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WPRIM Management System>
DCMS
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Electrolytes & Blood Pressure
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2016
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14
Volume:
14
1. A Case of Isolated Glycosuria Mediated by an SLC5A2 Gene Mutation and Characterized by Postprandial Heavy Glycosuria Without Salt Wasting.
Page:35—37
2. Genetic Variations of Tyrosine Hydroxylase in the Pathogenesis of Hypertension.
Page:21—26
3. Severe Hypernatremia Caused by Acute Exogenous Salt Intake Combined with Primary Hypothyroidism.
Page:27—30
4. A Case Report of Syndrome of Inappropriate Antidiuretic Hormone Induced by Pregabalin.
Page:31—34
5. Confronting Practical Problems for Initiation of On-line Hemodiafiltration Therapy.
Page:1—4
6. A Rare Case of Polyneuropathy and Monoclonalgammopathy with Recurrent Acute Kidney Injury.
Page:5—10
7. Hypokalemic Hypertension Leading to a Diagnosis of Autosomal Dominant Polycystic Kidney Disease.
Page:11—15
8. A Pedigree with c.179 Cytosine to Threonine Missense Mutation of SLC12A3 Gene Presenting Gitelman's Syndrome.
Page:16—19
