19 results on '"Cheon, Chong-Kun"'
Search Results
2. Pediatric management challenges of hyperglycemic hyperosmolar state: case series of Korean adolescents with type 2 diabetes.
3. Identification of a novel mutation of the SHOX gene in a patient with Leri-Weill dyschondrosteosis accompanied by growth hormone deficiency.
4. The impacts of COVID-19 on childhood obesity: prevalence, contributing factors, and implications for management.
5. A novel compound heterozygous variant of the COL11A1 gene in a patient with fibrochondrogenesis type I: the first case in Korea.
6. The first case of hyperosmolar diabetic ketoacidosis in a patient diagnosed with MODY 5 (maturity-onset diabetes of the young type 5) and 17q12 microdeletion syndrome.
7. Commentary on "Glycemic control and complications of type 2 diabetes mellitus in children and adolescents during the COVID-19 outbreak".
8. A Korean child with DICER1 syndrome presenting with thyroid manifestations accompanied by other types of neoplasms: a case report and literature review.
9. The first case of novel variants of the FSHR mutation causing primary amenorrhea in 2 siblings in Korea.
10. Pediatric management challenges of hyperglycemic hyperosmolar state: case series of Korean adolescents with type 2 diabetes.
11. Response to growth hormone according to provocation test results in idiopathic short stature and idiopathic growth hormone deficiency.
12. Commentary on "Effects of gonadotropin-releasing hormone agonist treatment on final adult height in boys with idiopathic central precocious puberty".
13. Clinical, endocrinological, and molecular features of four Korean cases of cytochrome P450 oxidoreductase deficiency.
14. Successful rapid weight reduction and the use of liraglutide for morbid obesity in adolescent Prader-Willi syndrome.
15. Evaluation and management of amenorrhea related to congenital sex hormonal disorders.
16. A rare case of multiple pituitary adenomas in an adolescent Cushing disease presenting as a vertebral compression fracture.
17. Genetics of Prader-Willi syndrome and Prader-Will-Like syndrome.
18. Incidence trends and associated factors of diabetes mellitus in Korean children and adolescents: a retrospective cohort study in Busan and Gyeongnam.
19. A novel de novo mutation within PHEX gene in a young girl with hypophosphatemic rickets and review of literature.
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