Zobrazeno 1 - 10
of 319
pro vyhledávání: '"Takashi, Koizumi"'
Autor:
Mao Mukai, Ai Hamano, Ikuko Mizuta, Isao Yokota, Akiko Watanabe-Hosomi, Hiraku Matsuura, Takashi Koizumi, Jun Matsuura, Tomoyuki Ohara, Shigenori Matsushima, Satoshi Teramukai, Kei Yamada, Toshiki Mizuno
Publikováno v:
Frontiers in Neurology, Vol 13 (2023)
BackgroundImpaired cerebrovasoreactivity is thought to play an important role in the pathophysiology of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). We aimed to clarify the association between
Externí odkaz:
https://doaj.org/article/8d5c042e35784a6a86b53058552e7ae3
Autor:
Takashi Koizumi, Katsutoshi Taguchi, Ikuko Mizuta, Hiroe Toba, Makoto Ohigashi, Okihiro Onishi, Kazuya Ikoma, Seiji Miyata, Tetsuo Nakata, Masaki Tanaka, Sébastien Foulquier, Harry W. M. Steinbusch, Toshiki Mizuno
Publikováno v:
Journal of Neuroinflammation, Vol 16, Iss 1, Pp 1-13 (2019)
Abstract Background Microglia play crucial roles in the maintenance of brain homeostasis. Activated microglia show a biphasic influence, promoting beneficial repair and causing harmful damage via M2 and M1 microglia, respectively. It is well-known th
Externí odkaz:
https://doaj.org/article/2ac3ba0aeded49a8a1a8a69f325d216d
Autor:
Takuma Ohmichi, Takashi Kasai, Makiko Shinomoto, Jun Matsuura, Takashi Koizumi, Fukiko Kitani-Morii, Harutsugu Tatebe, Hidenao Sasaki, Toshiki Mizuno, Takahiko Tokuda
Publikováno v:
Frontiers in Neurology, Vol 11 (2020)
Caffeine is considered to be a neuroprotective agent against Parkinson's disease (PD) and is expected to offer a blood-based biomarker for the disease. We herein investigated the ability of this biomarker to discriminate between PD and neurodegenerat
Externí odkaz:
https://doaj.org/article/9fd87767385e4b8eb25577f7a1f5ef65
Autor:
Takashi Okada, Kazuo Washida, Kenichi Irie, Satoshi Saito, Michio Noguchi, Tsutomu Tomita, Masatoshi Koga, Kazunori Toyoda, Shuhei Okazaki, Takashi Koizumi, Ikuko Mizuta, Toshiki Mizuno, Masafumi Ihara
Publikováno v:
Frontiers in Aging Neuroscience, Vol 12 (2020)
Objectives: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is the most common hereditary small vessel disease, with reported frequencies of 2-5/100,000 individuals. Recently, it has been reported
Externí odkaz:
https://doaj.org/article/b048d0036cc44c1aad29dd14abfc0e82
Publikováno v:
Frontiers in Aging Neuroscience, Vol 12 (2020)
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a hereditary cerebral small vessel disease caused by mutations in NOTCH3, is characterized by recurrent stroke without vascular risk factors, mood d
Externí odkaz:
https://doaj.org/article/d1618f9321554437bb1370feb1d20e3b
Autor:
Takashi Koizumi, Danielle Kerkhofs, Toshiki Mizuno, Harry W. M. Steinbusch, Sébastien Foulquier
Publikováno v:
Frontiers in Neuroscience, Vol 13 (2019)
Cerebral small vessels feed and protect the brain parenchyma thanks to the unique features of the blood–brain barrier. Cerebrovascular dysfunction is therefore seen as a detrimental factor for the initiation of several central nervous system (CNS)
Externí odkaz:
https://doaj.org/article/25cf3c6eb2764dd19fba4b6839b7be6b
Publikováno v:
京都府立医科大学附属北部医療センター誌 = Journal of North Medical Center Kyoto Prefectural University of Medicine. 7(1):44-49
京都府立医科大学附属北部医療センター 神経内科
Department of Neurology, North Medical Center, Kyoto Prefectural University of Medicine
症例は63歳女性。3日前からの異常言動を主訴に救急受診した。
Department of Neurology, North Medical Center, Kyoto Prefectural University of Medicine
症例は63歳女性。3日前からの異常言動を主訴に救急受診した。
Publikováno v:
Rinsho shinkeigaku = Clinical neurology. 62(5)
A 63-year-old woman with no medical history of note developed acute-onset abnormal behavior persisting for one week. Mild disturbance of consciousness was noted on physical examination. Her blood and spinal fluid test results were normal. On brain MR
Autor:
Yuki Yoshimura, Takashi Koizumi
Publikováno v:
AIJ Journal of Technology and Design. 26:655-660
Autor:
Akiko Watanabe-Hosomi, Ai Hamano, Toshiki Mizuno, Ikuko Mizuta, Mao Mukai, Jun Matsuura, Hidekazu Tomimoto, Takashi Koizumi
Publikováno v:
Journal of Human Genetics. 65:637-646