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Martin Konrad

Showing results (11-20 of 141) with videos related to

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Journal of Pediatric Endocrinology & Metabolism : JPEM|September 1, 2020
Idiopathic infantile hypercalcemia: mutations in SLC34A1 and CYP24A1 in two siblings and fathersAyla Güven, Martin Konrad, Karl P Schlingmann
Pediatric Nephrology (Berlin, Germany)|November 25, 2003
Genetics of hereditary disorders of magnesium homeostasisKarl P Schlingmann, Martin Konrad, Hannsjörg W Seyberth
European Journal of Pediatrics|June 13, 2008
Long-term follow-up of a patient with primary hypomagnesaemia and secondary hypocalcaemia due to a novel TRPM6 mutationDolors Esteban-Oliva, Guillem Pintos-Morell, Martin Konrad
Kidney International Reports|December 22, 2025
Response to the Letter to the Editor Entitled "From Variant of Unknown Significance to Likely Pathogenic: Adult-Onset - Nephronophthisis Linked to NPHP4 p.T680M"Jens Christian König, Mareike Dahmer-Heath, Martin Konrad
Hormone Research|January 5, 2006
A Spanish founder mutation in the chloride channel gene, CLCNKB, as a cause of atypical Bartter syndrome in adult ageJuan José Gorgojo, Sergio Donnay, Nikola Jeck, et al.
Kidney International|January 2, 2014
The case | hypercalcemia in a 60-year-old maleAnnette Helmuth, Martin Konrad, Karl P Schlingmann, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 17, 2004
Growth failure in a girl with Fanconi syndrome and growth hormone deficiencyChristian Plank, Martin Konrad, Helmut G Dörr, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 4, 2026
Essential but elusive: the availability of suitable salt treatments for tubulopathiesDetlef Bockenhauer, Gema Ariceta, Francesco Emma, et al.
Pediatric Nephrology (Berlin, Germany)|January 4, 2020
Distribution and management of the pediatric refugee population with renal replacement: A German pediatric cohortJohanna Lemke, Raphael Schild, Martin Konrad, et al.
Pediatric Nephrology (Berlin, Germany)|April 28, 2005
Hypomagnesemia with hypercalciuria and nephrocalcinosis: case report and a family studyVelibor Tasic, Donco Dervisov, Svetlana Koceva, et al.
Pageof 15

Showing results (11-20 of 141) with videos related to

Sort By:
Pageof 15
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 1, 2020
Idiopathic infantile hypercalcemia: mutations in SLC34A1 and CYP24A1 in two siblings and fathersAyla Güven, Martin Konrad, Karl P Schlingmann
Pediatric Nephrology (Berlin, Germany)|November 25, 2003
Genetics of hereditary disorders of magnesium homeostasisKarl P Schlingmann, Martin Konrad, Hannsjörg W Seyberth
European Journal of Pediatrics|June 13, 2008
Long-term follow-up of a patient with primary hypomagnesaemia and secondary hypocalcaemia due to a novel TRPM6 mutationDolors Esteban-Oliva, Guillem Pintos-Morell, Martin Konrad
Kidney International Reports|December 22, 2025
Response to the Letter to the Editor Entitled "From Variant of Unknown Significance to Likely Pathogenic: Adult-Onset - Nephronophthisis Linked to NPHP4 p.T680M"Jens Christian König, Mareike Dahmer-Heath, Martin Konrad
Hormone Research|January 5, 2006
A Spanish founder mutation in the chloride channel gene, CLCNKB, as a cause of atypical Bartter syndrome in adult ageJuan José Gorgojo, Sergio Donnay, Nikola Jeck, et al.
Kidney International|January 2, 2014
The case | hypercalcemia in a 60-year-old maleAnnette Helmuth, Martin Konrad, Karl P Schlingmann, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 17, 2004
Growth failure in a girl with Fanconi syndrome and growth hormone deficiencyChristian Plank, Martin Konrad, Helmut G Dörr, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 4, 2026
Essential but elusive: the availability of suitable salt treatments for tubulopathiesDetlef Bockenhauer, Gema Ariceta, Francesco Emma, et al.
Pediatric Nephrology (Berlin, Germany)|January 4, 2020
Distribution and management of the pediatric refugee population with renal replacement: A German pediatric cohortJohanna Lemke, Raphael Schild, Martin Konrad, et al.
Pediatric Nephrology (Berlin, Germany)|April 28, 2005
Hypomagnesemia with hypercalciuria and nephrocalcinosis: case report and a family studyVelibor Tasic, Donco Dervisov, Svetlana Koceva, et al.
Pageof 15