論文・総説 - 森 崇寧
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Umene R, Kitamura M, Arai H, Matsumura K, Ishimaru Y, Maeda K, Uramatsu T, Obata Y, Mori T, Sohara E, Uchida S, Nishino T. Bartter syndrome representing digenic-based salt-losing tubulopathies presumably accelerated by renal insufficiency. CEN case reports. 2020.06; 9 (4): 375-379. ( PubMed, DOI )
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Furusho Taisuke, Sohara Eisei, Mandai Shintaro, Kikuchi Hiroaki, Takahashi Naohiro, Fujimaru Takuya, Hashimoto Hiroko, Arai Yohei, Ando Fumiaki, Zeniya Moko, Mori Takayasu, Susa Koichiro, Isobe Kiyoshi, Nomura Naohiro, Yamamoto Kohei, Okado Tomokazu, Rai Tatemitsu, Uchida Shinichi. Renal TNF alpha activates the WNK phosphorylation cascade and contributes to salt-sensitive hypertension in chronic kidney disease KIDNEY INTERNATIONAL. 2020.04; 97 (4): 713-727. ( PubMed, DOI )
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Mori Tetsuya, Sekimizu Masahiro, Fukano Reiji, Choi Ilseung, Takeuchi Kengo, Tateishi Ukihide, Terauchi Takashi, Kada Akiko, Saito Akiko, Asada Ryuta, Horibe Keizo, Nagai Hirokazu. Alectinib in Children with Recurrent or Refractory ALK-positive ALCL: Phase 2 Trial in Both Children and Adults PEDIATRIC BLOOD & CANCER. 2019.12; 66 S12-S13.
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Ikeda Takashi, Mori Keita, Kawamura Koji, Mori Takehiko, Hagiwara Shotaro, Ueda Yasunori, Kahata Kaoru, Uchida Naoyuki, Tsukada Nobuhiro, Murakami Satoshi, Yamamoto Masahide, Takahashi Tsutomu, Ichinohe Tatsuo, Onizuka Makoto, Atsuta Yoshiko, Kanda Yoshinobu, Okamoto Shinichiro, Sunami Kazutaka, Takamatsu Hiroyuki. Comparison between autologous and allogeneic stem cell transplantation as salvage therapy for multiple myeloma relapsing/progressing after autologous stem cell transplantation HEMATOLOGICAL ONCOLOGY. 2019.12; 37 (5): 586-594. ( DOI )
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Chinen T, Saeki E, Mori T, Sohara E, Uchida S, Akimoto T. A case of Gitelman syndrome: our experience with a patient treated in clinical practice on a local island. Journal of rural medicine : JRM. 2019.11; 14 (2): 258-262. ( PubMed, DOI )
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Furuto Yoshitaka, Kawamura Mariko, Namikawa Akio, Takahashi Hiroko, Shibuya Yuko, Mori Takayasu, Sohara Eisei. Non-urate transporter 1, non-glucose transporter member 9-related renal hypouricemia and acute renal failure accompanied by hyperbilirubinemia after anaerobic exercise: a case report BMC NEPHROLOGY. 2019.11; 20 (1): 433. ( PubMed, DOI )
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Akihisa T, Sato M, Wakayama Y, Taneda S, Horita S, Hirose O, Makabe S, Kataoka H, Mori T, Sohara E, Uchida S, Nitta K, Mochizuki T. Glomerular Basement Membrane Protein Expression and the Diagnosis and Prognosis of Autosomal Dominant Alport Syndrome. Kidney medicine. 2019.11; 1 (6): 391-396. ( PubMed, DOI )
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Yoshiaki Matsuura, Naohiro Nomura, Wakana Shoda, Takayasu Mori, Kiyoshi Isobe, Koichiro Susa, Fumiaki Ando, Eisei Sohara, Tatemitsu Rai, Shinichi Uchida. Tacrolimus ameliorates the phenotypes of type 4 Bartter syndrome model mice through activation of sodium-potassium-2 chloride cotransporter and sodium-chloride cotransporter. Biochem. Biophys. Res. Commun.. 2019.09; 517 (2): 364-368. ( PubMed, DOI )
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Nagai Norihiro, Ayaki Masahiko, Yanagawa Tatsuo, Hattori Atsuhiko, Negishi Kazuno, Mori Takuro, Nakamura Takahiro J., Tsubota Kazuo. Suppression of Blue Light at Night Ameliorates Metabolic Abnormalities by Controlling Circadian Rhythms INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. 2019.09; 60 (12): 3786-3793. ( DOI )
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Sakoh Takashi, Sekine Akinari, Mori Takayasu, Mizuno Hiroki, Kawada Masahiro, Hiramatsu Rikako, Hasegawa Eiko, Hayami Noriko, Yamanouchi Masayuki, Suwabe Tatsuya, Sawa Naoki, Ubara Yoshifumi, Fujimaru Takuya, Sohara Eisei, Shinichi Uchida, Hoshino Junichi, Takaichi Kenmei. A familial case of pseudohypoaldosteronism type II (PHA2) with a novel mutation (D564N) in the acidic motif in WNK4 MOLECULAR GENETICS & GENOMIC MEDICINE. 2019.06; 7 (6): e705. ( PubMed, DOI )
