Search Results - "Shoji, Yasuko"

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    Renal function in short‐statured children born small for gestational age and treated with growth hormone by Koizumi, Mikiko, Ida, Shinobu, Shoji, Yasuko, Etani, Yuri, Kawai, Masanobu

    Published in Pediatrics international (01-07-2021)
    “…Background Children born small for gestational age (SGA), particularly when associated with an extremely low birthweight (ELBW), have a higher risk of renal…”
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    Journal Article
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    Genotype-phenotype correlation analysis in Japanese patients with Noonan syndrome by Shoji, Yasuko, Ida, Shinobu, Niihori, Tetsuya, Aoki, Yoko, Okamoto, Nobuhiko, Etani, Yuri, Kawai, Masanobu

    Published in Endocrine Journal (01-01-2019)
    “…Noonan syndrome (NS) is a heterogeneous disorder with multiple congenital malformations. Recent advances in molecular and genetic approaches have identified a…”
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    Journal Article
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    Visceral adipose tissue resides within the reference range in children with Prader-Willi syndrome receiving nutritional intervention on a regular basis by Koizumi, Mikiko, Ida, Shinobu, Shoji, Yasuko, Nishimoto, Yukiko, Etani, Yuri, Kawai, Masanobu

    Published in Endocrine Journal (01-01-2020)
    “…Nutritional intervention for maintaining an appropriate body composition is central to the management of Prader-Willi syndrome (PWS). Despite evidence that…”
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    Journal Article
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    Fat distribution in short‐stature children born small for gestational age by Maeyama, Takatoshi, Ida, Shinobu, Onuma, Shinsuke, Shoji, Yasuko, Yamamoto, Takehisa, Etani, Yuri, Kawai, Masanobu

    Published in Pediatrics international (01-12-2020)
    “…Background Children born small for gestational age (SGA) with catch‐up growth are at high risk for developing obesity; however, the characteristics of body…”
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    Growth hormone treatment for extremely low birthweight children born small for gestational age by Onuma, Shinsuke, Ida, Shinobu, Maeyama, Takatoshi, Shoji, Yasuko, Etani, Yuri, Kawai, Masanobu

    Published in Pediatrics international (01-01-2021)
    “…Background The effectiveness of growth hormone (GH) treatment for height gain in short‐stature children born small for gestational age (SGA) with extremely low…”
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    Visceral adipose tissue increases shortly after the cessation of GH therapy in adults with Prader-Willi syndrome by Koizumi, Mikiko, Ida, Shinobu, Shoji, Yasuko, Nishimoto, Yukiko, Etani, Yuri, Kawai, Masanobu

    Published in Endocrine Journal (01-01-2018)
    “…GH therapy in pediatric patients with Prader-Willi syndrome (PWS) improves body composition, but discontinuation of GH after achieving adult height has been…”
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    MIRAGE syndrome caused by a novel missense variant (p.Ala1479Ser) in the SAMD9 gene by Onuma, Shinsuke, Wada, Tamaki, Araki, Ryosuke, Wada, Kazuko, Tanase-Nakao, Kanako, Narumi, Satoshi, Fukui, Miho, Shoji, Yasuko, Etani, Yuri, Ida, Shinobu, Kawai, Masanobu

    Published in Human genome variation (05-03-2020)
    “…MIRAGE syndrome is a recently identified disorder characterized by myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital phenotypes,…”
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    Thyroid hormone status in patients with severe selenium deficiency by Kawai, Masanobu, Shoji, Yasuko, Onuma, Shinsuke, Etani, Yuri, Ida, Shinobu

    Published in Clinical Pediatric Endocrinology (01-01-2018)
    “…Selenium (Se) is an essential trace element that is involved in numerous biological processes in the form of a selenoprotein such as iodothyronine deiodinase…”
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    Genetic backgrounds and genotype-phenotype relationships in anthropometric parameters of 116 Japanese individuals with Noonan syndrome by Shoji, Yasuko, Hata, Ayaha, Maeyama, Takatoshi, Wada, Tamaki, Hasegawa, Yuiko, Nishi, Eriko, Ida, Shinobu, Etani, Yuri, Niihori, Tetsuya, Aoki, Yoko, Okamoto, Nobuhiko, Kawai, Masanobu

