Detalles de la búsqueda
1.
Combination therapy of liothyronine and levothyroxine for hypothyroidism-induced dilated cardiomyopathy
Annals of Pediatric Endocrinology & Metabolism
; : 144-148, 2023.
Artículo
en Inglés
| WPRIM | ID: wpr-999358
2.
Changes in the Prevalences of Obesity, Abdominal Obesity, and Non-Alcoholic Fatty Liver Disease among Korean Children during the COVID-19 Outbreak
Yonsei Medical Journal
; : 269-277, 2023.
Artículo
en Inglés
| WPRIM | ID: wpr-977428
3.
Bone Age Estimation and Prediction of Final Adult Height Using Deep Learning
Yonsei Medical Journal
; : 679-686, 2023.
Artículo
en Inglés
| WPRIM | ID: wpr-1003232
4.
Clinical practice guidelines for optimizing bone health in Korean children and adolescents
Annals of Pediatric Endocrinology & Metabolism
; : 5-14, 2022.
Artículo
en Inglés
| WPRIM | ID: wpr-925472
5.
Two cases of 17α-hydroxylase/17,20-lyase deficiency caused by the CYP17A1 mutation
Annals of Pediatric Endocrinology & Metabolism
; : 66-70, 2021.
Artículo
en Inglés
| WPRIM | ID: wpr-896885
6.
Identification of a novel point mutation in DAX-1 gene in a patient with adrenal hypoplasia congenita
Annals of Pediatric Endocrinology & Metabolism
; : 126-129, 2021.
Artículo
en Inglés
| WPRIM | ID: wpr-896874
7.
Two cases of 17α-hydroxylase/17,20-lyase deficiency caused by the CYP17A1 mutation
Annals of Pediatric Endocrinology & Metabolism
; : 66-70, 2021.
Artículo
en Inglés
| WPRIM | ID: wpr-889181
8.
Identification of a novel point mutation in DAX-1 gene in a patient with adrenal hypoplasia congenita
Annals of Pediatric Endocrinology & Metabolism
; : 126-129, 2021.
Artículo
en Inglés
| WPRIM | ID: wpr-889170
9.
Ten-Year Trends of Metabolic Syndrome Prevalence and Nutrient Intake among Korean Children and Adolescents: A Population-Based Study
Yonsei Medical Journal
; : 344-351, 2021.
Artículo
en Inglés
| WPRIM | ID: wpr-875578
10.
Cushing syndrome with acute kidney injury due to ureteral stones in a 6-year-old boy
Annals of Pediatric Endocrinology & Metabolism
; : 277-281, 2020.
Artículo
en Inglés
| WPRIM | ID: wpr-896868
11.
Cushing syndrome with acute kidney injury due to ureteral stones in a 6-year-old boy
Annals of Pediatric Endocrinology & Metabolism
; : 277-281, 2020.
Artículo
en Inglés
| WPRIM | ID: wpr-889164
12.
Incidence and Prevalence of Type 1 Diabetes Mellitus among Korean Children and Adolescents between 2007 and 2017: An Epidemiologic Study Based on a National Database
Diabetes & Metabolism Journal
; : 866-874, 2020.
Artículo
en Inglés
| WPRIM | ID: wpr-898029
13.
A case of primary hyperparathyroidism due to an intrathymic ectopic parathyroid adenoma in a 15-year-old boy
Annals of Pediatric Endocrinology & Metabolism
; : 187-191, 2020.
Artículo
| WPRIM | ID: wpr-830472
14.
Incidence and Prevalence of Type 1 Diabetes Mellitus among Korean Children and Adolescents between 2007 and 2017: An Epidemiologic Study Based on a National Database
Diabetes & Metabolism Journal
; : 866-874, 2020.
Artículo
en Inglés
| WPRIM | ID: wpr-890325
15.
A novel compound heterozygous mutation of the AIRE gene in a patient with autoimmune polyendocrine syndrome type 1
Annals of Pediatric Endocrinology & Metabolism
; : 248-252, 2019.
Artículo
| WPRIM | ID: wpr-785405
16.
Respiratory failure in a diabetic ketoacidosis patient with severe hypophosphatemia
Annals of Pediatric Endocrinology & Metabolism
; : 103-106, 2018.
Artículo
en Inglés
| WPRIM | ID: wpr-714970
17.
Effect of the Orally Active Growth Hormone Secretagogue MK-677 on Somatic Growth in Rats
Yonsei Medical Journal
; : 1174-1180, 2018.
Artículo
en Inglés
| WPRIM | ID: wpr-718494
18.
Clinical manifestations of Rathke’s cleft cysts and their natural progression during 2 years in children and adolescents
Annals of Pediatric Endocrinology & Metabolism
; : 164-169, 2017.
Artículo
en Inglés
| WPRIM | ID: wpr-99771
19.
Insulin resistance and bone age advancement in girls with central precocious puberty
Annals of Pediatric Endocrinology & Metabolism
; : 176-182, 2017.
Artículo
en Inglés
| WPRIM | ID: wpr-99769
20.
A 1-month-old infant with chylomicronemia due to GPIHBP1 gene mutation treated by plasmapheresis
Annals of Pediatric Endocrinology & Metabolism
; : 68-71, 2017.
Artículo
en Inglés
| WPRIM | ID: wpr-226720