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Ohkubo Atsushi, Okado Tomokazu, Sakurasawa Takatoshi, Maeda Takuma, Itagaki Ayako, Yamamoto Hiroko, Miyamoto Satoko, Seshima Hiroshi, Kurashima Naoki, Mori Takayasu, Iimori Soichiro, Sohara Eisei, Rai Tatemitsu, Uchida Shinichi, Naito Shotaro. Removal Characteristics of Immunoadsorption with the Tryptophan-Immobilized Column Using Conventional and Selective Plasma Separators in the Treatment of Myasthenia Gravis THERAPEUTIC APHERESIS AND DIALYSIS. 2019.06; 23 (3): 271-278. ( PubMed, DOI )
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Fujiki Tamami, Ando Fumiaki, Murakami Kana, Isobe Kiyoshi, Mori Takayasu, Susa Koichiro, Nomura Naohiro, Sohara Eisei, Rai Tatemitsu, Uchida Shinichi. Tolvaptan activates the Nrf2/HO-1 antioxidant pathway through PERK phosphorylation SCIENTIFIC REPORTS. 2019.06; 9 (1): 9245. ( PubMed, DOI )
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Ohkubo Atsushi, Okado Tomokazu, Sakurasawa Takatoshi, Maeda Takuma, Itagaki Ayako, Yamamoto Hiroko, Miyamoto Satoko, Seshima Hiroshi, Kurashima Naoki, Mori Takayasu, Iimori Soichiro, Sohara Eisei, Rai Tatemitsu, Uchida Shinichi, Naito Shotaro. 重症筋無力症の治療における通常型および選択的血漿分離器を用いたトリプトファン固定化カラムによる免疫吸着の除去特性(Removal Characteristics of Immunoadsorption with the Tryptophan-Immobilized Column Using Conventional and Selective Plasma Separators in the Treatment of Myasthenia Gravis) Therapeutic Apheresis and Dialysis. 2019.06; 23 (3): 271-278. ( 医中誌 )
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Asanomi Yuya, Shigemizu Daichi, Miyashita Akinori, Mitsumori Risa, Mori Taiki, Hara Norikazu, Ito Kaoru, Niida Shumpei, Ikeuchi Takeshi, Ozaki Kouichi. A rare functional variant of SHARPIN attenuates the inflammatory response and associates with increased risk of late-onset Alzheimer's disease MOLECULAR MEDICINE. 2019.06; 25 ( DOI )
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Tanaka Tatsuhiko, Oki Eishin, Mori Takayasu, Tsuruga Kazushi, Sohara Eisei, Uchida Shinichi, Tanaka Hiroshi. COMPLETE CLINICAL RESOLUTION OF A JAPANESE FAMILY WITH RENAL PSEUDOHYPOALDOSTERONISM TYPE 1 DUE TO A NOVEL NR3C2 MUTATION NEPHROLOGY. 2019.04; 24 (4): 489-+. ( PubMed, DOI )
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Saki Watanabe, Jun Ino, Takuya Fujimaru, Sekiko Taneda, Taro Akihisa, Shiho Makabe, Hiroshi Kataoka, Takayasu Mori, Eisei Sohara, Shinichi Uchida, Kosaku Nitta, Toshio Mochizuki. PKD1 mutation may epistatically ameliorate nephronophthisis progression in patients with NPHP1 deletion. Clin Case Rep. 2019.02; 7 (2): 336-339. ( PubMed, DOI )
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Kikuchi Hiroaki, Sasaki Emi, Nomura Naohiro, Mori Takayasu, Minamishima Yoji Andrew, Yoshizaki Yuki, Takahashi Naohiro, Furusho Taisuke, Arai Yohei, Mandai Shintaro, Yamashita Takahiro, Ando Fumiaki, Maejima Yasuhiro, Isobe Kiyoshi, Okado Tomokazu, Rai Tatemitsu, Uchida Shinichi, Sohara Eisei. Failure to sense energy depletion may be a novel therapeutic target in chronic kidney disease KIDNEY INTERNATIONAL. 2019.01; 95 (1): 123-137. ( PubMed, DOI )
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Mandai Shintaro, Sato Hidehiko, Iimori Soichiro, Naito Shotaro, Tanaka Haruna, Ando Fumiaki, Susa Koichiro, Isobe Kiyoshi, Mori Takayasu, Nomura Naohiro, Sohara Eisei, Okado Tomokazu, Uchida Shinichi, Fushimi Kiyohide, Rai Tatemitsu. Nationwide in-hospital mortality following major fractures among hemodialysis patients and the general population: An observational cohort BONE. 2019.01; 130 115122. ( PubMed, DOI )
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Sekine Akinari, Fujimaru Takuya, Hoshino Junichi, Suwabe Tatsuya, Oguro Masahiko, Mizuno Hiroki, Kawada Masahiro, Sumida Keiichi, Hiramatsu Rikako, Hasegawa Eiko, Yamanouchi Masayuki, Hayami Noriko, Mandai Shintaro, Chiga Motoko, Kikuchi Hiroaki, Ando Fumiaki, Mori Takayasu, Sohara Eisei, Uchida Shinichi, Sawa Naoki, Takaichi Kenmei, Ubara Yoshifumi. Genotype-Clinical Correlations in Polycystic Kidney Disease with No Apparent Family History AMERICAN JOURNAL OF NEPHROLOGY. 2019; 49 (3): 233-240. ( PubMed, DOI )
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Ayumi Matsumoto, Isao Matsui, Takayasu Mori, Yusuke Sakaguchi, Masayuki Mizui, Yoshiyasu Ueda, Atsushi Takahashi, Yohei Doi, Karin Shimada, Satoshi Yamaguchi, Keiichi Kubota, Nobuhiro Hashimoto, Tatsufumi Oka, Yoshitsugu Takabatake, Eisei Sohara, Takayuki Hamano, Shinichi Uchida, Yoshitaka Isaka. Severe Osteomalacia with Dent Disease Caused by a Novel Intronic Mutation of the CLCN5 gene. Intern. Med.. 2018.12; 57 (24): 3603-3610.