Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Natsuko Koita"'
Autor:
Erina Ono, Akira Ishii, Yoshiaki Higashi, Natsuko Koita, Takashi Ayaki, Katsuya Tanigaki, Shunsuke Takayanagi, Naoya Kondo, Kaoru Sakai, Shuichiro Endo, Hideki Yokoi, Takeshi Matsubara, Sachiko Minamiguchi, Ichizo Nishino, Ryosuke Takahashi, Motoko Yanagita
Publikováno v:
BMC Nephrology, Vol 22, Iss 1, Pp 1-8 (2021)
Abstract Background Lately, monoclonal gammopathy of renal significance (MGRS) has been defined as a group of renal disorders that are strongly associated with monoclonal protein, including amyloid immunoglobulin light chain (AL) amyloidosis. Amyloid
Externí odkaz:
https://doaj.org/article/3494f0f0d62b4d5bafcbe09b66373f12
Autor:
Naoya Kondo, Natsuko Koita, Shuichiro Endo, Erina Ono, Takeshi Matsubara, Shunsuke Takayanagi, Ryosuke Takahashi, Katsuya Tanigaki, Ichizo Nishino, Takashi Ayaki, Motoko Yanagita, Hideki Yokoi, Kaoru Sakai, Yoshiaki Higashi, Akira Ishii, Sachiko Minamiguchi
Publikováno v:
BMC Nephrology, Vol 22, Iss 1, Pp 1-8 (2021)
BMC Nephrology
BMC Nephrology
Background Lately, monoclonal gammopathy of renal significance (MGRS) has been defined as a group of renal disorders that are strongly associated with monoclonal protein, including amyloid immunoglobulin light chain (AL) amyloidosis. Amyloid myopathy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fc56192eb7f5288131599965a605969
https://doaj.org/article/3494f0f0d62b4d5bafcbe09b66373f12
https://doaj.org/article/3494f0f0d62b4d5bafcbe09b66373f12
Autor:
Akio Ikeda, Akifumi Takaori-Kondo, Naoki Goda, Takashi Ayaki, Toshiyuki Kitano, Momoko Nishikori, Ryosuke Takahashi, Masahiro Nagano, Natsuko Koita, Sachiko Minamiguchi
Publikováno v:
Internal Medicine
Primary central nervous system lymphoma (PCNSL) and chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids (CLIPPERS) can share clinical features and may be indistinguishable, even after brain biopsy. We encount
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2983fbd9c9f4f34b8b0d4a817597f571
http://hdl.handle.net/2433/240900
http://hdl.handle.net/2433/240900
Autor:
Takakuni Maki, Ran Nakashima, Kosaku Murakami, Hironori Haga, Yuri Nakamura, Takeshi Iwasaki, Shinnosuke Nakayama, Koichiro Ohmura, Hajime Yoshifuji, Yoshiki Iemura, Natsuko Koita, Nobuo Kuramoto, Tsutomu Okada, Tsuneyo Mimori, Shuji Akizuki
Publikováno v:
Modern Rheumatology Case Reports. 2:214-220
Thrombocytopenia, anasarca, fever, reticulin fibrosis and organomegaly (TAFRO) syndrome is a recently proposed disease entity that is considered to be a variant of Castleman’s disease. Here, we rep...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::79b5319d3367cfd7be0aa8b236d88aa0
https://doi.org/10.1080/24725625.2018.1469819
https://doi.org/10.1080/24725625.2018.1469819
Autor:
Hiromichi Kawai, Makoto Urushitani, Akihiro Hashiguchi, Tomoya Terashima, Ryota Hikiami, Hirofumi Yamashita, Nobuyuki Oka, Natsuko Koita, Nobukatsu Sawamoto, Hiroshi Takashima, Ryosuke Takahashi, Kaoru Furukawa, Naoto Jingami
Publikováno v:
Journal of human genetics. 63(1)
Axonal Charcot-Marie-Tooth disease (CMT) is most frequently caused by mutations in the MFN2 gene (CMT2A) that can lead to various clinical phenotypes. The age at disease onset varies, but most cases occur before adolescence. We report two Japanese si
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ab742b00e09fd531027a8f89d9a3da5
https://pubmed.ncbi.nlm.nih.gov/29215088
https://pubmed.ncbi.nlm.nih.gov/29215088