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Utility of glomerular Gd-IgA1 staining for indistinguishable cases of IgA nephropathy or Alport syndrome

Ishiko, S; Tanaka, A; Takeda, A; Hara, M; Hamano, N; Koizumi, M; Ueno, T; Hayashi, H; Kondo, A; Nagai, S; Aoto, Y; Sakakibara, N; Nagano, C; Horinouchi, T; Yamamura, T; Ninchoji, T; Shima, Y; Nakanishi, K; Yoshikawa, N; Iijima, K; Nozu, K

Ishiko, S (corresponding author), Kobe Univ, Grad Sch Med, Dept Pediat, Chuo Ku, 7-5-1 Kusunoki Cho, Kobe, Hyogo 6500017, Japan.

CLINICAL AND EXPERIMENTAL NEPHROLOGY, ; ():

Abstract

Background Pathological findings in Alport syndrome frequently show mesangial proliferation and sometimes incidental IgA deposition, in addition to un......

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