Publications by authors named "Yusuke Mitani"

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Sleep variability and learning outcomes in preterm and full-term children: An observational study.
Yusuke Mitani, Yuko Yoshimura, Shinichiro Mizutomi, Tetsujiro Shirahashi, Hidenori Iwasaki

Early Hum Dev· January 2026

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Synthesis and herbicidal activity of C5-substituted cinmethylin analogs.
Narihito Ogawa, Kakeru Hasegawa, Masaru Kawakami, Chihiro Uematsu, Tatsuya Hirano, Yusuke Mitani

J Pestic Sci· May 2025

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Language and sensory characteristics are reflected in voice-evoked responses in low birth weight children.
Yuko Yoshimura, Yusuke Mitani, Takashi Ikeda, Sanae Tanaka, Momoka Suda

Pediatr Res· January 2025

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Preterm toddlers have low nighttime sleep quality and high daytime activity.
Yoko Asaka, Yusuke Mitani, Hidenobu Ohta, Takayo Nakazawa, Rika Fukutomi

Sci Rep· November 2022

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Prenatal clinical manifestations in individuals with variants.
Toshiyuki Itai, Satoko Miyatake, Masataka Taguri, Fumihito Nozaki, Masayasu Ohta, Yusuke Mitani

J Med Genet· August 2021

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Sleep maturation influences cognitive development of preterm toddlers.
Akiko Ando, Hidenobu Ohta, Yuko Yoshimura, Machiko Nakagawa, Yoko Asaka, Yusuke Mitani

Sci Rep· August 2021

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Daytime nap and nighttime breastfeeding are associated with toddlers' nighttime sleep.
Machiko Nakagawa, Hidenobu Ohta, Rinshu Shimabukuro, Yoko Asaka, Takayo Nakazawa, Yusuke Mitani

Sci Rep· February 2021

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Wavy Floating Greater Omentum Findings Are Useful for Differentiating the Etiology of Fetal Ascites.
Takashi Iizuka, Masanori Ono, Rena Yamazaki, Kyosuke Kagami, Yusuke Mitani

Diagnostics (Basel)· February 2021

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The Japanese experience and pharmacokinetics of antenatal maternal high-dose immunoglobulin treatment as a prophylaxis for neonatal hemochromatosis in siblings.
Noriki Okada, Aiko Sasaki, Jumpei Saito, Yusuke Mitani, Akihiro Yachie

J Matern Fetal Neonatal Med· January 2020

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Prenatal diagnosis facilitated prompt enzyme replacement therapy for prenatal benign hypophosphatasia.
Yuka Ishijima, Takashi Iizuka, Kyosuke Kagami, Sakiko Masumoto, Kyohei Nakade, Yusuke Mitani

J Obstet Gynaecol· January 2020

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Amniotic epithelial cells damage by oxidative stress in cases of diffuse chorioamniotic hemosiderosis.
Takashi Iizuka, Masanori Ono, Sakiko Masumoto, Yusuke Mitani, Rena Yamazaki

J Obstet Gynaecol Res· October 2019

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Twin anemia-polycythemia sequence with blood chimerism in monochorionic dizygotic opposite-sex twins.
Takuma Suzuki, Kyosuke Kagami, Yusuke Mitani, Rena Yamazaki, Masanori Ono

J Obstet Gynaecol Res· June 2019

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Deep spontaneous molecular remission in a patient with congenital acute myeloid leukemia expressing a novel MOZ-p300 fusion transcript.
Yasuhiro Ikawa, Ryosei Nishimura, Hideaki Maeba, Toshihiro Fujiki, Rie Kuroda, Yusuke Mitani

Leuk Lymphoma· October 2018

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A successful case of neoadjuvant chemotherapy and radical hysterectomy during pregnancy for advanced uterine cervical cancer accompanied by neonatal erythroderma.
Kayo Kayahashi, Yasunari Mizumoto, Subaru Myojo, Yusuke Mitani, Atsushi Tajima

J Obstet Gynaecol Res· October 2018

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XL-EDA-ID Presenting with Congenital Duodenal Atresia and Perforations.
Yusuke Mitani, Taizo Wada, Yusuke Matsuda, Seisho Sakai, Akihiro Yachie

J Clin Immunol· October 2018

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Pyridoxal 5'-phosphate and related metabolites in hypophosphatasia: Effects of enzyme replacement therapy.
Tomoyuki Akiyama, Takuo Kubota, Keiichi Ozono, Toshimi Michigami, Daisuke Kobayashi, Yusuke Mitani

Mol Genet Metab· September 2018

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A Say-Barber-Biesecker-Young-Simpson variant of Ohdo syndrome with a KAT6B 10-base pair palindromic duplication: A recurrent mutation causing a severe phenotype mixed with genitopatellar syndrome.
Yo Niida, Yusuke Mitani, Mondo Kuroda, Ayano Yokoi, Hiroyasu Nakagawa

Congenit Anom (Kyoto)· May 2017

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Reply to: Uniparental disomy of chromosome 1 unmasks recessive mutations of PPT1 in a boy with neuronal ceroid lipofuscinosis type 1.
Yo Niida, Ayano Yokoi, Mondo Kuroda, Yusuke Mitani, Hiroyasu Nakagawa

Brain Dev· February 2017

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A girl with infantile neuronal ceroid lipofuscinosis caused by novel PPT1 mutation and paternal uniparental isodisomy of chromosome 1.
Yo Niida, Ayano Yokoi, Mondo Kuroda, Yusuke Mitani, Hiroyasu Nakagawa

Brain Dev· August 2016

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Mutational analysis of TSC1 and TSC2 in Japanese patients with tuberous sclerosis complex revealed higher incidence of TSC1 patients than previously reported.
Yo Niida, Akiko Wakisaka, Takanori Tsuji, Hiroshi Yamada, Mondo Kuroda, Yusuke Mitani

J Hum Genet· April 2013

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Applying and testing the conveniently optimized enzyme mismatch cleavage method to clinical DNA diagnosis.
Yo Niida, Mondo Kuroda, Yusuke Mitani, Akiko Okumura, Ayano Yokoi

Mol Genet Metab· November 2012

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Paternal uniparental isodisomy of chromosome 22 in a patient with metachromatic leukodystrophy.
Yo Niida, Mondo Kuroda, Yusuke Mitani, Ayano Yokoi, Mamoru Ozaki

J Hum Genet· October 2012

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