Zobrazeno 1 - 10
of 506
pro vyhledávání: '"Ohara Akira"'
Autor:
Haga, Yoichi1 (AUTHOR) masaki.matsuoka@med.toho-u.ac.jp, Ohara, Akira1 (AUTHOR) hiroyuki.takahashi@med.toho-u.ac.jp, Yakuwa, Tsuneyoshi2 (AUTHOR), Yamashita, Akari1 (AUTHOR), Udo, Midori1 (AUTHOR), Matsuoka, Masaki1 (AUTHOR), Ohara, Hiroshi3 (AUTHOR) h.ohara@med.toho-u.ac.jp, Yasumoto, Atsushi4 (AUTHOR) yasuatsu0219@huhp.hokudai.ac.jp, Takahashi, Hiroyuki1 (AUTHOR)
Publikováno v:
Hematology Reports. Sep2024, Vol. 16 Issue 3, p504-511. 8p.
Publikováno v:
Journal of Orthopaedic Surgery and Research, Vol 5, Iss 1, p 33 (2010)
Abstract Paget's disease of the bone is a common metabolic bone disease in most European countries, Australia, New Zealand, and North America. Conversely, this disease is rare in Scandinavia, Asia, and Africa. In Japan, it is extremely rare, with a p
Externí odkaz:
https://doaj.org/article/163a206f5c2c4b97a83b6dc25f6084b6
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Yoshida, Masanori, Nakabayashi, Kazuhiko, Yang, Wentao, Sato-Otsubo, Aiko, Tsujimoto, Shin-ichi, Ogata-Kawata, Hiroko, Kawai, Tomoko, Ishiwata, Keisuke, Sakamoto, Mika, Okamura, Kohji, Yoshida, Kaoru, Shirai, Ryota, Osumi, Tomoo, Moriyama, Takaya, Nishii, Rina, Takahashi, Hiroyuki, Kiyotani, Chikako, Shioda, Yoko, Terashima, Keita, Ishimaru, Sae, Yuza, Yuki, Takagi, Masatoshi, Arakawa, Yuki, Kinoshita, Akitoshi, Hino, Moeko, Imamura, Toshihiko, Hasegawa, Daisuke, Nakazawa, Yozo, Okuya, Mayuko, Kakuda, Harumi, Takasugi, Nao, Inoue, Akiko, Ohki, Kentaro, Yoshioka, Takako, Ito, Shuichi, Tomizawa, Daisuke, Koh, Katsuyoshi, Matsumoto, Kimikazu, Sanada, Masashi, Kiyokawa, Nobutaka, Ohara, Akira, Ogawa, Seishi, Manabe, Atsushi, Niwa, Akira, Hata, Kenichiro, Yang, Jun J., Kato, Motohiro *
Publikováno v:
In Blood Advances 14 December 2021 5(23):5420-5428
Autor:
Sigurdsson, Valgardur, Haga, Youichi, Takei, Hajime, Mansell, Els, Okamatsu-Haga, Chizuko, Suzuki, Mitsuyoshi, Radulovic, Visnja, van der Garde, Mark, Koide, Shuhei, Soboleva, Svetlana, Gåfvels, Mats, Nittono, Hiroshi, Ohara, Akira, Miharada, Kenichi
Publikováno v:
In Blood Advances 12 May 2020 4(9):1833-1843
Publikováno v:
In Journal of Infection and Chemotherapy February 2017 23(2):96-100
Autor:
Shikama, Yoshiaki, Yokoya, Chiemi, Ohara, Akira, Yamashita, Megumi, Shimizu, Yuichi, Imagawa, Tomoyuki
Publikováno v:
Antimicrobial Stewardship & Healthcare Epidemiology; 2024, Vol. 4 Issue 1, p1-6, 6p
Autor:
Utsugisawa, Taiju, Uchiyama, Toshitaka, Toki, Tsutomu, Ogura, Hiromi, Aoki, Takako, Hamaguchi, Isao, Ishiguro, Akira, Ohara, Akira, Kojima, Seiji, Ohga, Shouichi, Ito, Etsuro, Kanno, Hitoshi
Publikováno v:
In Blood Cells, Molecules and Diseases July 2016 59:31-36
Autor:
Yamamoto, Keiko Shimojima, Utshigisawa, Taiju, Ogura, Hiromi, Aoki, Takako, Kawakami, Takahiro, Ohga, Shoichi, Ohara, Akira, Ito, Etsuro, Yamamoto, Toshiyuki, Kanno, Hitoshi
Publikováno v:
Human Genome Variation, Vol 9, Iss 1, Pp 1-5 (2022)
Human Genome Variation
Human Genome Variation
Hereditary spherocytosis is the most frequent cause of hereditary hemolytic anemia and is classified into five subtypes (SPH1-5) according to OMIM. Because the clinical and laboratory features of patients with SPH1-5 are variable, it is difficult to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f437e7435632fe79d158445926c6945
https://doaj.org/article/bd96da2165d44c4086f36908541d61a1
https://doaj.org/article/bd96da2165d44c4086f36908541d61a1
Autor:
Kiyokawa, Nobutaka, Iijima, Kazutoshi, Tomita, Osamu, Miharu, Masashi, Hasegawa, Daisuke, Kobayashi, Kenichiro, Okita, Hajime, Kajiwara, Michiko, Shimada, Hiroyuki, Inukai, Takeshi, Makimoto, Atsushi, Fukushima, Takashi, Nanmoku, Toru, Koh, Katsuyoshi, Manabe, Atsushi, Kikuchi, Akira, Sugita, Kanji, Fujimoto, Junichiro, Hayashi, Yasuhide, Ohara, Akira
Publikováno v:
In Leukemia Research January 2014 38(1):42-48