- Secondary renal tubular dysgenesis in a newborn exposed to angiotensin Ⅱ receptor antagonist during gestation
-
Gang MH, Lee YW, Chang My
- KMID: 2513269
- Clin Exp Pediatr.
- 2021 Mar;64(3):136-138.
- doi: 10.3345/cep.2020.00752
-
- CITED
-
- Close
- SHARE
-
- Close
- 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
- 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... -
- CITED
-
- Close
- SHARE
-
- Close
- Effects of Horticultural Therapy Program on State-Anxiety, Fatigue and Quality of Life among Women Cancer Survivors
-
Oh KO, Gang MH, Jung KS
- KMID: 2269518
- Asian Oncol Nurs.
- 2012 Jun;12(2):125-131.
- doi: 10.5388/aon.2012.12.2.125
PURPOSE: This study was designed to examine the effects of horticultural therapy program on state-anxiety, fatigue and quality of life (QoL) of among women cancer survivors. METHODS: Quasi-experimental study was used... -
- CITED
-
- Close
- SHARE
-
- Close
- 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
- 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... -
- CITED
-
- Close
- SHARE
-
- Close
- Perception of Patient Safety Culture and Safety Care Activity of Entry-level Nurses
-
Cho SS, Gang MH
- KMID: 2270114
- Korean J Occup Health Nurs.
- 2013 Feb;22(1):24-34.
PURPOSE: We investigated the relationship between patient safety culture and safety care activity, and identified factors for safety care activity of entry-level nurses. METHODS: The subjects of the study were 204... -
- CITED
-
- Close
- SHARE
-
- Close
- Neonatal Thrombocytopenia due to MYH9 Missense Mutation: A Case Report
-
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... -
- CITED
-
- Close
- SHARE
-
- Close
- 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
- 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... -
- CITED
-
- Close
- SHARE
-
- Close
- Infratentorial and Intraparenchymal Subependymoma in the Cerebellum: Case Report
-
Kim Y, Lee SY, Yi KS, Cha SH, Gang MH, Cho BS, Lee YM
- KMID: 1711491
- Korean J Radiol.
- 2014 Feb;15(1):151-155.
- doi: 10.3348/kjr.2014.15.1.151
Subependymomas are rare benign tumors located in the ventricular system. Intraparenchymal subependymoma is extremely rare; only 6 cases have been reported, and all were located in the supratentorial region. We... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Langerhans Cell Histiocytosis Involving the Thyroid Gland: Ultrasonographic Finding
-
Kim Y, Lee SY, Cha SH, Lee GS, Cho BS, Gang MH
- KMID: 2096945
- J Korean Soc Ultrasound Med.
- 2013 Mar;32(1):67-70.
Langerhans cell histiocytosis is a rare, proliferative monoclonal histiocytic disease of unknown cause. Primary involvement of the thyroid gland by LCH is very rare, and most cases show evidence of... -
- CITED
-
- Close
- SHARE
-
- Close
- A neonate with Say–Barber–Biesecker–Young– Simpson syndrome with a novel pathogenic mutation in KAT6B gene: A case report
-
Shin JH, Lim HH, Gang MH, Kim SY, Yang Ss, Chang My
- KMID: 2524743
- J Genet Med.
- 2021 Dec;18(2):147-151.
- doi: 10.5734/JGM.2021.18.2.147
The Say–Barber–Biesecker–Young–Simpson variant of Ohdo syndrome (SBBYSS) (Online Mendelian Inheritance in Man #603736) is a rare autosomal dominant disorder and clinically features blepharophimosis with ptosis, a mask-like facial appearance, cryptorchidism,... -
- CITED
-
- Close
- SHARE
-
- Close
- Short-Term Complications of Percutaneous Endoscopic Gastrostomy according to the Type of Technique
-
Gang MH, Kim JY
- KMID: 2315495
- Pediatr Gastroenterol Hepatol Nutr.
- 2014 Dec;17(4):214-222.
- doi: 10.5223/pghn.2014.17.4.214
PURPOSE: The method of percutaneous endoscopic gastrostomy (PEG) tube placement can be divided into the pull and introducer techniques. We compared short-term complications and prognosis between patients who underwent the... -
- CITED
-
- Close
- SHARE
-
- Close
- A 10-Year Single-Center Experience of Catheter-Related Thrombosis in Neonates
-
Shin JH, Gang MH, Lee YW, Kil HR, Chang My
- KMID: 2522527
- Perinatology.
