Huey Yin, Tsurusaki, Yoshinori, Mizuguchi, Takeshi, Miyatake, Satoko, Miyake, Noriko, Ogata, Kazuhiro, Saitsu, Hirotomo, Matsumoto, Naomichi

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Whole blood transcriptome analysis for age- and gender-specific gene expression profiling in Japanese individuals von Aoki, Yu-Ichi, Taguchi, Keiko, Anzawa, Hayato, Kawashima, Junko, Ishida, Noriko, Otuki, Akihito, Hasegawa, Atsushi, Baird, Liam, Suzuki, Takafumi, Motoike, Ikuko N, Ohneda, Kinuko, Kumada, Kazuki, Katsuoka, Fumiki, Kinoshita, Kengo, Yamamoto, Masayuki

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A summary of the Clinical Practice Guideline for the Diagnosis and Management of Voice Disorders, 2018 in Japan von Umeno, Hirohito, Hyodo, Masamitsu, Haji, Tomoyuki, Hara, Hirotaka, Imaizumi, Mitsuyoshi, Ishige, Miyoko, Kumada, Masanobu, Makiyama, Kiyoshi, Nishizawa, Noriko, Saito, Koichiro, Shiromoto, Osamu, Suehiro, Atsushi, Takahashi, Goro, Tateya, Ichiro, Tsunoda, Koichi, Shiotani, Akihiro, Omori, Koichi

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Landscape of electrophilic and inflammatory stress-mediated gene regulation in human lymphoblastoid cell lines von Ishida, Noriko, Aoki, Yuichi, Katsuoka, Fumiki, Nishijima, Ichiko, Nobukuni, Takahiro, Anzawa, Hayato, Bin, Li, Tsuda, Miyuki, Kumada, Kazuki, Kudo, Hisaaki, Terakawa, Takahiro, Otsuki, Akihito, Kinoshita, Kengo, Yamashita, Riu, Minegishi, Naoko, Yamamoto, Masayuki

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A practical program for responding to epileptic seizures including buccal midazolam administration in schools: Effectiveness evaluation for Yogo teachers in Japan von Ozawa, Noriko, Tomisaki, Etsuko, Sou, Hikaru, Miyagawa, Shoko, Yoshioka, Junki, Horie, Hiroko, Kandatsu, Ayaka, Deguchi, Naoko Kumada, Soeda, Etsuko

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Usefulness of Attenuation Imaging with an Ultrasound Scanner for the Evaluation of Hepatic Steatosis von Tada, Toshifumi, Iijima, Hiroko, Kobayashi, Natsuko, Yoshida, Masahiro, Nishimura, Takashi, Kumada, Takashi, Kondo, Reiichiro, Yano, Hirohisa, Kage, Masayoshi, Nakano, Chikage, Aoki, Tomoko, Aizawa, Nobuhiro, Ikeda, Naoto, Takashima, Tomoyuki, Yuri, Yukihisa, Ishii, Noriko, Hasegawa, Kunihiro, Takata, Ryo, Yoh, Kazunori, Sakai, Yoshiyuki, Nishikawa, Hiroki, Iwata, Yoshinori, Enomoto, Hirayuki, Hirota, Seiichi, Fujimoto, Jiro, Nishiguchi, Shuhei

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De Novo Mutations in GNAO1, Encoding a Gαo Subunit of Heterotrimeric G Proteins, Cause Epileptic Encephalopathy von Nakamura, Kazuyuki, Kodera, Hirofumi, Akita, Tenpei, Shiina, Masaaki, Kato, Mitsuhiro, Hoshino, Hideki, Terashima, Hiroshi, Osaka, Hitoshi, Nakamura, Shinichi, Tohyama, Jun, Kumada, Tatsuro, Furukawa, Tomonori, Iwata, Satomi, Shiihara, Takashi, Kubota, Masaya, Miyatake, Satoko, Koshimizu, Eriko, Nishiyama, Kiyomi, Nakashima, Mitsuko, Tsurusaki, Yoshinori, Miyake, Noriko, Hayasaka, Kiyoshi, Ogata, Kazuhiro, Fukuda, Atsuo, Matsumoto, Naomichi, Saitsu, Hirotomo

