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Karl Peter Schlingmann

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Endocrinology and Metabolism Clinics of North America|November 14, 2021
Vitamin D-dependent HypercalcemiaKarl Peter Schlingmann
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 29, 2014
Inherited disorders of renal hypomagnesaemiaMartin Konrad, Karl Peter Schlingmann
Journal of Clinical Research in Pediatric Endocrinology|January 14, 2016
A Novel Homozygous Mutation in the Transient Receptor Potential Melastatin 6 Gene: A Case ReportAyça Altıncık, Karl Peter Schlingmann, Mahya Sultan Tosun
Endocrinology and Metabolism Clinics of North America|October 30, 2017
Genetic Diseases of Vitamin D Metabolizing EnzymesGlenville Jones, Marie Laure Kottler, Karl Peter Schlingmann
European Journal of Pediatrics|September 25, 2012
Severe hypercalcemic crisis in an infant with idiopathic infantile hypercalcemia caused by mutation in CYP24A1 geneFilip Fencl, Květa Bláhová, Karl Peter Schlingmann, et al.
Iranian Journal of Kidney Diseases|March 15, 2013
Intravenous pamidronate in the treatment of severe idiopathic infantile hypercalcemiaSylva Skalova, Lucie Cerna, Milan Bayer, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 14, 2021
A novel synonymous homozygous variant [c.2538G>A (p.Thr846Thr)] in <i>TRPM6</i> in a patient with hypomagnesemia with secondary hypocalcemiaSezer Acar, Karl Peter Schlingmann, Özlem Nalbantoğlu, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 28, 2010
The role of tight junctions in paracellular ion transport in the renal tubule: lessons learned from a rare inherited tubular disorderLea Haisch, Jorge Reis Almeida, Paulo Roberto Abreu da Silva, et al.
Kidney & Blood Pressure Research|August 26, 2015
Discordant Clinical Course of Vitamin-D-Hydroxylase (CYP24A1) Associated Hypercalcemia in Two Adult Brothers With NephrocalcinosisTilman Jobst-Schwan, Andrea Pannes, Karl Peter Schlingmann, et al.
The Journal of Clinical Endocrinology and Metabolism|January 16, 2014
A lifetime of hypercalcemia and hypercalciuria, finally explainedThomas P Jacobs, Martin Kaufman, Glenville Jones, et al.
Pageof 4

Showing results (1-10 of 39) with videos related to

Sort By:
Pageof 4
Endocrinology and Metabolism Clinics of North America|November 14, 2021
Vitamin D-dependent HypercalcemiaKarl Peter Schlingmann
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 29, 2014
Inherited disorders of renal hypomagnesaemiaMartin Konrad, Karl Peter Schlingmann
Journal of Clinical Research in Pediatric Endocrinology|January 14, 2016
A Novel Homozygous Mutation in the Transient Receptor Potential Melastatin 6 Gene: A Case ReportAyça Altıncık, Karl Peter Schlingmann, Mahya Sultan Tosun
Endocrinology and Metabolism Clinics of North America|October 30, 2017
Genetic Diseases of Vitamin D Metabolizing EnzymesGlenville Jones, Marie Laure Kottler, Karl Peter Schlingmann
European Journal of Pediatrics|September 25, 2012
Severe hypercalcemic crisis in an infant with idiopathic infantile hypercalcemia caused by mutation in CYP24A1 geneFilip Fencl, Květa Bláhová, Karl Peter Schlingmann, et al.
Iranian Journal of Kidney Diseases|March 15, 2013
Intravenous pamidronate in the treatment of severe idiopathic infantile hypercalcemiaSylva Skalova, Lucie Cerna, Milan Bayer, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 14, 2021
A novel synonymous homozygous variant [c.2538G>A (p.Thr846Thr)] in <i>TRPM6</i> in a patient with hypomagnesemia with secondary hypocalcemiaSezer Acar, Karl Peter Schlingmann, Özlem Nalbantoğlu, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 28, 2010
The role of tight junctions in paracellular ion transport in the renal tubule: lessons learned from a rare inherited tubular disorderLea Haisch, Jorge Reis Almeida, Paulo Roberto Abreu da Silva, et al.
Kidney & Blood Pressure Research|August 26, 2015
Discordant Clinical Course of Vitamin-D-Hydroxylase (CYP24A1) Associated Hypercalcemia in Two Adult Brothers With NephrocalcinosisTilman Jobst-Schwan, Andrea Pannes, Karl Peter Schlingmann, et al.
The Journal of Clinical Endocrinology and Metabolism|January 16, 2014
A lifetime of hypercalcemia and hypercalciuria, finally explainedThomas P Jacobs, Martin Kaufman, Glenville Jones, et al.
Pageof 4