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The Boy:Girl Ratio of Children Diagnosed with Growth Hormone Deficiency-Induced Short Stature Is Associated with the Boy:Girl Ratio of Children Visiting Short Stature Clinics.
Tanaka T, Soneda S, Sato N, Kishi K, Noda M, Ogasawara A, Nose O, Nakano Y, Kinoshita E, Mochizuki T, Konda S, Murashita M, Tanizawa T, Nozue H, Tokuda M, Kubota K, Araki K, Kitanaka S, Inomata H, Miyagi C, Ishizu K, Miyagawa S. Tanaka T, et al. Among authors: soneda s. Horm Res Paediatr. 2021;94(5-6):211-218. doi: 10.1159/000518995. Epub 2021 Aug 23. Horm Res Paediatr. 2021. PMID: 34425577
Cytochrome P450 oxidoreductase gene mutations and Antley-Bixler syndrome with abnormal genitalia and/or impaired steroidogenesis: molecular and clinical studies in 10 patients.
Fukami M, Horikawa R, Nagai T, Tanaka T, Naiki Y, Sato N, Okuyama T, Nakai H, Soneda S, Tachibana K, Matsuo N, Sato S, Homma K, Nishimura G, Hasegawa T, Ogata T. Fukami M, et al. Among authors: soneda s. J Clin Endocrinol Metab. 2005 Jan;90(1):414-26. doi: 10.1210/jc.2004-0810. Epub 2004 Oct 13. J Clin Endocrinol Metab. 2005. PMID: 15483095
Usefulness of insulin detemir in Japanese children with type 1 diabetes.
Jinno K, Urakami T, Horikawa R, Kawamura T, Kikuchi N, Kikuchi T, Kizu R, Kosaka K, Mizuno H, Mochizuki T, Nishii A, Ohki Y, Soneda S, Sugihara S, Tatematsu T, Amemiya S; Japanese Study Group of Insulin Therapy for Childhood and Adolescent Diabetes. Jinno K, et al. Among authors: soneda s. Pediatr Int. 2012 Dec;54(6):773-9. doi: 10.1111/j.1442-200X.2012.03687.x. Epub 2012 Sep 17. Pediatr Int. 2012. PMID: 22726205 Clinical Trial.
Systematic molecular analyses of SHOX in Japanese patients with idiopathic short stature and Leri-Weill dyschondrosteosis.
Shima H, Tanaka T, Kamimaki T, Dateki S, Muroya K, Horikawa R, Kanno J, Adachi M, Naiki Y, Tanaka H, Mabe H, Yagasaki H, Kure S, Matsubara Y, Tajima T, Kashimada K, Ishii T, Asakura Y, Fujiwara I, Soneda S, Nagasaki K, Hamajima T, Kanzaki S, Jinno T, Ogata T, Fukami M; Japanese SHOX study group. Shima H, et al. Among authors: soneda s. J Hum Genet. 2016 Jul;61(7):585-91. doi: 10.1038/jhg.2016.18. Epub 2016 Mar 17. J Hum Genet. 2016. PMID: 26984564
(Epi)genetic defects of MKRN3 are rare in Asian patients with central precocious puberty.
Suzuki E, Shima H, Kagami M, Soneda S, Tanaka T, Yatsuga S, Nishioka J, Oto Y, Kamiya T, Naiki Y, Ogata T, Fujisawa Y, Nakamura A, Kawashima S, Morikawa S, Horikawa R, Sano S, Fukami M. Suzuki E, et al. Among authors: soneda s. Hum Genome Var. 2019 Jan 21;6:7. doi: 10.1038/s41439-019-0039-9. eCollection 2019. Hum Genome Var. 2019. PMID: 30675365 Free PMC article.
FUT2 non-secretor status is associated with Type 1 diabetes susceptibility in Japanese children.
Ihara K, Fukano C, Ayabe T, Fukami M, Ogata T, Kawamura T, Urakami T, Kikuchi N, Yokota I, Takemoto K, Mukai T, Nishii A, Kikuchi T, Mori T, Shimura N, Sasaki G, Kizu R, Takubo N, Soneda S, Fujisawa T, Takaya R, Kizaki Z, Kanzaki S, Hanaki K, Matsuura N, Kasahara Y, Kosaka K, Takahashi T, Minamitani K, Matsuo S, Mochizuki H, Kobayashi K, Koike A, Horikawa R, Teno S, Tsubouchi K, Mochizuki T, Igarashi Y, Amemiya S, Sugihara S; Japanese Study Group of Insulin Therapy for Childhood and Adolescent Diabetes (JSGIT). Ihara K, et al. Among authors: soneda s. Diabet Med. 2017 Apr;34(4):586-589. doi: 10.1111/dme.13288. Epub 2016 Dec 15. Diabet Med. 2017. PMID: 27859559
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