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8 papers found.
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Value of adding the renal pathological score to the kidney failure risk equation in advanced diabetic nephropathy

, Miho Shimizu, Kengo Furuichi. Formal analysis: Masayuki Yamanouchi, Junichi Hoshino. Investigation: Masayuki Yamanouchi. Methodology: Masayuki Yamanouchi, Junichi Hoshino, Kengo Furuichi. Project ... administration: Takashi Wada. Supervision: Junichi Hoshino, Yoshifumi Ubara, Kenmei Takaichi, Miho Shimizu, Kengo Furuichi, Takashi Wada. Validation: Junichi Hoshino. Writing ± original draft: Masayuki

Paratubular basement membrane insudative lesions predict renal prognosis in patients with type 2 diabetes and biopsy-proven diabetic nephropathy

, Yoshifumi Ubara. Data curation: Koki Mise, Junichi Hoshino, Toshiharu Ueno, Akinari Sekine, Keiichi Sumida, Masayuki Yamanouchi, Noriko Hayami, Tatsuya Suwabe, Rikako Hiramatsu, Eiko Hasegawa, Naoki Sawa ... , Masayuki Yamanouchi, Takeshi Fujii, Shigeko Hara, Jun Wada, Kenichi Ohashi, Kenmei Takaichi, Yoshifumi Ubara. Methodology: Koki Mise, Yutaka Yamaguchi, Junichi Hoshino, Takeshi Fujii, Jun Wada, Kenichi

Effect of Proteinuria and Glomerular Filtration Rate on Renal Outcome in Patients with Biopsy-Proven Benign Nephrosclerosis

Background Reduced estimated glomerular filtration rate (eGFR) and proteinuria are risk factors for end-stage renal disease (ESRD), of which benign nephrosclerosis is a common cause. However, few biopsy-based studies have assessed these associations. Methods We performed retrospective cohort study of 182 Japanese patients who underwent renal biopsy from June 1985 through March 2014 ...

Renal prognosis a long time after renal biopsy on patients with diabetic nephropathy

Background A new classification of diabetic nephropathy was reported by Tervaert et al., but the association between pathological findings and the clinical outcomes remains unclear.

Quality of life of patients with ADPKD—Toranomon PKD QOL study: cross-sectional study

Background The quality of life (QOL) of patients with autosomal dominant polycystic kidney disease (ADPKD) has not been investigated well. This study was performed to clarify the QOL of patients with ADPKD and to identify factors that affected their QOL. Methods The present cross-sectional study is part of a prospective observational study on the QOL of ADPKD patients. Patients ...

Membranoproliferative glomerulonephritis and circulating cryoglobulins

Background Previous studies on membranoproliferative glomerulonephritis (MPGN) and cryoglobulinemic glomerulopathy (CG) were based upon case series that were performed before hepatitis C virus (HCV) infection was routinely investigated. Therefore, it remains unknown how far HCV contributes to MPGN or CG, and there have only been a few reports about HCV-negative idiopathic MPGN. ...

Myeloperoxidase-antineutrophil cytoplasmic antibody-associated crescentic glomerulonephritis in autosomal dominant polycystic kidney disease

Background Autosomal dominant polycystic kidney disease (ADPKD) is an inherited disorder that is characterized by the development of cysts in the kidneys and other organs. Urinary protein excretion is usually less than 1 g/day, and ADPKD is rarely associated with nephrotic syndrome or rapidly progressive glomerulonephritis (RPGN). To date, myeloperoxidase (MPO)-antineutrophil ...

Long term follow up of congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome) on hemodialysis for 19 years: a case report

Background Thrombotic thrombocytopenic purpura (TTP) is frequently associated with renal abnormalities, but there have been few reports about renal abnormalities in patients with hereditary TTP. In particular, little is known about the long-term prognosis of patients with childhood-onset congenital TTP. Case presentation We report a Japanese patient with congenital TTP ...