Acute Kidney Injury Associated with Minimal Change Nephrotic Syndrome in an Elderly Patient Successfully Treated with both Fluid Management and Specific Therapy Based on Kidney Bio...

gan Oyama, Yuko, Iwafuchi, Yoichi, Morioka, Tetsuo, Narita, Ichiei
Cyhoeddwyd yn Case Rep Nephrol Dial (2020)

Ectopic ossification in the cranial dura mater in dialysis patients with secondary hyperparathyroidism

gan Oyama, Yuko, Kazama, Junichiro J., Fukagawa, Mitsutoshi, Arakawa, Yasuaki, Ezuka, Isamu
Cyhoeddwyd yn NDT Plus (2010)

Nephrotic Syndrome without Hematuria due to Infection-Related Glomerulonephritis Mimicking Minimal-Change Disease in a Child

gan Iwafuchi, Yoichi, Morioka, Tetsuo, Morita, Takashi, Watanabe, Kanako, Oyama, Yuko, Narita, Ichiei
Cyhoeddwyd yn Case Rep Nephrol Dial (2016)

A Case of Transforming Growth Factor-β-Induced Gene-Related Oculorenal Syndrome: Granular Corneal Dystrophy Type II with a Unique Nephropathy

gan Iwafuchi, Yoichi, Morioka, Tetsuo, Oyama, Yuko, Nozu, Kandai, Iijima, Kazumoto, Narita, Ichiei
Cyhoeddwyd yn Case Rep Nephrol Dial (2016)

De novo acute hepatitis B in myeloperoxidase-specific anti-neutrophil cytoplasmic autoantibody-related microscopic polyangiitis treated with corticosteroids

gan Iwafuchi, Yoichi, Oyama, Yuko, Morita, Takashi, Kamimura, Akira, Miyazaki, Shigeru, Narita, Ichiei
Cyhoeddwyd yn CEN Case Rep (2012)

Combined membranous nephropathy and crescentic glomerulonephritis with concurrent anti-glomerular basement membrane antibody and myeloperoxidase-specific anti-neutrophil cytoplasmi...

gan Iwafuchi, Yoichi, Morita, Takashi, Oyama, Yuko, Kamimura, Akira, Miyazaki, Shigeru, Narita, Ichiei
Cyhoeddwyd yn CEN Case Rep (2013)

Enzyme replacement therapy in a patient of heterozygous Fabry disease: clinical and pathological evaluations by repeat kidney biopsy and a successful pregnancy

gan Iwafuchi, Yoichi, Maruyama, Hiroki, Morioka, Tetsuo, Noda, Seiko, Nagata, Hiroshi, Oyama, Yuko, Narita, Ichiei
Cyhoeddwyd yn CEN Case Rep (2017)

Diverse Renal Phenotypes Observed in a Single Family with a Genetic Mutation in Paired Box Protein 2

gan Iwafuchi, Yoichi, Morioka, Tetsuo, Morita, Takashi, Yanagihara, Toshio, Oyama, Yuko, Morisada, Naoya, Iijima, Kazumoto, Narita, Ichiei
Cyhoeddwyd yn Case Rep Nephrol Dial (2016)