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Detlef Bockenhauer

Showing results (101-110 of 233) with videos related to

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Nephron. Physiology|October 10, 2009
Vasopressin type 2 receptor V88M mutation: molecular basis of partial and complete nephrogenic diabetes insipidusDetlef Bockenhauer, Eric Carpentier, Driss Rochdi, et al.
Nature Reviews. Nephrology|April 9, 2020
Diagnoses of uncertain significance: kidney genetics in the 21st centuryDaniel P Gale, Andrew Mallett, Chirag Patel, et al.
Annals of Saudi Medicine|January 14, 2014
Steroid-resistant nephrotic syndrome: impact of genetic testingJameela A Kari, Sherif M El-Desoky, Mamdooh Gari, et al.
Pediatric Nephrology (Berlin, Germany)|February 9, 2011
A patient with polyuria and hydronephrosis: questionGraciana Jaureguiberry, William Van't Hoff, Imran Mushtaq, et al.
Clinical Kidney Journal|June 13, 2015
Aquaporin-2: new mutations responsible for autosomal-recessive nephrogenic diabetes insipidus-update and epidemiologyDaniel G Bichet, Abdulah El Tarazi, Jessica Matar, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|June 16, 2023
Syndrome of inappropriate secretion of anti-diuretic hormone due to hypothalamic hamartoma: use of tolvaptanRebecca Jane Moon, Maisara Soliman, Lieke Hoogenboom, et al.
Pediatric Nephrology (Berlin, Germany)|February 12, 2017
Clinical and molecular aspects of distal renal tubular acidosis in childrenMartine T P Besouw, Marc Bienias, Patrick Walsh, et al.
Kidney International Reports|February 23, 2023
Shockwaves and the Rolling Stones: An Overview of Pediatric Stone DiseaseNaima Smeulders, Alexander Cho, Abdulelah Alshaiban, et al.
Pediatric Transplantation|April 12, 2019
Plasma electrolyte imbalance in pediatric kidney transplant recipientsWesley Hayes, Catherine Longley, Nicola Scanlon, et al.
Hormone Research in Paediatrics|June 8, 2020
Co-Existence of Congenital Adrenal Hyperplasia and Bartter Syndrome due to Maternal Uniparental Isodisomy of HSD3B2 and CLCNKB MutationsDinesh Giri, Detlef Bockenhauer, Charu Deshpande, et al.
Pageof 24

Showing results (101-110 of 233) with videos related to

Sort By:
Pageof 24
Nephron. Physiology|October 10, 2009
Vasopressin type 2 receptor V88M mutation: molecular basis of partial and complete nephrogenic diabetes insipidusDetlef Bockenhauer, Eric Carpentier, Driss Rochdi, et al.
Nature Reviews. Nephrology|April 9, 2020
Diagnoses of uncertain significance: kidney genetics in the 21st centuryDaniel P Gale, Andrew Mallett, Chirag Patel, et al.
Annals of Saudi Medicine|January 14, 2014
Steroid-resistant nephrotic syndrome: impact of genetic testingJameela A Kari, Sherif M El-Desoky, Mamdooh Gari, et al.
Pediatric Nephrology (Berlin, Germany)|February 9, 2011
A patient with polyuria and hydronephrosis: questionGraciana Jaureguiberry, William Van't Hoff, Imran Mushtaq, et al.
Clinical Kidney Journal|June 13, 2015
Aquaporin-2: new mutations responsible for autosomal-recessive nephrogenic diabetes insipidus-update and epidemiologyDaniel G Bichet, Abdulah El Tarazi, Jessica Matar, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|June 16, 2023
Syndrome of inappropriate secretion of anti-diuretic hormone due to hypothalamic hamartoma: use of tolvaptanRebecca Jane Moon, Maisara Soliman, Lieke Hoogenboom, et al.
Pediatric Nephrology (Berlin, Germany)|February 12, 2017
Clinical and molecular aspects of distal renal tubular acidosis in childrenMartine T P Besouw, Marc Bienias, Patrick Walsh, et al.
Kidney International Reports|February 23, 2023
Shockwaves and the Rolling Stones: An Overview of Pediatric Stone DiseaseNaima Smeulders, Alexander Cho, Abdulelah Alshaiban, et al.
Pediatric Transplantation|April 12, 2019
Plasma electrolyte imbalance in pediatric kidney transplant recipientsWesley Hayes, Catherine Longley, Nicola Scanlon, et al.
Hormone Research in Paediatrics|June 8, 2020
Co-Existence of Congenital Adrenal Hyperplasia and Bartter Syndrome due to Maternal Uniparental Isodisomy of HSD3B2 and CLCNKB MutationsDinesh Giri, Detlef Bockenhauer, Charu Deshpande, et al.
Pageof 24