Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Yukari Morita"'
Publikováno v:
Rigakuryoho Kagaku. 37:9-13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee3d4ab3528aaaf11cece781da726e88
https://doi.org/10.1589/rika.37.9
https://doi.org/10.1589/rika.37.9
Autor:
Yukari Morita, Tomomi Furushima, Konosuke Furuta, Yuka Miyamoto, Yasushi Osaki, Hirokazu Furuya
Publikováno v:
Neurology and Clinical Neuroscience. 9:83-90
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::32a916e15ccddd5c82667e9ffa6e9716
https://doi.org/10.1111/ncn3.12468
https://doi.org/10.1111/ncn3.12468
Autor:
Tomomi Furushima, Yasushi Osaki, Yuka Miyamoto, Hirokazu Furuya, Yukari Morita, Tomohiro Shogase, Sho Ohtsuru
Publikováno v:
Acta Neurologica Scandinavica
Objectives A pre-possible multiple system atrophy (MSA) phase, that is, the period between symptom onset and satisfying the second consensus diagnostic criteria for possible or probable MSA, may exist. The aim of the study was to identify the pre-pos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d64597f6709686b1d428be106441f12
https://pubmed.ncbi.nlm.nih.gov/33111976
https://pubmed.ncbi.nlm.nih.gov/33111976
Autor:
Yuka Miyamoto, Masanori P. Takahashi, Shu‐ichi Nagamatsu, Tomomi Furushima, Tomoya Kubota, Itsuki Mori, Hirokazu Furuya, Yasushi Osaki, Yukari Morita
Publikováno v:
Neurology and Clinical Neuroscience. 7:354-356
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::695d7873aa4828c7480873fa4adf00b5
https://doi.org/10.1111/ncn3.12328
https://doi.org/10.1111/ncn3.12328
Publikováno v:
Neurology and Clinical Neuroscience
Background and Aim Early clinical diagnosis of progressive supranuclear palsy (PSP) remains challenging. Aim We attempted to identify any sign or symptom to diagnose PSP earlier. Methods A total of 401 patients, 40 with PSP and 361 with other neurode
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b859859afa041d22b2d9f4841c0daf78
https://doi.org/10.1111/ncn3.12122
https://doi.org/10.1111/ncn3.12122
Autor:
Yoshiaki, Nishida, Masayuki, Nakamura, Yuka, Urata, Kei, Kasamo, Hanae, Hiwatashi, Izumi, Yokoyama, Masahiro, Mizobuchi, Kotaro, Sakurai, Yasushi, Osaki, Yukari, Morita, Masako, Watanabe, Kenji, Yoshida, Kiyomi, Yamane, Natsuki, Miyakoshi, Ryouichi, Okiyama, Takehiro, Ueda, Noritaka, Wakasugi, Yuji, Saitoh, Takashi, Sakamoto, Yuji, Takahashi, Ken, Shibano, Hideki, Tokuoka, Atsushi, Hara, Kazunari, Monma, Katsuhisa, Ogata, Keita, Kakuda, Hideki, Mochizuki, Takeo, Arai, Manabu, Araki, Takeshi, Fujii, Kazuto, Tsukita, Haruhi, Sakamaki-Tsukita, Akira, Sano
Publikováno v:
Neurology: Genetics
Objective To identify mutations in vacuolar protein sorting 13A (VPS13A) for Japanese patients with suspected chorea-acanthocytosis (ChAc). Methods We performed a comprehensive mutation screen, including sequencing and copy number variation (CNV) ana
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::73304f1eea3a125cb07b05e3aa847e05
https://pubmed.ncbi.nlm.nih.gov/31192303
https://pubmed.ncbi.nlm.nih.gov/31192303
Autor:
Asa Takahashi, Katsutoshi Tanioka, Yasushi Osaki, Naohito Yamasaki, Toru Kubo, Kenta Sugiura, Hiroaki Kitaoka, Yukari Morita, Hirokazu Furuya
Publikováno v:
Nihon Naika Gakkai Zasshi. 104:2589-2594
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf611bdb3d68cec8dd01f8dfbd1149bc
https://doi.org/10.2169/naika.104.2589
https://doi.org/10.2169/naika.104.2589
Autor:
Masako Watanabe, Kenji Yoshida, Kazuto Tsukita, Noritaka Wakasugi, Hideki Mochizuki, Ryouichi Okiyama, Yasushi Osaki, Atsushi Hara, Kiyomi Yamane, Katsuhisa Ogata, Kotaro Sakurai, Kei Kasamo, Yuka Urata, Kazunari Monma, Ken Shibano, Yukari Morita, Takehiro Ueda, Yuji Saitoh, Hanae Hiwatashi, Manabu Araki, Yuji Takahashi, Natsuki Miyakoshi, Masahiro Mizobuchi, Keita Kakuda, Akira Sano, Masayuki Nakamura, Haruhi Sakamaki-Tsukita, Takashi Sakamoto, Takeo Arai, Yoshiaki Nishida, Izumi Yokoyama, Takeshi Fujii, Hideki Tokuoka
Publikováno v:
Neurology Genetics. 5(3):e332-e332
ObjectiveTo identify mutations in vacuolar protein sorting 13A (VPS13A) for Japanese patients with suspected chorea-acanthocytosis (ChAc).MethodsWe performed a comprehensive mutation screen, including sequencing and copy number variation (CNV) analys
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a51e7aaa2b19ba7c02f702d9d25c2ea2
https://hdl.handle.net/20.500.14094/90006874
https://hdl.handle.net/20.500.14094/90006874
Publikováno v:
Acta Neurologica Scandinavica. 124:182-187
Osaki Y, Morita Y, Kuwahara T, Miyano I, Doi Y. Prevalence of Parkinson’s disease and atypical parkinsonian syndromes in a rural Japanese district. Acta Neurol Scand: 2011: 124: 182–187. © 2010 John Wiley & Sons A/S. Objectives – To investigat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::981e08962f8ff2083c38cd30a24544a0
https://doi.org/10.1111/j.1600-0404.2010.01442.x
https://doi.org/10.1111/j.1600-0404.2010.01442.x
Publikováno v:
Movement Disorders. 24:1475-1480
Although dementia is increasingly recognized as a common feature in Parkinson's disease (PD), its pathological substrate remains unknown. We conducted cross-sectional and longitudinal brain perfusion SPECT analyses to explore changes during the cours
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd844997a1569f75a24b11c3b41703e6
https://doi.org/10.1002/mds.22623
https://doi.org/10.1002/mds.22623