- A novel compound variant in GNRHR causing congenital idiopathic hypogonadotropic hypogonadism in a young male Korean patient
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Lee G, Lee MS, Lee R, Moon JE
- KMID: 2549334
- Ann Pediatr Endocrinol Metab.
- 2023 Dec;28(Suppl 1):S20-S22.
- doi: 10.6065/apem.2244070.035
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- Subcutaneous emphysema, pneumomediastinum, pneumoretroperitoneum, and pneumoperitoneum secondary to colonic perforation during colonoscopy
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Kim BH, Yoon SJ, Lee JY, Moon JE, Chung IS
- KMID: 1965374
- Korean J Anesthesiol.
- 2013 Dec;65(6 Suppl):S103-S104.
- doi: 10.4097/kjae.2013.65.6S.S103
No abstract available. -
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- Esthetic restorations of maxillary anterior teeth with orthodontic treatment and porcelain laminate veneers: a case report
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Moon JE, Kim SH, Han JS, Yang JH, Lee JB
- KMID: 1456763
- J Adv Prosthodont.
- 2010 Jun;2(2):61-63.
- doi: 10.4047/jap.2010.2.2.61
If orthodontists and restorative dentists establish the interdisciplinary approach to esthetic dentistry, the esthetic and functional outcome of their combined efforts will be greatly enhanced. This article describes satisfying esthetic... -
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- Bilateral Tension Pneumothorax and Bronchospasm in the Patients with Recent History of Croup: A case report
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Moon JE, Ahn HJ, Kim JA
- KMID: 2299171
- Korean J Anesthesiol.
- 2007 Jun;52(6):724-727.
- doi: 10.4097/kjae.2007.52.6.724
Tension pneumothorax is a rare but critical complication of mechanical ventilation. Many researchers regard elevated peak inspiratory pressure as a major etiology for pneumothorax during ventilatory care. Bronchospasm is another... -
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- De novo a novel variant of CaSR gene in a neonate with congenital hypoparathyroidism
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Moon JE, Lee SJ, Park SH, Kim J, Jin DK, Ko CW
- KMID: 2417769
- Ann Pediatr Endocrinol Metab.
- 2018 Jun;23(2):107-111.
- doi: 10.6065/apem.2018.23.2.107
Autosomal-dominant hypocalcemia with hypercalciuria (ADHH) is a genetic disease characterized by hypoparathyroidism with hypercalciuria. Most patients with ADHH have calcium-sensing receptor (CaSR) gene mutations. The CaSR gene controls parathyroid secretions,... -
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- Tension pneumothorax occurred by tumescent solution injection during delay extended latissimus dorsi flap : A case report
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Lee JY, Moon JE, Lee SM
- KMID: 2263354
- Anesth Pain Med.
- 2009 Jan;4(1):36-39.
Tension pneumothorax is known as a rare complication of breast augmentation surgery, but can occur more than expected. This is a case of a 34-year-old woman who was to receive... -
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- Digital intraoral impression for immediate provisional restoration of maxillary single implant: A case report
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Chang YJ, Kim HJ, Song MK, Moon JE, Lee HL, Park CI
- KMID: 2195254
- J Korean Acad Prosthodont.
- 2015 Jul;53(3):234-243.
- doi: 10.4047/jkap.2015.53.3.234
Developing of digital technique, it is possible to fabricate implant prostheses for edentulous area using intraoral 3-dimentional information throughout implant diagnosis and treatment process. It is being changed that from... -
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- Hyperuricemia is Associated With an Increased Prevalence of Metabolic Syndrome in a General Population and a Decreased Prevalence of Diabetes in Men
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Jeong H, Moon JE, Jeon CH
- KMID: 2506978
- J Rheum Dis.
- 2020 Oct;27(4):247-260.
- doi: 10.4078/jrd.2020.27.4.247
Objective. Elevated uric acid is associated with cardiovascular disease and metabolic syndrome. However, uric acid is also an antioxidant with beneficial effect on comorbidities. The aim of this study was... -
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- An Alport syndrome boy with Van Wyk-Grumbach syndrome induced by prolonged untreated congenital hypothyroidism
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Lee SJ, Moon JE, Lee GM, Cho MH, Ko CW
- KMID: 2503365
- Ann Pediatr Endocrinol Metab.
- 2020 Jun;25(2):132-136.
- doi: 10.6065/apem.1938074.037
Alport syndrome (AS) is a rare genetic disorder that causes progressive nephritis and is more common among males. Studies have reported an association between thyroid antibodies and hypothyroidism in patients... -
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- Full mouth rehabilitation with fixed implant-supported prosthesis using temporary denture and double digital scanning technique: a case report
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Shin SH, Park CI, Kang SH, Moon JE, Oh MS, Park CM, Jeon WJ, Han SG, Kim SJ, Choi SJ
- KMID: 2544978
- J Korean Acad Prosthodont.
- 2023 Jul;61(3):245-256.
- doi: 10.4047/jkap.2023.61.3.245
When restoring with a dental digital system for implant-supported prosthesis, a double digital scanning technique is required: an intraoral scan of the three-dimensional implant location and intraoral scan after placement... -
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- Severe recurrent nocturnal hypoglycemia during chemotherapy with 6-mercaptopurine in a child with acute lymphoblastic leukemia
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Cho EM, Moon JE, Lee SJ, Ko CW
- KMID: 2432275
- Ann Pediatr Endocrinol Metab.
