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See Latest ArticlesRare F311L CFTR Gene Mutation in a Child Presented with Recurrent Electrolyte Abnormalities and Metabolic Alkalosis
Journal of The Medical Association of Thailand, 04/28/09
Lumpaopong A et al. - The authors report a rare case of CF with Delta F508/ F311L genotype presented with recurrent hyponatremia and metabolic alkalosis. Awareness of electrolyte abnormalities during febrile illness, proper genetic counseling, and long-term follow up are necessary in this patient.
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Today in Acid-Base...keeping you current
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Activation of p53 Promotes Renal Injury in Acute Aristolochic Acid Nephropathy
Journal of the American Society of Nephrology, 11/23/09
Torsades de Pointes induced by a combination of garenoxacin and disopyramide and other cytochrome P450, family 3, subfamily A polypeptide-4-influencing drugs during hypokalemia due to licorice
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WNK4 Enhances the Degradation of NCC through a Sortilin-Mediated Lysosomal Pathway
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A comprehensive study of cardiovascular risk factors, cardiac function and vascular disease in children with chronic renal failure
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