AOYAMA Kouhei

Researcher Information

Research funding number

• 40812095

J-Global ID

• 201701006698674007

Research Interests

• 先天性甲状腺機能低下症   低ゴナドトロピン性性腺機能低下症   

Research Areas

• Life sciences / Metabolism and endocrinology

Academic & Professional Experience

• 2024/04 - Today  Nagoya City UniversityGraduate School of Medical Sciences講師

Published Papers

• Relationship between Birth Order and Postnatal Growth until 4 Years of Age: The Japan Environment and Children’s Study

  Aya Yoshida; Kayo Kaneko; Kohei Aoyama; Naoya Yamaguchi; Atsushi Suzuki; Sayaka Kato; Takeshi Ebara; Mayumi Sugiura-Ogasawara; Michihiro Kamijima; Shinji Saitoh

  Children MDPI AG 10 (3) 557 - 557 2023/03 [Refereed]
  
• An infant with a heterozygous variant of ABCG5 presented with hypercholesterolemia only during breastfeeding.

  Aya Yoshida; Kohei Aoyama; Naoya Yamaguchi; Atsushi Suzuki; Haruo Mizuno; Hayato Tada; Shinji Saitoh

  Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology 32 (2) 114 - 118 2023
• The iodide transporter Slc26a7 impacts thyroid function more strongly than Slc26a4 in mice

  Naoya Yamaguchi; Atsushi Suzuki; Aya Yoshida; Tatsushi Tanaka; Kohei Aoyama; Hisashi Oishi; Yuichiro Hara; Tomoo Ogi; Izuki Amano; Satomi Kameo; Noriyuki Koibuchi; Yasuhiro Shibata; Shinya Ugawa; Haruo Mizuno; Shinji Saitoh

  Scientific Reports Springer Science and Business Media LLC 12 (1) 2022/12
• An infant case of pseudohypoaldosteronism type1A caused by a novel NR3C2 variant

  Saki Noda; Kohei Aoyama; Yuto Kondo; Jun Okamura; Atsushi Suzuki; Naoya Yamaguchi; Aya Yoshida; Yoshishige Miyake

  Human Genome Variation Springer Science and Business Media LLC 8 (1) 2021/12
• Peripheral nerves are involved in hypomyelinating leukodystrophy-3 caused by a homozygous AIMP1 variant.

  Ikumi Hori; Daisuke Ieda; Shogo Ito; Seimi Ebe; Yuji Nakamura; Kei Ohashi; Kohei Aoyama; Ayako Hattori; Minoru Kokubo; Shinji Saitoh

  Brain & development 43 (4) 590 - 595 2021/04
• 発達の遅れで来院し,急激に退行した4歳女児

  武内 温子; 堀 いくみ; 田中 達之; 青山 幸平; 根岸 豊; 伊藤 孝一; 服部 文子; 坂 京子; 岡崎 康司; 村山 圭; 齋藤 伸治

  脳と発達 (一社)日本小児神経学会 52 (Suppl.) S129 - S129 0029-0831 2020/08
• Clinical and genetic investigation of 136 Japanese patients with congenital hypothyroidism.

  Tatsushi Tanaka; Kohei Aoyama; Atsushi Suzuki; Shinji Saitoh; Haruo Mizuno

  Journal of pediatric endocrinology & metabolism : JPEM 33 (6) 691 - 701 2020/05 [Refereed]
  
• De novo 2q36.3q37.1 deletion encompassing TRIP12 and NPPC yields distinct phenotypes.

  Yuto Kondo; Kohei Aoyama; Hisato Suzuki; Ayako Hattori; Ikumi Hori; Koichi Ito; Aya Yoshida; Mari Koroki; Kentaro Ueda; Kenjiro Kosaki; Shinji Saitoh

  Human genome variation 7 19 - 19 2020 [Refereed]
  
• Congenital goitrous hypothyroidism is caused by dysfunction of the iodide transporter SLC26A7

  Jun Ishii; Atsushi Suzuki; Toru Kimura; Michihiro Tateyama; Tatsushi Tanaka; Takuya Yazawa; Yu Arimasu; I-Shan Chen; Kohei Aoyama; Yoshihiro Kubo; Shinji Saitoh; Haruo Mizuno; Hiroshi Kamma

  Communications Biology Springer Science and Business Media LLC 2 (1) 270  2019/12 [Refereed]
  
• Transition from Leigh syndrome to MELAS syndrome in a patient with heteroplasmic MT-ND3 m.10158T>C.

