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CEN Case Reports|January 13, 2026
A case of chronic Campylobacter fetus infection-related glomerulonephritis, mimicking systemic autoimmune diseasesMinami Matsumoto, Yuichiro Kitai, Shinya Yamamoto, et al.
CEN Case Reports|January 20, 2026
Coincidence of autosomal dominant polycystic kidney disease and Alport syndrome: a case report and literature reviewRui Liu, Fei Liu
CEN Case Reports|February 15, 2026
An autopsy-proven case of normotensive scleroderma renal crisis with refractory pleuroperitoneal effusionHideki Uedono, Katsuhito Mori, Shinya Nakatani, et al.
CEN Case Reports|February 15, 2026
Successful living kidney transplantation in a T-cell flow cytometry crossmatch-positive patient with atypical hemolytic uremic syndrome treated with an anti-C5 antibody: a case reportMasayoshi Okumi, Natsuko Okuno, Ryo Kurose, et al.
CEN Case Reports|February 15, 2026
Recurrent obturator hernia in a patient with autosomal dominant polycystic kidney disease undergoing peritoneal dialysis: a case reportKoichiro Okumura, Tomoko Kawanishi, Yasutomo Abe, et al.
CEN Case Reports|February 5, 2026
Relapse of minimal change nephrotic syndrome after initiation of sulfamethoxazole-trimethoprim combination therapy: a case reportTakuya Sugiura, Shun Ito, Naohiro Sakaguchi, et al.
CEN Case Reports|February 6, 2025
Case of maternal uniparental isodisomy with autosomal recessive Alport syndrome combined with congenital myasthenia and Oguchi diseaseMisaki Akiyama, Keiko Matsubara, Hiroshi Terashima, et al.
CEN Case Reports|December 29, 2024
A case of neuron-derived neurotrophic factor-positive, syphilis-related membranous nephropathy that achieved spontaneous remissionYuko Yoshida, Kenji Ueki, Yuta Matsukuma, et al.
CEN Case Reports|December 31, 2024
The application of omalizumab in children with atopic diseases complicated by nephrotic syndrome: a case reportYi Mao, Jialu Lu, Lei Yin, et al.
CEN Case Reports|December 11, 2024
Fanconi syndrome following administration of oral supplements containing red yeast rice: several months follow-up of three casesReina Matsui-Hosoya, Koji Sato, Motohiro Yagasaki, et al.
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