Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Hiroyo Kourakata"'
Autor:
Shinichi Shiona, Shoichiro Kanda, Shuichi Ito, Ryoko Harada, Satoshi Tazoe, Motoshi Hattori, Shinichiro Ohara, Shogo Minamikawa, Naoya Morisada, Kenji Ishikura, Tomohiko Yamamura, Yukiko Mori, Daisuke Aotani, Mayumi Enseki, Hiroyo Kourakata, Katsuaki Kasahara, Miki Washiyama, China Nagano, Kazumoto Iijima, Kandai Nozu, Nana Sakakibara, Yoshinori Araki, Koichi Kamei, Takeshi Yamada, Kenichiro Miura, Ryojiro Tanaka, Akane Seo, Chieko Matsumura, Keisuke Sugimoto
Publikováno v:
Clinical and Experimental Nephrology. 23(9):1119-1129
Background Hepatocyte nuclear factor 1β(HNF1B), located on chromosome 17q12, causes renal cysts and diabetes syndrome (RCAD). Moreover, various phenotypes related to congenital anomalies of the kidney and urinary tract (CAKUT) or Bartter-like electr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff1808fa9ad048ab66aa9d7a9b2658b6
https://hdl.handle.net/20.500.14094/90007295
https://hdl.handle.net/20.500.14094/90007295
Autor:
Shogo Minamikawa, Daisuke Ichikawa, Tomohiko Yamamura, Hiroyo Kourakata, Yoshimi Nozu, China Nagano, Ming Juan Ye, Naoya Morisada, Satoshi Tazoe, Hiroshi Kaito, Keita Nakanishi, Junya Fujimura, Ryojiro Tanaka, Tomoko Horinouchi, Kazumoto Iijima, Nana Sakakibara, Keita Numasawa, Chieko Matsumura, Kandai Nozu, Masahiko Yazawa
Publikováno v:
Clinical and Experimental Nephrology. 22(4):881-888
Background: Comprehensive genetic approaches for diagnosing inherited kidney diseases using next-generation sequencing (NGS) have recently been established. However, even with these approaches, we are still failing to detect gene defects in some pati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a58a58f34c05e280b3ced40c48cbcde2
http://www.lib.kobe-u.ac.jp/handle_kernel/90005938
http://www.lib.kobe-u.ac.jp/handle_kernel/90005938
Publikováno v:
Clinical Rheumatology. 23:76-80
Two cases of hypertrophic pachymeningitis (HP) associated with pulmonary silicosis in tunnel workers are described. In both cases the myeloperoxidase antineutrophil cytoplasmic autoantibody (MPO-ANCA) was positive. Two patients with pulmonary silicos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01d5a0779aaace4746d7bdf5b6c150bc
https://doi.org/10.1007/s10067-003-0815-1
https://doi.org/10.1007/s10067-003-0815-1
Autor:
Masaaki Arakawa, Katsumi Enomoto, Eiichi Suzuki, Hiroki Tsukada, Toshinori Takada, Yoko Taguchi, Isao Saito, Hiroyo Kourakata, Masaaki Nakano
Publikováno v:
Respirology. 4:223-228
Objective: Interstitial lung disease (ILD) is a complication occurring in 10–30% of patients with polymyositis/dermatomyositis (PM/DM) as well as in those with progressive systemic sclerosis (PSS). Clinical features are different between these two
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f3d80c5949278f776c18105dff6dbd4
https://doi.org/10.1046/j.1440-1843.1999.00179.x
https://doi.org/10.1046/j.1440-1843.1999.00179.x
Autor:
Tomoyuki Ito, Ichiei Narita, Hajime Yamazaki, Tadashi Koike, Naoko Sato, Silvia Ferrari, Takako Saeki, Akira Youkou, Hajime Ishiguro, Friedrich Scheiflinger, Hiroyo Kourakata
Publikováno v:
Arthritis careresearch. 63(8)
IgG4-related disease is a recently recognized group characterized by elevated serum IgG4 levels and prominent lymphoplasmacytic infiltration of IgG4-positive cells into multiple organs (1). The condition was first described in relation to the pancrea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e697b829d38affbd7ef1760ef66d3a79
https://pubmed.ncbi.nlm.nih.gov/21523922
https://pubmed.ncbi.nlm.nih.gov/21523922