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Editorial : Genetic diagnosis of Alport syndrome
Clinical and Experimental Pediatrics
2019 .01
양극성장애로 오인된 윌슨병
신경정신의학
2016 .01
Successful pregnancy outcome in a Korean patient with symptomatic Wilson’s disease
Obstetrics & Gynecology Science
2015 .01
Clinical Characteristics, Genetic Features, and Long-Term Outcome of Wilson’s Disease in a Taiwanese Population: An 11-Year Follow-Up Study in a Taiwanese Population: An 11-Year Follow-Up Study
Journal Of Movement Disorders
2023 .05
Morning Glory Syndrome associated with Autosomal Dominant Alport Syndrome with a Heterozygous COL4A4 Mutation
Childhood Kidney Diseases
2021 .12
Clinical Characteristics and Long-Term Prognosis of Alport Syndrome: A Retrospective Single-Center Study
Childhood Kidney Diseases
2020 .01
Copper Deficiency Myeloneuropathy in a Patient With Wilson’s Disease
Journal Of Movement Disorders
2024 .01
Fracture in a Young Male Patient Leading to the Diagnosis of Wilson’s Disease: A Case Report
대한골대사학회지
2015 .01
A rare case of Wilson disease associated with intracerebral hemorrhage
Korean Journal of Anesthesiology
2020 .01
Hypopituitarism Presenting as Adrenal Insufficiency and Hypothyroidism in a Patient with Wilson’s Disease: A Case Report
Journal of Korean Medical Science
2016 .01
suspi진단이지연된 비전형적 Mowat-Wilson syndrome 1예
Laboratory Medicine Online
2016 .01
Mechanism-based histological characteristics of animal disease models and their applications in evaluating pharmaceutical effects
한국실험동물학회 학술발표대회 논문집
2025 .02
Wilson Disease Comorbid with Hereditary Sensory Autonomic Neuropathy Type IV and Gitelman Syndrome
Pediatric Gastroenterology, Hepatology & Nutrition
2019 .01
An Alport syndrome boy with Van Wyk-Grumbach syndrome induced by prolonged untreated congenital hypothyroidism
Annals of Pediatirc Endocrinology & Metabolism
2020 .01
Genetic background, recent advances in molecular biology, and development of novel therapy in Alport syndrome
Kidney Research and Clinical Practice
2020 .01
Prevalence, Incidence, and Treatment Pattern of Wilson’s Disease Using National Health Insurance Data From 2010-2020, Korea
Journal of Korean Medical Science
2024 .04
An Adult Case of Bartter Syndrome Type III Presenting with Proteinuria
Journal of Pathology and Translational Medicine
2016 .01
Late Diagnosis of Wilson Disease, Initially Presenting as Cerebellar Atrophy Mimicking Spinocerebellar Ataxia, by Multigene Panel Testing
Annals of Laboratory Medicine
2020 .01
Could Urinary Copper/Zinc Ratio Be a Newer Tool to Replace 24-Hour Urinary Copper Excretion for Diagnosing Wilson Disease in Children?
Pediatric Gastroenterology, Hepatology & Nutrition
2024 .01
Clinical Approach to Children with Proteinuria
Childhood Kidney Diseases
2017 .01
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