Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Megumi Nihonmatsu"'
Autor:
Hiroaki Nozaki, Ryoko Koike, Toshiki Mizuno, Akihide Koyama, Ayuka Murakami, Akio Yokoseki, Masahiro Makino, Ikuko Mizuta, Yohei Saito, Suzuko Moritani, Muichi Kaito, Osamu Onodera, Atsushi Shiga, Yumi Sekine, Kazuhide Miyazaki, Kenju Hara, Takeshi Momotsu, Tomoko Noda, Taisuke Kato, Shoichi Ito, Megumi Nihonmatsu, Masatoyo Nishizawa, Naoto Endo, Ryozo Kuwano, Mari Yoshida, Masahiro Uemura
Publikováno v:
Neurology. 86:1964-1974
Objective: To elucidate the molecular mechanism of mutant HTRA1-dependent cerebral small vessel disease in heterozygous individuals. Methods: We recruited 113 unrelated index patients with clinically diagnosed cerebral small vessel disease. The codin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae77e394fdff4fdcb644052f72b4a9c0
https://doi.org/10.1212/wnl.0000000000002694
https://doi.org/10.1212/wnl.0000000000002694
Autor:
Suzuko Moritani, Akihide Koyama, Atsushi Shiga, Osamu Onodera, Toshiki Mizuno, Mari Yoshida, Tomoko Noda, Kenju Hara, Muichi Kaito, Yumi Sekine, Takeshi Momotsu, Masatoyo Nishizawa, Masahiro Makino, Hiroaki Nozaki, Taisuke Kato, Ryozo Kuwano, Shoichi Ito, Kazuhide Miyazaki, Ikuko Mizuta, Ryoko Koike, Masahiro Uemura, Yohei Saito, Naoto Endo, Ayuka Murakami, Akio Yokoseki, Megumi Nihonmatsu
Publikováno v:
Stroke. 48
Introduction: Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL), an autosomal recessive inherited cerebral small vessel disease (CSVD), involves severe leukoaraiosis, multiple lacunar infarcts, earl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::33d726d96daae8feb00419af77e13bd5
https://doi.org/10.1161/str.48.suppl_1.tp269
https://doi.org/10.1161/str.48.suppl_1.tp269
Autor:
Takeshi Ikeuchi, Yasuko Toyoshima, Shinichi Katada, Akihide Koyama, Masatoyo Nishizawa, Imaharu Nakano, Megumi Nihonmatsu, Hitoshi Takahashi, Hiroaki Nozaki, Akira Tanaka, Atsushi Shiga, Akio Yokoseki, Mari Ikeda, Taisuke Kato, Hirotoshi Kawata, Kunimasa Arima, Osamu Onodera
Publikováno v:
Human Molecular Genetics. 20:1800-1810
Cerebral small-vessel disease is a common disorder in elderly populations; however, its molecular basis is not well understood. We recently demonstrated that mutations in the high-temperature requirement A (HTRA) serine peptidase 1 (HTRA1) gene cause
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c73c6b4c84eee76d5286b50a7831d0ff
https://doi.org/10.1093/hmg/ddr063
https://doi.org/10.1093/hmg/ddr063
Autor:
Hiroaki Nozaki, Taisuke Kato, Megumi Nihonmatsu, Yohei Saito, Ikuko Mizuta, Tomoko Noda, Ryoko Koike, Kazuhide Miyazaki, Muichi Kaito, Shoichi Ito, Masahiro Makino, Akihide Koyama, Atsushi Shiga, Masahiro Uemura, Yumi Sekine, Ayuka Murakami, Suzuko Moritani, Kenju Hara, Akio Yokoseki, Ryozo Kuwano
Publikováno v:
Neurology; 5/24/2016, Vol. 86 Issue 21, p1964-1974, 11p