  Atsuko Kori; Ikumi Hori; Tatsushi Tanaka; Kohei Aoyama; Koichi Ito; Ayako Hattori; Kyoko Ban; Yasushi Okazaki; Kei Murayama; Shinji Saitoh

  Brain & development 41 (9) 803 - 807 0387-7604 2019/10 [Refereed]
  
• 思春期早発症を契機に診断された副腎皮質癌の一例

  郡 温子; 岩淵 英人; 亀井 美智; 武田 理沙; 吉田 悟; 中野 さつき; 山口 直哉; 鈴木 敦詞; 田中 達之; 青山 幸平; 高木 大輔; 近藤 知史; 山下 依子; 齋藤 伸治

  日本小児血液・がん学会雑誌 (一社)日本小児血液・がん学会 56 (2) 247 - 248 2187-011X 2019/09
• m.10158T>C変異によるミトコンドリア病の4歳女児

  郡 温子; 堀 いくみ; 田中 達之; 青山 幸平; 伊藤 孝一; 服部 文子; 齋藤 伸治; 坂 京子; 村山 圭

  日本小児科学会雑誌 (公社)日本小児科学会 123 (5) 910 - 910 0001-6543 2019/05 [Refereed]
  
• Individual Clinically Diagnosed with CHARGE Syndrome but with a Mutation in KMT2D, a Gene Associated with Kabuki Syndrome: A Case Report

  Sonoko Sakata; Satoshi Okada; Kohei Aoyama; Keiichi Hara; Chihiro Tani; Reiko Kagawa; Akari Utsunomiya-Nakamura; Shinichiro Miyagawa; Tsutomu Ogata; Haruo Mizuno; Masao Kobayashi

  FRONTIERS IN GENETICS FRONTIERS MEDIA SA 8 210  1664-8021 2017/12 [Refereed]
  
• Combined genetic analyses can achieve efficient diagnostic yields for subjects with Alagille syndrome and incomplete Alagille syndrome

  Kei Ohashi; Takao Togawa; Tokio Sugiura; Koichi Ito; Takeshi Endo; Kohei Aoyama; Yutaka Negishi; Toyoichiro Kudo; Reiko Ito; Shinji Saitoh

  ACTA PAEDIATRICA WILEY 106 (11) 1817 - 1824 0803-5253 2017/11 [Refereed]
  
• Molecular genetic and clinical delineation of 22 patients with congenital hypogonadotropic hypogonadism

  Kohei Aoyama; Haruo Mizuno; Tatsushi Tanaka; Takao Togawa; Yutaka Negishi; Kei Ohashi; Ikumi Hori; Masako Izawa; Takashi Hamajima; Shinji Saitoh

  JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM WALTER DE GRUYTER GMBH 30 (10) 1111 - 1118 0334-018X 2017/10 [Refereed]
  
• A combination of genetic and biochemical analyses for the diagnosis of PI3K-AKT-mTOR pathway-associated megalencephaly

  Yutaka Negishi; Fuyuki Miya; Ayako Hattori; Yoshikazu Johmura; Motoo Nakagawa; Naoki Ando; Ikumi Hori; Takao Togawa; Kohei Aoyama; Kei Ohashi; Shinobu Fukumura; Seiji Mizuno; Ayako Umemura; Yoko Kishimoto; Nobuhiko Okamoto; Mitsuhiro Kato; Tatsuhiko Tsunoda; Mami Yamasaki; Yonehiro Kanemura; Kenjiro Kosaki; Makoto Nakanishi; Shinji Saitoh

  BMC MEDICAL GENETICS BIOMED CENTRAL LTD 18 (1) 4  1471-2350 2017/01 [Refereed]
  
