The reliability and validity of joint range of motion measurement using zoom and a smartphone application von Tozawa, Ryosuke, Ishii, Narumi, Onuma, Ryo, Kawasaki, Tsubasa

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Dietary Fructo-Oligosaccharides Attenuate Early Activation of CD4+ T Cells Which Produce both Th1 and Th2 Cytokines in the Intestinal Lymphoid Tissues of a Murine Food Allergy Mode... von Tsuda, Masato, Arakawa, Haruka, Ishii, Narumi, Ubukata, Chihiro, Michimori, Mana, Noda, Masanari, Takahashi, Kyoko, Kaminogawa, Shuichi, Hosono, Akira

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Weight Perception and Diet Behavior of Japanese and Russian Adolescent Girls von Inaba, Hiromi, Rziankina, Marina F., Kostromina, Svetlana A., Sakauchi, Genki, Ito, Reina, Kaiwa, Misaki, Natsui, Saya, Ishii, Narumi, Saito, Toshiko, Takano, Kousuke, Zhmerenetsky, Konstantin V., Ishigami, Kazuo

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GnRH(1-5), a metabolite of gonadotropin-releasing hormone, enhances luteinizing hormone release via activation of kisspeptin neurons in female rats von Ieda, Nahoko, Assadullah, Minabe, Shiori, Ikegami, Kana, Watanabe, Youki, Sugimoto, Yusuke, Sugimoto, Arisa, Kawai, Narumi, Ishii, Hirotaka, Inoue, Naoko, Uenoyama, Yoshihisa, Tsukamura, Hiroko

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Response to Letter to the Editor From Janot et al: “Single-Exon Deletions of ZNRF3 Exon 2 Cause Congenital Adrenal Hypoplasia” von Amano, Naoko, Narumi, Satoshi, Ishii, Tomohiro, Hasegawa, Tomonobu

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Effective situation-based delirium simulation training using flipped classroom approach to improve interprofessional collaborative practice competency: a mixed-methods study von Shikino, Kiyoshi, Ide, Narumi, Kubota, Yoko, Ishii, Itsuko, Ito, Shoichi, Ikusaka, Masatomi, Sakai, Ikuko

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GWAS of thyroid dysgenesis identifies a risk locus at 2q33.3 linked to regulation of Wnt signaling von Narumi, Satoshi, Opitz, Robert, Nagasaki, Keisuke, Muroya, Koji, Asakura, Yumi, Adachi, Masanori, Abe, Kiyomi, Sugisawa, Chiho, Kühnen, Peter, Ishii, Tomohiro, Nöthen, Markus M, Krude, Heiko, Hasegawa, Tomonobu

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Efficacy and tolerability of 100 mg of lasmiditan for migraine: A multi-center, prospective observational real-world study in Japan von Ishii, Ryotaro, Ishizuchi, Kei, Watanabe, Narumi, Fukazawa, Ryosuke, Trivedi, Meesha, Nakahara, Jin, Takizawa, Tsubasa

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Single-Exon Deletions of ZNRF3 Exon 2 Cause Congenital Adrenal Hypoplasia von Amano, Naoko, Narumi, Satoshi, Aizu, Katsuya, Miyazawa, Mari, Okamura, Kohji, Ohashi, Hirofumi, Katsumata, Noriyuki, Ishii, Tomohiro, Hasegawa, Tomonobu

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Letter to the Editor regarding “Serum steroid metabolite profiling by LC-MS/MS in two phenotypic male patients with HSD17B3 deficiency: Implications for hormonal diagnosis” von Sato, Takeshi, Nakano, Satsuki, Honda, Misa, Narumi, Satoshi, Ishii, Tomohiro, Hasegawa, Tomonobu

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Association Between Sarcopenia And Brain Amyloid-Β Positivity Among Community-dwelling Older Adults: 328 von Ohta, Takahisa, Shida, Takashi, Kojima, Narumi, Osuka, Yosuke, Ishii, Kenji, Shinkai, Shoji, Kim, Hunkyung, Tanaka, Kiyoji, Sasai, Hiroyuki

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Design of an apertureless two-stage acceleration lens for a single-ion implantation system von Ishii, Y., Ohkubo, T., Miyawaki, N., Yuri, Y., Onoda, S., Narumi, K., Saitoh, Y.

