Search Results - "飯島, 誠"

肺血栓塞栓症を合併した膝窩静脈静脈性血管瘤の1例 by 稗田, 哲也, 牧野, 裕, 東, 亮太, 飯島, 誠, 村上, 達哉

“…膝窩静脈静脈性血管瘤（popliteal venous aneurysm; PVA）は稀な疾患で，肺血栓塞栓症（pulmonary thromboembolism;…”
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P72-4. 特発性胸腹部大動脈破裂の一例 by 牧野裕, 伊藤和, 村瀬亮太, 飯島誠

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OAC-038 PPAR γ活性と石灰化抑制効果に関する脱細胞化弁付き導管移植実験モデルでの基礎的検討 by 飯島誠, 宋建国, Eric Johansson, Sun Suwan, Roberto Magistri, 鈴木良和, Antonio Ballarin

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P48-3. 治療に難渋し胸腹部置換術を要したEVAR術後type V endoleakの1例 by 牧野裕, 東亮太, 新井洋輔, 飯島誠

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P33-2. ハイブリット治療を行った外傷性右鎖骨下動脈瘤の1例 by 牧野裕, 東亮太, 稗田哲也, 飯島誠

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O14-6. EVAR術後の瘤径変化におけるType II EL発症時期の意義 by 東亮太, 稗田哲也, 飯島誠, 牧野裕

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PA04-02 閉鎖チャンバー式静脈血リザーバ併用PCPS閉鎖回路による左心室前負荷軽減効果の実験的検討 by 飯島誠, 内藤祐嗣, 新宮康栄, 若狭哲, 大岡智学, 橘剛, 久保田卓, 松居喜郎

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OA-115 非虚血性心筋症においてQuantitative Gated SPECTによる術前左室壁thickeningは術後心事故を予測しうる - 術前のQGS, 酢酸PET, 心臓MRIによる左室局所解析の検討から by 久保田卓, 関達也, 浅井英嗣, 加藤伸康, 飯島誠, 内藤祐嗣, 新宮康栄, 若狭哲, 大岡智学, 橘剛, 松居喜郎

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SYA3-03 脳梗塞を伴った活動性感染性心内膜炎症例の手術介入時期に対する検討 by 小林一哉, 安藤悟央, 関達也, 浅井英嗣, 加藤伸康, 飯島誠, 内藤祐嗣, 新宮康栄, 若狭哲, 加藤裕貴, 大岡智学, 橘剛, 久保田卓, 松居喜郎

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SP06-04 胸部大動脈―食道瘻の治療戦略 by 久保田卓, 関達也, 飯島誠, 内藤祐嗣, 新宮康栄, 若狭哲, 大岡智学, 橘剛, 山内英智, 大畑俊裕, 大場淳一, 松居喜郎

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An updated view of the pathogenesis of steroid-sensitive nephrotic syndrome by Horinouchi, Tomoko, Nozu, Kandai, Iijima, Kazumoto

“…  Idiopathic nephrotic syndrome is the most common childhood glomerular disease. Most forms of this syndrome respond to corticosteroids at standard doses and…”
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Rituximab in steroid-sensitive nephrotic syndrome: lessons from clinical trials by Iijima, Kazumoto, Sako, Mayumi, Kamei, Koichi, Nozu, Kandai

“…Idiopathic nephrotic syndrome is the most common chronic glomerular disease in children. A total of 80–90% of patients with childhood idiopathic nephrotic…”
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Comprehensive genetic diagnosis of Japanese patients with severe proteinuria by Nagano, China, Yamamura, Tomohiko, Horinouchi, Tomoko, Aoto, Yuya, Ishiko, Shinya, Sakakibara, Nana, Shima, Yuko, Nakanishi, Koichi, Nagase, Hiroaki, Iijima, Kazumoto, Nozu, Kandai

“…Numerous disease-causing gene mutations have been identified in proteinuric diseases, such as nephrotic syndrome and glomerulosclerosis. This report describes…”
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Serum cardiac troponin I is a candidate biomarker for cardiomyopathy in Duchenne and Becker muscular dystrophies by Yamaguchi, Hiroshi, Awano, Hiroyuki, Yamamoto, Tetsushi, Nambu, Yoshinori, Iijima, Kazumoto

