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Kidney International
|
February 20, 2026
Disruption of the human cystin-1 myristoyl-electrostatic switch causes polycystic kidney disease that phenocopies autosomal recessive polycystic kidney disease
Chaozhe Yang, Naoe Harafuji, Jacob A Watts, et al.
The Journal of Pediatrics
|
July 13, 2014
Consensus expert recommendations for the diagnosis and management of autosomal recessive polycystic kidney disease: report of an international conference
Lisa M Guay-Woodford, John J Bissler, Michael C Braun, et al.
Kidney International
|
March 23, 2019
Health-related quality of life in glomerular disease
Pietro A Canetta, Jonathan P Troost, Shannon Mahoney, et al.
The Journal of Clinical Investigation
|
September 3, 2024
Increased risk of kidney failure in patients with genetic kidney disorders
Mark D Elliott, Natalie Vena, Maddalena Marasa, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
November 14, 2018
CureGN Study Rationale, Design, and Methods: Establishing a Large Prospective Observational Study of Glomerular Disease
Laura H Mariani, Andrew S Bomback, Pietro A Canetta, et al.
Nature Genetics
|
September 14, 2010
Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy
Edgar A Otto, Toby W Hurd, Rannar Airik, et al.
Kidney International Reports
|
November 20, 2018
Clinical Characteristics and Treatment Patterns of Children and Adults With IgA Nephropathy or IgA Vasculitis: Findings From the CureGN Study
David T Selewski, Josephine M Ambruzs, Gerald B Appel, et al.
Kidney International
|
March 23, 2025
Insights from ADPedKD, ERKReg and RaDaR registries provide a multi-national perspective on the presentation of childhood autosomal dominant polycystic kidney disease in high- and middle-income countries
Charlotte Gimpel, Steffen Fieuws, Jonas Hofstetter, et al.
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Search research articles
Search
Showing results (191-200 of 198) with videos related to
Sort By:
Page
of 20
You have reached the last page of results.
This site can display upto 198 results.
Kidney International
|
February 20, 2026
Disruption of the human cystin-1 myristoyl-electrostatic switch causes polycystic kidney disease that phenocopies autosomal recessive polycystic kidney disease
Chaozhe Yang, Naoe Harafuji, Jacob A Watts, et al.
The Journal of Pediatrics
|
July 13, 2014
Consensus expert recommendations for the diagnosis and management of autosomal recessive polycystic kidney disease: report of an international conference
Lisa M Guay-Woodford, John J Bissler, Michael C Braun, et al.
Kidney International
|
March 23, 2019
Health-related quality of life in glomerular disease
Pietro A Canetta, Jonathan P Troost, Shannon Mahoney, et al.
The Journal of Clinical Investigation
|
September 3, 2024
Increased risk of kidney failure in patients with genetic kidney disorders
Mark D Elliott, Natalie Vena, Maddalena Marasa, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
November 14, 2018
CureGN Study Rationale, Design, and Methods: Establishing a Large Prospective Observational Study of Glomerular Disease
Laura H Mariani, Andrew S Bomback, Pietro A Canetta, et al.
Nature Genetics
|
September 14, 2010
Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy
Edgar A Otto, Toby W Hurd, Rannar Airik, et al.
Kidney International Reports
|
November 20, 2018
Clinical Characteristics and Treatment Patterns of Children and Adults With IgA Nephropathy or IgA Vasculitis: Findings From the CureGN Study
David T Selewski, Josephine M Ambruzs, Gerald B Appel, et al.
Kidney International
|
March 23, 2025
Insights from ADPedKD, ERKReg and RaDaR registries provide a multi-national perspective on the presentation of childhood autosomal dominant polycystic kidney disease in high- and middle-income countries
Charlotte Gimpel, Steffen Fieuws, Jonas Hofstetter, et al.
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of 20