Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Philip J G M Voets"'
Publikováno v:
PLoS ONE, Vol 16, Iss 3, p e0248445 (2021)
[This corrects the article DOI: 10.1371/journal.pone.0245499.].
Externí odkaz:
https://doaj.org/article/e4eb4d9986a5484d8874c021ce31a5f5
Publikováno v:
PLoS ONE, Vol 16, Iss 1, p e0245499 (2021)
BackgroundThe syndrome of inappropriate antidiuretic hormone secretion (SIADH) is one of the most common causes of hypotonic hyponatremia. In our previous work, we have derived a novel model (Voets equation) that can be used by clinicians to predict
Externí odkaz:
https://doaj.org/article/2f959f19d6764fffa3fa3c91354f56e1
Autor:
Philip J. G. M. Voets
Publikováno v:
Physiological Reports, Vol 12, Iss 7, Pp n/a-n/a (2024)
Abstract Clinical hyponatremia guidelines, protocols and flowcharts are a convenient means for clinicians to quickly establish an etiological diagnosis for hyponatremia, and facilitate its often complex analysis. Unfortunately, they often erroneously
Externí odkaz:
https://doaj.org/article/2f7fbabb8ee24d3e813882182968e5aa
Publikováno v:
Journal of Nephrology, 35, 1, pp. 339-342
Journal of Nephrology
Journal of Nephrology, 35, 339-342
Journal of Nephrology
Journal of Nephrology, 35, 339-342
Contains fulltext : 248875.pdf (Publisher’s version ) (Open Access)
Publikováno v:
Clinical Kidney Journal
Disorders of water and sodium homeostasis in the human body—or dysnatraemias—are frequently encountered in clinical practice, but their analysis is often complex and their management is often troublesome. For many clinicians, it remains challengi
Publikováno v:
Journal of Clinical Monitoring and Computing
Dysnatremia—either hyponatremia or hypernatremia—is frequently encountered in the clinical practice and often poses a diagnostic and therapeutic challenge for physicians. Despite their frequent occurrence, disorders of the water and sodium balanc
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 157(49)
Iron overload disorders are common and, if left untreated, severe systemic diseases that can have both genetic and acquired causes. Hereditary haemochromatosis, β-thalassaemia, myelodysplastic syndromes and sickle cell disease are among the most imp