Association between treatment for retinopathy of prematurity and blood monocyte counts von Obata, Shumpei, Matsumoto, Riko, Kakinoki, Masashi, Sawada, Osamu, Sawada, Tomoko, Saishin, Yoshitsugu, Yanagi, Takahide, Maruo, Yoshihiro, Ohji, Masahito

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Natural course of congenital hypothyroidism by dual oxidase 2 mutations from the neonatal period through puberty von Maruo, Yoshihiro, Nagasaki, Keisuke, Matsui, Katsuyuki, Mimura, Yu, Mori, Asami, Fukami, Maki, Takeuchi, Yoshihiro

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Genotype of UGT1A1 and phenotype correlation between Crigler-Najjar syndrome type II and Gilbert syndrome von Maruo, Yoshihiro, Nakahara, Sayuri, Yanagi, Takahide, Nomura, Akitaka, Mimura, Yu, Matsui, Katsuyuki, Sato, Hiroshi, Takeuchi, Yoshihiro

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Bilirubin Uridine Diphosphate-glucuronosyltransferase Polymorphism as a Risk Factor for Prolonged Hyperbilirubinemia in Japanese Preterm Infants von Yanagi, Takahide, Nakahara, Sayuri, Maruo, Yoshihiro

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Fasting-associated urticaria and/or anaphylaxis: A case report von Kunitsu, Tomoaki, Ueba, Satoko, Nakajima, Ryo, Nonomura, Kazuo, Maruo, Yoshihiro, Hide, Michihiro

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A nationwide survey of bilirubin encephalopathy in preterm infants in Japan von Okumura, Akihisa, Morioka, Ichiro, Arai, Hiroshi, Hayakawa, Masahiro, Maruo, Yoshihiro, Kusaka, Takashi, Kunikata, Tetsuya, Kumada, Satoko

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Highest concentration of breast‐milk‐derived exosomes in colostrum von Ohta, Motoki, Koshida, Shigeki, Jimbo, Itsuki, Oda, Machi, Inoue, Ryo, Tsukahara, Takamitsu, Terahara, Masaki, Nakamura, Yoshitaka, Maruo, Yoshihiro

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Citrullinated fibrinogen is a target of auto-antibodies in interstitial lung disease in mice with collagen-induced arthritis von Sato, Tomomi, Satooka, Hiroki, Ichioka, Satoko, Maruo, Yoshihiro, Hirata, Takako

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Bilirubin Uridine Diphosphate-Glucuronosyltransferase Variation Is a Genetic Basis of Breast Milk Jaundice von Maruo, Yoshihiro, MD, PhD, Morioka, Yoriko, MD, PhD, Fujito, Hiroshi, MD, Nakahara, Sayuri, MD, Yanagi, Takahide, MD, Matsui, Katsuyuki, MD, PhD, Mori, Asami, MD, PhD, Sato, Hiroshi, PhD, Tukey, Robert H., PhD, Takeuchi, Yoshihiro, MD, PhD

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Contribution of UGT1A1 variations to chemotherapy-induced unconjugated hyperbilirubinemia in pediatric leukemia patients von Nomura, Akitaka, Maruo, Yoshihiro, Taga, Takashi, Takeuchi, Yoshihiro

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The KCNQ channel inhibitor XE991 suppresses nicotinic acetylcholine receptor-mediated responses in rat intracardiac ganglion neurons von Sato, Aya, Kojima, Fumiaki, Hayashi, Toru, Arichi, Shiho, Maruo, Yoshihiro, Ishibashi, Hitoshi, Eto, Kei

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Systemic adverse events after screening of retinopathy of prematurity with mydriatic von Obata, Shumpei, Imamura, Taku, Kakinoki, Masashi, Yanagi, Takahide, Maruo, Yoshihiro, Ohji, Masahito

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Intestinal UDP-Glucuronosyltransferase 1A1 and Protection against Irinotecan-Induced Toxicity in a Novel UDP-Glucuronosyltransferase 1A1 Tissue-Specific Humanized Mouse Model von Mennillo, Elvira, Yang, Xiaojing, Weber, Andre A, Maruo, Yoshihiro, Verreault, Melanie, Barbier, Olivier, Chen, Shujuan, Tukey, Robert H

