Effectiveness of mRNA COVID-19 Vaccines in Japan during the Nationwide Pandemic of the Delta Variant

Autor: Tetsuya, Akaishi, Shigeki, Kushimoto, Yukio, Katori, Noriko, Sugawara, Kaoru, Igarashi, Motoo, Fujita, Shigeo, Kure, Shin, Takayama, Michiaki, Abe, Akiko, Kikuchi, Kota, Ishizawa, Yoshiko, Abe, Hiroyuki, Imai, Yohei, Inaba, Yoko, Iwamatsu-Kobayashi, Takashi, Nishioka, Ko, Onodera, Tadashi, Ishii

Publikováno v: The Tohoku Journal of Experimental Medicine. 257:1-6

The coronavirus disease 2019 (COVID-19) pandemic, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), remained a major global health concern in 2021. To suppress the spread of infection, mass vaccinations have been performed acros

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::303f4359eacba45967548cc700c7a3be
https://doi.org/10.1620/tjem.2022.j012

Impacts of Natural Environmental Factors and Prevalence of Airway Symptoms on the Local Spread of COVID-19: A Time-Series Analysis in Regional COVID-19 Epidemics

Autor: Shigeki Kushimoto, Michiaki Abe, Yohei Inaba, Shigeo Kure, Tadashi Ishii, Yoshiko Abe, Motoo Fujita, Tetsuya Akaishi, Noriko Sugawara, Kaoru Igarashi, Takashi Nishioka, Shin Takayama, Junichi Tanaka, Akiko Kikuchi, Yukio Katori, Hiroyuki Imai, Ko Onodera, Yoko Iwamatsu-Kobayashi

Publikováno v: The Tohoku Journal of Experimental Medicine. 254:89-100

Coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is the world's largest public health concern in 2021. This study evaluated the associations of the prevalence of airway symptoms among the te

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8fe38b7adf0d10b2ee1a8821aa58082b
https://doi.org/10.1620/tjem.254.89

The Japanese Society for Apheresis clinical practice guideline for therapeutic apheresis

Autor: Takaya Abe, Hidenori Matsuo, Ryuzo Abe, Shinji Abe, Hiroaki Asada, Akira Ashida, Akiyasu Baba, Kei Eguchi, Yutaka Eguchi, Yoshihiro Endo, Yoshihiro Fujimori, Kengo Furuichi, Yutaka Furukawa, Mayumi Furuya, Tomoki Furuya, Norio Hanafusa, Wataru Hara, Mariko Harada‐Shiba, Midori Hasegawa, Noriyuki Hattori, Motoshi Hattori, Sumi Hidaka, Toshihiko Hidaka, Chika Hirayama, Shigaku Ikeda, Hideaki Imamura, Kazuaki Inoue, Keita Ishizuka, Kiyonobu Ishizuka, Takafumi Ito, Hitomi Iwamoto, Syoko Izaki, Maki Kagitani, Shuzo Kaneko, Naoto Kaneko, Takuro Kanekura, Kiyoki Kitagawa, Makio Kusaoi, Youwei Lin, Takeshi Maeda, Hisashi Makino, Shigeki Makino, Kenichi Matsuda, Takao Matsugane, Yusuke Minematsu, Michio Mineshima, Kenichiro Miura, Katsuichi Miyamoto, Takeshi Moriguchi, Mayumi Murata, Makoto Naganuma, Hajime Nakae, Shinya Narukawa, Atsushi Nohara, Kyoichi Nomura, Hirofumi Ochi, Atsushi Ohkubo, Takayasu Ohtake, Kazuya Okada, Tomokazu Okado, Yoshiki Okuyama, Susumu Omokawa, Satoru Oji, Norihiko Sakai, Yuichiro Sakamoto, Shigeru Sasaki, Motoyoshi Sato, Mariko Seishima, Hidetoshi Shiga, Homare Shimohata, Noriko Sugawara, Kohei Sugimoto, Yasushi Suzuki, Masato Suzuki, Takashi Tajima, Yasuhiro Takikawa, Satoru Tanaka, Kenjiro Taniguchi, Satoko Tsuchida, Tatsuo Tsukamoto, Kenji Tsushima, Yasunori Ueda, Takashi Wada, Hiromichi Yamada, Hiroyuki Yamada, Toshihiko Yamaka, Ken'ichiro Yamamoto, Yoko Yokoyama, Norihito Yoshida, Toyokazu Yoshioka, Ken Yamaji

Publikováno v: Therapeutic apheresis and dialysis : official peer-reviewed journal of the International Society for Apheresis, the Japanese Society for Apheresis, the Japanese Society for Dialysis TherapyREFERENCE. 25(6)

Most of the diseases for which apheresis therapy is indicated are intractable and rare, and each patient has a different background and treatment course prior to apheresis therapy initiation. Therefore, it is difficult to conduct large-scale randomiz

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::839074705f684480f34330c769c39233
https://pubmed.ncbi.nlm.nih.gov/34877777

Clear Evidence of LAMA5 Gene Biallelic Truncating Variants Causing Infantile Nephrotic Syndrome

Autor: Tomoko Horinouchi, Yuya Aoto, Sadayuki Nagai, Hiroaki Nagase, China Nagano, Atsushi Kondo, Kiyotoshi Sekiguchi, Atsushi Tashiro, Jeffrey H. Miner, Kazumoto Iijima, Nana Sakakibara, Noriko Sugawara, Tomohiko Yamamura, Shinya Ishiko, Chisato Umeda, Haruhide Sakaguchi, Kandai Nozu, Rini Rossanti, Yukimasa Taniguchi

Publikováno v: Kidney360

BACKGROUND: Pathogenic variants in single genes encoding podocyte-associated proteins have been implicated in about 30% of steroid-resistant nephrotic syndrome (SRNS) patients in children. However, LAMA5 gene biallelic variants have been identified i

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cdbb08e3bdb5e5d4f4c74af2471e397e
https://europepmc.org/articles/PMC8986055/

Diversity of renal phenotypes in patients withWDR19mutations: Two case reports

Autor: Noriko Sugawara, Michio Nagata, Takako Yoshioka, Osamu Miyazaki, Shuichi Ito, Kenji Ishikura, Mai Sato, Hiroko Nagata, Yuko Hamasaki, Shuji Kondo, Masao Ogura, Kiyonobu Ishizuka, Kazumoto Iijima, Seiichiro Shishido, Koichi Kamei, Kentaro Ogata, Ken Saida, Naoya Morisada, Maki Urushihara, Takahisa Yoshikawa

Publikováno v: Nephrology. 22:566-571

WDR19 has been reported as a causative gene of nephronophthisis-related ciliopathies. Patients with WDR19 mutations can show various extrarenal manifestations such as skeletal disorders, Caroli disease, and retinal dystrophy, and typically display ne

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6febf9bc064ced63709039f1c8378981
https://doi.org/10.1111/nep.12996