Zobrazeno 1 - 10
of 96
pro vyhledávání: '"Kazushige DOBASHI"'
Autor:
Keiko Nagahara MD, PhD, Yoshifusa Abe MD, PhD, Akira Hojo MD, Kazushige Dobashi MD, PhD, Motoko Chiga, Kiyoshi Isobe MD, PhD, Shinichi Uchida MD, PhD, Kazuo Itabashi MD, PhD
Publikováno v:
Global Pediatric Health, Vol 1 (2014)
Externí odkaz:
https://doaj.org/article/47820263a93948c7aa86ddc1099c4d7a
Autor:
Mariko Harada-Shiba, Hidenori Arai, Hirotoshi Ohmura, Hiroaki Okazaki, Daisuke Sugiyama, Hayato Tada, Kazushige Dobashi, Kota Matsuki, Tetsuo Minamino, Shizuya Yamashita, Koutaro Yokote
Publikováno v:
Journal of Atherosclerosis and Thrombosis. 30:558-586
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::745fcec34c411bfaf065eec7883d04ec
https://doi.org/10.5551/jat.cr005
https://doi.org/10.5551/jat.cr005
Autor:
Mariko Harada-Shiba, Akira Ohtake, Daisuke Sugiyama, Hayato Tada, Kazushige Dobashi, Kota Matsuki, Tetsuo Minamino, Shizuya Yamashita, Yukiyo Yamamoto
Publikováno v:
Journal of Atherosclerosis and Thrombosis. 30:531-557
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af163daa431106eae6bc902644b1b121
https://doi.org/10.5551/jat.cr006
https://doi.org/10.5551/jat.cr006
Autor:
Masa-aki Kawashiri, Tomohiro Hirao, Jun Kunikata, Tsuyoshi Sasaki, Keiji Matsunaga, Takuji Fujisawa, Kazushige Dobashi, Yoichi Hoshikawa, Katsunori Yokoyama, Shigeru Ito, Takashi Kusaka, Ichiro Yokota, Asako Mizobuchi, Shohei Ishikawa, Hayato Tada, Takashi Iwase, Tetsuo Minamino, Hai Ying Fu
Publikováno v:
Journal of Atherosclerosis and Thrombosis. 29:839-849
Aim Familial hypercholesterolemia (FH) is an underdiagnosed autosomal dominant genetic disorder characterized by high levels of plasma low-density lipoprotein cholesterol (LDL-C) from birth. This study aimed to assess the genetic identification of FH
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b6bcd056113f9b91bb461e2875625af
https://doi.org/10.5551/jat.62780
https://doi.org/10.5551/jat.62780
Autor:
Kazushige Dobashi, Mika Hori, Shinji Yokoyama, Yasushi Ishigaki, Kyoko Inagaki, Katsunori Ikewaki, Kimitoshi Nakamura, Masatsune Ogura, Shizuya Yamashita, Kota Matsuki, Hayato Tada, Masa-aki Kawashiri, Kazuhisa Tsukamoto, Akihiro Nomura, Mariko Harada-Shiba
Publikováno v:
Journal of Atherosclerosis and Thrombosis
Sitosterolemia is an inherited metabolic disorder characterized by increased levels of plant sterols, such as sitosterol. This disease is caused by loss-of-function genetic mutations in ATP-binding cassette (ABC) subfamily G member 5 or member 8 ( AB
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ae36980d0a203e097b3ce741fe0e560
https://doi.org/10.5551/jat.rv17052
https://doi.org/10.5551/jat.rv17052
Autor:
Kazushige Dobashi
Publikováno v:
Journal of Atherosclerosis and Thrombosis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ac9f4e6806350c2323d9489043b4b62
https://doi.org/10.5551/jat.ed163
https://doi.org/10.5551/jat.ed163
Autor:
Kazushige Dobashi
Publikováno v:
Journal of atherosclerosis and thrombosis. 29(12)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::757f6281dd90258ae1bb0f8e966f76d3
https://pubmed.ncbi.nlm.nih.gov/35095055
https://pubmed.ncbi.nlm.nih.gov/35095055
Autor:
Yasuko Ogiwara, Yukihiro Hasegawa, Masa-aki Kawashiri, Ayako Ochi, Katsumi Mizuno, Kento Ikegawa, Tsuyoshi Nishibukuro, Masanori Adachi, Keiko Nagahara, Hayato Tada, Yuya Nakano, Junya Toyoda, Masakazu Yamagishi, Kazushige Dobashi
Publikováno v:
Journal of atherosclerosis and thrombosis. 29(5)
Aim This study aimed to elucidate the gene and lipid profiles of children clinically diagnosed with familial hypercholesterolemia (FH). Methods A total of 21 dyslipidemia-related Mendelian genes, including FH causative genes (LDLR, APOB, and PCSK9) a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7508546c63ceae071e8310eeeead44f
https://pubmed.ncbi.nlm.nih.gov/35249907
https://pubmed.ncbi.nlm.nih.gov/35249907
Autor:
Koh Ono, Hitoshi Shimano, Hiroyuki Daida, Shinji Yokoyama, Kota Matsuki, Mariko Harada-Shiba, Hayato Tada, Toshio Hayashi, Sachiko Okazaki, Atsushi Nohara, Tetsuo Minamino, Masatsune Ogura, Mika Hori, Kazushige Dobashi
Publikováno v:
Journal of Atherosclerosis and Thrombosis
Familial hypercholesterolemia (FH) is an inherited disorder with retarded clearance of plasma LDL caused by mutations of the genes involved in the LDL receptor-mediated pathway and most of them exhibit autosomal dominant inheritance. Homozygotes of F
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::429b7977fa24fc390626959c6d716257
https://doi.org/10.5551/jat.rv17050
https://doi.org/10.5551/jat.rv17050
Autor:
Atsutoshi Shiratori, Satoshi Hibino, Kazushige Dobashi, Yoshifusa Abe, Yoshitaka Watanabe, Shuichiro Watanabe, Satomi Nimura, Tsuneki Watanabe, Yuya Nakano, Katsumi Mizuno, Yasuko Nakano, Kaori Kamijo, Kazuo Itabashi, Tetsuro Tamai, Hirokazu Ikeda, Shunsuke Sakurai, Takaaki Takayanagi
Publikováno v:
Clinical and Experimental Nephrology
Background Serum adiponectin circulates in three multimeric isoforms: high-molecular-weight (HMW), middle-molecular-weight (MMW), and low-molecular-weight (LMW) isoforms. Potential change in the circulating adiponectin levels in patients with nephrot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::262c437eb0f5eb98e27ebcd665a92bff
https://doi.org/10.21203/rs.3.rs-28091/v1
https://doi.org/10.21203/rs.3.rs-28091/v1
