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Pediatric Nephrology (Berlin, Germany)|May 29, 2016
Genetic causes of hypomagnesemia, a clinical overviewDaan H H M Viering, Jeroen H F de Baaij, Stephen B Walsh, et al.Journal of the American Society of Nephrology : JASN|September 7, 2023
Electrolyte Disorders in Mitochondrial Cytopathies: A Systematic ReviewDaan H H M Viering, Lars Vermeltfoort, René J M Bindels, et al.Plos One|June 3, 2016
P2X6 Knockout Mice Exhibit Normal Electrolyte HomeostasisJeroen H F de Baaij, Andreas Kompatscher, Daan H H M Viering, et al.Journal of Hypertension|September 5, 2020
Genetics of renovascular hypertension in childrenDaan H H M Viering, Melanie M Y Chan, Lieke Hoogenboom, et al.Journal of Hypertension|February 8, 2022
Higher SBP in female patients with mitochondrial diseaseDaan H H M Viering, Marjolein D van Borselen, Jaap Deinum, et al.Pediatric Nephrology (Berlin, Germany)|March 26, 2021
Functional tests to guide management in an adult with loss of function of type-1 angiotensin II receptorDaan H H M Viering, Anneke P Bech, Jeroen H F de Baaij, 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.Journal of the American Society of Nephrology : JASN|April 5, 2017
Polycystic Kidney Disease with Hyperinsulinemic Hypoglycemia Caused by a Promoter Mutation in Phosphomannomutase 2Oscar Rubio Cabezas, Sarah E Flanagan, Horia Stanescu, et al.Pageof 1