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Erratum: Possible Role of Single Stranded DNA Binding Protein 3 on Skin Hydration by Regulating Epidermal Differentiation

Choi MR, Shin JM, Shin YA, Chang YH, Chang MY, Lim CA, Sohn KC, Seo YJ, Kim CD, Lee JH, Lee Y

The authors would like to change the corresponding author of the article.
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Two cases of Korean hemorrhagic fever complicated with pregnancy

Chun SH, Chang MY, Kim YJ, Woo BH

  • KMID: 1696928
  • Korean J Obstet Gynecol.
  • 1992 May;35(5):778-782.
No abstract available.
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Secondary renal tubular dysgenesis in a newborn exposed to angiotensin Ⅱ receptor antagonist during gestation

Gang MH, Lee YW, Chang My

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significance of serum CA-125 concentrations as tumor markers in patients with ovarian tumors

Yoo EH, Lee MJ, Kim YJ, Chang MY, Ahn JJ, Woo BH

  • KMID: 2259570
  • Korean J Obstet Gynecol.
  • 1993 Jul;36(7):1734-1743.
No abstract available.
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Revascularization of Concurrent Renal and Cerebral Artery Stenosis in a 14-Year-Old Girl with Takayasu Arteritis and Moyamoya Syndrome

Lee ML, Chang MY, Chang TM, Yang RC, Chang MC, Yang AD

Concurrent involvement of bilateral renal and cerebral arteries, usually incurred as stenosis, is rare in childhood-onset Takayasu arteritis (c-TA). We report the case of a 14-year-old girl, with c-TA, presenting...
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Trisomy 12p Syndrome Secondary to a Balanced Maternal Translocation [46,XX, t(12;22)(p11.2;p13)]

Gang MH, Lee YW, Lim HH, Chang MY

Trisomy 12p is a rare chromosomal anomaly. It causes dysmorphic features, multiple congenital anomalies, neonatal complications, and mental retardation. We present a case of complete and pure trisomy 12p syndrome...
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A Case of Tuberous Sclerosis Associated with Multiple Tumorous Condition

Kim MJ, Chang MY, Lee KS, An RZ

  • KMID: 1544437
  • J Korean Child Neurol Soc.
  • 2000 May;8(1):126-126.
Tuberous Sclerosis is a neurocutaneous syndrome, which is characterized by seizure, mental retardation, angiofibroma and various tumorous conditions. We report a case of 15 year old girl with Tuberous Sclerosis...
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Endoscopic Hemoclipping Treatment for Gastric Dieulafoy Lesion in a Newborn

Lee YW, Shin JH, Chang MY, Kim JY

Dieulafoy's lesion is defined as a small mucosal defect overlying an abnormal, large caliber submucosal artery that protrudes through the gastrointestinal mucosa. This lesion is a rare cause of massive...
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Possible Role of Single Stranded DNA Binding Protein 3 on Skin Hydration by Regulating Epidermal Differentiation

Choi MR, Shin JM, Shin YA, Chang YH, Chang MY, Lim CA, Sohn KC, Seo YJ, Kim CD, Lee JH, Lee Y

BACKGROUND: Skin hydration is a common problem both in elderly and young people as dry skin may cause irritation, dermatological disorders, and wrinkles. While both genetic and environmental factors seem...
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A Case of Neonatal Sepsis with Meningitis due to Gardnerella vaginalis

Jin HY, Oh SM, Chang MY

  • KMID: 2280606
  • Korean J Perinatol.
  • 2007 Jun;18(2):182-185.
Gardnerella vaginalis is a normal component of the vaginal flora and is one of the organisms associated with bacterial vaginosis. It is rarely involved in neonatal infection. Although it is...
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Congenital Hydrocolpos Mimicking a Mature Cystic Teratoma in the Pelvis

Chang MY

Neonatal hydrocolpos is a rare condition that involves fluid accumulation in the vagina. On diagnostic imaging, the dilated vagina, along with the compressed uterus, can simulate a mature cystic teratoma...
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Post-Intubation Tracheoesophageal Fistula with Posterior Glottic Web

Lee JE, Chang MY, Kim KH, Jung YH

  • KMID: 2166452
  • Clin Exp Otorhinolaryngol.
  • 2011 Jun;4(2):105-108.
Tracheoesophageal fistula (TEF) after prolonged intubation could present as chronic aspiration and could be mistaken as unilateral or bilateral vocal fold palsy, especially when there was combined posterior glottic synechia....
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Comparison of Hematologic and Serum Biochemistric Values at 1 Month of Age between Breast-fed and Formula-fed Infants

Byun SH, Chang MY

  • KMID: 2099012
  • J Korean Soc Neonatol.
  • 2000 May;7(1):17-23.
PURPOSE: We compared the hematologic data, serum biochemical and immunoglobulin values at 1 month of age and anthropometric variables at 1, 4, and 6 months of age between breast-fed and...
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Clinical Observation on Poor R-Wave Progression

Won KH, Chang MY, Oh KS, Kim YC, Lee HC

Poor R-Wave Progression(PRWP) of precordial leads is frequently encountered electrocardiographic findings of uncertain significance and has simply been deemed as suggestion of anterior myocardial infarction without concrete ground. 217 cases...
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Brain Injuries Due to Neonatal Hypoglycemia: Case Report

Kim DB, Song CJ, Chang MY, Youn HW

Although hypoglycemia may be common among neonates, brain injuries resulting from isolated neonatal hypoglycemia are rare. The condition may cause neurological symptoms such as stupor, jitteriness, and seizures, though...
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Therapeutic Exercises for Strengthening Suprahyoid Muscles

Park JS, Hwang NK, Oh DH, Chang MY

Suprahyoid muscles play an important role in normal swallowing by providing muscle contractions involved in airway protection and upper esophageal sphincter opening. However, these muscles can be weakened by neurological...
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Pfeiffer Syndrome Type 2 with Sporadic Fibroblast Growth Factor Receptor 2 Mutation and Coccygeal Anomaly

Lee JS, Choi JH, Lee YW, Gang MH, You SK, Shin HD, Chang MY

Pfeiffer syndrome is a rare genetic disorder characterized by premature fusion of certain skull bones (craniosynostosis) and anomalies of the face and extremities. A female newborn showing ocular proptosis and...
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Removal of non-palpable Implanon(TM) by ultrasound guidance

Kim SY, Huh JS, Chang MY, Hong Y, Choi BR, Baek JH, Seo K

OBJECTIVE: This study was designed to analyze outcome of removal of non-palpable Implanon(TM) by ultrasound guidance. METHODS: This is retrospective study of patients who were referred from local clinic where removal...
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Neonatal Thrombocytopenia due to MYH9 Missense Mutation: A Case Report

Shin JH, Chang My, Lee E, Lee YW, Yoo JW, Gang MH

Myosin heavy chain 9 (MYH9)-related disorders (MYH9RD) are autosomal-dominant disorders charac terized by macrothrombocytopenia with or without leukocyte inclusion bodies or extra-hematolo gical manifestations, such as sensorineural deafness, cataract, and...
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Leri-Weill dyschondrosteosis in a newborn presenting with respiratory failure due to severe micrognathia

Gang MH, Lee J, Lee YW, Shin JH, Lim HH, Kim YM, Chang My

Short stature homeobox-containing gene (SHOX) is a well-known causative gene for the short stature in Turner syndrome. The clinical manifestation of SHOX gene related disorders varies from SHOX haploinsufficiency, presenting...
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