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Detlef Bockenhauer

Showing results (91-100 of 233) with videos related to

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Acta Paediatrica (Oslo, Norway : 1992)|March 31, 2016
Tolvaptan is successful in treating inappropriate antidiuretic hormone secretion in infantsDaniela Marx-Berger, David V Milford, Meenakshi Bandhakavi, et al.
Pflugers Archiv : European Journal of Physiology|January 12, 2011
The salt-wasting phenotype of EAST syndrome, a disease with multifaceted symptoms linked to the KCNJ10 K+ channelSascha Bandulik, Katharina Schmidt, Detlef Bockenhauer, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 14, 2011
A family with hyponatremia and the nephrogenic syndrome of inappropriate antidiuresisDetlef Bockenhauer, Michael D Penney, David Hampton, et al.
Pediatric Nephrology (Berlin, Germany)|May 29, 2016
Genetic causes of hypomagnesemia, a clinical overviewDaan H H M Viering, Jeroen H F de Baaij, Stephen B Walsh, et al.
Nephron. Clinical Practice|May 16, 2012
Mutation analysis of NPHS1 in a worldwide cohort of congenital nephrotic syndrome patientsBugsu Ovunc, Shazia Ashraf, Virginia Vega-Warner, et al.
Children (Basel, Switzerland)|November 10, 2020
A Rare Cause of Chronic Hypokalemia with Metabolic Alkalosis: Case Report and Differential DiagnosisCristina Bertulli, Marguerite Hureaux, Chiara De Mutiis, et al.
Kidney International|July 1, 2014
The case | Renal tubular acidosis and eye findingsJameela A Kari, Sherif M El Desoky, Ajay K Singh, et al.
Clinical Journal of the American Society of Nephrology : CJASN|May 16, 2008
Renal phenotype in Lowe Syndrome: a selective proximal tubular dysfunctionDetlef Bockenhauer, Arend Bokenkamp, William van't Hoff, et al.
BMC Nephrology|July 12, 2017
Fainting Fanconi syndrome clarified by proxy: a case reportStephen Benedict Walsh, Robert Unwin, Robert Kleta, et al.
Pediatric Nephrology (Berlin, Germany)|May 2, 2026
Renal Fanconi syndrome and vitamin D deficiency: chicken or egg?Samia Zerrouki, Gonenc Soyalp, Lucie Taillandier, et al.
Pageof 24

Showing results (91-100 of 233) with videos related to

Sort By:
Pageof 24
Acta Paediatrica (Oslo, Norway : 1992)|March 31, 2016
Tolvaptan is successful in treating inappropriate antidiuretic hormone secretion in infantsDaniela Marx-Berger, David V Milford, Meenakshi Bandhakavi, et al.
Pflugers Archiv : European Journal of Physiology|January 12, 2011
The salt-wasting phenotype of EAST syndrome, a disease with multifaceted symptoms linked to the KCNJ10 K+ channelSascha Bandulik, Katharina Schmidt, Detlef Bockenhauer, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 14, 2011
A family with hyponatremia and the nephrogenic syndrome of inappropriate antidiuresisDetlef Bockenhauer, Michael D Penney, David Hampton, et al.
Pediatric Nephrology (Berlin, Germany)|May 29, 2016
Genetic causes of hypomagnesemia, a clinical overviewDaan H H M Viering, Jeroen H F de Baaij, Stephen B Walsh, et al.
Nephron. Clinical Practice|May 16, 2012
Mutation analysis of NPHS1 in a worldwide cohort of congenital nephrotic syndrome patientsBugsu Ovunc, Shazia Ashraf, Virginia Vega-Warner, et al.
Children (Basel, Switzerland)|November 10, 2020
A Rare Cause of Chronic Hypokalemia with Metabolic Alkalosis: Case Report and Differential DiagnosisCristina Bertulli, Marguerite Hureaux, Chiara De Mutiis, et al.
Kidney International|July 1, 2014
The case | Renal tubular acidosis and eye findingsJameela A Kari, Sherif M El Desoky, Ajay K Singh, et al.
Clinical Journal of the American Society of Nephrology : CJASN|May 16, 2008
Renal phenotype in Lowe Syndrome: a selective proximal tubular dysfunctionDetlef Bockenhauer, Arend Bokenkamp, William van't Hoff, et al.
BMC Nephrology|July 12, 2017
Fainting Fanconi syndrome clarified by proxy: a case reportStephen Benedict Walsh, Robert Unwin, Robert Kleta, et al.
Pediatric Nephrology (Berlin, Germany)|May 2, 2026
Renal Fanconi syndrome and vitamin D deficiency: chicken or egg?Samia Zerrouki, Gonenc Soyalp, Lucie Taillandier, et al.
Pageof 24