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Detlef Böckenhauer

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Clinical Kidney Journal|February 20, 2026
Improving precision diagnosis in unexplained CKDMax C Liebau, Detlef Böckenhauer, Peter Boor
Pediatric Nephrology (Berlin, Germany)|November 20, 2025
Failure to thrive in children with tubulopathiesGiulio Rivetti, Francesco Emma, Faidra Veligratli, et al.
The Journal of Pediatrics|June 30, 2009
Dent-2 disease: a mild variant of Lowe syndromeArend Bökenkamp, Detlef Böckenhauer, Hae Il Cheong, et al.
Biochemia Medica|October 22, 2024
A case of alkaptonuria presenting with unexplained dark-stained diapers and spurious hyperoxaluria and proteinuria due to homogentisic acid interferenceThibault Vanhove, Margo Aertgeerts, Peter Witters, et al.
Journal of Pediatric Genetics|September 15, 2016
Novel OCRL mutations in patients with Dent-2 diseaseDetlef Böckenhauer, Arend Bökenkamp, Matti Nuutinen, et al.
Kidney International|July 6, 2023
Rare variants in the sodium-dependent phosphate transporter gene SLC34A3 explain missing heritability of urinary stone diseaseOmid Sadeghi-Alavijeh, Melanie M Y Chan, Shabbir H Moochhala, et al.
Pediatric Nephrology (Berlin, Germany)|April 28, 2020
Rituximab versus cyclophosphamide as first steroid-sparing agent in childhood frequently relapsing and steroid-dependent nephrotic syndromeJameela A Kari, Khalid A Alhasan, Amr S Albanna, et al.
Human Genetics|February 11, 2023
Phosphomannomutase 2 (PMM2) variants leading to hyperinsulinism-polycystic kidney disease are associated with early-onset inflammatory bowel disease and gastric antral foveolar hyperplasiaFevronia Kiparissi, Antonia Dastamani, Liina Palm, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 10, 2025
Dent disease: clinical practice recommendationsArend Bökenkamp, Gema Ariceta, Detlef Böckenhauer, et al.
Science Translational Medicine|February 11, 2026
Metabolic acidosis causes a Fanconi-like syndrome with intracellular trafficking defects and proximal tubule dysfunctionJ Christopher Hennings, Keerthana S Murthy, Nicolas Picard, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Clinical Kidney Journal|February 20, 2026
Improving precision diagnosis in unexplained CKDMax C Liebau, Detlef Böckenhauer, Peter Boor
Pediatric Nephrology (Berlin, Germany)|November 20, 2025
Failure to thrive in children with tubulopathiesGiulio Rivetti, Francesco Emma, Faidra Veligratli, et al.
The Journal of Pediatrics|June 30, 2009
Dent-2 disease: a mild variant of Lowe syndromeArend Bökenkamp, Detlef Böckenhauer, Hae Il Cheong, et al.
Biochemia Medica|October 22, 2024
A case of alkaptonuria presenting with unexplained dark-stained diapers and spurious hyperoxaluria and proteinuria due to homogentisic acid interferenceThibault Vanhove, Margo Aertgeerts, Peter Witters, et al.
Journal of Pediatric Genetics|September 15, 2016
Novel OCRL mutations in patients with Dent-2 diseaseDetlef Böckenhauer, Arend Bökenkamp, Matti Nuutinen, et al.
Kidney International|July 6, 2023
Rare variants in the sodium-dependent phosphate transporter gene SLC34A3 explain missing heritability of urinary stone diseaseOmid Sadeghi-Alavijeh, Melanie M Y Chan, Shabbir H Moochhala, et al.
Pediatric Nephrology (Berlin, Germany)|April 28, 2020
Rituximab versus cyclophosphamide as first steroid-sparing agent in childhood frequently relapsing and steroid-dependent nephrotic syndromeJameela A Kari, Khalid A Alhasan, Amr S Albanna, et al.
Human Genetics|February 11, 2023
Phosphomannomutase 2 (PMM2) variants leading to hyperinsulinism-polycystic kidney disease are associated with early-onset inflammatory bowel disease and gastric antral foveolar hyperplasiaFevronia Kiparissi, Antonia Dastamani, Liina Palm, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 10, 2025
Dent disease: clinical practice recommendationsArend Bökenkamp, Gema Ariceta, Detlef Böckenhauer, et al.
Science Translational Medicine|February 11, 2026
Metabolic acidosis causes a Fanconi-like syndrome with intracellular trafficking defects and proximal tubule dysfunctionJ Christopher Hennings, Keerthana S Murthy, Nicolas Picard, et al.
Pageof 2