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Clinical and Experimental Nephrology|July 13, 2024
A review of the genetic background in complicated WT1-related disordersChina Nagano, Kandai Nozu
BMC Nephrology|July 16, 2017
Warfarin-induced toxic epidermal necrolysis in combination therapy of Henoch-Schönlein purpura nephritis: a case reportKatsuaki Kasahara, Yoshimitsu Gotoh, Yoshiyuki Kuroyanagi, et al.
BMC Nephrology|November 6, 2015
Case report: anti-glomerular basement membrane antibody disease with normal renal functionChina Nagano, Yoshimitu Goto, Katuaki Kasahara, et al.
Arerugi = [Allergy]|March 28, 2013
[Anaphylaxis and biphasic reaction in a children hospital]China Nagano, Akira Ishiguro, Nobuyuki Yotani, et al.
Pediatric Nephrology (Berlin, Germany)|January 24, 2024
WT1 exon 10 missense variant in a pediatric patient with focal segmental glomerulosclerosis with embryonal hyperplasiaMari Kurokawa, Manao Nishimura, Kei Nishiyama, et al.
CEN Case Reports|February 2, 2024
A case of pseudo-Bartter/Gitelman syndrome caused by long-term laxative abuse, leading to end-stage kidney diseaseAtsushi Kondo, Kunihiko Yoshiya, Nana Sakakibara, et al.
CEN Case Reports|August 6, 2025
A case of Frasier syndrome achieved complete remission by cyclosporine A for steroid-resistant nephrotic syndromeYasuhiro Inaba, Akinori Miyazono, Takuro Mitsunobu, et al.
CEN Case Reports|July 8, 2020
A different clinical manifestation in a Japanese family with autosomal dominant distal renal tubular acidosis caused by SLC4A1 mutationKoji Sakuraya, Kandai Nozu, Itsuhiro Oka, et al.
CEN Case Reports|January 21, 2021
An extremely mild clinical course in a case with LAMB2-associated nephritis diagnosed with next-generation sequencingKoji Sakuraya, Kandai Nozu, Hitohiko Murakami, et al.
Minerva Pediatrics|November 14, 2018
Steroid- and immunosuppressant-based protocol of Henoch-Schönlein purpura nephritis without angiotensin inhibitors in the acute phaseKatsuaki Kasahara, Yoshimitsu Gotoh, Yoshiyuki Kuroyanagi, et al.
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