“…Introduction/Aims Serum cardiac troponin I (cTnI), its relation to cardiomyopathy, and the contribution of the ACTN3 genotype to serum levels of cTnI in…”
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Rituximab for nephrotic syndrome in children by Iijima, Kazumoto, Sako, Mayumi, Nozu, Kandai

“…Idiopathic nephrotic syndrome is the most common chronic glomerular disease in children. At least 20 % of children with this syndrome show frequent relapses…”
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Mycophenolate Mofetil after Rituximab for Childhood-Onset Complicated Frequently-Relapsing or Steroid-Dependent Nephrotic Syndrome by Iijima, Kazumoto, Sako, Mayumi, Oba, Mari, Tanaka, Seiji, Hamada, Riku, Sakai, Tomoyuki, Ohwada, Yoko, Ninchoji, Takeshi, Yamamura, Tomohiko, Machida, Hiroyuki, Shima, Yuko, Tanaka, Ryojiro, Kaito, Hiroshi, Araki, Yoshinori, Morohashi, Tamaki, Kumagai, Naonori, Gotoh, Yoshimitsu, Ikezumi, Yohei, Kubota, Takuo, Kamei, Koichi, Fujita, Naoya, Ohtsuka, Yasufumi, Okamoto, Takayuki, Yamada, Takeshi, Tanaka, Eriko, Shimizu, Masaki, Horinochi, Tomoko, Konishi, Akihide, Omori, Takashi, Nakanishi, Koichi, Ishikura, Kenji, Ito, Shuichi, Nakamura, Hidefumi, Nozu, Kandai

“…Rituximab is the standard therapy for childhood-onset complicated frequently relapsing or steroid-dependent nephrotic syndrome (FRNS/SDNS). However, most…”
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In steroid-resistant nephrotic syndrome that meets the strict definition, monogenic variants are less common than expected by Ichikawa, Yuta, Sakakibara, Nana, Nagano, China, Inoki, Yuta, Tanaka, Yu, Ueda, Chika, Kitakado, Hideaki, Kondo, Atsushi, Ishimori, Shingo, Horinouchi, Tomoko, Iijima, Kazumoto, Nozu, Kandai

“…Background In patients with steroid-resistant nephrotic syndrome (SRNS), the presence of monogenic variants influences therapeutic strategies. Large cohort…”
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The ACTN3 577XX Null Genotype Is Associated with Low Left Ventricular Dilation-Free Survival Rate in Patients with Duchenne Muscular Dystrophy by Nagai, Masashi, Awano, Hiroyuki, Yamamoto, Tetsushi, Bo, Ryosuke, Matsuo, Masafumi, Iijima, Kazumoto

“…•The ACTN3 genotype is a genetic modifier for Duchenne muscular dystrophy.•The ACTN3 genotype with risk of dilated cardiomyopathy in patients was studied.•The…”
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Detailed characteristics of acute encephalopathy with biphasic seizures and late reduced diffusion: 18-year data of a single-center consecutive cohort by Yamaguchi, Hiroshi, Nishiyama, Masahiro, Tokumoto, Shoichi, Ishida, Yusuke, Tomioka, Kazumi, Aoki, Kazunori, Seino, Yusuke, Toyoshima, Daisaku, Takeda, Hiroki, Kurosawa, Hiroshi, Nozu, Kandai, Maruyama, Azusa, Tanaka, Ryojiro, Iijima, Kazumoto, Nagase, Hiroaki

“…Acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) is a syndrome characterized by biphasic seizures with impaired consciousness…”
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Assessment of catabolic state in infants with the use of urinary titin N-fragment by Fukushima, Sachiyo, Nakanishi, Nobuto, Fujioka, Kazumichi, Suga, Kenichi, Shirakawa, Taku, Osawa, Kayo, Hara, Kanako, Tsutsumi, Rie, Urushihara, Maki, Nakagawa, Ryuji, Awano, Hiroyuki, Oto, Jun, Sakaue, Hiroshi, Iijima, Kazumoto, Matsuo, Masafumi

“…Background Urinary titin N-fragment levels have been used to assess the catabolic state, and we used this biomarker to evaluate the catabolic state of infants…”
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