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Erratum: Clinical, radiologic, and genetic features of Korean patients with Mucopolysaccharidosis IVA

Lee NH, Cho SY, Maeng SH, Jeon TY, Sohn YB, Kim SJ, Park HD, Jin DK

This erratum is being published to correct of page 435 and Table 4.
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Inflammation as the Potential Basis in Depression

Maeng SH, Hong H

There is growing evidence of the association between inflammation and stress-related disorders including depression. The positive correlation between the increased levels of inflammatory cytokines observed in patients with other diseases...
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Giant Aneurysm of a Congenital Coronary Arteriovenous Fistula Arising from the Left Coronary Artery

Shin MS, Maeng SH, Lee HJ, Cho HK, Chung IM, Shin GJ

  • KMID: 2434662
  • Korean Circ J.
  • 1999 Jul;29(7):740-746.
Congenital coronary arteriovenous fistula is a rare condition which is an abnormal communication of the coronary artery with the right ventricle, right atrium, left atrium or left ventricle. Coronary artery...
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A Case of Dermatomyositis Manifestated by the Paroxysmal Supraventricular Tachycardia

Kim YS, Maeng SH, Cho HK, Park SH, Shin GJ

Dermatomyositis is a disease of unknown etiology characterized by inflammation and degeneration of skeletal muscles and cutaneous abnormalities. Cardiac involvement in dermatomyositis-polymyositis is thought to be rare. In recent year,...
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The Clinical Efficacy and Safety of TAGOCIN(R) inj

Yu M, Maeng SH, Cho YJ

OBJECTIVES: We studied the open clinical trial to evaluate the efficacy and safety of TAGOCIN(R), teicoplanin, glycopeptide anti microbial agent, which was manufactured in one Korean pharmacy. METHODS: We selected 15...
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Two Cases of Tension Pneumopericardium in Mechanically Ventilated Preterm Infants

Maeng SH, Seo HJ, Shin J, Jung J, Kim JK, Yoo HS, Ahn SY, Kim ES, Chang YS, Park WS

Pneumopericardium is a rare form of neonatal air leakage. Tension pneumopericardium is much more infrequent, but can cause a cardiovascular deterioration with high mortality up to 80% and neurodevelopmental morbidity...
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A Case of Acute Respiratory Failure Presenting Lobar Consolidation

Shin TR, Maeng SH, Lee HK, Kim HY, Chang JH

Pulmonary embolism is one of the most common acute pulmonary disease in the adult general hospital populalion. However, the disease is still frequenfly unsuspected and underdiagnosed due to the...
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A case of acetaminophen induced anaphylaxis without aspirin sensitivity

Kim YJ, Ryu KH, Yu M, Oh HJ, Park CH, Maeng SH, Cho YJ

  • KMID: 2252784
  • Korean J Med.
  • 2003 Nov;65(Suppl 3):S926-S930.
Acetaminophen is a world-wide used analgesic and anti-pyretic drug with less anti-in-flammatory effect, available without prescription in most countries. Allergic-like reactions to this drug, including urticaria, angioedema, and anaphylactic reactions...
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One Case of Buckwheat Allergy Proved by Oral Provacation Test

Hong ES, Park JA, Shin TR, Seo KY, Woo GE, Lee NY, Kim MS, Maeng SH, Cho YJ

Buckwheat belongs to the Polygonacea or buckwheat family and is not a true cereral since it does not belong to the Graminiae, or grain family. Its products have long been...
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Growth Hormone Treatment and Its Effect on Height in Pediatric Patients with Different Genotypes of Prader-Willi Syndrome

Kwun C, Cho SY, Maeng SH, Jung YJ, Jin DK

PURPOSE: Differences in phenotypes between the two most common subtypes of Prader-Willi syndrome (PWS) indicate that a distinct response to growth hormone (GH) treatment may exist. To test this hypothesis,...
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The effect of Der p 2 antigen on the production of interferon gamma by CD3+T, CD56+NK and CD3+CD56+TNK cells from patients with mild persistent allergic asthma

Maeng SH, Lee JS, Park CW, Cho YJ

  • KMID: 2285850
  • J Asthma Allergy Clin Immunol.
  • 2003 Jun;23(2):341-348.
BACKGROUND: Asthma is a chronic inflammatory disease of the bronchial mucosa and is associated with excess production of Th2 cytokines (IL-4, IL-5) relative to Th1 cytokine (IFN-V). The NK cell...
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Osteogenesis Imperfecta Type VI with Severe Bony Deformities Caused by Novel Compound Heterozygous Mutations in SERPINF1

