Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Mayuri Ichinose"'
Publikováno v:
BMC Nephrology, Vol 20, Iss 1, Pp 1-5 (2019)
Abstract Background Thrombophilia due to protein C (PC) and protein S (PS) deficiencies is highly prevalent among patients with stage 5 chronic kidney disease and is reported to arise due to extracorporeal circulation during hemodialysis (HD). This s
Externí odkaz:
https://doaj.org/article/0e4e44d5a8564da791aaa2de20248a58
Publikováno v:
BMC Nephrology, Vol 20, Iss 1, Pp 1-5 (2019)
BMC Nephrology
BMC Nephrology
Background Thrombophilia due to protein C (PC) and protein S (PS) deficiencies is highly prevalent among patients with stage 5 chronic kidney disease and is reported to arise due to extracorporeal circulation during hemodialysis (HD). This study aime
Publikováno v:
Internal Medicine
Thrombophilia is a serious unpredictable complication caused by gene mutations, resulting in anticoagulant deficiencies. We herein report a single-family case series of protein C (PC) deficiency. Case 1 involved a Japanese man whose PC deficiency res
Autor:
Yasunori Utsunomiya, Mayuri Ichinose, Masahisa Kobayashi, Yoshikatsu Eto, Masaaki Nakayama, Toya Ohashi
Publikováno v:
Clinical and Experimental Nephrology. 9:228-232
Fabry disease is an X-linked disorder resulting from a deficiency of the lysosomal enzyme alpha-galactosidase A(alpha-Gal A). Renal insufficiency is a very important manifestation and affects the prognosis of patients. Recently, a renal variant type
Autor:
Yoshindo Kawaguchi, Hiroyasu Yamamoto, Masaaki Nakayama, Stuart C. Sealfon, Mayuri Ichinose, Katsuyoshi Tojo, Osamu Sakai, Hasegawa T
Publikováno v:
Endocrine Journal. 42:367-376
The association of familial hypogonadism with progressive cerebellar ataxia is only rarely encountered, and the exact link between the symptoms remains unknown. We report here two sisters presenting with Holmes type cerebellar ataxia, hypogonadotropi
Autor:
Osamu Sakai, Yoshindo Kawaguchi, Mayuri Ichinose, Hasegawa T, Masaaki Nakayama, Katsuyoshi Tojo
Publikováno v:
Internal Medicine. 34:18-23
A 52-year-old woman was diagnosed as having cerebellar ataxia, hypogonadotropic hypogonadism and retinochoroidal degeneration, the so-called, "Boucher-Neuhauser" syndrome proposed by Limber et al (Am J Med Genet 33:409, 1989). In addition, laboratory
Autor:
Akira, Saito, Yoriko, Ohta, Kazuhiro, Sato, Mayuri, Ichinose, Tatsuro, Arii, Katsuhide, Toyama
Publikováno v:
Contributions to nephrology. 177
Three times weekly home hemodialysis (HHD) was introduced shortly after the initiation of chronic hemodialysis (HD) treatment in 1960. HHD eliminates the need of transportation to and from the dialysis unit and by allowing patients to set their own d
Autor:
Tetsuya Kawamura, Nobuo Tsuboi, Tatsuo Hosoya, Kensuke Joh, Yasunori Utsunomiya, Mayuri Ichinose
Publikováno v:
Clinical and experimental nephrology. 14(5)
The clinical course of cryoglobulinemic glomerulonephritis (CGGN) is usually slowly progressive, and only a minority of these patients progress to end-stage renal failure. This report describes an atypical case of a patient with CGGN who demonstrated
Autor:
Kenji Kasai, Eiko Kataoka, Yoshindo Kawaguchi, Mayuri Ichinose, Tatsuo Hosoya, Masahide Koremoto, Takayuki Sohka, Takasi Shirai, Hideo Okonogi, Mari Suzuki, Kazuyoshi Nakamura, Takeshi Ohno, Masaya Sumita
Publikováno v:
Blood purification. 24(2)
Background/Aims: Hemodialysis (HD) therapy may lead to functional changes in patient leukocytes. For example, the upregulation of inflammatory cytokines, such as IL-1β and TNFα, has been well characterized. However, these findings do not explain th
Autor:
Shinya, Kawamoto, Mayuri, Ichinose, Yoriko, Ito, Hajime, Takahashi, Tetsuya, Kawamura, Tatsuo, Hosoya
Publikováno v:
Nihon Jinzo Gakkai shi. 47(4)
A Sixty eight-year-old man complained of shortness of breath on exercise since the spring of 2001. An abnormal lung shadow was pointed out on chest X-ray and progression of renal dysfunction and high gamma globulinemia were detected out on blood exam