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Journal of the American Society of Nephrology : JASN
|
September 4, 2010
SPAK-knockout mice manifest Gitelman syndrome and impaired vasoconstriction
Sung-Sen Yang, Yi-Fen Lo, Chin-Chen Wu, et al.
Journal of the American Society of Nephrology : JASN
|
November 8, 2014
Discovery of Novel SPAK Inhibitors That Block WNK Kinase Signaling to Cation Chloride Transporters
Eriko Kikuchi, Takayasu Mori, Moko Zeniya, et al.
Internal Medicine (Tokyo, Japan)
|
October 8, 2025
Delayed Therapeutic Response to Oral Corticosteroids and Rituximab Leading to Dialysis Independence in a Patient with Treatment-resistant C3 Glomerulonephritis
Yuki Nakao, Junko Kunieda, Towako Taguchi, et al.
Kidney Diseases (Basel, Switzerland)
|
June 15, 2022
Echocardiographic Findings and Genotypes in Autosomal Dominant Polycystic Kidney Disease
Ryohei Miyamoto, Akinari Sekine, Takuya Fujimaru, et al.
Hypertension (Dallas, Tex. : 1979)
|
October 11, 2023
National Trends in Mortality and Urgent Dialysis after Acute Hypertension in Japan From 2010 Through 2019
Hisazumi Matsuki, Taku Genma, Shintaro Mandai, et al.
International Journal of Surgery (London, England)
|
August 9, 2022
Nationwide mortality associated with perioperative acute dialysis requirement in major surgeries
Yuta Nakano, Shintaro Mandai, Taku Genma, et al.
CEN Case Reports
|
July 11, 2018
Ruptured infected aneurysm of the thoracic aorta associated with tunneled dialysis catheter-related methicillin-resistant Staphylococcus aureus bacteremia in a hemodialysis patient
Fumiko Katsuragawa, Kiyotaka Nagahama, Shotaro Naito, et al.
Cell Metabolism
|
May 10, 2007
Molecular pathogenesis of pseudohypoaldosteronism type II: generation and analysis of a Wnk4(D561A/+) knockin mouse model
Sung-Sen Yang, Tetsuji Morimoto, Tatemitsu Rai, et al.
Internal Medicine (Tokyo, Japan)
|
April 5, 2021
A Novel Mutation in LMX1B (p.Pro219Ala) Causes Focal Segmental Glomerulosclerosis with Alport Syndrome-like Phenotype
Yuji Oe, Eikan Mishima, Takayasu Mori, et al.
JCI Insight
|
September 9, 2021
Impairment in renal medulla development underlies salt wasting in Clc-k2 channel deficiency
Meng-Hsuan Lin, Jen-Chi Chen, Xuejiao Tian, et al.
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of 29
Search research articles
Search
Showing results (201-210 of 288) with videos related to
Sort By:
Page
of 29
Journal of the American Society of Nephrology : JASN
|
September 4, 2010
SPAK-knockout mice manifest Gitelman syndrome and impaired vasoconstriction
Sung-Sen Yang, Yi-Fen Lo, Chin-Chen Wu, et al.
Journal of the American Society of Nephrology : JASN
|
November 8, 2014
Discovery of Novel SPAK Inhibitors That Block WNK Kinase Signaling to Cation Chloride Transporters
Eriko Kikuchi, Takayasu Mori, Moko Zeniya, et al.
Internal Medicine (Tokyo, Japan)
|
October 8, 2025
Delayed Therapeutic Response to Oral Corticosteroids and Rituximab Leading to Dialysis Independence in a Patient with Treatment-resistant C3 Glomerulonephritis
Yuki Nakao, Junko Kunieda, Towako Taguchi, et al.
Kidney Diseases (Basel, Switzerland)
|
June 15, 2022
Echocardiographic Findings and Genotypes in Autosomal Dominant Polycystic Kidney Disease
Ryohei Miyamoto, Akinari Sekine, Takuya Fujimaru, et al.
Hypertension (Dallas, Tex. : 1979)
|
October 11, 2023
National Trends in Mortality and Urgent Dialysis after Acute Hypertension in Japan From 2010 Through 2019
Hisazumi Matsuki, Taku Genma, Shintaro Mandai, et al.
International Journal of Surgery (London, England)
|
August 9, 2022
Nationwide mortality associated with perioperative acute dialysis requirement in major surgeries
Yuta Nakano, Shintaro Mandai, Taku Genma, et al.
CEN Case Reports
|
July 11, 2018
Ruptured infected aneurysm of the thoracic aorta associated with tunneled dialysis catheter-related methicillin-resistant Staphylococcus aureus bacteremia in a hemodialysis patient
Fumiko Katsuragawa, Kiyotaka Nagahama, Shotaro Naito, et al.
Cell Metabolism
|
May 10, 2007
Molecular pathogenesis of pseudohypoaldosteronism type II: generation and analysis of a Wnk4(D561A/+) knockin mouse model
Sung-Sen Yang, Tetsuji Morimoto, Tatemitsu Rai, et al.
Internal Medicine (Tokyo, Japan)
|
April 5, 2021
A Novel Mutation in LMX1B (p.Pro219Ala) Causes Focal Segmental Glomerulosclerosis with Alport Syndrome-like Phenotype
Yuji Oe, Eikan Mishima, Takayasu Mori, et al.
JCI Insight
|
September 9, 2021
Impairment in renal medulla development underlies salt wasting in Clc-k2 channel deficiency
Meng-Hsuan Lin, Jen-Chi Chen, Xuejiao Tian, et al.
Page
of 29