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Reninoma: a rare cause of curable hypertension

Kim JH, Kim JH, Cho MH, Park E, Hyun HS, Ahn YH, Kang HG, Moon KC, Ha IS, Cheong HI

The most common type of refractory hypertension found in children is secondary hypertension, which is a potentially curable disease. Reninoma, a renin-secreting juxtaglomerular cell tumor, is a rare cause of...
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Approach to the Patient with Metabolic Alkalosis Accompanied by Hypokalemia

Yi JH, Han SW

No abstract available.
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Alteration of Akt, p-Akt, ERK, and p-ERK Proteins Expression in the Kidney of Hypokalemic Rat

Bae CS, Cho HJ, Ahn KY

Hypokalemia causes metabolic alkalosis and morphological changes of the kidney. K⁺ balance is regulated not only by ion channels or pump gene, but also by various genes including NF-E2-related factor...
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Rheumatoid arthritis accompanied by Gitelman syndrome

Park MG, Lee JH, Kim SJ, Park SH, Park SK, Choi JS, Hwang JY

Gitelman syndrome is a condition caused by a mutation of the thiazide sensitive Na-Cl cotransporter gene on the distal convoluted tubule. It results in a variety of clinical features, including...
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HELLP syndrome in a pregnant patient with Gitelman syndrome

Lee M, Kim DI, Lee KH, Byun JH, Hwang J, Hwang WM, Yun SR, Yoon SH

Gitelman syndrome is characterized by hypokalemia, metabolic alkalosis, hypocalciuria, and hypomagnesemia. The clinical course of Gitelman syndrome in pregnant women remains unclear, but it is thought to be benign. We...
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Renal intercalated cells and blood pressure regulation

Wall SM

Type B and non-A, non-B intercalated cells are found within the connecting tubule and the cortical collecting duct. Of these cell types, type B intercalated cells are known to mediate...
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The impact of high serum bicarbonate levels on mortality in hemodialysis patients

Chang KY, Kim HW, Kim WJ, Kim YK, Kim SH, Song HC, Kim YO, Jin DC, Choi EJ, Yang CW, Kim YL, Kim NH, Kang SW, Kim YS, Kim YS

BACKGROUND/AIMS: The optimal serum bicarbonate level is controversial for patients who are undergoing hemodialysis (HD). In this study, we analyzed the impact of serum bicarbonate levels on mortality among HD...
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Extreme Metabolic Alkalosis Caused by Gastrostomy Tube Malposition Treated Using Conventional Hemodialysis

Bae EH, Ma SK, Kim SW

No abstract available.
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Gitelman's Syndrome Associated with Chondrocalcinosis

Song ST, Lim YJ, Park JS, Song Y, Lee S, Choi J, Jun JB

Gitelman's syndrome (GS), a hereditary disease characterized by hypokalemia, hypomagnesemia, and hypocalciuria, is a salt-losing renal tubulopathy. Herein, we describe a case of a 28-year-old woman diagnosed with atypical GS...
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A Pedigree with c.179 Cytosine to Threonine Missense Mutation of SLC12A3 Gene Presenting Gitelman's Syndrome

Kim Y, Kang SS, Park WY, Jin K, Kim DK, Han S

A 42-year-old man came to the hospital presenting chest discomfort and general weakness. He had come to the hospital with the same symptoms 3 months ago and 12 years prior....
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Milk-alkali syndrome secondary to the intake of calcium supplements

Lee IH, Noh SY, Kang GW

Milk-alkali syndrome (MAS), a triad of hypercalcemia, metabolic alkalosis, and renal failure, is associated with ingestion of large amounts of calcium and absorbable alkali. MAS is the third most common...
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Oral Proton Pump Inhibitor for Treatment of Congenital Chloride Diarrhea

Jo HC, Yoon JS, Jang JY, Sohn YB, Lee JH, Cheong HI, Park MS

Congenital chloride diarrhea (CCD) is a rare autosomal recessive disease, which is characterized by electrolyte absorption defect due to impaired function of the Cl-/HCO3 - exchanger in the ileum and the...
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A novel mutation of CLCNKB in a Korean patient of mixed phenotype of Bartter-Gitelman syndrome

Cho HW, Lee ST, Cho H, Cheong HI

Bartter syndrome (BS) is an inherited renal tubular disorder characterized by low or normal blood pressure, hypokalemic metabolic alkalosis, and hyperreninemic hyperaldosteronism. Type III BS is caused by loss-of-function mutations...
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A Case of Secondary FSGS due to Chronic Chloride Diarrhea

Kim BK, Lee HS, Yim HE, Cheong HI, Yoo KH

Congenital chloride diarrhea (CLD) is a rare autosomal recessive disease that is difficult to diagnose. CLD requires early treatment to correct electrolyte imbalance and alkalosis and to prevent severe dehydration....
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Acute Kidney Injury Arising from Severe Hyperemesis Gravidarum: Case Report with a Review of Literatures

Shim SM, Ryu AL, Kim YS

Severe hyperemesis gravidarum is a rare but potentially life-threatening it left untreated. Its serious complications are dehydration, ketosis, alkalosis from loss of hydrochloric acid, hypokalemia, and compromised pre-renal acute kidney...
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A Case of Ectopic Adrenocorticotropic Hormone Syndrome in Small Cell Lung Cancer

Jeong C, Lee J, Ryu S, Lee HY, Shin AY, Kim JS, Ahn JH, Kang HS

Small cell lung cancer (SCLC), which originated from neuroendocrine tissue, can develop into paraneoplastic endocrine syndromes, such as Cushing syndrome, because of an inappropriate secretion of ectopic adrenocorticotropic hormone (ACTH)....
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A Case of Milk-Alkali Syndrome in a Patient with Hypoparathyroidism after Total Thyroidectomy

Joo BY, Park HS, Hong JC

Milk-alkali syndrome (MAS) is a disorder featuring hypercalcemia, renal failure and metabolic alkalosis due to ingestion of large amounts of calcium and absorbable alkali. MAS was first reported after Milk-alkali...
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Furosemide induced medullary nephrocalcinosis mimicking Bartter syndrome

Kim S, Kyung C, Kim YH, Cho JH, Hwang C, Lee JE

  • KMID: 2319925
  • Yeungnam Univ J Med.
  • 2014 Jun;31(1):21-24.
Clinical presentation of Bartter syndrome is similar to surrepitious vomiting or use of diuretics. Therefore, precise differential diagnosis of Bartter syndrome is crucial. We report a case of medullary nephrocalcinosis...
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A Case of Adult onset Bartter Syndrome with Nephrocalcinosis

Park MG, Lim TW, Oh HT, Song SU, Heo D, Rim H

Bartter syndrome is a renal tubular defect in electrolyte transport characterized by hypokalemia, metabolic alkalosis, hyperreninemia, hyperaldosteronism, normal blood pressure, and other clinical symptoms. As a clinical and genetical heterogeneous disorder,...
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Hyperventilation due to Incision & Drainage under Inadequate Psychosedation & Local Anesthesia in Advanced Odontogenic Infectious Lesion

Oh JH, Son JS, Yoo JH, Kim JB

Extension of advanced odontogenic infection from deep neck fascial spaces into the mediastinum is heralded by chest pain, dyspnea, fever, and radiographic demonstration of mediastinal widening. The critical care should...
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