- 2021 Sep;32(3):117-124.
- doi: 10.14734/PN.2021.32.3.117
Objective: Central catheterization is one of the major iatrogenic risk factors of neonatal thrombosis. We conducted this study to investigate the clinical features of neonatal catheter-related thrombosis. Methods: This is a... -
- CITED
-
- Close
- SHARE
-
- Close
- Clinical Characteristics and Outcomes of Mothers and Newborn Babies at an Inte grated Perinatal Center for High-risk Preg nancy and Neonatal Care
-
Park Y, Gang MH, Lee YW, Kang BH, Lee MA, Chang My
- KMID: 2510393
- Perinatology.
- 2020 Dec;31(4):199-208.
- doi: 10.14734/PN.2020.31.4.199
Objective: The appropriate perinatal care and safe delivery of high-risk pregnant women have a sig nificant impact on the prognosis of newborn. The purpose of this study is to analyze... -
- CITED
-
- Close
- SHARE
-
- Close
- Postoperative Complications of Esophageal Atresia and Role of Endoscopic Balloon Dilatation in Anastomotic Strictures
-
Cho JY, Chang My, Gang MH, Lee YW, Park JB, Kim JY, Kim HJ
- KMID: 2535162
- Pediatr Gastroenterol Hepatol Nutr.
- 2022 Nov;25(6):453-460.
- doi: 10.5223/pghn.2022.25.6.453
Purpose: Esophageal atresia (EA) with or without tracheoesophageal fistula (TEF) is a congenital anomaly that can cause frequent digestive and nutritional problems, even after repair. The most common complication is... -
- CITED
-
- Close
- SHARE
-
- Close
- Breast Milk-Transmitted Cytomegalovirus Infection in Preterm Infants
-
Gang MH, Chang MY
- KMID: 2437899
- Neonatal Med.
- 2018 May;25(2):58-65.
- doi: 10.5385/nm.2018.25.2.58
PURPOSE: The purpose of this study is to describe the rate of cytomegalovirus (CMV) virolactia, and the prevalence of breast milk (BM)-transmitted postnatal CMV infection among premature infants after freeze-thawing... -
- CITED
-
- Close
- SHARE
-
- Close
- Successful Management of Visceral Kaposiform Hemangioendothelioma with Kasabach‐Merritt Phenomenon Using Corticosteroids and Vincristine
-
Gang MH, Lim YJ, Chang My
- KMID: 2502092
- Neonatal Med.
- 2020 Feb;27(1):37-43.
- doi: 10.5385/nm.2020.27.1.37
Kaposiform hemangioendothelioma (KHE) is a rare, locally aggressive vascular neoplasm that often develops a coagulopathy known as KasabachMerritt phenomenon (KMP). Visceral involvement denotes a poor prognosis. We report a case... -
- CITED
-
- Close
- SHARE
-
- Close
- Clinical Characteristics of Children with Lobar Pneumonia Caused by Mycoplasma pneumoniae
-
Yang EA, Gang MH, You SY, Kim JH, Lee JH
- KMID: 2315272
- Pediatr Allergy Respir Dis.
- 2012 Sep;22(3):256-264.
PURPOSE: This study was conducted to evaluate the prevalence, clinical characteristics and laboratory findings of lobar pneumonia in children caused by Mycoplasma pneumonia and to find a diagnostic tool for... -
- CITED
-
- Close
- SHARE
-
- Close
- A neonate with hyperornithinemia-hyperammonemia-homocitrullinuria syndrome from a consanguineous Pakistani family
-
Kim YM, Lim HH, Gang MH, Lee YW, Kim SZ, Kim GH, Yoo HW, Ko JM, Chang M
- KMID: 2470104
- J Genet Med.
- 2019 Dec;16(2):85-89.
- doi: 10.5734/JGM.2019.16.2.85
Hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome is a rare autosomal recessive urea cycle disorder. HHH is caused by a deficiency of the mitochondrial ornithine transporter protein, which is encoded by the solute carrier... -
- CITED
-
- Close
- SHARE
-
- Close
