Diagnosis and management of Bartter syndrome: executive summary of the consensus and recommendations from the European Rare Kidney Disease Reference Network Working Group for Tubular Disorders
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Síndrome de Bartter; Hipopotasemia hereditaria; Tubulopatía perdedora de sal
Citación recomendada
Konrad M, Nijenhuis T, Ariceta G, Bertholet-Thomas A, Calo LA, Capasso G, et al. Diagnosis and management of Bartter syndrome: executive summary of the consensus and recommendations from the European Rare Kidney Disease Reference Network Working Group for Tubular Disorders. Kidney Int. 2021 Feb;99(2):324–335.
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https://hdl.handle.net/11351/6145Este elemento aparece en las siguientes colecciones
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