- Erratum: Possible Role of Single Stranded DNA Binding Protein 3 on Skin Hydration by Regulating Epidermal Differentiation
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Choi MR, Shin JM, Shin YA, Chang YH, Chang MY, Lim CA, Sohn KC, Seo YJ, Kim CD, Lee JH, Lee Y
- KMID: 2428947
- Ann Dermatol.
- 2018 Dec;30(6):761-761.
- doi: 10.5021/ad.2018.30.6.761
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
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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
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Gang MH, Lee YW, Chang My
- KMID: 2513269
- Clin Exp Pediatr.
- 2021 Mar;64(3):136-138.
- doi: 10.3345/cep.2020.00752
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- significance of serum CA-125 concentrations as tumor markers in patients with ovarian tumors
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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
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Lee ML, Chang MY, Chang TM, Yang RC, Chang MC, Yang AD
- KMID: 2405008
- J Korean Med Sci.
- 2018 Mar;33(10):e76.
- doi: 10.3346/jkms.2018.33.e76
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)]
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Gang MH, Lee YW, Lim HH, Chang MY
- KMID: 2468549
- Perinatology.
- 2019 Dec;30(4):254-259.
- doi: 10.14734/PN.2019.30.4.254
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
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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
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Lee YW, Shin JH, Chang MY, Kim JY
- KMID: 2277711
- Korean J Pediatr Gastroenterol Nutr.
- 2011 Dec;14(4):393-397.
- doi: 10.5223/kjpgn.2011.14.4.393
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
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Choi MR, Shin JM, Shin YA, Chang YH, Chang MY, Lim CA, Sohn KC, Seo YJ, Kim CD, Lee JH, Lee Y
- KMID: 2457520
- Ann Dermatol.
- 2018 Aug;30(4):432-440.
- doi: 10.5021/ad.2018.30.4.432
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
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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
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Chang MY
- KMID: 2164928
- Neonatal Med.
- 2016 May;23(2):127-130.
- doi: 10.5385/nm.2016.23.2.127
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
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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
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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
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Won KH, Chang MY, Oh KS, Kim YC, Lee HC
- KMID: 2229787
- Korean Circ J.
- 1983 Jun;13(1):195-201.
- doi: 10.4070/kcj.1983.13.1.195
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
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Kim DB, Song CJ, Chang MY, Youn HW
- KMID: 2199942
- J Korean Radiol Soc.
- 2003 Oct;49(4):359-362.
- doi: 10.3348/jkrs.2003.49.4.359
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
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Park JS, Hwang NK, Oh DH, Chang MY
- KMID: 2406776
- J Korean Dysphagia Soc.
- 2018 Jan;8(1):8-14.
- doi: 10.0000/jkdps.2018.8.1.8
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
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Lee JS, Choi JH, Lee YW, Gang MH, You SK, Shin HD, Chang MY
- KMID: 2421578
- Perinatology.
- 2018 Sep;29(3):128-132.
- doi: 10.14734/PN.2018.29.3.128
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
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Kim SY, Huh JS, Chang MY, Hong Y, Choi BR, Baek JH, Seo K
- KMID: 2273890
- Korean J Obstet Gynecol.
- 2010 Jun;53(6):506-511.
- doi: 10.5468/kjog.2010.53.6.506
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
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Shin JH, Chang My, Lee E, Lee YW, Yoo JW, Gang MH
- KMID: 2527757
- Perinatology.
- 2022 Mar;33(1):48-52.
- doi: 10.14734/PN.2022.33.1.48
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
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Gang MH, Lee J, Lee YW, Shin JH, Lim HH, Kim YM, Chang My
- KMID: 2510004
- J Genet Med.
- 2020 Dec;17(2):108-111.
- doi: 10.5734/JGM.2020.17.2.108
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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