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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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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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Hypercalcemia Associated with Acute Kidney Injury and Metabolic Alkalosis

Jeong JH, Bae EH

  • KMID: 2406200
  • Electrolyte Blood Press.
  • 2010 Dec;8(2):92-94.
Most cases of hypercalcaemia are secondary to malignancy or primary hyperparathyroidism. We report a patient presenting with a triad of hypercalcemia, metabolic alkalosis, and renal failure secondary to treatment of...
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Acid-Base Disorders in ICU Patients

Oh YK

  • KMID: 2406196
  • Electrolyte Blood Press.
  • 2010 Dec;8(2):66-71.
Metabolic acid-base disorders are comnom clinical problems in ICU patients. Arterial blood gas analysis and anion gap (AG) are important laboratory data in approaching acid-base interpretation. When measuring the AG,...
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Role of Pendrin in Acid: base Balance

Chang JH, Kim S

Pendrin (SLC26A4) is a Na+-independent Cl-/HCO3- exchanger which is expressed in the apical membranes of type B and non-A, non-B intercalated cells within the distal convoluted tubule, the connecting tubule,...
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Mannitol-induced Metabolic Alkalosis

Kang KP, Lee S, Lee KH, Kang SK

Mannitol is an osmotic diuretic agent useful in a variety of clinical conditions. This study is based on acid-base and electrolyte changes seen after the intravenous infusion of hypertonic mannitol...
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A Case of Neonatal Bartter Syndrome

Ryu JM, Lee JH, Han HW, Park YS

  • KMID: 1627752
  • J Korean Soc Pediatr Nephrol.
  • 2005 Oct;9(2):255-262.
Bartter and Bartter-like syndromes, which include classic Bartter syndrome(type III), neonatal Bartter syndrome(type I, II or IV) and Gitelman syndrome, are autosomal - recessively inherited renal tubular disorders characterized by...
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Severe Hypochloremic Metabolic Alkalosis: A case report

Kim EC, Lee JS, Cho YS, Lee HS, Jang DJ, Shin CS

Chloride is the most abundant negative charge ion in extracellular fluid. In plasma it combines with sodium as sodium chloride and with potassium as potassium chloride. Chloride also is found...
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A Case of Juxtaglomerular Cell Tumor

Lee JH, Kim JY, Seok HJ, Choi JM, Yi MZ, Son HY, Kim HJ, Yang WS, Kim CS

  • KMID: 2079407
  • Korean J Nephrol.
  • 2004 May;23(3):484-487.
The juxtaglomerular cell tumor is a rare benign tumor which causes surgically correctable hypertension. We report a case of hypertension caused by juxtaglomerular cell tumor in a 17-year old man....
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A Case of Congenital Chloride Diarrhea in Premature Infant

Yoon SK, Kim EY, Moon KR, Park SK

  • KMID: 2104628
  • J Korean Pediatr Soc.
  • 2003 Mar;46(3):308-311.
Congenital chloride diarrhea is a serious autosomal recessive disease, and defect of intestinal electrolyte absorption that involves, specifically, Cl-/HCO3- exchange in the distal part of the ileum and colon. The...
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Clinical Feature and Response to Plasma Exchange in Adult Patients with Diarrhea-associated Hemolytic Uremic Syndrome (D+HUS)

Kim HY, Kang WH, Kim B, Lee YH, Huh W, Kim DJ, Kim YG, Oh HY

  • KMID: 1990098
  • Korean J Nephrol.
  • 1998 Nov;17(6):887-895.
Diarrea-associated hemolytic uremic syndrome (HUS) is very rare in adults. Few reports are available on clinical features and plasma exchange in adult patients with diarrhea-associated HUS in Korea. We retrospectively...
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A Case of Liddle's Syndrome Associated with Muscle Weakness

Kang JH, Lee CH, Han SM, Kim WY, Park HK, Kwack KK, So SC, Rhee DH, Kim JH, Shin HM, Imm EW

  • KMID: 2307362
  • Korean J Nephrol.
  • 1998 Jan;17(1):124-127.
Liddle's syndrome was described in 1963 by Liddle, et al., as the disease featuring a hypertension and hypokalemia but with negligible secretion of aldosterone. This syndrome, which morphologically belongs to...
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Metabolic alkalosis induced by plasmapheresis in a patient with systemic lupus erythematosus

Choi MY, Lee JD, Lee SH, Park IS, Woo JY, Choi EJ, Chang YS, Bang BK

We report a patient with systemic lupus erythematosus (SLE), who had developed metabolic alkalosis during plasmapheresis. The metabolic alkalosis could be promptly corrected by reducing the amount of citrate load....
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Congenital chloridorrhea in Korean infants

Lee YD, Lee HJ, Moon HR

The present paper describes two Korean male infants, 1. 16 year old and newly born neonate from two families who were diagnosed and managed for one of very rare...
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