An international cohort study of autosomal dominant tubulointerstitial kidney disease due to REN mutations identifies distinct clinical subtypes

M Živná, K Kidd, M Zaidan, P Vyleťal, V Barešová… - Kidney international, 2020 - Elsevier
There have been few clinical or scientific reports of autosomal dominant tubulointerstitial
kidney disease due to REN mutations (ADTKD-REN), limiting characterization. To further …
被引用次数：37 相关文章

An international cohort study of autosomal dominant tubulointerstitial kidney disease due to REN mutations identifies distinct clinical subtypes

M Živná, K Kidd, M Zaidan, P Vyleťal… - Kidney …, 2020 - kidney-international.org
There have been few clinical or scientific reports of autosomal dominant tubulointerstitial
kidney disease due to REN mutations (ADTKD-REN), limiting characterization. To further …

An international cohort study of autosomal dominant tubulointerstitial kidney disease due to REN mutations identifies distinct clinical subtypes

M Živná, K Kidd, M Zaidan… - Kidney …, 2020 - utsouthwestern.elsevierpure.com
There have been few clinical or scientific reports of autosomal dominant tubulointerstitial
kidney disease due to REN mutations (ADTKD-REN), limiting characterization. To further …

An international cohort study of autosomal dominant tubulointerstitial kidney disease due to REN mutations identifies distinct clinical subtypes

M Živná, K Kidd, M Zaidan, P Vyleťal… - Kidney …, 2020 - pubmed.ncbi.nlm.nih.gov
There have been few clinical or scientific reports of autosomal dominant tubulointerstitial
kidney disease due to REN mutations (ADTKD-REN), limiting characterization. To further …
[HTML] nih.gov

[HTML][HTML] An International Cohort Study of Autosomal Dominant Tubulointerstitial Kidney Disease due to REN Mutations Identifies Distinct Clinical Subtypes

M Živná, K Kidd, M Zaidan, P Vyleťal… - Kidney …, 2020 - ncbi.nlm.nih.gov
There have been few clinical or scientific reports of autosomal dominant tubulointerstitial
kidney disease due to REN mutations (ADTKD-REN), limiting characterization. To further …

An international cohort study of autosomal dominant tubulointerstitial kidney disease due to REN mutations identifies distinct clinical subtypes

M Živná, K Kidd, M Zaidan, P Vyleťal… - Kidney …, 2020 - eprints.whiterose.ac.uk
There have been few clinical or scientific reports of autosomal dominant tubulointerstitial
kidney disease due to REN mutations (ADTKD-REN), limiting characterization. To further …

An international cohort study of autosomal dominant tubulointerstitial kidney disease due to REN mutations identifies distinct clinical subtypes

M Zivna, K Kidd, M Zaidan, P Vyletal, V Baresova… - Kidney Int …, 2020 - kups.ub.uni-koeln.de
There have been few clinical or scientific reports of autosomal dominant tubulointerstitial
kidney disease due to REN mutations (ADTKD-REN), limiting characterization. To further …
[PDF] academia.edu

[PDF][PDF] This is a repository copy of An international cohort study of autosomal dominant tubulointerstitial kidney disease due to REN mutations identifies distinct clinical …

M Živná, K Kidd, M Zaidan - academia.edu
ABSTRACT 1 There have been few clinical or scientific reports of autosomal dominant
tubulo-interstitial kidney 2 disease due to REN mutations (ADTKD-REN), limiting …

An international cohort study of autosomal dominant tubulointerstitial kidney disease due to REN mutations identifies distinct clinical subtypes.

M Živná, K Kidd, M Zaidan, P Vyleťal… - Kidney …, 2020 - europepmc.org
There have been few clinical or scientific reports of autosomal dominant tubulointerstitial
kidney disease due to REN mutations (ADTKD-REN), limiting characterization. To further …
[PDF] iupui.edu

[PDF][PDF] An International Cohort Study of Autosomal Dominant Tubulointerstitial Kidney Disease due to REN Mutations Identifies Distinct Clinical Subtypes

M Živná, K Kidd, M Zaidan, P Vyleťal, V Barešová… - 2020 - scholarworks.iupui.edu
There have been few clinical or scientific reports of autosomal dominant tubulointerstitial
kidney disease due to REN mutations (ADTKD-REN), limiting characterization. To further …