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Kidney Diseases (Basel, Switzerland)|June 15, 2022
Echocardiographic Findings and Genotypes in Autosomal Dominant Polycystic Kidney DiseaseRyohei Miyamoto, Akinari Sekine, Takuya Fujimaru, et al.
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|May 11, 2018
[Transplantation-associated thrombotic microangiopathy confirmed by renal biopsy]Satoshi Miyamoto, Shunsuke Kimura, Yosuke Hosoya, et al.
Nephron|September 13, 2021
A Novel LMX1B Variant Identified in a Patient Presenting with Severe Renal Involvement and Thin Glomerular Basement MembraneNobuhisa Morimoto, Kiyotaka Nagahama, Takayasu Mori, et al.
Internal Medicine (Tokyo, Japan)|June 8, 2022
Different Clinical Courses of Nephronophthisis in Dizygotic TwinsYutaro Oki, Ai Katsuma, Masahiro Okabe, et al.
Molecular Genetics & Genomic Medicine|May 3, 2019
A familial case of pseudohypoaldosteronism type II (PHA2) with a novel mutation (D564N) in the acidic motif in WNK4Takashi Sakoh, Akinari Sekine, Takayasu Mori, et al.
Kidney International|February 16, 2020
Renal TNFα activates the WNK phosphorylation cascade and contributes to salt-sensitive hypertension in chronic kidney diseaseTaisuke Furusho, Eisei Sohara, Shintaro Mandai, et al.
Clinical and Experimental Nephrology|February 17, 2021
Deletion of Alox15 improves kidney dysfunction and inhibits fibrosis by increased PGD<sub>2</sub> in the kidneyNaohiro Takahashi, Hiroaki Kikuchi, Ayaka Usui, et al.
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