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Helen M Stuart

Showing results (1-10 of 20) with videos related to

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Pediatric Nephrology (Berlin, Germany)|November 29, 2017
Genetic testing in steroid-resistant nephrotic syndrome: why, who, when and how?Rebecca Preston, Helen M Stuart, Rachel Lennon
Pediatric Nephrology (Berlin, Germany)|April 16, 2013
Genetics of human congenital urinary bladder diseaseAdrian S Woolf, Helen M Stuart, William G Newman
Pediatric Nephrology (Berlin, Germany)|September 30, 2024
Detection of Alport gene variants in children and young people with persistent haematuriaNatasha Su Lynn Ng, Tomohiko Yamamura, Mohan Shenoy, et al.
Pediatric Nephrology (Berlin, Germany)|July 9, 2013
Urofacial syndrome: a genetic and congenital disease of aberrant urinary bladder innervationAdrian S Woolf, Helen M Stuart, Neil A Roberts, et al.
Human Molecular Genetics|April 3, 2014
Heparanase 2, mutated in urofacial syndrome, mediates peripheral neural development in XenopusNeil A Roberts, Adrian S Woolf, Helen M Stuart, et al.
Scientific Reports|August 14, 2023
Predicting congenital renal tract malformation genes using machine learningMitra Kabir, Helen M Stuart, Filipa M Lopes, et al.
American Journal of Medical Genetics. Part A|January 11, 2019
22q11.2 duplications in a UK cohort with bladder exstrophy-epispadias complexGlenda M Beaman, Adrian S Woolf, Raimondo M Cervellione, et al.
Kidney International Reports|October 26, 2020
Early B-cell Factor 3-Related Genetic Disease Can Mimic Urofacial SyndromeJ Robert Harkness, Glenda M Beaman, Keng W Teik, et al.
Clinical Genetics|August 24, 2019
A homozygous missense variant in CHRM3 associated with familial urinary bladder diseaseGlenda M Beaman, Gabriella Galatà, Keng W Teik, et al.
Pediatric Nephrology (Berlin, Germany)|March 6, 2015
Coinheritance of COL4A5 and MYO1E mutations accentuate the severity of kidney diseaseRachel Lennon, Helen M Stuart, Agnieszka Bierzynska, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Pediatric Nephrology (Berlin, Germany)|November 29, 2017
Genetic testing in steroid-resistant nephrotic syndrome: why, who, when and how?Rebecca Preston, Helen M Stuart, Rachel Lennon
Pediatric Nephrology (Berlin, Germany)|April 16, 2013
Genetics of human congenital urinary bladder diseaseAdrian S Woolf, Helen M Stuart, William G Newman
Pediatric Nephrology (Berlin, Germany)|September 30, 2024
Detection of Alport gene variants in children and young people with persistent haematuriaNatasha Su Lynn Ng, Tomohiko Yamamura, Mohan Shenoy, et al.
Pediatric Nephrology (Berlin, Germany)|July 9, 2013
Urofacial syndrome: a genetic and congenital disease of aberrant urinary bladder innervationAdrian S Woolf, Helen M Stuart, Neil A Roberts, et al.
Human Molecular Genetics|April 3, 2014
Heparanase 2, mutated in urofacial syndrome, mediates peripheral neural development in XenopusNeil A Roberts, Adrian S Woolf, Helen M Stuart, et al.
Scientific Reports|August 14, 2023
Predicting congenital renal tract malformation genes using machine learningMitra Kabir, Helen M Stuart, Filipa M Lopes, et al.
American Journal of Medical Genetics. Part A|January 11, 2019
22q11.2 duplications in a UK cohort with bladder exstrophy-epispadias complexGlenda M Beaman, Adrian S Woolf, Raimondo M Cervellione, et al.
Kidney International Reports|October 26, 2020
Early B-cell Factor 3-Related Genetic Disease Can Mimic Urofacial SyndromeJ Robert Harkness, Glenda M Beaman, Keng W Teik, et al.
Clinical Genetics|August 24, 2019
A homozygous missense variant in CHRM3 associated with familial urinary bladder diseaseGlenda M Beaman, Gabriella Galatà, Keng W Teik, et al.
Pediatric Nephrology (Berlin, Germany)|March 6, 2015
Coinheritance of COL4A5 and MYO1E mutations accentuate the severity of kidney diseaseRachel Lennon, Helen M Stuart, Agnieszka Bierzynska, et al.
Pageof 2