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Changes in fetal growth restriction and retinopathy of prematurity during the coronavirus disease 2019 pandemic: A cross-sectional study von Obata, Shumpei, Matsumoto, Riko, Kakinoki, Masashi, Tsuji, Shunichiro, Murakami, Takashi, Yanagi, Takahide, Maruo, Yoshihiro, Ohji, Masahito

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Phosphatase and tensin homolog ( PTEN ) mutation can cause activated phosphatidylinositol 3-kinase δ syndrome–like immunodeficiency von Tsujita, Yuki, MD, Mitsui-Sekinaka, Kanako, MD, Imai, Kohsuke, MD, PhD, Yeh, Tzu-Wen, MSc, Mitsuiki, Noriko, MD, PhD, Asano, Takaki, MD, Ohnishi, Hidenori, MD, PhD, Kato, Zenichiro, MD, PhD, Sekinaka, Yujin, MD, Zaha, Kiyotaka, MD, Kato, Tamaki, MD, PhD, Okano, Tsubasa, MD, Takashima, Takehiro, MD, Kobayashi, Kaoru, MD, PhD, Kimura, Mitsuaki, MD, PhD, Kunitsu, Tomoaki, MD, Maruo, Yoshihiro, MD, PhD, Kanegane, Hirokazu, MD, PhD, Takagi, Masatoshi, MD, PhD, Yoshida, Kenichi, MD, PhD, Okuno, Yusuke, MD, PhD, Muramatsu, Hideki, MD, PhD, Shiraishi, Yuichi, PhD, Chiba, Kenichi, BA, Tanaka, Hiroko, BSc, Miyano, Satoru, PhD, Kojima, Seiji, MD, PhD, Ogawa, Seishi, MD, PhD, Ohara, Osamu, PhD, Okada, Satoshi, MD, PhD, Kobayashi, Masao, MD, PhD, Morio, Tomohiro, MD, PhD, Nonoyama, Shigeaki, MD, PhD

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Blood neutrophil-to-lymphocyte ratio as a risk factor in treatment for retinopathy of prematurity von Obata, Shumpei, Matsumoto, Riko, Kakinoki, Masashi, Sawada, Osamu, Sawada, Tomoko, Saishin, Yoshitsugu, Yanagi, Takahide, Maruo, Yoshihiro, Ohji, Masahito

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Effect of intravitreal bevacizumab for retinopathy of prematurity on weight gain von Obata, Shumpei, Ichiyama, Yusuke, Matsumoto, Riko, Kakinoki, Masashi, Saishin, Yoshitsugu, Yanagi, Takahide, Maruo, Yoshihiro, Ohji, Masahito

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Postweaning Iron Deficiency in Male Rats Leads to Long-Term Hyperactivity and Decreased Reelin Gene Expression in the Nucleus Accumbens von Nishikura, Noriko, Hino, Kodai, Kimura, Tomoko, Uchimura, Yasuhiro, Hino, Shinjiro, Nakao, Mitsuyoshi, Maruo, Yoshihiro, Udagawa, Jun

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Ketogenic diet for refractory epilepsy with MEHMO syndrome: Caution for acute necrotizing pancreatitis von Mori, Mioko, Kumada, Tomohiro, Inoue, Kenji, Nozaki, Fumihito, Matsui, Katsuyuki, Maruo, Yoshihiro, Yamada, Mamiko, Suzuki, Hisato, Kosaki, Kenjiro, Shibata, Minoru

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Transient Congenital Hypothyroidism Caused by Biallelic Mutations of the Dual Oxidase 2 Gene in Japanese Patients Detected by a Neonatal Screening Program von Maruo, Yoshihiro, Takahashi, Hiroko, Soeda, Ikumi, Nishikura, Noriko, Matsui, Katsuyuki, Ota, Yoriko, Mimura, Yu, Mori, Asami, Sato, Hiroshi, Takeuchi, Yoshihiro

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