Chong Kun Cheon at Pusan National University School of Medicine - Research Interests, Publications & Academic Profile - ApplyKite

Chong Kun Cheon

Associate Professor

Pusan National University School of Medicine

South Korea

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Research Interests

Internal Medicine

60%

Pediatric Nutrition

80%

Rare Disease

90%

Medical Science

80%

Endocrinology

50%

Pediatric Endocrinology

40%

Osteogenesis Imperfecta

30%

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Articles17

The impacts of COVID-19 on childhood obesity: prevalence, contributing factors, and implications for management

Year:

2024

The first case of hyperosmolar diabetic ketoacidosis in a patient diagnosed with MODY 5 (maturity-onset diabetes of the young type 5) and 17q12 microdeletion syndrome

Year:

2024

NANS‐CDG: Expanding clinical insights with a novel patient with novel variants

Year:

2024

Identification of a novel mutation of the SHOX gene in a patient with Leri-Weill dyschondrosteosis accompanied by growth hormone deficiency

Year:

2024

A novel compound heterozygous variant of the COL11A1 gene in a patient with fibrochondrogenesis type I: the first case in Korea

Year:

2024

A heterozygous mutation in UBE2H in a patient with developmental delay leads to an aberrant brain development in zebrafish

Year:

2023

Pediatric management challenges of hyperglycemic hyperosmolar state: case series of Korean adolescents with type 2 diabetes

Year:

2023

The first case of novel variants of the FSHR mutation causing primary amenorrhea in 2 siblings in Korea

Year:

2023

Haploinsufficiency A20 misdiagnosed as PFAPA (periodic fever, aphthous stomatitis, pharyngitis, and cervical adenitis) syndrome with Kikuchi disease

Year:

2023

A Korean child with DICER1 syndrome presenting with thyroid manifestations accompanied by other types of neoplasms: a case report and literature review

Year:

2023

Commentary on "Glycemic control and complications of type 2 diabetes mellitus in children and adolescents during the COVID-19 outbreak"

Year:

2023

Prospective evaluation of the clinical utility of whole-exome sequencing using buccal swabbing for undiagnosed rare diseases

Year:

2022

From diagnosis to treatment of mucopolysaccharidosis type VI: A case report with a novel variant, c.1157C>T (p.Ser386Phe), in ARSB gene

Year:

2022

Response to growth hormone according to provocation test results in idiopathic short stature and idiopathic growth hormone deficiency

Year:

2022

Fabry nephropathy before and after enzyme replacement therapy: important role of renal biopsy in patients with Fabry disease

Year:

2021

Commentary on "Effects of gonadotropin-releasing hormone agonist treatment on final adult height in boys with idiopathic central precocious puberty"

Year:

2021

Clinical relevance of targeted exome sequencing in patients with rare syndromic short stature

Year:

2021

Collaborators7

YongBeom Shin

Section chief / Professor

Pusan National University Yangsan Hospital

SOUTH KOREA

Hyun Jung Lee

Clinical Professor

Pusan National University Yangsan Hospital

SOUTH KOREA

Seung Hwan Oh

Pusan National University Yangsan Hospital

SOUTH KOREA

Ju Young Yoon

Pusan National University Yangsan Hospital

SOUTH KOREA

Il Young Kim

Pusan National University Yangsan Hospital

SOUTH KOREA

Su Eun Park

Pusan National University Yangsan Hospital

SOUTH KOREA

Yoo-Mi Kim

Pusan National University Yangsan Hospital

SOUTH KOREA

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