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Use of fludrocortisone for intradialytic hypotension

Seo Y, Jeung S, Kang SM, Yang WS, Kim H, Kim SB

Intradialytic hypotension during dialysis adversely affects a patient's prognosis and increases mortality. We report a case in which intradialytic hypotension that persisted after the administration of midodrine was relieved after...
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Cerebral Salt Wasting Treated with Fludrocortisone in a 17-Year-Old Boy

Choi MJ, Oh YS, Park SJ, Kim JH, Shin JI

Cerebral salt wasting is characterized by inappropriate natriuresis and volume contraction with associated cerebral pathology. It is distinct from the syndrome of inappropriate antidiuretic hormone secretion, which is characterized by...
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Management of a 25-day-old Male Presenting with a First Episode of Acute Pyelonephritis, and Persistent Hyperkalemia with Normal Serum Aldosterone

Kang YS, Choi JY, Lee JH

Hyperkalemia is often detected in young infants, particularly in association with acute pyelonephritis or a urinary tract anomaly. Cases of hyperkalemia in this population may also be due to transient...
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Persistent Autonomic Dysfunction in Guillain-Barre Syndrome: A case report

Lee SJ, Choi ES, Jung SH, Cho YR, Han ZA, Yu IH

  • KMID: 2325198
  • J Korean Acad Rehabil Med.
  • 2008 Oct;32(5):586-590.
Autonomic dysfunction is a common manifestation in Guillain-Barre syndrome (GBS), but it rarely persists. We report a case involving a 22-year-old man who presented with glove-and-stocking type sensory loss, symmetric...
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Effect of Corticosteroids Instillation on Intraocular Pressure and on Intraocular Pressure-lowering Action of Acetazolamide in Rabbit

Paek US, Cho BH, Che KC

  • KMID: 2107051
  • J Korean Ophthalmol Soc.
  • 1974 Mar;15(1):1-8.
This study was undertaken to clarify the effects of glucocorticosteroids on intraocular pressure and the combined effects of acetazolamide and glucocorticosteroid on ocular pressure. Male and female rabbits, weighing 1.7-2.2kg,...
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Orthostatic Hypotension: Mechanisms, Causes, Management

Low PA, Tomalia VA

Orthostatic hypotension (OH) occurs when mechanisms for the regulation of orthostatic BP control fails. Such regulation depends on the baroreflexes, normal blood volume, and defenses against excessive venous pooling. OH...
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A Case of Cerebral Salt Wasting Syndrome Associated with Tuberculous Meningitis

Lee JY, Lee ES, Lee JH, Lim EJ, Kim HS, Jang JS, Kim HK, Kim DM, Park YB, Lee JY, Mo EK

  • KMID: 2318668
  • Tuberc Respir Dis.
  • 2005 Sep;59(3):306-310.
Hyponatremia which is due to excessive sodium loss in the urine and decrease in extracellular fluid volume following an acute or chronic central nervous system injury, has been conjunctively described...
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Long-term Follow up of Congenital Adrenal Hyperplasia Patients with Hyponatremia

Song JH, Lee KH, Kim SD, Cho BS

Congenital adrenal hyperplasia (CAH) caused by 21-hydroxylase deficiency is an autosomal recessive disease, which leads to cortisol and aldosterone deficiency and hyperandrogenism. Typical medical treatment includes oral glucocorticoid and mineralocorticoid...
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Effect of Corticosteroids on Renal Excretion of Lithium

Oh SY, Ha JH, Lee KY, Kim WJ

Lithium salts are being used increasingly to treat patient with affective disorders, especially acute mania, or bipolar manic-depressive illness. For therapeutic effect the lithium content must be maintained at or...
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Cerebral salt-wasting syndrome after hematopoietic stem cell transplantation in adolescents: 3 case reports

Jeon YJ, Lee HY, Jung IA, Cho WK, Cho B, Suh BK

Cerebral salt-wasting syndrome (CSWS) is a rare disease characterized by a extracellular volume depletion and hyponatremia induced by marked natriuresis. It is mainly reported in patients who experience a central...
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Usefulness of tilt training in patients with neurocardiogenic syncope