• Molecular Genetic Dissection and Neonatal/Infantile Intrahepatic Cholestasis Using Targeted Next-Generation Sequencing

  Takao Togawa; Tokio Sugiura; Koichi Ito; Takeshi Endo; Kohei Aoyama; Kei Ohashi; Yutaka Negishi; Toyoichiro Kudo; Reiko Ito; Atsuo Kikuchi; Natsuko Arai-Ichinoi; Shigeo Kure; Shinji Saitoh

  JOURNAL OF PEDIATRICS MOSBY-ELSEVIER 171 171 - + 0022-3476 2016/04 [Refereed]
  

MISC

• Homozygous loss-of-function mutation in the SLC26A7 gene coding a novel iodide transporter causes goitrous congenital hypothyroidism

  Atsushi Suzuki; Jun Ishii; Aya Yoshida; Naoya Yamguchi; Tatsushi Tanaka; Kohei Aoyama; Michihiro Tateyama; I-Shan Chen; Yoshihiro Kubo; Toru Kimura; Takuya Yazawa; Yu Arimasu; Hiroshi Kamma; Shinji Saitoh; Haruo Mizuno  HORMONE RESEARCH IN PAEDIATRICS  91-  36  -36  2019/09
• 日齢0から酵素補充療法を開始し良好な経過をたどっている周産期重症型低ホスファターゼ症の1例

  田中 達之; 山本 和之; 岩脇 由希子; 鈴木 敦詞; 青山 幸平; 加藤 晋; 伊藤 孝一; 杉浦 時雄; 長崎 理香; 水野 晴夫; 道上 敏美; 立川 加奈子; 大薗 恵一  日本内分泌学会雑誌  93-  (1)  372  -372  2017/04
• 治療方針に苦悩する小児期発症巨大後腹膜神経芽腫群腫瘍の1例

  高木 大輔; 近藤 知史; 藤井 義敬; 伊藤 康彦; 亀井 美智; 青山 幸平; 齋藤 伸治  日本小児血液・がん学会雑誌  52-  (5)  462  -463  2016/02
• Molecular Genetic Diagnosis of Idiopathic Hypogonadotropic Hypogonadism by Using Targeted Next-Generation Sequencing

  Kohei Aoyama; Atsushi Suzuki; Tatsushi Tanaka; Haruo Mizuno; Shinji Saitoh  HORMONE RESEARCH IN PAEDIATRICS  86-  108  -108  2016
• 肺炎球菌ワクチン接種後に侵襲性肺炎球菌感染症に罹患した3例

  大下 裕法; 青山 幸平; 加藤 沙耶香; 根岸 豊; 鈴木 一孝; 伊藤 孝一; 遠藤 剛; 服部 文子; 犬飼 幸子; 水野 晴夫; 伊藤 哲哉; 齋藤 伸治; 坂 京子  日本小児科学会雑誌  118-  (3)  554  -554  2014/03
• 先天性副腎過形成症の初期治療はどのように行うべきか?

  水野 晴夫; 青山 幸平; 岩山 秀之; 根岸 豊; 遠藤 剛; 服部 文子; 安藤 直樹; 伊藤 哲哉; 齋藤 伸治  日本小児科学会雑誌  117-  (5)  932  -932  2013/05
• Primary angiitis of the central nervous system in children(PACNS)が疑われた1例

  粟屋 梨沙; 青山 幸平; 根岸 豊; 鈴木 一孝; 遠藤 剛; 岩山 秀之; 伊藤 哲哉; 服部 文子; 安藤 直樹; 齋藤 伸治; 豊田 剛成; 櫻井 圭太; 中川 基生; 本田 茂  日本小児科学会雑誌  116-  (1)  108  -108  2012/01
• 著明な胆汁うっ滞を認めたZelleweger症候群の1例

  青山 幸平; 遠藤 剛; 伊藤 孝一; 杉浦 時雄  日本小児栄養消化器肝臓学会雑誌  25-  (Suppl.)  91  -91  2011/09

Other link

researchmap

https://researchmap.jp/aoyamakohei