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  1. No Access

    Article

    An unusual kidney presentation of severe proteinuria in a 2-year-old girl: Questions

    Aya Nawata, Takahiro Morishita, Satoshi Hisano, Kaneyasu Nakagawa in Pediatric Nephrology (2021)

  2. No Access

    Article

    An unusual kidney presentation of severe proteinuria in a 2-year-old girl: Answers

    Aya Nawata, Takahiro Morishita, Satoshi Hisano, Kaneyasu Nakagawa in Pediatric Nephrology (2021)

  3. No Access

    Article

    A cross-sectional study in patients with IgA nephropathy of correlations between clinical data and pathological findings at the time of renal biopsy: a Japanese prospective cohort study

    The correlations between clinical data and pathological findings at the time of renal biopsy were investigated in IgA nephropathy patients.

    Chisako Kamano, Akira Shimizu, Kensuke Joh in Clinical and Experimental Nephrology (2021)

  4. Article

    Correction to: Validation of the diagnostic criteria for IgG4‑related kidney disease (IgG4‑RKD) 2011, and proposal of a new 2020 version

    A correction to this paper has been published: https://doi.org/10.1007/s10157-021-02040-9

    Takako Saeki, Mitsuhiro Kawano, Tasuku Nagasawa in Clinical and Experimental Nephrology (2021)

  5. No Access

    Article

    Concurrent minimal change disease and retroperitoneal liposarcoma successfully treated by tumor resection and steroid therapy

    A 54-year-old Japanese woman developed simultaneous abdominal distension and bilateral leg edema. Her medical history and results of periodic medical check-up were unremarkable. Blood tests revealed severe hyp...

    Yuki Yasui, Ryoko Shibata, Natsumi Morita, Naoko Himuro, Aki Hamauchi in CEN Case Reports (2021)

  6. No Access

    Article

    Two cases of idiopathic multicentric Castleman disease with nephrotic syndrome treated with tocilizumab

    We report two cases of idiopathic multicentric Castleman disease (iMCD) with nephrotic syndrome (NS) treated with tocilizumab. Case 1 was a 58-year-old man diagnosed with iMCD prior to the onset of NS. Renal b...

    Norihiro Furutera, Naoya Fukunaga, Jun Okita, Tomoko Suzuki in CEN Case Reports (2021)

  7. Article

    Open Access

    Validation of the diagnostic criteria for IgG4-related kidney disease (IgG4-RKD) 2011, and proposal of a new 2020 version

    In 2011, the IgG4-related kidney disease (IgG4-RKD) working group of the Japanese Society of Nephrology proposed diagnostic criteria for IgG4-RKD. The aim of the present study was to validate those criteria an...

    Takako Saeki, Mitsuhiro Kawano, Tasuku Nagasawa in Clinical and Experimental Nephrology (2021)

  8. Article

    Open Access

    IgM monoclonal gammopathy with heavy-and-light-chain amyloidosis resembling fibrillary glomerulonephritis determined by tandem mass spectrometry: a case report

    Fibrillary glomerulonephritis (FGN) is distinguished from amyloidosis by thicker fibrils and the lack of staining with histochemical dyes typically reactive with amyloid. However, congophilic FGN has been prop...

    Misa Adachi, Mineaki Kitamura, Kumiko Muta, Akihiro Maekawa in BMC Nephrology (2020)

  9. No Access

    Article

    A case of denosumab-associated membranous nephropathy in a patient with rheumatoid arthritis

    We herein report a case of anti-RANKL monoclonal antibody-associated membranous nephropathy (MN). A 67-year-old woman with a history of rheumatoid arthritis treated with prednisolone and methotrexate for more ...

    Miyuki Kimoto, Naoya Fukunaga, Nahomi Yamaguchi, Misaki Maruo in CEN Case Reports (2020)

  10. Article

    Open Access

    Clinicopathological characteristics of thrombospondin type 1 domain-containing 7A-associated membranous nephropathy

    Thrombospondin type 1 domain-containing 7A (THSD7A) is a recently identified target antigen of idiopathic membranous nephropathy (iMN). The clinicopathological characteristics of THSD7A-associated MN are poorl...

    Shigeo Hara, Takahiro Tsuji, Yuichiro Fukasawa, Satoshi Hisano in Virchows Archiv (2019)

  11. Article

    Open Access

    A grading system that predicts the risk of dialysis induction in IgA nephropathy patients based on the combination of the clinical and histological severity

    Histological classification is essential in the clinical management of immunoglobulin A nephropathy (IgAN). However, there are limitations in predicting the prognosis of IgAN based on histological information ...