Choe WH, Kim JS, Hong SH, Jeon CH, Kim JS, Kim HS, Kwon HC, Park SW, Kim DK, Lee SH, Hong KP, Park JE, Seo JD, Lee WR

Neurocardiogenic syncope is a relatively common cause of syncope and is diagnosed by head-up tilt test. A wide variety of medical treatment has been proposed, such as beta-blocker, vasoconstrictor, fludrocortisone,...
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A case of POEMS syndrome associated with amyloidosis

Lee EJ, Ju HR, Ra SH, Han JY, An WS, Kim SE, Kim KH

  • KMID: 1652691
  • Korean J Med.
  • 2004 Apr;66(4):425-431.
POEMS syndrome (polyneuropathy, organomegaly, endocrinopathy, monoclonal M protein, and skin lesion) is a rare multisystemic disease of unknown cause with varying clinical manifestations. Amyloidosis-associated POEMS Syndrome is also rare condition....
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A Case of Cerebral Salt Wasting Syndrome associated with Tuberculous Meningitis

Rho SH, Choi JY, Nam TM, Kim HK, Lee SJ, Jeong IK, Hong EG, Choi CS, Kim DM, Yu JM, Ihm SH, Choi MG, Yoo HJ, Park SW, Kim HC

  • KMID: 2200051
  • J Korean Soc Endocrinol.
  • 2002 Oct;17(5):698-704.
Hyponatremia in patients with central nervous system disorders is suggestive of the syndrome of inappropriate secretion of antidiuretic hormone (SIADH), and volume restriction is recommended for its correction. However, if...
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Spontaneous Bilateral Renal Rupture in an End-stage Renal Disease Patient Treated with Hemodialysis

Chung S, Choi DE, Na KR, Sul CK, Lee KW, Shin YT

  • KMID: 2252996
  • Korean J Nephrol.
  • 2010 Sep;29(5):670-674.
Bilateral spontaneous renal rupture is a rare event that has been documented in only a few reports. We report a spontaneous, but not simultaneous rupture of both kidneys in a...
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Two cases of Antley-Bixler syndrome caused by mutations in different genes, FGFR2 and POR

Woo H, Ko JM, Shin CH, Yang SW

Antley-Bixler syndrome (ABS) is a rare form of syndromic craniosynostosis with additional systemic synostosis, including radiohumeral or radioulnar synostosis. Another characteristic feature of ABS is mid-facial hypoplasia that leads to...
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Characteristics of Korean Patients with Primary Adrenal Insufficiency: A Registry-Based Nationwide Survey in Korea

Hong AR, Ryu OH, Kim SY, Kim SW, The Korean Adrenal Gland and Endocrine Hypertension Study Group, Korean Endocrine Society

BACKGROUND: Primary adrenal insufficiency (PAI) is a rare, potentially life-threatening condition. There are few Korean studies on PAI, and most have had small sample sizes. We aimed to examine the...
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Manifestation of Giant Bilateral Symptomatic Adrenal Myelolipomas in an Adult Patient with Congenital Adrenal Hyperplasia

Kim YM, Choi JH, Lee BH, Kim GH, Hong BS, Ryu YJ, Yoo HW

Adrenal myelolipoma is an uncommon non-functioning tumor that is composed of variable amounts of mature adipose tissue and scattered islands of hematopoietic elements, including erythroid, myeloid, lymphoid series, and megakaryocytes....
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Central precocious puberty in a patient with X-linked adrenal hypoplasia congenita and Xp21 contiguous gene deletion syndrome

Koh JW, Kang SY, Kim GH, Yoo HW, Yu J

X-linked adrenal hypoplasia congenita is caused by the mutation of DAX-1 gene (dosage-sensitive sex reversal, adrenal hypoplasia critical region, on chromosome X, gene 1), and can occur as part of...
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