- 2018 Dec;23(4):226-228.
- doi: 10.6065/apem.2018.23.4.226
Various endocrine dysfunctions occur during chemotherapy, including hypoglycemia. However, reports of hypoglycemia associated with 6-mercaptopurine (6-MP) are rare. Herein, we report an 8-year-old boy with severe symptomatic hypoglycemia likely due... -
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- Failed recanalization mediates the association of women with poor outcomes after thrombectomy: a single-center experience
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Lee SJ, Lee TK, Moon JE
- KMID: 2538767
- J Neurocrit Care.
- 2022 Dec;15(2):104-112.
- doi: 10.18700/jnc.220054
Background: Whether thrombectomy benefits differ according to sex remains debatable. We aimed to investigate whether there was a difference in stroke outcomes between men and women treated with thrombectomy. Methods: We... -
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- A Korean male with Kleefstra syndrome presented with micropenis
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Lee R, Lee Ms, Moon JE
- KMID: 2549325
- Ann Pediatr Endocrinol Metab.
- 2023 Dec;28(4):308-311.
- doi: 10.6065/apem.2244174.087
Kleefstra syndrome is caused by chromosome 9q34.3 deletion or heterozygous mutations in the euchromatin histone methyl transferase 1 (EHMT1) gene. It can be accompanied by intellectual disability, distinctive facial features,... -
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- One-year experience of oral substrate reduction therapy in three patients with Gaucher disease type I
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Sohn YB, Kim Y, Moon JE
- KMID: 2509985
- J Genet Med.
- 2020 Dec;17(2):62-67.
- doi: 10.5734/JGM.2020.17.2.62
Purpose: Eliglustat is an oral substrate reduction therapy (SRT) approved for adults with Gaucher disease type I (GD1) who are extensive, intermediate, or poor CYP2D6 metabolizers. Here we report one-year... -
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- Increase in blood glucose level and incidence of diabetic ketoacidosis in children with type 1 diabetes mellitus in the Daegu-Gyeongbuk area during the coronavirus disease 2019 (COVID-19) pandemic: a retrospective cross-sectional study
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Lee MS, Lee R, Ko CW, Moon JE
- KMID: 2525027
- J Yeungnam Med Sci.
- 2022 Jan;39(1):46-52.
- doi: 10.12701/yujm.2021.01221
Background: The coronavirus disease 2019 (COVID-19) outbreak in the Daegu-Gyeongbuk area in 2020 has caused difficulties in the daily life and hospital care of children with type 1 diabetes mellitus... -
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- Metanephrine negative pheochromocytoma: a rare case report of dopamine-secreting tumor in an adolescent neurofibromatosis type 1 patient
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Lee MS, Lee R, Park SH, Kwon SH, Park JY, Lee SW, Lee SM, Moon JE
- KMID: 2549324
- Ann Pediatr Endocrinol Metab.
- 2023 Dec;28(4):302-307.
- doi: 10.6065/apem.2244016.008
Pheochromocytoma (PCC) occurs in 4% of pediatric neurofibromatosis type 1 (NF1) patients and is characterized by epinephrine and norepinephrine secretion. Herein, we report the first case of dopamine-secreting PCC in... -
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- Action Research in Hospital Settings: A Literature Review of International Nursing Journals
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Moon JE, Song MO, Kim HY, Park HY, Kim EA, Kim YM, Jang KS
- KMID: 2153277
- J Korean Acad Nurs Adm.
- 2016 Jan;22(1):46-56.
- doi: 10.11111/jkana.2016.22.1.46
PURPOSE: Purpose of this study was to identify major trends of action research from 2006 to 2013 and suggest directions for activating and advancing domestic action research in nursing. METHODS: A... -
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- A cell function study on calcium regulation of a novel calcium-sensing receptor mutation (p.Tyr825Phe)
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Moon JE, Yang HY, Wee G, ParK SH, Ko CW
- KMID: 2514149
- Ann Pediatr Endocrinol Metab.
- 2021 Mar;26(1):24-30.
- doi: 10.6065/apem.2040022.011
Purpose: Autosomal dominant hypocalcemia with hypercalciuria is a genetic disease characterized by hypoparathyroidism with hypercalciuria. We discovered a novel variant (p.Tyr825Phe[Y825F]) of the CASR gene in a neonate with congenital... -
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- Severe vitamin D deficiency in preterm infants: maternal and neonatal clinical features
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Park SH, Lee GM, Moon JE, Kim HM
- KMID: 2129735
- Korean J Pediatr.
- 2015 Nov;58(11):427-433.
- doi: 10.3345/kjp.2015.58.11.427
PURPOSE: We investigated the vitamin D status of preterm infants to determine the incidence of vitamin D deficiency. METHODS: A total of 278 preterm infants delivered at Kyungpook National University Hospital... -
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- Vitamin D in Full-term Neonates in Daegu and Gyeongbuk Province of Korea and the Association with Maternal and Neonatal Diseases
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Moon JE, Lee JM, Ro DE, Kim HM
- KMID: 2164188
- Korean J Perinatol.
- 2015 Dec;26(4):329-335.
- doi: 10.14734/kjp.2015.26.4.329
PURPOSE: This study aimed to evaluate serum 25-hydroxyvitamin D [25(OH)D3] levels of full-term neonates in Daegu and Gyeongbuk province of Korea to determine the association between maternal and neonatal diseases,... -
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