Zobrazeno 1 - 10
of 108
pro vyhledávání: '"Kouichi, Hirayama"'
Autor:
Masatoshi Sega, Marina Yamashita, Hiroshi Maruyama, Yuji Taya, Kentaro Ohgi, Rei Haraoka, Kouichi Hirayama
Publikováno v:
Medicina, Vol 60, Iss 5, p 694 (2024)
Renal embolisms due to cardiac myxomas are extremely rare; the clinical course, treatment, and prognosis of this disease are not established. A 69-year-old Japanese woman who underwent a nephrectomy for renal cell carcinoma 3 years earlier was hospit
Externí odkaz:
https://doaj.org/article/100c24ed025148a28fc80c06baefbc3a
Publikováno v:
Medicina, Vol 59, Iss 11, p 2014 (2023)
Combination therapy with glucocorticoids, cyclophosphamide, and plasmapheresis is recommended as the standard treatment for anti-glomerular basement membrane (anti-GBM) disease, but the prognosis of this disease remains poor. Several immunobiological
Externí odkaz:
https://doaj.org/article/a128901410414206be95918202f0ae2a
Publikováno v:
Medicina, Vol 59, Iss 8, p 1478 (2023)
Fabry disease is an X-linked inherited lysosomal storage disorder with a deficiency of α-galactosidase A activity, which results in the intracellular accumulation of globotriaosylceramide (Gb3) and related glycosphingolipids in various organs. Fabry
Externí odkaz:
https://doaj.org/article/4ea40d587a10456299f54e110c92d432
Autor:
Hiroshi Maruyama, Kouichi Hirayama, Marina Yamashita, Kentaro Ohgi, Ryuji Tsujimoto, Mamiko Takayasu, Homare Shimohata, Masaki Kobayashi
Publikováno v:
BMC Rheumatology, Vol 4, Iss 1, Pp 1-7 (2020)
Abstract Background Proteasomes are found in both the cell nucleus and cytoplasm and play a major role in the ubiquitin-dependent and -independent non-lysosomal pathways of intracellular protein degradation. Proteasomes are also involved in the turno
Externí odkaz:
https://doaj.org/article/34529ed02da44a7ea932fcf069ca1f59
Autor:
Homare Shimohata, Marina Yamashita, Kentaro Ohgi, Ryuji Tsujimoto, Hiroshi Maruyama, Mamiko Takayasu, Kouichi Hirayama, Masaki Kobayashi
Publikováno v:
Renal Replacement Therapy, Vol 5, Iss 1, Pp 1-6 (2019)
Abstract Background Although individuals undergoing maintenance hemodialysis are a major sarcopenic population, there are few methods to assess their skeletal muscle mass conveniently. Here, we investigated the usefulness of serum myostatin and insul
Externí odkaz:
https://doaj.org/article/2395c9b5c9e24218a1b4e6c00796dc70
Autor:
Yasunori Miyamoto, Kouichi Hirayama, Hiroshi Maruyama, Kentaro Ohgi, Mamiko Takayasu, Homare Shimohata, Masaki Kobayashi
Publikováno v:
BMC Nephrology, Vol 20, Iss 1, Pp 1-7 (2019)
Abstract Background Thymic hyperplasia and thymic epithelial tumor (thymoma) have been associated with a variety of autoimmune diseases. Renal involvement has been reported in patients with thymoma. Minimal change disease and membranous nephropathy a
Externí odkaz:
https://doaj.org/article/595dc9b3316b4d8d823bae341ce1baec
Autor:
Akinori Hara, Ken-ei Sada, Takashi Wada, Koichi Amano, Hiroaki Dobashi, Tatsuya Atsumi, Takahiko Sugihara, Kouichi Hirayama, Shogo Banno, Yohko Murakawa, Midori Hasegawa, Kunihiro Yamagata, Yoshihiro Arimura, Hirofumi Makino, Masayoshi Harigai
Publikováno v:
Modern Rheumatology; Mar2024, Vol. 34 Issue 2, p382-390, 9p
Autor:
Akinori Hara, Ken-ei Sada, Takashi Wada, Koichi Amano, Hiroaki Dobashi, Tatsuya Atsumi, Takahiko Sugihara, Kouichi Hirayama, Shogo Banno, Yohko Murakawa, Midori Hasegawa, Kunihiro Yamagata, Yoshihiro Arimura, Hirofumi Makino, Masayoshi Harigai
Publikováno v:
Modern Rheumatology.
ObjectivesThis study elucidated the prognosis and risk factors associated with damage accrual during long-term remission maintenance therapy for patients with antineutrophil cytoplasmic antibody–associated vasculitis (AAV).MethodsWe obtained data f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9ad08497aef7bb91d4f661118e342326
https://doi.org/10.1093/mr/road029
https://doi.org/10.1093/mr/road029
Autor:
Homare Shimohata, Kentaro Ohgi, Hiroshi Maruyama, Yasunori Miyamoto, Mamiko Takayashu, Kouichi Hirayama, Masaki Kobayashi
Publikováno v:
Case Reports in Nephrology, Vol 2017 (2017)
In 2004, the novel category of monoclonal IgG deposition disease has been proposed and termed “proliferative glomerulonephritis with monoclonal IgG deposits” (PGNMID). This disease is characterized by membranoproliferative glomerulonephritis and
Externí odkaz:
https://doaj.org/article/bdc6ba26fa7c4498a2916babb87d0960
Autor:
Masaki Kobayashi, Hiroshi Maruyama, Marina Yamashita, Kouichi Hirayama, Kentaro Ohgi, Mamiko Takayasu, Homare Shimohata
Publikováno v:
CEN Case Rep
Fabry disease is an X-linked inherited lysosomal storage disorder caused by a deficiency of α-galactosidase A activity, resulting in the intracellular accumulation of globotriaosylceramide and related glycosphingolipids. The phenotypes of Fabry dise
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab9a175e18104553f3e3a30fb80d48b4
https://doi.org/10.1007/s13730-020-00463-z
https://doi.org/10.1007/s13730-020-00463-z