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More articles from Acid/Base and Electrolyte Disorders

  • Trajectories of Serum Sodium on In-Hospital and 1-Year Survival among Hospitalized Patients
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    Trajectories of Serum Sodium on In-Hospital and 1-Year Survival among Hospitalized Patients
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    Tubular Acidification Defect in Adults with Sickle Cell Disease
    Maud Cazenave, Vincent Audard, Jean-Philippe Bertocchio, Anoosha Habibi, Stéphanie Baron, Caroline Prot-Bertoye, Jugurtha Berkenou, Gérard Maruani, Thomas Stehlé, Nicolas Cornière, Hamza Ayari, Gérard Friedlander, Frédéric Galacteros, Pascal Houillier, Pablo Bartolucci and Marie Courbebaisse
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  • Derivation and Validation of a Novel Risk Score to Predict Overcorrection of Severe Hyponatremia
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    Derivation and Validation of a Novel Risk Score to Predict Overcorrection of Severe Hyponatremia
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  • Sodium Zirconium Cyclosilicate among Individuals with Hyperkalemia
    Open Access
    Sodium Zirconium Cyclosilicate among Individuals with Hyperkalemia
    Bruce S. Spinowitz, Steven Fishbane, Pablo E. Pergola, Simon D. Roger, Edgar V. Lerma, Javed Butler, Stephan von Haehling, Scott H. Adler, June Zhao, Bhupinder Singh, Philip T. Lavin, Peter A. McCullough, Mikhail Kosiborod, David K. Packham and on behalf of the ZS-005 Study Investigators
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  • Rate of Correction of Hypernatremia and Health Outcomes in Critically Ill Patients
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    Rate of Correction of Hypernatremia and Health Outcomes in Critically Ill Patients
    Kinsuk Chauhan, Pattharawin Pattharanitima, Niralee Patel, Aine Duffy, Aparna Saha, Kumardeep Chaudhary, Neha Debnath, Tielman Van Vleck, Lili Chan, Girish N. Nadkarni and Steven G. Coca
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  • Urea for the Treatment of Hyponatremia
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    Urea for the Treatment of Hyponatremia
    Helbert Rondon-Berrios, Srijan Tandukar, Maria K. Mor, Evan C. Ray, Filitsa H. Bender, Thomas R. Kleyman and Steven D. Weisbord
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  • Risk Factors and Outcomes of Rapid Correction of Severe Hyponatremia
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    Risk Factors and Outcomes of Rapid Correction of Severe Hyponatremia
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    Prevalence and Correlates of Metabolic Acidosis among Patients with Homozygous Sickle Cell Disease
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