    Hideo Okonogi, Tetsuya Kawamura, Kensuke Joh in Clinical and Experimental Nephrology (2019)

  12. No Access

    Article

    Focal segmental glomerulosclerosis with heterozygous apolipoprotein E5 (Glu3Lys)

    Apolipoprotein (apo) E5 is a rare apoE isoform. The apoE5 (Glu3Lys) variant, which is caused by the substitution of lysine with glutamic acid at codon 3, has a relative frequency of 0.1% in Japan. Previous stu...

    Masaru Sasaki, Tetsuhiko Yasuno, Kenji Ito, Akira Matsunaga in CEN Case Reports (2018)

  13. Article

    Open Access

    Long-term desensitization for ABO-incompatible living related kidney transplantation recipients with high refractory and rebound anti-blood type antibody: case report

    ABO-incompatible living related kidney transplantation (ABO-iLKT) has increased the possibilities for kidney transplantation in patients with end stage renal disease. Due to advancements in immunosuppressive a...

    Hiroaki Nishimura, Yasutoshi Yamada, Satoshi Hisano, Akihiko Mitsuke in BMC Nephrology (2018)

  14. No Access

    Article

    Nationwide multicenter kidney biopsy study of Japanese patients with hypertensive nephrosclerosis

    Nephrosclerosis is an increasingly reason for dialysis in Japan. However, kidney biopsy specimens for hypertensive nephrosclerosis are very limited; thus, the pathologic evaluation of hypertensive nephrosclero...

    Kengo Furuichi, Miho Shimizu, Yukio Yuzawa in Clinical and Experimental Nephrology (2018)

  15. No Access

    Article

    Clinicopathological analysis of biopsy-proven diabetic nephropathy based on the Japanese classification of diabetic nephropathy

    The Japanese classification of diabetic nephropathy reflects the risks of mortality, cardiovascular events and kidney prognosis and is clinically useful. Furthermore, pathological findings of diabetic nephropa...

    Kengo Furuichi, Miho Shimizu, Yukio Yuzawa in Clinical and Experimental Nephrology (2018)

  16. No Access

    Article

    Reproducibility for pathological prognostic parameters of the Oxford classification of IgA nephropathy: the authors reply

    Satoshi Hisano, Kensuke Joh, Ritsuko Katafuchi in Clinical and Experimental Nephrology (2017)

  17. No Access

    Article

    Tubulointerstitial nephritis as adverse effect of programmed cell death 1 inhibitor, nivolumab, showed distinct histological findings

    Immune-checkpoint inhibitor nivolumab (anti-PD-1 antibody) blocks T cell inhibition and stimulate immunologic response toward cancer cells. It was also revealed that PD-1/PD-L1 interaction crucially controls t...

    Ai Uchida, Maho Watanabe, Aya Nawata, Yosuke Ikari, Masaru Sasaki in CEN Case Reports (2017)

  18. Article

    Open Access

    Fibronectin glomerulopathy complicated with persistent cloaca and congenital esophageal atresia: a case report and literature review

    Fibronectin glomerulopathy is a rare, inherited, autosomal dominant, glomerular disease characterized by proteinuria, microscopic hematuria, hypertension, massive glomerular deposits of fibronectin, and slow p...

    Misaki Takii, Takaichi Suehiro, Aya Shima, Hideki Yotsueda in BMC Nephrology (2017)

  19. No Access

    Article

    Reproducibility for pathological prognostic parameters of the Oxford classification of IgA nephropathy: a Japanese cohort study of the Ministry of Health, Labor and Welfare

    The Oxford classification of IgA nephropathy (IgAN) was proposed by international working group in 2009. Interobserver reproducibility of each pathological definition was already evaluated, but that of four pa...

    Satoshi Hisano, Kensuke Joh, Ritsuko Katafuchi in Clinical and Experimental Nephrology (2017)

  20. Article

    Open Access

    Estimation of the number of histological diagnosis for IgG4-related kidney disease referred to the data obtained from the Japan Renal Biopsy Registry (J-RBR) questionnaire and cases reported in the Japanese Society of Nephrology Meetings

    More than 2 years have passed since the proposal of the diagnostic criteria for IgG4-related kidney disease (IgG4-RKD). The aim of this study was to estimate the number of histological diagnosis for IgG4-RKD t...

    Hitoshi Nakashima, Mitsuhiro Kawano, Takako Saeki in Clinical and Experimental Nephrology (2017)

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