Showing results (401-410 of 1,081) with videos related to
Sort By:
Pageof 109
CEN Case Reports|May 13, 2022
IgA nephropathy with glomerular capillary IgA deposition following SARS-CoV-2 mRNA vaccination: a report of three casesShinya Yokote, Hiroyuki Ueda, Akihiro Shimizu, et al.CEN Case Reports|July 20, 2021
Tubulointerstitial nephritis in antineutrophil cytoplasmic antibody-associated vasculitis with monoclonal gammopathyErika Hishida, Takahisa Kobayashi, Yuko Ono, et al.CEN Case Reports|July 25, 2021
A case of early recurrent immunoglobulin A nephropathy and T-cell-mediated rejection in a transplant patient with Wiskott-Aldrich syndromeKosei Yamaguchi, Mineaki Kitamura, Yuki Kawaguchi, et al.CEN Case Reports|March 19, 2020
Isolated nephrocalcinosis due to compound heterozygous mutations in renal outer medullary potassium channelPriyanka Khandelwal, Jasintha Sabanadesan, Aditi Sinha, et al.CEN Case Reports|January 25, 2020
Plasma exchange combined with bortezomib-based chemotherapy is effective for early renal recovery in a patient with IgD-λ type multiple myelomaHiroyuki Ueda, Hideaki Kuno, Daisuke Takahashi, et al.CEN Case Reports|January 4, 2021
Nodular glomerulosclerosis in a kidney transplant recipient with impaired glucose tolerance: diabetic or idiopathic? A case report and literature reviewZhong Hong Liew, Puay Hoon Tan, Marjorie Foo, et al.CEN Case Reports|January 5, 2021
Spontaneous remission of minimal change nephrotic syndrome in an elderly manYuki Chiba, Tasuku Nagasawa, Saori Kin, et al.CEN Case Reports|January 2, 2021
Fecal microbiota transplantation for membranous nephropathyGuanzhou Zhou, Jiaqi Zeng, Lihua Peng, et al.CEN Case Reports|April 8, 2020
Bardet-Biedl syndrome in two unrelated patients with identical compound heterozygous SCLT1 mutationsNaoya Morisada, Riku Hamada, Kenichiro Miura, et al.CEN Case Reports|October 30, 2020
A patient with congenital nephrogenic diabetes insipidus due to AVPR2 mutation complicated by persisting polydipsia under hemodialysis treatmentTakashi Iijima, Takayasu Mori, Eisei Sohara, et al.Pageof 109