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Multisystem Inflammatory Syndrome in Children Related to COVID-19: the First Case in Korea

Journal of Korean Medical Science, 2020, 35(43), , pp.1-8

2020

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Impact of Nontreatment Duration and Keratopathy on Major Adverse Cardiovascular Events in Fabry Disease: A Nationwide Cohort Study

Journal of clinical medicine, 2024-01, Vol.13 (2), p.479

2024

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Prevalence and risk factors for type 2 diabetes mellitus with Prader-Willi syndrome: a single center experience

Orphanet journal of rare diseases, 2017-08, Vol.12 (1), p.146-146, Article 146

2017

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Identification of a novel KAT6A variant in an infant presenting with facial dysmorphism and developmental delay: a case report and literature review

BMC medical genomics, 2021-12, Vol.14 (1), p.297-297, Article 297

2021

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Effects of recombinant human growth hormone treatment on growth, body composition, and safety in infants or toddlers with Prader-Willi syndrome: a randomized, active-controlled trial

Orphanet journal of rare diseases, 2019-09, Vol.14 (1), p.216-216, Article 216

2019

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Multisystem Inflammatory Syndrome in Children Related to COVID-19: the First Case in Korea

Journal of Korean medical science, 2020, Vol.35 (43)

2020

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Measuring the Differentiated Impact of New Low-Income Housing Tax Credit (LIHTC) Projects on Households’ Movements by Income Level within Urban Areas

Urban science, 2021-12, Vol.5 (4), p.79

2021

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Cardiac Evaluation before and after Oral Propranolol Treatment for Infantile Hemangiomas

Journal of clinical medicine, 2024-06, Vol.13 (11), p.3332

2024

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Association Between Non-invasive Diagnostic Methods of Liver Fibrosis and Type 2 Diabetes in Pediatric Patients With Non-alcoholic Fatty Liver Disease

Frontiers in pediatrics, 2022-02, Vol.10, p.825141-825141

2022

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Impact of 6-month triptorelin formulation on predicted adult height and basal gonadotropin levels in patients with central precocious puberty

Frontiers in endocrinology (Lausanne), 2023-02, Vol.14, p.1134977-1134977

2023

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Two Novel Mutations of ANKRD11 Gene and Wide Clinical Spectrum in KBG Syndrome: Case Reports and Literature Review

Frontiers in genetics, 2020-11, Vol.11, p.579805

2020

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Clinical, Hormonal, and Neuroradiological Characteristics and Therapeutic Outcomes of Prolactinomas in Children and Adolescents at a Single Center

Frontiers in endocrinology (Lausanne), 2020-08, Vol.11, p.527-527

2020

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Development and Validation of Pediatric-Youth Hyperphagia Assessment for Prader-Willi Syndrome

Epidemiology and Health, 2022, 44(0), , pp.1-8

2022

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Femtosecond Electron Solvation at the Ionic Liquid/Metal Electrode Interface

Journal of the American Chemical Society, 2013-07, Vol.135 (29), p.10646-10653

2013

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Case of Chronic Active Epstein-Barr Virus Infection Developed Hemophagocytic Lymphohistiocytosis after COVID-19 Infection

Clinical pediatric hematology-oncology, 2023-10, Vol.30 (2), p.80-84

2023

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2022 Clinical practice guidelines for central precocious puberty of Korean children and adolescents

Annals of pediatric endocrinology & metabolism, 2023-09, Vol.28 (3), p.168-177

2023

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Etiological trends in male central precocious puberty

Annals of Pediatric Endocrinology & Metabolism, 2018, 23(2), , pp.75-80

2018

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HDR syndrome with a novel mutation in GATA3 mimicking a congenital X-linked stapes gusher: a case report

BMC medical genetics, 2017-10, Vol.18 (1), p.121-121, Article 121

2017

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

Journal of personalized medicine, 2022-04, Vol.12 (5), p.665

2022

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A case of de novo 18p deletion syndrome with panhypopituitarism

