国際健康推進医学分野

27  件  
※ 登録方法の違いにより重複して表示されている場合があります。

  1. Tomoko Mizuno, Tadashi Kanouchi, Yumie Tamura, Ko Hirata, Runa Emoto, Tomonori Suzuki, Kenichi Kashimada, Tomohiro Morio: Changes in electrophysiological findings of spinal muscular atrophy type I after the administration of nusinersen and onasemnogene abeparvovec: two case reports. BMC Neurol. 2023.10; 23 (1): 392. ( PubMed , DOI )

  2. Moriyama K, Mizuno T, Suzuki T, Inaji M, Maehara T, Fujita A, Kato M, Matsumoto N: ATP1A3-related early childhood onset developmental and epileptic encephalopathy responding to corpus callosotomy: A case report. Brain & development. 2023.01; 45 (1): 77-81. ( PubMed , DOI )

  1. Katagiri A, Nawa N, Fujiwara T*: Association Between Length of Only-Child Period During Early Childhood and Overweight at Age 8-A Population-Based Longitudinal Study in Japan. Front Pediatr. 2022.06; 10 782940. ( PubMed , DOI )

  2. Haitian Nan, Tomoko Mizuno, Atsuko Arisaka, Kenshi Sei, Yoshihisa Takiyama: A p.Glu420Gln mutation in SPAST is associated with infantile onset spastic paraplegia complicated by cerebella ataxia, epilepsy, peripheral neuropathy, and hypoplasia of the corpus callosum. Neurol Sci. 2022.03; 43 (3): 2123-2126. ( PubMed , DOI )

  1. Katagiri A, Nawa N, Fujiwara T: Association Between Paternal Separation During Early Childhood and Pubertal Timing Among Girls Using Longitudinal Birth Cohort in Japan. Frontiers in Endocrinology. 2021.12; 12 766728. ( PubMed , DOI )

  2. Tomohiro Tago, Tomonori Suzuki, Ayako Kashimada, Masatoshi Takagi, Tomoko Mizuno: Two case reports of KBG syndrome with Dandy-Walker variant. Pediatr Int. 2021.12; 63 (12): 1530-1532. ( PubMed , DOI )

  3. Haitian Nan, Hiroshi Shiraku, Tomoko Mizuno, Yoshihisa Takiyama: A p.Arg499His mutation in SPAST is associated with infantile-onset complicated spastic paraplegia: a case report and review of the literature. BMC Neurol. 2021.11; 21 (1): 439. ( PubMed , DOI )

  4. Mizuno T, Miyata R, Hojo A, Tamura Y, Nakashima M, Mizuguchi T, Matsumoto N, Kato M: Clinical variations of epileptic syndrome associated with PACS2 variant. Brain & development. 2021.02; 43 (2): 343-347. ( PubMed , DOI )

  1. Sugawara Y, Mizuno T, Moriyama K, Ishiwata H, Kato M, Nakashima M, Mizuguchi T, Matsumoto N: Cerebrospinal fluid abnormalities in developmental and epileptic encephalopathy with a de novo CDK19 variant. Neurology. Genetics. 2020.12; 6 (6): e527. ( PubMed , DOI )

  1. Setsuko Hasegawa, Satoko Kumada, Naoyuki Tanuma, Atsumi Tsuji-Hosokawa, Ayako Kashimada, Tomoko Mizuno, Kengo Moriyama, Yuji Sugawara, Ikuko Shirai, Yohane Miyata, Hiroya Nishida, Hideaki Mashimo, Takeshi Hasegawa, Takatoshi Hosokawa, Hiroaki Hisakawa, Mitsugu Uematsu, Akio Fujine, Rie Miyata, Hiroshi Sakuma, Kenichi Kashimada, Kohsuke Imai, Tomohiro Morio, Masaharu Hayashi, Shuki Mizutani, Masatoshi Takagi: Long-Term Evaluation of Low-Dose Betamethasone for Ataxia Telangiectasia. Pediatr Neurol. 2019.11; 100 60-66. ( PubMed , DOI )

  2. Tomoko Mizuno, Ayako Kashimada, Toshihiro Nomura, Kengo Moriyama, Haruna Yokoyama, Setsuko Hasegawa, Masatoshi Takagi, Shuki Mizutani: Infantile-onset spinocerebellar ataxia type 5 associated with a novel SPTBN2 mutation: A case report. Brain Dev. 2019.08; 41 (7): 630-633. ( PubMed , DOI )

  3. Ayako Kashimada, Setsuko Hasegawa, Toshihiro Nomura, Hiroshi Shiraku, Kengo Moriyama, Tomonori Suzuki, Keisuke Nakajima, Tomoko Mizuno, Kohsuke Imai, Yuji Sugawara, Tomohiro Morio, Satoko Kumada, Masatoshi Takagi: Genetic analysis of undiagnosed ataxia-telangiectasia-like disorders. Brain Dev. 2019.02; 41 (2): 150-157. ( PubMed , DOI )

  1. Nagatsuma M, Takasawa K, Yamauchi T, Nakagawa R, Mizuno T, Tanaka E, Yamamoto K, Uemura N, Kashimada K, Morio T: A postzygotic KRAS mutation in a patient with Schimmelpenning syndrome presenting with lipomatosis, renovascular hypertension, and diabetes mellitus. Journal of human genetics. 2018.11; ( PubMed , DOI )

