Zobrazeno 1 - 10
of 101
pro vyhledávání: '"Makoto, Ide"'
Autor:
Makoto Ide, Noriyuki Sonoda, Tomoaki Inoue, Shinichiro Kimura, Yohei Minami, Hiroaki Makimura, Eiichi Hayashida, Fuminori Hyodo, Mayumi Yamato, Ryoichi Takayanagi, Toyoshi Inoguchi
Publikováno v:
PLoS ONE, Vol 15, Iss 2, p e0228750 (2020)
OBJECTIVE:Accumulating epidemiological studies have demonstrated that diabetes is an important risk factor for dementia. However, the underlying pathological and molecular mechanisms, and effective treatment, have not been fully elucidated. Herein, w
Externí odkaz:
https://doaj.org/article/fe7dd10d348043fbad54de8f350e3f3b
Autor:
Peter M. Voorhees, Angela Dispenzieri, Alexander Fosså, Amy Chadburn, Megan S. Lim, Makoto Ide, Joshua D Brandstadter, David Wu, Frits van Rhee, Amy D Greenway, Gordan Srkalovic, Wilbur B. Bowne, Thomas S. Uldrick, Sheila K Pierson, Raymond S.M. Wong, Stephen Schey, Mary Jo Lechowicz, Shanmuganathan Chandrakasan, Kazuyuki Yoshizaki, Kojo S.J. Elenitoba-Johnson, Ivan Maillard, Sunita D. Nasta, Razelle Kurzrock, David C. Fajgenbaum, Nikhil C. Munshi, Eric Oksenhendler, Matthew Streetly, Sophia A. T. Parente, Corey Casper
Publikováno v:
Blood Adv
Castleman disease (CD) includes a group of rare and heterogeneous disorders with characteristic lymph node histopathological abnormalities. CD can occur in a single lymph node station, which is referred to as unicentric CD (UCD). CD can also involve
Autor:
Masahiko Taniguchi, Yuki Yorishima, Hiroshi Shoji, Makoto Ide, Yusuke Kumura, Keisuke Kunisaki
Publikováno v:
Rinsho shinkeigaku = Clinical neurology. 62(2)
We conducted a survey of 16 Japanese patients (9 males, 7 females) aged 48-70 years in the advanced-stage Okinawa-type neurogenic muscular atrophy (i.e. hereditary motor and sensory neuropathy with proximal dominant involvement: HMSN-P) by a question
Publikováno v:
European journal of haematologyREFERENCES. 108(4)
Autor:
Tetsuya Fukumoto, Makoto Ide, Makiko Uemura, Yukiko Hamasaki Kubo, Osamu Imataki, Haruyuki Fujita, Hirofumi Ohno, Hiroaki Ohnishi, Jun-ichiro Kida, Hiroyuki Kubo, Norimitsu Kadowaki, Maki Oku, Tomoya Ishida
Publikováno v:
Transplantation and cellular therapy. 27(11)
Pericardial effusion (PE) is a rare complication after allogeneic hematopoietic stem cell transplantation (allo-HSCT). Although the mechanisms underlying the onset of PE remain unclear, patients with PE after allo-HSCT have poor clinical outcomes. Ho
Autor:
Waki, Fusako, Shumpei, Uchida, Tetsuya, Fukumoto, Makoto, Ide, Yoichiro, Izumi, Yasunori, Kawachi, Hiroaki, Ohnishi
Publikováno v:
In Annals of Oncology November 2015 26 Supplement 7:vii97-vii97
Publikováno v:
International journal of dermatologyReferences. 60(1)
Autor:
Amy Chadburn, Dale Frank, Michele Paessler, Mary Jo Lechowicz, Gordan Srkalovic, Sheila K Pierson, Makoto Ide, Gisele W. B. Colleoni, Adam Bagg, Ahmet Dogan, Thomas S. Uldrick, Raymond S.M. Wong, Razelle Kurzrock, Peter M. Voorhees, Frits van Rhee, Elaine S. Jaffe, Michael P. Croglio, Alexander Suarez, Megan S. Lim, Vera P. Krymskaya, Raj Jayanthan, Sunita D. Nasta, David C. Fajgenbaum, David Simpson, Angela Dispenzieri, Corey Casper, David Wu, David M. Menke, Shanmuganathan Chandrakasan, Eric Oksenhendler, Alexander Fosså, Jean François Rossi, Amy Y. Liu, Jason R. Ruth, Kazuyuki Yoshizaki, Kojo S.J. Elenitoba-Johnson, Dermot Kelleher, Christopher S. Nabel
Publikováno v:
Blood. 129:1646-1657
Human herpesvirus-8 (HHV-8)-negative, idiopathic multicentric Castleman disease (iMCD) is a rare and life-threatening disorder involving systemic inflammatory symptoms, polyclonal lymphoproliferation, cytopenias, and multiple organ system dysfunction
Autor:
Tomoaki Inoue, Mayumi Yamato, Ryoichi Takayanagi, Shinichiro Kimura, Yohei Minami, Hiroaki Makimura, Eiichi Hayashida, Fuminori Hyodo, Toyoshi Inoguchi, Makoto Ide, Noriyuki Sonoda
Publikováno v:
PLoS ONE, Vol 15, Iss 2, p e0228750 (2020)
PLoS ONE
PLoS ONE
Objective Accumulating epidemiological studies have demonstrated that diabetes is an important risk factor for dementia. However, the underlying pathological and molecular mechanisms, and effective treatment, have not been fully elucidated. Herein, w
Autor:
Tomoyuki Sakai, Shino Fujimoto, Makoto Ide, Sohsuke Yamada, Junya Kuroda, Toshihiro Fukushima, Shuichi Mizuta, Takafumi Kawanami, Haruka Iwao-Kawanami, Yasufumi Masaki, Sadao Aoki, Nozomu Kurose, Hiroshi Kawabata, Norifumi Tsukamoto, Kazue Takai, Keigo Setoguchi
Publikováno v:
American journal of hematologyREFERENCES. 94(9)
Castleman disease (CD) is a rare lymphoproliferative disorder that can be unicentric or multicentric. Multicentric CD (MCD) is further subdivided into human herpesvirus type-8-associated, POEMS syndrome-associated, and idiopathic (iMCD). TAFRO syndro