Suchergebnisse - "Kim, Ja Hye"

PubPharm (67)

1

Growth trajectories of children born preterm and full term with low birth weight to preschool ages : A nationwide study

enthalten in: The Journal of clinical endocrinology and metabolism | 2024

von Cha, J. | Kang, E. | Na, J. | +3

2

Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency through molecular genetic analysis of the CYP21A2 gene

enthalten in: Annals of pediatric endocrinology & metabolism | 2024

von Yoon, J. | Hwang, S. | Kim, J. | +3

3

Long-term endocrine sequelae after hematopoietic stem cell transplantation in children and adolescents

enthalten in: Annals of pediatric endocrinology & metabolism | 2024

von Hwang, S. | Lee, Y. | Yoon, J. | +6

4

Impact of Early Diagnostic and Therapeutic Interventions and Clinical Course in Children and Adolescents with Multiple Endocrine Neoplasia Types 1 and 2

enthalten in: Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association | 2024

von Kim, J. | Lee, Y. | Hwang, S. | +4

5

Applications of genomic research in pediatric endocrine diseases

enthalten in: Clinical and experimental pediatrics | 2023

von Kim, J. | Choi, J.

6

Clinical Characteristics and Long-Term Outcomes of Adrenal Tumors in Children and Adolescents

enthalten in: Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association | 2023

von Kim, J. | Choi, Y. | Hwang, S. | +4

7

Clinical outcomes and genotype-phenotype correlations in patients with complete and partial androgen insensitivity syndromes

enthalten in: Annals of pediatric endocrinology & metabolism | 2023

von Lee, N. | Kim, J. | Yoon, J. | +4

8

Ultra-Low Level Somatic Mutations and Structural Variations in Focal Cortical Dysplasia Type II

enthalten in: Annals of neurology | 2023

von Kim, J. | Park, J. | Lee, J. | +7

9

Molecular basis and genetic testing strategies for diagnosing 21-hydroxylase deficiency, including CAH-X syndrome

enthalten in: Annals of pediatric endocrinology & metabolism | 2023

von Kim, J. | Kim, G. | Yoo, H. | +1

10

Pediatric hepatocellular carcinoma associated with Niemann-Pick disease type C : Case report and literature review

enthalten in: JIMD reports | 2023

von Hwang, S. | Choi, Y. | Lee, B. | +3

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