    Published in Clinical Pediatric Endocrinology (2024)
    “…Noonan syndrome (NS) is caused by pathogenic variants in genes encoding components of the RAS/MAPK pathway and presents with a number of symptoms, including…”
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    Safety, tolerability, and immunogenicity of a novel 4-antigen Staphylococcus aureus vaccine (SA4Ag) in healthy Japanese adults by Inoue, Megumi, Yonemura, Takuma, Baber, James, Shoji, Yasuko, Aizawa, Masakazu, Cooper, David, Eiden, Joseph, Gruber, William C., Jansen, Kathrin U., Anderson, Annaliesa S., Gurtman, Alejandra

    Published in Human vaccines & immunotherapeutics (02-11-2018)
    “…A novel Staphylococcus aureus 4-antigen vaccine (SA4Ag) is under development, comprising capsular polysaccharide serotypes 5 and 8 (CP5 and CP8) conjugated to…”
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    Endocrine status of patients with septo-optic dysplasia: fourteen Japanese cases by Koizumi, Mikiko, Ida, Shinobu, Shoji, Yasuko, Etani, Yuri, Hatsukawa, Yoshikazu, Okamoto, Nobuhiko

    Published in Clinical Pediatric Endocrinology (01-01-2017)
    “…A clinical diagnosis of septo-optic dysplasia (SOD) is made when two or more of the classical triad of optic nerve hypoplasia, pituitary hormone abnormalities…”
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    Late onset of injection site reactions after vaccination with the 13-valent pneumococcal conjugate vaccine in adult study populations by Juergens, Christine, Trammel, James, Shoji, Yasuko, Patterson, Scott, Watson, Wendy, Webber, Chris, Gruber, William C., Scott, Daniel A., Schmoele-Thoma, Beate

    Published in Human vaccines & immunotherapeutics (01-01-2018)
    “…Injection site reactions (ISRs; redness, swelling and pain) commonly occur within 1-2 days after vaccination. After administration of toxoid vaccines including…”
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    Ovarian insufficiency following allogeneic hematopoietic stem cell transplantation by Kawano, Mahiru, Komura, Hiroko, Kawaguchi, Haruna, Shimizu, Shoko, Yada-Hashimoto, Namiko, Shimizu, Mariko, Sato, Maho, Inoue, Masami, Ida, Shinobu, Etani, Yuri, Shoji, Yasuko, Nakacho, Mariko, Sawada, Kenjiro, Kimura, Tadashi, Mitsuda, Nobuaki, Kurachi, Hirohisa

    Published in Gynecological endocrinology (01-02-2017)
    “…Ovarian insufficiency is a serious complication for young women who undergo hematopoietic stem cell transplantation (HSCT). Reduced-intensity conditioning…”
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    Endocrinological Characteristics of 25 Japanese Patients with CHARGE Syndrome by Shoji, Yasuko, Ida, Shinobu, Etani, Yuri, Yamada, Hiroyuki, Kayatani, Futoshi, Suzuki, Yasuhiro, Kosaki, Kenjiro, Okamoto, Nobuhiko

    Published in Clinical Pediatric Endocrinology (01-04-2014)
    “…CHARGE syndrome is a congenital disorder caused by mutation of the chromodomain helicase DNA binding protein 7 (CHD7) gene and is characterized by multiple…”
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    Visceral adipose tissue resides within the reference range in children with Prader-Willi syndrome receiving nutritional intervention on a regular basis by Mikiko Koizumi, Shinobu Ida, Yasuko Shoji, Yukiko Nishimoto, Yuri Etani, Masanobu Kawai

    Published in ENDOCRINE JOURNAL (2020)
    “…[Abstract.] Nutritional intervention for maintaining an appropriate body composition is central to the management of Prader-Willi syndrome (PWS). Despite…”
    Get full text
    Journal Article
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    Genotype-phenotype correlation analysis in Japanese patients with Noonan syndrome by Yasuko Shoji, Shinobu Ida, Tetsuya Niihori, Yoko Aoki, Nobuhiko Okamoto, Yuri Etani, Masanobu Kawai

    Published in ENDOCRINE JOURNAL (2019)
    “…[Abstract.] Noonan syndrome (NS) is a heterogeneous disorder with multiple congenital malformations. Recent advances in molecular and genetic approaches have…”
    Get full text
    Journal Article