Mutation spectrum of the dystrophin gene in 442 Duchenne Becker muscular dystrophy cases from one Japanese referral center
Takeshima, Yasuhiro, Yagi, Mariko, Okizuka, Yo, Awano, Hiroyuki, Zhang, Zhujun, Yamauchi, Yumiko, Nishio, Hisahide, Matsuo, Masafumi
Published in Journal of human genetics (01.06.2010)
Published in Journal of human genetics (01.06.2010)
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Predictive factors of continuous negative extrathoracic pressure management failure in children with moderate to severe respiratory syncytial virus infection
Ishimori, Shingo, Okizuka, Yo, Onishi, Satoshi, Shinomoto, Tadashi, Minami, Hirotaka
Published in Scientific reports (13.04.2021)
Published in Scientific reports (13.04.2021)
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Sonographic temporary nephromegaly in children during their first febrile urinary tract infection is a significant prognostic factor for recurrent infection
Ishimori, Shingo, Fujimura, Junya, Nakanishi, Keita, Hattori, Kengo, Hirase, Satoshi, Matsunoshita, Natsuki, Kamiyoshi, Naohiro, Okizuka, Yo
Published in Scientific reports (20.08.2024)
Published in Scientific reports (20.08.2024)
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The Combination of Binding Avidity of Ovomucoid-Specific IgE Antibody and Specific IgG4 Antibody Can Predict Positive Outcomes of Oral Food Challenges during Stepwise Slow Oral Immunotherapy in Children with Hen's Egg Allergy
Taniuchi, Shoichiro, Sakai, Rika, Nishida, Takahiro, Goma, Meguru, Mitomori, Masatoshi, Imaide, Aya, Enomoto, Masahiro, Nishino, Masamitsu, Okizuka, Yo, Kido, Hiroshi
Published in Nutrients (01.06.2023)
Published in Nutrients (01.06.2023)
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A case of neonatal Proteus mirabilis meningitis with multiple brain abscesses
Matsuura, So, Utsugi, Reina, Arita, Hideyuki, Maeno, Kazushige, Yabumoto, Kanako, Saito, Taeko, Onishi, Satoshi, Ishimori, Shingo, Okizuka, Yo, Harada, Atsuko
Published in Nervous System in Children (2022)
Published in Nervous System in Children (2022)
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Surgical management for intracranial hemorrhage in neonates and infants with hemophilia
Wada, Yuki, Yamanaka, Takumi, Toyoda, Saori, Kawamoto, Saki, Fukuya, Shogo, Maeno, Kazushige, Hattori, Yuka, Onishi, Satoshi, Ishimori, Shingo, Okizuka, Yo, Harada, Atsuko
Published in Nervous System in Children (2023)
Published in Nervous System in Children (2023)
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Complicated post-operative care of infant craniopharyngioma: A case report
Utsugi, Reina, Kimoto, Yuki, Fukuya, Shogo, Arita, Hideyuki, Maeno, Kazushige, Ekuni, Satoshi, Onishi, Satoshi, Okizuka, Yo, Utsunomiya, Hidetsuna, Harada, Atsuko
Published in Nervous System in Children (2020)
Published in Nervous System in Children (2020)
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Effect of CPS14217C>A genotype on valproic-acid-induced hyperammonemia
Yagi, Mariko, Nakamura, Tsutomu, Okizuka, Yo, Oyazato, Yoshinobu, Kawasaki, Yoko, Tsuneishi, Shuichi, Sakaeda, Toshiyuki, Matsuo, Masafumi, Okumura, Katsuhiko, Okamura, Noboru
Published in Pediatrics international (01.10.2010)
Published in Pediatrics international (01.10.2010)
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Insertion of the IL1RAPL1 gene into the duplication junction of the dystrophin gene
Zhang, Zhujun, Yagi, Mariko, Okizuka, Yo, Awano, Hiroyuki, Takeshima, Yasuhiro, Matsuo, Masafumi
Published in Journal of human genetics (01.08.2009)
Published in Journal of human genetics (01.08.2009)
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Journal Article
Treatment of preterm infants with West syndrome: Differences due to etiology
Mure, Takeo, Nakagawa, Taku, Okizuka, Yo, Takami, Yuichi, Oyazato, Yoshinobu, Nagase, Hiroaki, Maruyama, Azusa, Adachi, Masao, Takada, Satoshi, Matsuo, Masafumi
Published in Pediatrics international (01.12.2012)
Published in Pediatrics international (01.12.2012)
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Small mutations detected by multiplex ligation-dependent probe amplification of the dystrophin gene
Okizuka, Yo, Takeshima, Yasuhiro, Awano, Hiroyuki, Zhang, Zhujun, Yagi, Mariko, Matsuo, Masafumi
Published in Genetic testing and molecular biomarkers (01.06.2009)
Published in Genetic testing and molecular biomarkers (01.06.2009)
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Journal Article
Tandem duplications of two separate fragments of the dystrophin gene in a patient with Duchenne muscular dystrophy
Zhang, Zhujun, Takeshima, Yasuhiro, Awano, Hiroyuki, Nishiyama, Atsushi, Okizuka, Yo, Yagi, Mariko, Matsuo, Masafumi
Published in Journal of human genetics (01.03.2008)
Published in Journal of human genetics (01.03.2008)
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Two Japanese infants with congenital generalized lipodystrophy due to BSCL2 mutations
Nishiyama, Atsushi, Yagi, Mariko, Awano, Hiroyuki, Okizuka, Yo, Maeda, Taro, Yoshida, Shinsaku, Takeshima, Yasuhiro, Matsuo, Masafumi
Published in Pediatrics international (01.12.2009)
Published in Pediatrics international (01.12.2009)
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Journal Article
Low incidence of limb-girdle muscular dystrophy type 2C revealed by a mutation study in Japanese patients clinically diagnosed with DMD
Okizuka, Yo, Takeshima, Yasuhiro, Itoh, Kyoko, Zhang, Zhujun, Awano, Hiroyuki, Maruyama, Koichi, Kumagai, Toshiyuki, Yagi, Mariko, Matsuo, Masafumi
Published in BMC genetics (30.03.2010)
Published in BMC genetics (30.03.2010)
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Mutation analysis of the ornithine transcarbamylase (OTC) gene in five Japanese OTC deficiency patients revealed two known and three novel mutations including a deep intronic mutation
Ogino, Wakako, Takeshima, Yasuhiro, Nishiyama, Atsushi, Okizuka, Yo, Yagi, Mariko, Tsuneishi, Shuichi, Saiki, Kayoko, Kugo, Masaaki, Matsuo, Masafumi
Published in Kobe journal of the medical sciences (2007)
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Published in Kobe journal of the medical sciences (2007)
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