Showing results (61-70 of 83) with videos related to

Sort By:
Pageof 9
Clinical and Experimental Nephrology|May 28, 2021
Clinical and histological features in pediatric and adolescent/young adult patients with renal disease: a cross-sectional analysis of the Japan Renal Biopsy Registry (J-RBR)Maki Urushihara, Hiroshi Sato, Akira Shimizu, et al.
Scientific Reports|December 3, 2021
Influenza virus vaccination in pediatric nephrotic syndrome significantly reduces rate of relapse and influenza virus infection as assessed in a nationwide surveyShingo Ishimori, Takashi Ando, Kaori Kikunaga, et al.
Kidney International Reports|February 2, 2026
Clinical and Genetic Insights Into Isolated Proteinuria With <i>CUBN</i> VariantsNana Sakakibara, Shinya Ishiko, Yu Tanaka, et al.
Transplant Infectious Disease : an Official Journal of the Transplantation Society|February 29, 2020
Kidney function of Japanese children undergoing kidney transplant with preemptive therapy for cytomegalovirus infectionYoshimitsu Gotoh, Seiichiro Shishido, Yuko Hamasaki, et al.
Pediatric Nephrology (Berlin, Germany)|August 11, 2022
Early predictive factors for progression to kidney failure in infants with severe congenital anomalies of the kidney and urinary tractKentaro Nishi, Osamu Uemura, Ryoko Harada, et al.
Clinical and Experimental Nephrology|September 18, 2021
Clinical features of autosomal recessive polycystic kidney disease in the Japanese population and analysis of splicing in PKHD1 gene for determination of phenotypesShinya Ishiko, Naoya Morisada, Atsushi Kondo, et al.
Clinical and Experimental Nephrology|November 1, 2016
Female X-linked Alport syndrome with somatic mosaicismKana Yokota, Kandai Nozu, Shogo Minamikawa, et al.
Kidney International Reports|August 13, 2021
Genotype-Phenotype Correlation in <i>WT1</i> Exon 8 to 9 Missense VariantsChina Nagano, Yutaka Takaoka, Koichi Kamei, et al.
American Journal of Medical Genetics. Part A|February 19, 2015
Renal complications in 6p duplication syndrome: microarray-based investigation of the candidate gene(s) for the development of congenital anomalies of the kidney and urinary tract (CAKUT) and focal segmental glomerular sclerosis (FSGS)Megumi Yoshimura-Furuhata, Akira Nishimura-Tadaki, Yoshiro Amano, et al.
Pediatric Nephrology (Berlin, Germany)|June 5, 2025
Relationship between clinical and pathologic findings and the presence of genetic variants in patients with steroid-resistant nephrotic syndromeKoichi Kamei, Kandai Nozu, Tomoko Horinouchi, et al.
Pageof 9