Cho SY, Ki CS, Sohn YB, Kim SJ, Maeng SH, Jin DK

Osteogenesis imperfecta (OI) comprises a heterogeneous group of disorders characterized by bone fragility, frequent fractures, and low bone mass. Dominantly inherited COL1A1 or COL1A2 mutations appear to be causative in...
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A novel MLL2 gene mutation in a Korean patient with Kabuki syndrome

Kim SJ, Cho SY, Maeng SH, Sohn YB, Kim SJ, Ki CS, Jin DK

Kabuki syndrome (KS) is a rare genetic disease with a distinctive dysmorphic face, intellectual disability, and multiple congenital abnormalities. KS is inherited in an autosomal dominant manner. As the primary...
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Comparison of Pharmacia CAP system and Auro Dex(R) Visual ENS(TM) screening test for detecting specific IgE in atopic patients

Kwak YG, Maeng SH, Kim HS, Cho YJ

  • KMID: 1618908
  • J Asthma Allergy Clin Immunol.
  • 2003 Mar;23(1):53-62.
BACKGROUND AND OBJECTIVE: Auro Dex(R) Visual ENS(TM) allergy screening test is a simplified and newly developed method for the detection of allergen-specific IgE in human serum. This system has advantages...
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Diagnosis and constitutional and laboratory features of Korean girls referred for precocious puberty

Kim D, Cho SY, Maeng SH, Yi ES, Jung YJ, Park SW, Sohn YB, Jin DK

  • KMID: 2409222
  • Korean J Pediatr.
  • 2012 Dec;55(12):481-486.
PURPOSE: Precocious puberty is defined as breast development before the age of 8 years in girls. The present study aimed to reveal the diagnosis of Korean girls referred for precocious...
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Study of dopamine transporter in the rat 6-hydroxydopamine Parkinson's disease model

Kim SY, Jung JM, Chang YS, Joo WS, Maeng SH, Ha CG, Kim JM, Kim YS, Lee MC, Lee SB, Jeon BS

  • KMID: 2342701
  • J Korean Neurol Assoc.
  • 1998 Aug;16(4):536-546.
BACKGROUND: Neuroprotective therapy is essential in the management of Parkinson's disease(PD). As symptomatic benefit of a treatment may clinically mask the disease progression, an evaluation of the effect of a...
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Clinical, radiologic, and genetic features of Korean patients with Mucopolysaccharidosis IVA

Lee NH, Cho SY, Maeng SH, Jeon TY, Sohn YB, Kim SJ, Park HD, Jin DK

PURPOSE: Mucopolysaccharidosis IVA (MPS IVA; Morquio A syndrome) is rare lysosomal storage disorder caused by N-acetylgalactosamine-6-sulfatase (GALNS) deficiency. Only a few MPS IVA cases have been reported in the Korean...
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Impact of Enzyme Replacement Therapy on Linear Growth in Korean Patients with Mucopolysaccharidosis Type II (Hunter Syndrome)

Cho SY, Huh R, Chang MS, Lee J, Kwun Y, Maeng SH, Kim SJ, Sohn YB, Park SW, Kwon EK, Han SJ, Jung J, Jin DK

Hunter syndrome (or mucopolysaccharidosis type II [MPS II]) arises because of a deficiency in the lysosomal enzyme iduronate-2-sulfatase. Short stature is a prominent and consistent feature in MPS II. Enzyme...
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White Coat Hypertension Diagnosed by 24-hour Ambulatory Blood Pressure Monitoring

Maeng SH, Cho H, Park SH, Shin GJ, Lee DS, Lim YH

OBJECTIVES: The Measurement of blood pressure by a doctor may trigger a pressor response, so there are marked differences between office and ambulatory or self-measured blood pressure and the subjects...
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Long-term Treatment with Oriental Medicinal Herb Artemisia princeps Alters Neuroplasticity in a Rat Model of Ovarian Hormone Deficiency

Kim HB, Kwon BJ, Cho HJ, Kim JW, Chon JW, Do MH, Park SY, Kim SY, Maeng SH, Park YK, Park JH

Artemisia princeps (AP) is a flowering perennial used as a traditional medicine and dietary supplement across East Asia. No study has yet assessed its effects on synaptic plasticity in hippocampus...
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