Annals of Pediatric Endocrinology & Metabolism, 2019, 24(1), , pp.60-63

2019

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Coexistence of Growth Hormone Deficiency and Pituitary Microadenoma in a Child with Unique Mosaic Turner Syndrome: A Case Report and Literature Review

Diagnostics (Basel), 2020-10, Vol.10 (10), p.783

2020

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Two-Photon Photoemission of Ultrathin Film PTCDA Morphologies on Ag(111)

Journal of physical chemistry. C, 2008-02, Vol.112 (7), p.2506-2513

2008

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Long-term follow-up on MURCS (Müllerian duct, renal, cervical somite dysplasia) association and a review of the literature

Annals of Pediatric Endocrinology & Metabolism, 2019, 24(3), , pp.207-211

2019

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A Case of Von Hippel-Lindau Disease Presented with Multiple Pancreatic Cysts and Medullary Hemangioblastoma

Clinical Pediatric Hematology-Oncology, 2020, 27(1), , pp.67-71

2020

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Long‐term cardiovascular outcomes and mortality with enzyme replacement therapy in patients with mucopolysaccharidosis type II

Journal of inherited metabolic disease, 2024-07

2024

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Multisystem Inflammatory Syndrome in Children Related to COVID-19: the First Case in Korea

Impact of Nontreatment Duration and Keratopathy on Major Adverse Cardiovascular Events in Fabry Disease: A Nationwide Cohort Study

Prevalence and risk factors for type 2 diabetes mellitus with Prader-Willi syndrome: a single center experience

Identification of a novel KAT6A variant in an infant presenting with facial dysmorphism and developmental delay: a case report and literature review

Effects of recombinant human growth hormone treatment on growth, body composition, and safety in infants or toddlers with Prader-Willi syndrome: a randomized, active-controlled trial

Multisystem Inflammatory Syndrome in Children Related to COVID-19: the First Case in Korea

Measuring the Differentiated Impact of New Low-Income Housing Tax Credit (LIHTC) Projects on Households’ Movements by Income Level within Urban Areas

Cardiac Evaluation before and after Oral Propranolol Treatment for Infantile Hemangiomas

Association Between Non-invasive Diagnostic Methods of Liver Fibrosis and Type 2 Diabetes in Pediatric Patients With Non-alcoholic Fatty Liver Disease

Impact of 6-month triptorelin formulation on predicted adult height and basal gonadotropin levels in patients with central precocious puberty

Two Novel Mutations of ANKRD11 Gene and Wide Clinical Spectrum in KBG Syndrome: Case Reports and Literature Review

Clinical, Hormonal, and Neuroradiological Characteristics and Therapeutic Outcomes of Prolactinomas in Children and Adolescents at a Single Center

Development and Validation of Pediatric-Youth Hyperphagia Assessment for Prader-Willi Syndrome

Femtosecond Electron Solvation at the Ionic Liquid/Metal Electrode Interface

Case of Chronic Active Epstein-Barr Virus Infection Developed Hemophagocytic Lymphohistiocytosis after COVID-19 Infection

2022 Clinical practice guidelines for central precocious puberty of Korean children and adolescents

Etiological trends in male central precocious puberty

HDR syndrome with a novel mutation in GATA3 mimicking a congenital X-linked stapes gusher: a case report

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

A case of de novo 18p deletion syndrome with panhypopituitarism

Coexistence of Growth Hormone Deficiency and Pituitary Microadenoma in a Child with Unique Mosaic Turner Syndrome: A Case Report and Literature Review

Two-Photon Photoemission of Ultrathin Film PTCDA Morphologies on Ag(111)

Long-term follow-up on MURCS (Müllerian duct, renal, cervical somite dysplasia) association and a review of the literature

A Case of Von Hippel-Lindau Disease Presented with Multiple Pancreatic Cysts and Medullary Hemangioblastoma

Long‐term cardiovascular outcomes and mortality with enzyme replacement therapy in patients with mucopolysaccharidosis type II

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