Genetic Analysis and Clinical Characteristics of Hereditary Pheochromocytoma and Paraganglioma Syndrome in Korean Population
Author:
Funder
Korea Health Industry Development Institute
Ministry of Health and Welfare
Publisher
Korean Endocrine Society
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Link
http://e-enm.org/upload/pdf/enm-2020-683.pdf
Reference41 articles.
1. Update on Adrenal Tumours in 2017 World Health Organization (WHO) of Endocrine Tumours
2. Differential Diagnosis of Pheochromocytomas and Paragangliomas
3. Pheochromocytoma: an update on genetics and management
4. Malignant and Metastatic Pheochromocytoma: Case Report and Review of the Literature
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1. Novel and recurrent genetic variants of VHL, SDHB, and RET genes in Chinese pheochromocytoma and paraganglioma patients;Frontiers in Genetics;2023-03-03
2. Genetic Study in Pheochromocytoma: Is It Possible to Stratify the Risk of Hereditary Pheochromocytoma?;Neuroendocrinology;2023
3. Bilateral Pheochromocytoma with Germline MAX Variant without Family History;Clinics and Practice;2022-05-07
4. The Role of VHL in the Development of von Hippel-Lindau Disease and Erythrocytosis;Genes;2022-02-17
5. Recurrent Germline Mutations of CHEK2 as a New Susceptibility Gene in Patients with Pheochromocytomas and Paragangliomas;International Journal of Endocrinology;2021-09-30
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