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Detlef Bockenhauer

Showing results (121-130 of 233) with videos related to

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Human Molecular Genetics|October 11, 2019
Functional assessment of variants associated with Wolfram syndromeMelissa Riachi, Sebahat Yilmaz, Erdal Kurnaz, et al.
European Journal of Pediatrics|May 5, 2019
Tolvaptan use in children and adolescents with autosomal dominant polycystic kidney disease: rationale and design of a two-part, randomized, double-blind, placebo-controlled trialFranz Schaefer, Djalila Mekahli, Francesco Emma, et al.
Pediatric Nephrology (Berlin, Germany)|May 21, 2011
Sotos syndrome, infantile hypercalcemia, and nephrocalcinosis: a contiguous gene syndromeJoanna Kenny, Melissa M Lees, Susan Drury, et al.
European Journal of Human Genetics : EJHG|May 30, 2020
Genetic aspects of congenital nephrotic syndrome: a consensus statement from the ERKNet-ESPN inherited glomerulopathy working groupBeata Stefania Lipska-Ziętkiewicz, Fatih Ozaltin, Tuula Hölttä, et al.
Nephron. Physiology|August 19, 2011
Familial autosomal recessive renal tubular acidosis: importance of early diagnosisAsaf Vivante, Danny Lotan, Naomi Pode-Shakked, et al.
Journal of Hypertension|September 5, 2020
Genetics of renovascular hypertension in childrenDaan H H M Viering, Melanie M Y Chan, Lieke Hoogenboom, et al.
Kidney International Reports|September 14, 2019
HNF1B Mutations Are Associated With a Gitelman-like Tubulopathy That Develops During ChildhoodShazia Adalat, Wesley N Hayes, William A Bryant, et al.
Kidney International|February 17, 2024
A Neanderthal haplotype introgressed into the human genome confers protection against membranous nephropathyCătălin D Voinescu, Monika Mozere, Giulio Genovese, et al.
Nephron. Physiology|August 19, 2011
KCNJ10 mutations disrupt function in patients with EAST syndromeBernard Freudenthal, Duvaraka Kulaveerasingam, Lokesh Lingappa, et al.
Nature Reviews. Nephrology|May 4, 2021
Publisher Correction: Management of congenital nephrotic syndrome: consensus recommendations of the ERKNet-ESPN Working GroupOlivia Boyer, Franz Schaefer, Dieter Haffner, et al.
Pageof 24

Showing results (121-130 of 233) with videos related to

Sort By:
Pageof 24
Human Molecular Genetics|October 11, 2019
Functional assessment of variants associated with Wolfram syndromeMelissa Riachi, Sebahat Yilmaz, Erdal Kurnaz, et al.
European Journal of Pediatrics|May 5, 2019
Tolvaptan use in children and adolescents with autosomal dominant polycystic kidney disease: rationale and design of a two-part, randomized, double-blind, placebo-controlled trialFranz Schaefer, Djalila Mekahli, Francesco Emma, et al.
Pediatric Nephrology (Berlin, Germany)|May 21, 2011
Sotos syndrome, infantile hypercalcemia, and nephrocalcinosis: a contiguous gene syndromeJoanna Kenny, Melissa M Lees, Susan Drury, et al.
European Journal of Human Genetics : EJHG|May 30, 2020
Genetic aspects of congenital nephrotic syndrome: a consensus statement from the ERKNet-ESPN inherited glomerulopathy working groupBeata Stefania Lipska-Ziętkiewicz, Fatih Ozaltin, Tuula Hölttä, et al.
Nephron. Physiology|August 19, 2011
Familial autosomal recessive renal tubular acidosis: importance of early diagnosisAsaf Vivante, Danny Lotan, Naomi Pode-Shakked, et al.
Journal of Hypertension|September 5, 2020
Genetics of renovascular hypertension in childrenDaan H H M Viering, Melanie M Y Chan, Lieke Hoogenboom, et al.
Kidney International Reports|September 14, 2019
HNF1B Mutations Are Associated With a Gitelman-like Tubulopathy That Develops During ChildhoodShazia Adalat, Wesley N Hayes, William A Bryant, et al.
Kidney International|February 17, 2024
A Neanderthal haplotype introgressed into the human genome confers protection against membranous nephropathyCătălin D Voinescu, Monika Mozere, Giulio Genovese, et al.
Nephron. Physiology|August 19, 2011
KCNJ10 mutations disrupt function in patients with EAST syndromeBernard Freudenthal, Duvaraka Kulaveerasingam, Lokesh Lingappa, et al.
Nature Reviews. Nephrology|May 4, 2021
Publisher Correction: Management of congenital nephrotic syndrome: consensus recommendations of the ERKNet-ESPN Working GroupOlivia Boyer, Franz Schaefer, Dieter Haffner, et al.
Pageof 24