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Microarray analysis of 50 patients reveals the critical chromosomal regions responsible for 1p36 deletion syndrome-related complications von Shimada, Shino, Shimojima, Keiko, Okamoto, Nobuhiko, Sangu, Noriko, Hirasawa, Kyoko, Matsuo, Mari, Ikeuchi, Mayo, Shimakawa, Shuichi, Shimizu, Kenji, Mizuno, Seiji, Kubota, Masaya, Adachi, Masao, Saito, Yoshiaki, Tomiwa, Kiyotaka, Haginoya, Kazuhiro, Numabe, Hironao, Kako, Yuko, Hayashi, Ai, Sakamoto, Haruko, Hiraki, Yoko, Minami, Koichi, Takemoto, Kiyoshi, Watanabe, Kyoko, Miura, Kiyokuni, Chiyonobu, Tomohiro, Kumada, Tomohiro, Imai, Katsumi, Maegaki, Yoshihiro, Nagata, Satoru, Kosaki, Kenjiro, Izumi, Tatsuro, Nagai, Toshiro, Yamamoto, Toshiyuki

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Genetic and clinical landscape of childhood cerebellar hypoplasia and atrophy von Sakamoto, Masamune, Iwama, Kazuhiro, Sasaki, Masayuki, Ishiyama, Akihiko, Komaki, Hirofumi, Saito, Takashi, Takeshita, Eri, Shimizu-Motohashi, Yuko, Haginoya, Kazuhiro, Kobayashi, Tomoko, Goto, Tomohide, Tsuyusaki, Yu, Iai, Mizue, Kurosawa, Kenji, Osaka, Hitoshi, Tohyama, Jun, Kobayashi, Yu, Okamoto, Nobuhiko, Suzuki, Yume, Kumada, Satoko, Inoue, Kenji, Mashimo, Hideaki, Arisaka, Atsuko, Kuki, Ichiro, Saijo, Harumi, Yokochi, Kenji, Kato, Mitsuhiro, Inaba, Yuji, Gomi, Yuko, Saitoh, Shinji, Shirai, Kentaro, Morimoto, Masafumi, Izumi, Yuishin, Watanabe, Yoriko, Nagamitsu, Shin-ichiro, Sakai, Yasunari, Fukumura, Shinobu, Muramatsu, Kazuhiro, Ogata, Tomomi, Yamada, Keitaro, Ishigaki, Keiko, Hirasawa, Kyoko, Shimoda, Konomi, Akasaka, Manami, Kohashi, Kosuke, Sakakibara, Takafumi, Ikuno, Masashi, Sugino, Noriko, Yonekawa, Takahiro, Gürsoy, Semra, Cinleti, Tayfun, Kim, Chong Ae, Teik, Keng Wee, Yan, Chan Mei, Haniffa, Muzhirah, Ohba, Chihiro, Ito, Shuuichi, Saitsu, Hirotomo, Saida, Ken, Tsuchida, Naomi, Uchiyama, Yuri, Koshimizu, Eriko, Fujita, Atsushi, Hamanaka, Kohei, Misawa, Kazuharu, Miyatake, Satoko, Mizuguchi, Takeshi, Miyake, Noriko, Matsumoto, Naomichi

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Periventricular small cystic lesions in a patient with Coffin-Lowry syndrome who exhibited a novel mutation in the RPS6KA3 gene von Miyata, Yohane, Saida, Ken, Kumada, Satoko, Miyake, Noriko, Mashimo, Hideaki, Nishida, Yuya, Shirai, Ikuko, Kurihara, Eiji, Nakata, Yasuhiro, Matsumoto, Naomichi

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