Familial MEN1 Syndrome Diagnosed on Functional Imaging: A Case Report with Clinical and Genetic Correlation
Author:
Affiliation:
1. Radiation Medicine Centre, Tata Memorial Hospital Annexe, BARC, Mumbai, Maharashtra, India
2. Radiation Medicine Centre, Homi Bhabha National Institute, Mumbai, Maharashtra, India
Abstract
Publisher
Georg Thieme Verlag KG
Link
http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0043-1768448.pdf
Reference11 articles.
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2. Multiple endocrine neoplasia type 1 (MEN1): an update and the significance of early genetic and clinical diagnosis;C DC Kamilaris;Front Endocrinol (Lausanne),2019
3. Multiple endocrine neoplasia type 1: from bedside to benchside;K Yoshimoto;J Med Invest,2000
4. 18F-FDOPA PET/CT accurately identifies MEN1-associated pheochromocytoma;A A Tepede;Endocrinol Diabetes Metab Case Rep,2020
5. Diagnostic challenges due to phenocopies: lessons from multiple endocrine neoplasia type1 (MEN1);J J Turner;Hum Mutat,2010
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