日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

A prospective cohort study of the factors associated with recurrence in young patients with thyroid cancer

一项关于年轻甲状腺癌患者复发相关因素的前瞻性队列研究

Shio, Koki; Suzuki, Satoshi; Matsumoto, Yoshiko; Kobashi, Yurie; Yamaya, Yukie; Sekino, Mizuki; Suzuki, Erina; Ozaki, Akihiko; Suzuki, Satoru; Shimura, Hiroki; Yokoya, Susumu; Hashimoto, Yuko; Ohira, Tetsuya; Furuya, Fumihiko; Suzuki, Shinichi

De novo retrotransposon insertion into the FGFR1 gene in a boy with congenital hypogonadotropic hypogonadism: a case report

先天性促性腺激素低下性性腺功能减退症患儿FGFR1基因中新发逆转录转座子插入:病例报告

Sawano, Kentaro; Nagasaki, Keisuke; Suzuki, Erina; Ogiwara, Yasuko; Kageyama, Ikuko; Fukami, Maki; Kuroki, Yoko

De Novo Splice Site Variant of TCF12 in a Boy With Isolated Kallmann Syndrome

一名患有孤立性卡尔曼综合征的男孩的TCF12基因新发剪接位点变异

Suzuki, Erina; Shima, Hirohito; Ueda, Aki; Nakabayashi, Kazuhiko; Matsubara, Keiko; Kuroki, Yoko; Kanno, Junko; Fukami, Maki

Surgical Resection with Posterior Rectus Sheath Preservation and Mesh Reconstruction without Pursuing Wide Negative Margins for an Abdominal Wall Desmoid in Familial Adenomatous Polyposis: A Case Report

家族性腺瘤性息肉病合并腹壁纤维瘤,采用保留腹直肌后鞘并进行网片重建的手术切除,不追求广泛阴性切缘:病例报告

Hasegawa, Makoto; Momma, Tomoyuki; Suzuki, Erina; Hashimoto, Yuko; Yago, Hiroki; Ito, Misato; Matsumoto, Takuro; Ujiie, Daisuke; Chida, Shun; Okayama, Hirokazu; Saito, Motonobu; Sakamoto, Wataru; Kono, Koji

DNA methylation changes in the genome of patients with hypogonadotropic hypogonadism

低促性腺激素性性腺功能减退症患者基因组中的DNA甲基化改变

Suzuki, Erina; Nakabayashi, Kazuhiko; Aoto, Saki; Ogata, Tsutomu; Kuroki, Yoko; Miyado, Mami; Fukami, Maki; Matsubara, Keiko

CHARGE syndrome in a child with a CHD7 variant and a novel pathogenic SOX2 variant: A case report

一例携带 CHD7 变异和新型致病性 SOX2 变异的儿童发生 CHARGE 综合征的病例报告

Kamimura, Miki; Shima, Hirohito; Suzuki, Erina; Sogi, Chisumi; Fujiwara, Ikuma; Adachi, Mika; Haruna, Hidenori; Takubo, Noriyuki; Fukami, Maki; Kikuchi, Atsuo; Kanno, Junko

Genetic variants of G-protein coupled receptors associated with pubertal disorders

与青春期障碍相关的G蛋白偶联受体基因变异

Suzuki, Erina; Miyado, Mami; Kuroki, Yoko; Fukami, Maki

Methylation status of genes escaping from X-chromosome inactivation in patients with X-chromosome rearrangements.

X染色体重排患者中逃脱X染色体失活的基因的甲基化状态

Kawashima Sayaka, Hattori Atsushi, Suzuki Erina, Matsubara Keiko, Toki Machiko, Kosaki Rika, Hasegawa Yukihiro, Nakabayashi Kazuhiko, Fukami Maki, Kagami Masayo

SOX10 Mutation Screening for 117 Patients with Kallmann Syndrome

对117例卡尔曼综合征患者进行SOX10基因突变筛查

Shima, Hirohito; Tokuhiro, Etsuro; Okamoto, Shingo; Nagamori, Mariko; Ogata, Tsutomu; Narumi, Satoshi; Nakamura, Akie; Izumi, Yoko; Jinno, Tomoko; Suzuki, Erina; Fukami, Maki

Labor dystocia and risk of histological chorioamnionitis and funisitis: a study from a single tertiary referral center

难产与组织学绒毛膜羊膜炎和脐带炎风险:来自单一三级转诊中心的研究

Kyozuka, Hyo; Murata, Tuyoshi; Fukuda, Toma; Suzuki, Erina; Yazawa, Riho; Yasuda, Shun; Kanno, Aya; Yamaguchi, Akiko; Hashimoto, Yuko; Fujimori, Keiya