  1. Tomoko Mizuno, Satoko Kumada, Rie Naito: Sleep-Related Laryngeal Stridor in Opsoclonus Myoclonus Syndrome. Pediatr. Neurol.. 2017.12; 77 91. ( PubMed , DOI )

  1. Tomoko Mizuno, Hirofumi Komaki, Masayuki Sasaki, Satoko Takanoha, Kenji Kuroda, Kiyokaku Kon, Shigeo Mamiya, Masaru Yoshioka, Kana Yatabe, Takashi Mikata, Tadayuki Ishihara, Takashi Nakajima, Hiroo Watanabe, Masaaki Konagaya, Maki Mitani, Tetsuro Konishi, Yasuko Tokita, Kiyotaka Fukuda, Katsunori Tatara, Kyoko Maruta, Shigehiro Imamura, Rie Shimazaki, Kiyoshi Ishikawa, Toshio Saito, Susumu Shinno: Efficacy and tolerance of gastrostomy feeding in Japanese muscular dystrophy patients. Brain Dev.. 2012.10; 34 (9): 756-762. ( PubMed , DOI )

  1. Tomoko Mizuno, Masayuki Sasaki, Hirofumi Komaki, Hiroshi Sakuma, Yoshiaki Saito, Eiji Nakagawa, Kenji Sugai, Yuko Saito, Ikuya Nonaka, Yukio Sawaishi: A case of congenital axonal neuropathy associated with West syndrome. Brain Dev.. 2011.09; 33 (8): 692-696. ( PubMed , DOI )

  2. Tomoko Mizuno, Eiji Nakagawa, Hiroshi Sakuma, Yoshiaki Saito, Hirofumi Komaki, Kenji Sugai, Masayuki Sasaki, Akio Takahashi, Taisuke Otsuki, Kotoe Sakihara, Masumi Inagaki: Multiple band frequency analysis in a child of medial temporal lobe ganglioglioma. Childs Nerv Syst. 2011.03; 27 (3): 479-483. ( PubMed , DOI )

  1. 片桐 碧海, 町田 宗仁: ワクチン未接種の子どもたち(Zero-dose children)の現状と課題　日本の国際保健への貢献の必要性 保健医療科学. 2024.10; 73 (4): 330-335. ( 医中誌 )

  1. 山内泰輔, 水野朋子: 【腫瘍随伴症候群】免疫学的機序によるもの　オプソクローヌス・ミオクローヌス症候群 臨床検査. 2023.11; 67 (11): 1272-1277.

  2. 水野 朋子: 【日常診療で見落としたくない神経疾患】新たな診断・治療が可能となった疾患　脊髄性筋萎縮症 小児科. 2023.10; 64 (10): 1012-1018. ( 医中誌 )

  3. 小笠原啓祐,水野朋子,神谷尚宏,平田航,田村友美恵,山内泰輔,鈴木智典,鹿島田彩子,水野裕貴,岡本健太郎,田中陽典,小林大輔,高木正稔,森尾友宏: 低ガンマグロブリン血症に対し免疫グロブリン療法を行っている乳児全身性ヒアリン症 日本小児科学会雑誌 . 2023.10; 127 (10): 1299-1305. ( 医中誌 )

  1. 森田俊平, 水野朋子, 清水一秀, 田村友美恵, 鈴木智典, 柳町昌克, 磯田健志, 高木正稔, 稲次基希, 前原健寿, 森尾友宏: 軽微な受傷機転から急性硬膜外血腫を発症し、Fanconi貧血の診断に至った1例. 小児科臨床. 2022.02; 75 (1): 142-146.

  1. 水野朋子: 【脳の感染症-脳炎と寄生虫】細菌性脳炎　マイコプラズマ脳炎(解説/特集) Clinical Neuroscience. 2020.10; 38 (10): 1238-1240.

  1. 金森透, 水野朋子, 長澤正之, 天野沙織, 足洗美穂, 岡田麻理, 恩田恵子, 今井雅子, 鈴木奈都子, 大柴晃洋: マイコプラズマ脳炎・脳症8例の臨床的検討 脳と発達. 2018.01; 50 50-54. ( 医中誌 )

  1. Mizuno T, Nakagawa E, Saito Y, Komaki H, Sugai K, Sasaki M, Otsuki T, Hasegawa T, Yamanouchi H, Kuramochi A: [A case of neurocutaneous melanosis associated with focal cortical dysplasia]. No to hattatsu = Brain and development. 2011.07; 43 (4): 300-3. ( PubMed )

  2. 水野朋子, 中川栄二, 斎藤義朗, 小牧宏文, 須貝研司, 佐々木征行, 大槻泰介, 長谷川毅, 山内秀雄, 倉持朗: 限局性皮質形成異常を合併した神経皮膚黒色症の1例 脳と発達. 2011.07; 43 (4): 300-303. ( 医中誌 )

  1. 片桐（水野）朋子, 山本敦子, 白井謙太朗, 渡辺章充, 荒木聡: 二相性の経過をとり、けいれん再発直前のMRIが正常であったヒトヘルペスウイルス(HHV)6による急性脳症 脳と発達. 2007.11; 39 (6): 458-459. ( 医中誌 )

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