삼성더클성장의원

Mixed diabetic ketoacidosis and hyperglycemic hyperosmolarity in a girl with nephronophthisis 4 presenting with rhabdomyolysis and pancreatitis.

Noh ES, Kim C, Cho SY.

Endocrine and Metabolic Illnesses in Young Adults with Prader-Willi Syndrome.

Noh ES, Kim MS, Kim C, Jeon K, Kim S, Cho SY, Jin DK.

Late-infantile GM1 gangliosidosis: A case report.

Noh ES, Park HM, Kim MS, Park HD, Cho SY, Jin DK.

Continuous Renal Replacement Therapy in Preterm Infants.

Noh ES, Kim HH, Kim HS, Han YS, Yang M, Ahn SY, Sung SI, Chang YS, Park WS.

Floating-Harbor Syndrome in a Korean Patient with Short Stature and Early Puberty: A Case Report.

Jeon J, Noh ES, Hwang IT.

Genomic Insights into Short Stature in Children Born Small for Gestational Age: A Korean Multicenter Exome Study.

Lee Y, Jeong HR, Kim EY, Noh ES, Jin HY, et al.

Differential microRNA Expression Profiles in Girls with Idiopathic Central Precocious Puberty and Premature Thelarche.

Lee HJ, Bae SJ, Noh ES, Jin HY, Hwang IT, Ryu S, Jeong HR.

Prediction of hepatic fibrosis using the aspartate transaminase-to-platelet ratio index in children and adolescents with metabolic dysfunction-associated steatotic liver disease.

Jin HY, Noh ES, Jeong H, Hwang IT.

Triglyceride Glucose Index is Associated with Ultrasonographic Fatty Liver Indicator in Children and Adolescents with Non-alcoholic Fatty Liver Disease.

Kim B, Jin HY, Yoon JS, Noh ES, Hwang IT.

α-Klotho levels in girls with central precocious puberty: potential as a diagnostic and monitoring marker.

Park JH, Noh ES, Hwang IT.

Resistance to thyroid hormone and nonfunctioning pituitary microadenoma in a 13-year-old boy with THRB mutation.

Kim J, Noh ES, Kim MS, Choi JM, Lee SM, Cho SY.

A Korean boy with a CHD8 mutation who presented with overgrowth, intellectual disability, and autism.

Kim C, Noh ES, Cho SY.

Diagnosis and Management of Osteoporosis in Children and Adolescents.

Jin HY, Noh ES, Hwang IT.

First female Korean child with Coffin-Lowry syndrome: a novel variant in RPS6KA3 diagnosed by exome sequencing and a literature review.

Song A, Im M, Kim MS, Noh ES, Kim C, Jang J, Lee SM, Ki CS, Cho SY, Jin DK.

Six-year clinical outcomes of enzyme replacement therapy for perinatal lethal and infantile hypophosphatasia in Korea: Two case reports.

Kim I, Noh ES, Kim MS, Jang JH, Jeon TY, Choi HW, Cho SY.

A novel splicing variant in GALNS in mucopolysaccharidosis IVA and the necessity of re-evaluating primer sequences.

Kim SM, Noh ES, Park JH, Park HD, Lee SY, Jang JH, Cho SY.

Multiple endocrine neoplasia type 2 and autoimmune polyendocrine syndromes in a 16-year-old male with Kabuki syndrome.

Park E, Kim MS, Noh ES, Lee JE, Kim SJ, Kwon YS, Cho SY.

The Youngest Infant to Be Diagnosed with Autosomal Dominant Hypocalcemia Type 2 Harboring a Novel Variant of GNA11.

Kwon EJ, Kim MS, Noh ES, Kim CW, Jang J, Choi JH, Cho SY, Jin DK.

Natural History and Molecular Characteristics of Korean Patients with Mucopolysaccharidosis Type III.

Kim MS, Yang A, Noh ES, Kim C, Bae GY, Lim HH, Park HD, Cho SY, Jin DK.

Development and validation of the Pediatric-Youth Hyperphagia Assessment for Prader-Willi syndrome.

Cho SY, Kang D, Im M, Yang A, Kim MS, Kim J, Noh ES, et al.