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Genetic defects in pediatric-onset adrenal insufficiency in Japan von Amano, Naoko, Narumi, Satoshi, Hayashi, Mie, Takagi, Masaki, Imai, Kazuhide, Nakamura, Toshiro, Hachiya, Rumi, Sasaki, Goro, Homma, Keiko, Ishii, Tomohiro, Hasegawa, Tomonobu

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MIRAGE syndrome is a rare cause of 46,XY DSD born SGA without adrenal insufficiency von Shima, Hirohito, Hayashi, Mie, Tachibana, Takashi, Oshiro, Makoto, Amano, Naoko, Ishii, Tomohiro, Haruna, Hidenori, Igarashi, Maki, Kon, Masafumi, Fukuzawa, Ryuji, Tanaka, Yukichi, Fukami, Maki, Hasegawa, Tomonobu, Narumi, Satoshi

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Calculation study of selective ion extraction from ion source with Paul-trap-type laser cooling device von Miyawaki, Nobumasa, Ishii, Yasuyuki, Yuri, Yosuke, Narumi, Kazumasa, Muroo, Kento, Ito, Kiyokazu, Okamoto, Hiromi

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Parathyroid adenoma with a somatic CASR pathogenic variant: A pediatric case report von Kawata, Kento, Sato, Takeshi, Honda, Misa, Narumi, Satoshi, Kameyama, Kaori, Ishii, Tomohiro, Hasegawa, Tomonobu

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SAMD9 mutations cause a novel multisystem disorder, MIRAGE syndrome, and are associated with loss of chromosome 7 von Narumi, Satoshi, Amano, Naoko, Ishii, Tomohiro, Katsumata, Noriyuki, Muroya, Koji, Adachi, Masanori, Toyoshima, Katsuaki, Tanaka, Yukichi, Fukuzawa, Ryuji, Miyako, Kenichi, Kinjo, Saori, Ohga, Shouichi, Ihara, Kenji, Inoue, Hirosuke, Kinjo, Tadamune, Hara, Toshiro, Kohno, Miyuki, Yamada, Shiro, Urano, Hironaka, Kitagawa, Yosuke, Tsugawa, Koji, Higa, Asumi, Miyawaki, Masakazu, Okutani, Takahiro, Kizaki, Zenro, Hamada, Hiroyuki, Kihara, Minako, Shiga, Kentaro, Yamaguchi, Tetsuya, Kenmochi, Manabu, Kitajima, Hiroyuki, Fukami, Maki, Shimizu, Atsushi, Kudoh, Jun, Shibata, Shinsuke, Okano, Hideyuki, Miyake, Noriko, Matsumoto, Naomichi, Hasegawa, Tomonobu

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Quantitative and sensitive detection of GNAS mutations causing mccune-albright syndrome with next generation sequencing von Narumi, Satoshi, Matsuo, Kumihiro, Ishii, Tomohiro, Tanahashi, Yusuke, Hasegawa, Tomonobu

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A novel missense variant of FGFR1 in a Japanese girl with Kallmann syndrome and holoprosencephaly von Uchida, Noboru, Mizuno, Yusuke, Seno, Shohei, Koyama, Yutaro, Takahashi, Tsutomu, Shibata, Hironori, Narumi, Satoshi, Hasegawa, Tomonobu, Ishii, Tomohiro

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Genetic and Clinical Characteristics of 185 Japanese Children with 46,XY Differences of Sex Development von Hayashi, Mie, Narumi, Satoshi, Sato, Takeshi, Amano, Naoko, Suwanai, Ayuko Suzuki, Haruna, Hidenori, Muroya, Koji, Adachi, Masanori, Asanuma, Hiroshi, Ohashi, Hirofumi, Ishii, Tomohiro, Hasegawa, Tomonobu

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