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Wyświetlanie 1-20 z 226
Tytuł:
Two pathways differentially linking tau depositions, oxidative stress, and neuronal loss to apathetic phenotypes in progressive supranuclear palsy
Autorzy:
Matsuoka, Kiwamu
Takado, Yuhei
Tagai, Kenji
Kubota, Manabu
Sano, Yasunori
Takahata, Keisuke
Ono, Maiko
Seki, Chie
Matsumoto, Hideki
Endo, Hironobu
Shinotoh, Hitoshi
Sahara, Yasuka
Obata, Takayuki
Near, Jamie
Kawamura, Kazunori
Zhang, Ming-Rong
Suhara, Tetsuya
Shimada, Hitoshi
Higuchi, Makoto
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Źródło:
In Journal of the Neurological Sciences 15 January 2023 444
Czasopismo naukowe
Szczegóły
Tytuł:
An optimized reference tissue method for quantification of tau protein depositions in diverse neurodegenerative disorders by PET with 18F-PM-PBB3 (18F-APN-1607)
Autorzy:
Tagai, Kenji
Ikoma, Yoko
Endo, Hironobu
Debnath, Oiendrila Bhowmik
Seki, Chie
Matsuoka, Kiwamu
Matsumoto, Hideki
Oya, Masaki
Hirata, Kosei
Shinotoh, Hitoshi
Takahata, Keisuke
Kurose, Shin
Sano, Yasunori
Ono, Maiko
Shimada, Hitoshi
Kawamura, Kazunori
Zhang, Ming-Rong
Takado, Yuhei
Higuchi, Makoto
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Źródło:
In NeuroImage 1 December 2022 264
Czasopismo naukowe
Szczegóły
Tytuł:
A Machine Learning–Based Approach to Discrimination of Tauopathies Using [F]PM‐PBB3 PET Images.
Autorzy:
Endo, Hironobu (AUTHOR)
Tagai, Kenji (AUTHOR)
Ono, Maiko (AUTHOR)
Ikoma, Yoko (AUTHOR)
Oyama, Asaka (AUTHOR)
Matsuoka, Kiwamu (AUTHOR)
Kokubo, Naomi (AUTHOR)
Hirata, Kosei (AUTHOR)
Sano, Yasunori (AUTHOR)
Oya, Masaki (AUTHOR)
Matsumoto, Hideki (AUTHOR)
Kurose, Shin (AUTHOR)
Seki, Chie (AUTHOR)
Shimizu, Hiroshi (AUTHOR)
Kakita, Akiyoshi (AUTHOR)
Takahata, Keisuke (AUTHOR)
Shinotoh, Hitoshi (AUTHOR)
Shimada, Hitoshi (AUTHOR)
Tokuda, Takahiko (AUTHOR)
Kawamura, Kazunori (AUTHOR)
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Źródło:
Movement Disorders. Nov2022, Vol. 37 Issue 11, p2236-2246. 11p.
Czasopismo naukowe
Szczegóły
Tytuł:
Immediate postnatal central hypothyroidism caused by maternal Graves' disease: Importance of early screening.
Autorzy:
Tochibora S; Department of Pediatrics, Graduate School of Medicine Gifu University Gifu Japan.; Division of Neonatal Intensive Care Unit Gifu University Hospital Gifu Japan.
Hori T; Department of Pediatrics, Graduate School of Medicine Gifu University Gifu Japan.; Division of Neonatal Intensive Care Unit Gifu University Hospital Gifu Japan.; Clinical Genetics Center Gifu University Hospital Gifu Japan.
Mori M; Department of Pediatrics, Graduate School of Medicine Gifu University Gifu Japan.; Division of Neonatal Intensive Care Unit Gifu University Hospital Gifu Japan.
Matsumoto H; Department of Pediatrics, Graduate School of Medicine Gifu University Gifu Japan.; Division of Neonatal Intensive Care Unit Gifu University Hospital Gifu Japan.
Otsuka H; Department of Pediatrics, Graduate School of Medicine Gifu University Gifu Japan.; Division of Neonatal Intensive Care Unit Gifu University Hospital Gifu Japan.; Clinical Genetics Center Gifu University Hospital Gifu Japan.
Sasai H; Department of Pediatrics, Graduate School of Medicine Gifu University Gifu Japan.; Division of Neonatal Intensive Care Unit Gifu University Hospital Gifu Japan.; Clinical Genetics Center Gifu University Hospital Gifu Japan.
Ito Y; Department of Pediatrics, Graduate School of Medicine Gifu University Gifu Japan.; Division of Neonatal Intensive Care Unit Gifu University Hospital Gifu Japan.
Kasahara Y; Department of Pediatrics, Graduate School of Medicine Gifu University Gifu Japan.; Division of Neonatal Intensive Care Unit Gifu University Hospital Gifu Japan.; Department of Pediatrics Matsunami General Hospital Gifu Japan.
Kawamoto N; Department of Pediatrics, Graduate School of Medicine Gifu University Gifu Japan.; Division of Neonatal Intensive Care Unit Gifu University Hospital Gifu Japan.
Ohnishi H; Department of Pediatrics, Graduate School of Medicine Gifu University Gifu Japan.; Division of Neonatal Intensive Care Unit Gifu University Hospital Gifu Japan.; Clinical Genetics Center Gifu University Hospital Gifu Japan.
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Źródło:
Clinical case reports [Clin Case Rep] 2022 Jul 14; Vol. 10 (7), pp. e6061. Date of Electronic Publication: 2022 Jul 14 (Print Publication: 2022).
