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Clinical Journal of the American Society of Nephrology : CJASN
|
November 21, 2022
Bardoxolone Methyl for Alport Syndrome: Opportunities and Challenges
Catherine Quinlan, Kushani Jayasinghe
Journal of Nephrology
|
October 9, 2024
Exploring new gene-disease associations in polycystic kidney disease: a case report highlighting the importance of a precise genomic diagnosis
Gemma Scholes, Yael Prawer, Jessica Ryan, et al.
Nephrology (Carlton, Vic.)
|
September 26, 2018
Recurrent oxalosis in a combined liver-kidney transplant patient with primary hyperoxaluria type 1 resulting in graft failure
Kushani Jayasinghe, Anna Haber, Kate Wyburn, et al.
Pediatric Nephrology (Berlin, Germany)
|
January 30, 2023
Clinical and diagnostic utility of genomic sequencing for children referred to a Kidney Genomics Clinic with microscopic haematuria
Josiah Shanks, Grainne Butler, Daryl Cheng, et al.
European Journal of Human Genetics : EJHG
|
February 12, 2025
Optimising the mainstreaming of renal genomics: Complementing empirical and theoretical strategies for implementation
Lin Cheng, Nathasha Kugenthiran, Catherine Quinlan, et al.
Pediatric Nephrology (Berlin, Germany)
|
February 13, 2025
Next-generation nephrology: part 1-an aid for genetic and genomic testing in pediatric nephrology
Asheeta Gupta, Kushani Jayasinghe, Amar Majmundar, et al.
Pediatric Nephrology (Berlin, Germany)
|
February 28, 2025
Next-generation nephrology: part 2-mainstreaming genomics in nephrology, a global perspective
Asheeta Gupta, Kushani Jayasinghe, Amar Majmundar, et al.
Human Genomics
|
February 1, 2018
Meeting report of the 2017 KidGen Renal Genetics Symposium
Kushani Jayasinghe, Cathy Quinlan, Zornitza Stark, et al.
Genes
|
October 27, 2022
Theory Designed Strategies to Support Implementation of Genomics in Nephrology
Arushi Kansal, Catherine Quinlan, Zornitza Stark, et al.
Archives of Disease in Childhood
|
October 23, 2024
Design and evaluation of a visual genomic explainer: a mixed-methods study
Grainne Butler, Camilla Andersen, Jim Buttery, et al.
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of 3
Search research articles
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Showing results (1-10 of 26) with videos related to
Sort By:
Page
of 3
Clinical Journal of the American Society of Nephrology : CJASN
|
November 21, 2022
Bardoxolone Methyl for Alport Syndrome: Opportunities and Challenges
Catherine Quinlan, Kushani Jayasinghe
Journal of Nephrology
|
October 9, 2024
Exploring new gene-disease associations in polycystic kidney disease: a case report highlighting the importance of a precise genomic diagnosis
Gemma Scholes, Yael Prawer, Jessica Ryan, et al.
Nephrology (Carlton, Vic.)
|
September 26, 2018
Recurrent oxalosis in a combined liver-kidney transplant patient with primary hyperoxaluria type 1 resulting in graft failure
Kushani Jayasinghe, Anna Haber, Kate Wyburn, et al.
Pediatric Nephrology (Berlin, Germany)
|
January 30, 2023
Clinical and diagnostic utility of genomic sequencing for children referred to a Kidney Genomics Clinic with microscopic haematuria
Josiah Shanks, Grainne Butler, Daryl Cheng, et al.
European Journal of Human Genetics : EJHG
|
February 12, 2025
Optimising the mainstreaming of renal genomics: Complementing empirical and theoretical strategies for implementation
Lin Cheng, Nathasha Kugenthiran, Catherine Quinlan, et al.
Pediatric Nephrology (Berlin, Germany)
|
February 13, 2025
Next-generation nephrology: part 1-an aid for genetic and genomic testing in pediatric nephrology
Asheeta Gupta, Kushani Jayasinghe, Amar Majmundar, et al.
Pediatric Nephrology (Berlin, Germany)
|
February 28, 2025
Next-generation nephrology: part 2-mainstreaming genomics in nephrology, a global perspective
Asheeta Gupta, Kushani Jayasinghe, Amar Majmundar, et al.
Human Genomics
|
February 1, 2018
Meeting report of the 2017 KidGen Renal Genetics Symposium
Kushani Jayasinghe, Cathy Quinlan, Zornitza Stark, et al.
Genes
|
October 27, 2022
Theory Designed Strategies to Support Implementation of Genomics in Nephrology
Arushi Kansal, Catherine Quinlan, Zornitza Stark, et al.
Archives of Disease in Childhood
|
October 23, 2024
Design and evaluation of a visual genomic explainer: a mixed-methods study
Grainne Butler, Camilla Andersen, Jim Buttery, et al.
Page
of 3