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期刊名:Electrolyte and blood pressure

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ISSN:1738-5997

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共收录本刊相关文章索引163
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Ibrahima Lyra Sarr,Abdou Khadir Sow,Baratou Coundoul et al. Ibrahima Lyra Sarr et al.
Background: Intradialytic hypotension (IDH) increases cardiovascular morbidity and mortality in chronic hemodialysis patients and cardiac autonomous neuropathy (CAN) might be involved. To assess cardiac autonomic control ...
Sunmin Lee,Hee Won Seo,Jiwon Lee et al. Sunmin Lee et al.
Hyponatremia is a common electrolyte disturbance with well-recognized neurological and gastrointestinal symptoms. However, it rarely presents with atypical manifestations, such as persistent hiccups. We report a case of a 36-year-old woman ...
Eunjin Bae Eunjin Bae
Clinical trials have found that sodium-glucose cotransporter-2 (SGLT2) inhibitors reduce serum urate levels by 0.6-1.5 mg/dL, which might contribute to cardiovascular protection. Urate is the final degradation product of purine nucleotides ...
Hye Jin Park,Su Hyun Song,Sang Heon Suh et al. Hye Jin Park et al.
Osmotic demyelination syndrome (ODS) is a rare neurological disorder associated with osmotic imbalances. Traditionally, ODS has been known to occur following the rapid correction of hyponatremia; however, ODS has also been reported concerni...
Hongran Moon,Sohyun Bae,Donghwan Yun et al. Hongran Moon et al.
Background: Effective blood pressure (BP) control is vital for preventing target organ damage, and combination therapy offers added benefits when single-agent treatment is insufficient. This cohort study examined whether ...
Sang Heon Suh,Su Hyun Song,Hong Sang Choi et al. Sang Heon Suh et al.
Cystinuria is an autosomal recessively inherited genetic disorder, and is typically classified into type A, caused by mutations in SLC3A1, or type B, caused by mutations in SLC7A9. While the predominance of the genotypes varies among countr...
Sangyub Han,Sejoong Kim Sangyub Han
Diabetic kidney disease (DKD) is a prevalent and complex disease among patients with diabetes in Korea, requiring comprehensive treatment strategies. Traditional management strategies targeting blood pressure, blood sugar, lipid, and lifest...
Hyung Eun Son Hyung Eun Son
Diabetic kidney disease (DKD) is a leading cause of chronic kidney disease (CKD). Recent advancements highlight the role of finerenone, a non-steroidal mineralocorticoid receptor antagonist (nsMRA), in DKD management. Studies like FIDELIO-D...
Eun Kyoung Lee,Won Seok Yang Eun Kyoung Lee
Background: Hyperkalemia is a frequent and potentially lethal complication of chronic kidney disease (CKD). We retrospectively examined the potassium-lowering effect of oral fludrocortisone and its adverse effects in hype...
In Hong Choi,Chang Seong Kim,Eun Hui Bae et al. In Hong Choi et al.
Although renal infarction (RI) is not a rare disease, its outcomes have not been well-documented. Furthermore, transient resolution and recurrence of RI have not been captured through imaging. We report a case of idiopathic RI that recurred...