소아청소년당뇨병의 관리 전략.
- Published in:
- Journal of Korean Diabetes, 2024, v. 25, n. 3, p. 145, doi. 10.4093/jkd.2024.25.3.145
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- Publication type:
- Article
Works by Ja Hyang Cho
Results: 17
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Short-term efficacy of N-carbamylglutamate in a patient with N-acetylglutamate synthase deficiency.
- Published in:
- Journal of Human Genetics, 2015, v. 60, n. 7, p. 395, doi. 10.1038/jhg.2015.30
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- Publication type:
- Article
3
A dynamin-like protein in Arabidopsis thaliana is involved in biogenesis of thylakoid membranes.
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- EMBO Journal, 1998, v. 17, n. 4, p. 859, doi. 10.1093/emboj/17.4.859
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- Publication type:
- Article
4
Growth plate closure and therapeutic interventions.
- Published in:
- Clinical & Experimental Pediatrics, 2024, v. 67, n. 11, p. 553, doi. 10.3345/cep.2023.00346
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- Publication type:
- Article
5
The Prevalence of Abdominal Obesity and Metabolic Syndrome in Korean Children and Adolescents.
- Published in:
- Journal of Obesity & Metabolic Syndrome, 2023, v. 32, n. 2, p. 103, doi. 10.7570/jomes23025
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- Publication type:
- Article
6
Near final height in Korean children referred for evaluation of short stature: clinical utility and analytical validity of height prediction methods.
- Published in:
- Annals of Pediatric Endocrinology & Metabolism, 2018, v. 23, n. 1, p. 28, doi. 10.6065/apem.2018.23.1.28
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- Publication type:
- Article
7
Etiology and therapeutic outcomes of children with gonadotropin-independent precocious puberty.
- Published in:
- Annals of Pediatric Endocrinology & Metabolism, 2016, v. 21, n. 3, p. 136, doi. 10.6065/apem.2016.21.3.136
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- Publication type:
- Article
8
Long-term clinical outcome and the identification of homozygous CYP27B1 gene mutations in a patient with vitamin D hydroxylation-deficient rickets type 1A.
- Published in:
- 2016
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- Publication type:
- Case Study
9
Endocrine dysfunctions in children with Williams- Beuren syndrome.
- Published in:
- Annals of Pediatric Endocrinology & Metabolism, 2016, v. 21, n. 1, p. 15, doi. 10.6065/apem.2016.21.1.15
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- Publication type:
- Article
10
Long-term efficacy of recombinant human growth hormone therapy in short-statured patients with Noonan syndrome.
- Published in:
- Annals of Pediatric Endocrinology & Metabolism, 2016, v. 21, n. 1, p. 26, doi. 10.6065/apem.2016.21.1.26
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- Publication type:
- Article
11
Turner syndrome presented with tall stature due to overdosage of the SHOX gene.
- Published in:
- 2015
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- Publication type:
- Case Study
12
Clinical, endocrinological, and molecular characterization of Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism: a single center experience.
- Published in:
- Annals of Pediatric Endocrinology & Metabolism, 2015, v. 20, n. 1, p. 27, doi. 10.6065/apem.2015.20.1.27
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- Publication type:
- Article
13
Long-term follow-up on Cushing disease patient after transsphenoidal surgery.
- Published in:
- 2014
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- Publication type:
- Case Study
14
Changes in Neonatal and Perinatal Vital Statistics during Last 5 Decades in Republic of Korea: Compared with OECD Nations.
- Published in:
- Neonatal Medicine, 2013, v. 20, n. 4, p. 402, doi. 10.5385/nm.2013.20.4.402
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- Publication type:
- Article
15
Diverse genetic aetiologies and clinical outcomes of paediatric hypoparathyroidism.
- Published in:
- Clinical Endocrinology, 2015, v. 83, n. 6, p. 790, doi. 10.1111/cen.12944
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- Publication type:
- Article
16
Variable Clinical Characteristics and Molecular Spectrum of Patients with Syndromes of Reduced Sensitivity to Thyroid Hormone: Genetic Defects in the THRB and SLC16A2 Genes.
- Published in:
- Hormone Research in Paediatrics, 2018, v. 90, n. 5, p. 283, doi. 10.1159/000493468
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- Publication type:
- Article
17
Phenotypic and molecular spectrum of Korean patients with Lesch-Nyhan syndrome and attenuated clinical variants.
- Published in:
- Metabolic Brain Disease, 2019, v. 34, n. 5, p. 1335, doi. 10.1007/s11011-019-00441-0
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- Publication type:
- Article