Je H. Han
Seocho, Republic of Korea
Last Updated: 09/26/2026
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Found 18 publications
The nature and pathological impact of the c.1748A > G variant of the neurofibromin 1 gene.
Journal: Gene
Published: September 04, 2024
Germline Mutations and Phenotypic Associations in Korean Patients With Pheochromocytoma and Paraganglioma: A Multicenter Study and Literature Review.
Journal: Annals of laboratory medicine
Published: September 21, 2023
USP37 Deubiquitinates CDC73 in HPT-JT Syndrome.
Journal: International journal of molecular sciences
Published: April 16, 2022
Clinical features and signaling effects of RET D631Y variant multiple endocrine neoplasia type 2 (MEN2).
Journal: The Korean journal of internal medicine
Published: July 06, 2021
Functional Identification of Compound Heterozygous Mutations in the CYP17A1 Gene Resulting in Combined 17α-Hydroxylase/17,20-Lyase Deficiency.
Journal: Endocrinology and metabolism (Seoul, Korea)
Published: March 21, 2018
Serum gamma-glutamyltransferase is not associated with subclinical atherosclerosis in patients with type 2 diabetes.
Journal: Cardiovascular diabetology
Published: April 30, 2016
A novel neurofibromatosis type 1 (NF1) mutation in a patient with NF1 and pheochromocytoma.
Journal: The Korean journal of internal medicine
Published: August 01, 2015
Mean Platelet Volume Is Closely Associated With Serum Glucose Level but Not With Arterial Stiffness and Carotid Atherosclerosis in Patients With Type 2 Diabetes.
Journal: The Journal of clinical endocrinology and metabolism
Published: June 30, 2015
Serum bilirubin levels are inversely associated with PAI-1 and fibrinogen in Korean subjects.
Journal: Atherosclerosis
Published: May 28, 2015
Identification and functional analysis of a novel CaSR mutation in a family with familial hypocalciuric hypercalcemia.
Journal: Journal of bone and mineral metabolism
Published: April 15, 2015
Last Updated: 09/26/2026