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Showing results (191-200 of 198) with videos related to

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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 diseaseChaozhe 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 conferenceLisa M Guay-Woodford, John J Bissler, Michael C Braun, et al.
Kidney International|March 23, 2019
Health-related quality of life in glomerular diseasePietro 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 disordersMark 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 DiseaseLaura 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 ciliopathyEdgar 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 StudyDavid 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 countriesCharlotte Gimpel, Steffen Fieuws, Jonas Hofstetter, et al.
Pageof 20

Showing results (191-200 of 198) with videos related to

Sort By:
Pageof 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 diseaseChaozhe 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 conferenceLisa M Guay-Woodford, John J Bissler, Michael C Braun, et al.
Kidney International|March 23, 2019
Health-related quality of life in glomerular diseasePietro 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 disordersMark 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 DiseaseLaura 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 ciliopathyEdgar 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 StudyDavid 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 countriesCharlotte Gimpel, Steffen Fieuws, Jonas Hofstetter, et al.
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