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Karl Peter Schlingmann

Showing results (11-20 of 39) with videos related to

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Journal of Immunology (Baltimore, Md. : 1950)|April 6, 2010
Plasma cells and nonplasma B cells express differing IgE repertoires in allergic sensitizationTobias Rogosch, Sebastian Kerzel, Larisa Sikula, et al.
Pediatric Nephrology (Berlin, Germany)|August 18, 2009
Functional analysis of BMP4 mutations identified in pediatric CAKUT patientsMansoureh Tabatabaeifar, Karl-Peter Schlingmann, Mieczyslaw Litwin, et al.
Molecular Genetics and Metabolism|July 17, 2022
Beneficial effects of starting oral cysteamine treatment in the first 2 months of life on glomerular and tubular kidney function in infantile nephropathic cystinosisKatharina Hohenfellner, Christina Nießl, Dieter Haffner, et al.
European Journal of Human Genetics : EJHG|August 15, 2013
New TRPM6 missense mutations linked to hypomagnesemia with secondary hypocalcemiaSergio Lainez, Karl Peter Schlingmann, Jenny van der Wijst, et al.
Pediatric Nephrology (Berlin, Germany)|May 25, 2005
Gene locus ambiguity in posterior urethral valves/prune-belly syndromeStefanie Weber, Sevgi Mir, Karl Peter Schlingmann, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|March 18, 2017
Improved Screening Test for Idiopathic Infantile Hypercalcemia Confirms Residual Levels of Serum 24,25-(OH)<sub>2</sub> D<sub>3</sub> in Affected PatientsMartin Kaufmann, Nicole Morse, Billy Joe Molloy, et al.
Nephron|May 24, 2018
A de novo KCNA1 Mutation in a Patient with Tetany and HypomagnesemiaJenny van der Wijst, Martin Konrad, Sjoerd A J Verkaart, et al.
Journal of the American Society of Nephrology : JASN|October 27, 2022
Long-Read Sequencing Identifies Novel Pathogenic Intronic Variants in Gitelman SyndromeDaan H H M Viering, Marguerite Hureaux, Kornelia Neveling, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 27, 2012
Loss of insulin-induced activation of TRPM6 magnesium channels results in impaired glucose tolerance during pregnancyAnil V Nair, Berthold Hocher, Sjoerd Verkaart, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 6, 2014
Retrospective cohort study of familial hypomagnesaemia with hypercalciuria and nephrocalcinosis due to CLDN16 mutationsPrzemysław Sikora, Marcin Zaniew, Lea Haisch, et al.
Pageof 4

Showing results (11-20 of 39) with videos related to

Sort By:
Pageof 4
Journal of Immunology (Baltimore, Md. : 1950)|April 6, 2010
Plasma cells and nonplasma B cells express differing IgE repertoires in allergic sensitizationTobias Rogosch, Sebastian Kerzel, Larisa Sikula, et al.
Pediatric Nephrology (Berlin, Germany)|August 18, 2009
Functional analysis of BMP4 mutations identified in pediatric CAKUT patientsMansoureh Tabatabaeifar, Karl-Peter Schlingmann, Mieczyslaw Litwin, et al.
Molecular Genetics and Metabolism|July 17, 2022
Beneficial effects of starting oral cysteamine treatment in the first 2 months of life on glomerular and tubular kidney function in infantile nephropathic cystinosisKatharina Hohenfellner, Christina Nießl, Dieter Haffner, et al.
European Journal of Human Genetics : EJHG|August 15, 2013
New TRPM6 missense mutations linked to hypomagnesemia with secondary hypocalcemiaSergio Lainez, Karl Peter Schlingmann, Jenny van der Wijst, et al.
Pediatric Nephrology (Berlin, Germany)|May 25, 2005
Gene locus ambiguity in posterior urethral valves/prune-belly syndromeStefanie Weber, Sevgi Mir, Karl Peter Schlingmann, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|March 18, 2017
Improved Screening Test for Idiopathic Infantile Hypercalcemia Confirms Residual Levels of Serum 24,25-(OH)<sub>2</sub> D<sub>3</sub> in Affected PatientsMartin Kaufmann, Nicole Morse, Billy Joe Molloy, et al.
Nephron|May 24, 2018
A de novo KCNA1 Mutation in a Patient with Tetany and HypomagnesemiaJenny van der Wijst, Martin Konrad, Sjoerd A J Verkaart, et al.
Journal of the American Society of Nephrology : JASN|October 27, 2022
Long-Read Sequencing Identifies Novel Pathogenic Intronic Variants in Gitelman SyndromeDaan H H M Viering, Marguerite Hureaux, Kornelia Neveling, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 27, 2012
Loss of insulin-induced activation of TRPM6 magnesium channels results in impaired glucose tolerance during pregnancyAnil V Nair, Berthold Hocher, Sjoerd Verkaart, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 6, 2014
Retrospective cohort study of familial hypomagnesaemia with hypercalciuria and nephrocalcinosis due to CLDN16 mutationsPrzemysław Sikora, Marcin Zaniew, Lea Haisch, et al.
Pageof 4