Genetic causes of hypomagnesemia, a clinical overview von Viering, Daan H. H. M, de Baaij, Jeroen H. F., Walsh, Stephen B., Kleta, Robert, Bockenhauer, Detlef

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Functional tests to guide management in an adult with loss of function of type-1 angiotensin II receptor von Viering, Daan H. H. M., Bech, Anneke P., de Baaij, Jeroen H. F., Steenbergen, Eric J., Danser, A. H. Jan, Wetzels, Jack F. M., Bindels, René J. M., Deinum, Jaap

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P2X6 Knockout Mice Exhibit Normal Electrolyte Homeostasis von de Baaij, Jeroen H F, Kompatscher, Andreas, Viering, Daan H H M, Bos, Caro, Bindels, René J M, Hoenderop, Joost G J

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Long-Read Sequencing Identifies Novel Pathogenic Intronic Variants in Gitelman Syndrome von Viering, Daan H H M, Hureaux, Marguerite, Neveling, Kornelia, Latta, Femke, Kwint, Michael, Blanchard, Anne, Konrad, Martin, Bindels, René J M, Schlingmann, Karl-Peter, Vargas-Poussou, Rosa, de Baaij, Jeroen H F

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Electrolyte Disorders in Mitochondrial Cytopathies: A Systematic Review von Viering, Daan H H M, Vermeltfoort, Lars, Bindels, René J M, Deinum, Jaap, de Baaij, Jeroen H F

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Polycystic Kidney Disease with Hyperinsulinemic Hypoglycemia Caused by a Promoter Mutation in Phosphomannomutase 2 von Cabezas, Oscar Rubio, Flanagan, Sarah E, Stanescu, Horia, García-Martínez, Elena, Caswell, Richard, Lango-Allen, Hana, Antón-Gamero, Montserrat, Argente, Jesús, Bussell, Anna-Marie, Brandli, Andre, Cheshire, Chris, Crowne, Elizabeth, Dumitriu, Simona, Drynda, Robert, Hamilton-Shield, Julian P, Hayes, Wesley, Hofherr, Alexis, Iancu, Daniela, Issler, Naomi, Jefferies, Craig, Jones, Peter, Johnson, Matthew, Kesselheim, Anne, Klootwijk, Enriko, Koettgen, Michael, Lewis, Wendy, Martos, José María, Mozere, Monika, Norman, Jill, Patel, Vaksha, Parrish, Andrew, Pérez-Cerdá, Celia, Pozo, Jesús, Rahman, Sofia A, Sebire, Neil, Tekman, Mehmet, Turnpenny, Peter D, Hoff, William Van't, Viering, Daan H H M, Weedon, Michael N, Wilson, Patricia, Guay-Woodford, Lisa, Kleta, Robert, Hussain, Khalid, Ellard, Sian, Bockenhauer, Detlef

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Gitelman-Like Syndrome Caused by Pathogenic Variants in mtDNA von Viering, Daan, Schlingmann, Karl P, Hureaux, Marguerite, Nijenhuis, Tom, Mallett, Andrew, Chan, Melanie M Y, van Beek, André, van Eerde, Albertien M, Coulibaly, Jean-Marie, Vallet, Marion, Decramer, Stéphane, Pelletier, Solenne, Klaus, Günter, Kömhoff, Martin, Beetz, Rolf, Patel, Chirag, Shenoy, Mohan, Steenbergen, Eric J, Anderson, Glenn, Bongers, Ernie M H F, Bergmann, Carsten, Panneman, Daan, Rodenburg, Richard J, Kleta, Robert, Houillier, Pascal, Konrad, Martin, Vargas-Poussou, Rosa, Knoers, Nine V A M, Bockenhauer, Detlef, de Baaij, Jeroen H F

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