Typ publikacji:
Case Reports
Raport
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Founder genetic variants of ABCC4 and ABCC11 in the Japanese population are not associated with the development of subacute myelo-optico-neuropathy (SMON).
Autorzy:
Matsumoto H; Department of Pediatrics, Gifu University Graduate School of Medicine, Gifu University, Gifu, Japan.
Sasai H; Department of Pediatrics, Gifu University Graduate School of Medicine, Gifu University, Gifu, Japan.; Clinical Genetics Center, Gifu University Hospital, Gifu, Japan.
Kawamoto N; Department of Pediatrics, Gifu University Graduate School of Medicine, Gifu University, Gifu, Japan.
Katsuyama M; Radioisotope Center, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Minamiyama M; Department of Neurology, National Hospital Organization Suzuka National Hospital, Mie, Japan.
Kuru S; Department of Neurology, National Hospital Organization Suzuka National Hospital, Mie, Japan.
Fukao T; Department of Pediatrics, Gifu University Graduate School of Medicine, Gifu University, Gifu, Japan.; Clinical Genetics Center, Gifu University Hospital, Gifu, Japan.
Ohnishi H; Department of Pediatrics, Gifu University Graduate School of Medicine, Gifu University, Gifu, Japan.; Clinical Genetics Center, Gifu University Hospital, Gifu, Japan.
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Corporate Authors:
SMON research group members
Źródło:
Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2022 Jan; Vol. 10 (1), pp. e1845. Date of Electronic Publication: 2021 Dec 24.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Clioquinol*
Peripheral Nervous System Diseases*
ATP-Binding Cassette Transporters ; Humans ; Japan ; Multidrug Resistance-Associated Proteins/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Dietary Supplementation with Monosodium Glutamate Suppresses Chemotherapy-Induced Downregulation of the T1R3 Taste Receptor Subunit in Head and Neck Cancer Patients.
Autorzy:
Shono, Hitoshi
Tsutsumi, Rie
Beppu, Kana
Matsushima, Rina
Watanabe, Suzuno
Fujimoto, Chisa
Kanamura, Ryo
Ohnishi, Hiroki
Kondo, Eiji
Azuma, Takahiro
Sato, Go
Kawai, Misako
Matsumoto, Hideki
Kitamura, Yoshiaki
Sakaue, Hiroshi
Takeda, Noriaki
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Źródło:
Nutrients; Sep2021, Vol. 13 Issue 9, p2921-2921, 1p
Czasopismo naukowe
Szczegóły
Tytuł:
Japanese patients with mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency: In vitro functional analysis of five novel HMGCS2 mutations.
Autorzy:
Ago Y; Department of Pediatrics, Graduate School of Medicine, Gifu University Hospital, Gifu, Gifu 501-1194, Japan.
Otsuka H; Department of Pediatrics, Graduate School of Medicine, Gifu University Hospital, Gifu, Gifu 501-1194, Japan.
Sasai H; Department of Pediatrics, Graduate School of Medicine, Gifu University Hospital, Gifu, Gifu 501-1194, Japan.; Clinical Genetics Center, Gifu University Hospital, Gifu, Gifu 501-1194, Japan.
Abdelkreem E; Department of Pediatrics, Faculty of Medicine, Sohag University, Sohag 82524, Egypt.
Nakama M; Department of Pediatrics, Graduate School of Medicine, Gifu University Hospital, Gifu, Gifu 501-1194, Japan.; Clinical Genetics Center, Gifu University Hospital, Gifu, Gifu 501-1194, Japan.
Aoyama Y; Department of Biomedical Sciences, College of Life and Health Sciences, Education and Training Center of Medical Technology, Chubu University, Kasugai, Aichi 487-8501, Japan.
Matsumoto H; Department of Pediatrics, Graduate School of Medicine, Gifu University Hospital, Gifu, Gifu 501-1194, Japan.
Fujiki R; Department of Applied Genomics, Kazusa DNA Research Institute, Kisarazu, Chiba 292-0818, Japan.
Ohara O; Department of Applied Genomics, Kazusa DNA Research Institute, Kisarazu, Chiba 292-0818, Japan.
Akiyama K; Akiyama Children's Clinic, Kitami, Hokkaido 090-0051, Japan.
Fukui K; Department of Pediatrics and Child Health, Kurume University School of Medicine, Kurume, Fukuoka 830-0011, Japan.
Watanabe Y; Department of Pediatrics and Child Health, Kurume University School of Medicine, Kurume, Fukuoka 830-0011, Japan.; Research Institute of Medical Mass Spectrometry, Kurume University School of Medicine, Kurume, Fukuoka 830-0011, Japan.
Nakajima Y; Department of Pediatrics, Fujita Health University School of Medicine, Toyoake, Aichi 470-1192, Japan.
Ohnishi H; Department of Pediatrics, Graduate School of Medicine, Gifu University Hospital, Gifu, Gifu 501-1194, Japan.
Ito T; Department of Pediatrics, Fujita Health University School of Medicine, Toyoake, Aichi 470-1192, Japan.
Fukao T; Department of Pediatrics, Graduate School of Medicine, Gifu University Hospital, Gifu, Gifu 501-1194, Japan.; Clinical Genetics Center, Gifu University Hospital, Gifu, Gifu 501-1194, Japan.
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Źródło:
Experimental and therapeutic medicine [Exp Ther Med] 2020 Nov; Vol. 20 (5), pp. 39. Date of Electronic Publication: 2020 Sep 01.
Typ publikacji:
Journal Article
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Wyświetlanie 1-20 z 226

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