PHAEOCHROMOCYTOMA: EXPERIENCE FROM A REFERRAL HOSPITAL IN SOUTHERN INDIA
Author:
Affiliation:
1. Departments of General Surgery Unit I (Surgical Endocrinology),,
2. Endocrinology and,
3. Nuclear Medicine, Christian Medical College and Hospital, Vellore 632002, Tamil Nadu, India
Publisher
Wiley
Subject
General Medicine,Surgery,Surgery
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1046/j.1440-1622.1999.01598.x
Reference16 articles.
1. LandsbergL&YoungJB. Pheochromocytoma. In: Fauci AS Braunwald E Isselbacher KJ Wilson JD Martin JB Kasper DL Hauser SL Longo DL. (eds)Harrison’s Principles of Internal Medicine 14th edn. New York: McGraw Hill Co. 1998; Chapter 333.
2. TierneyLM&McPheeSJ.Current Medical Diagnosis and Treatment 36th edn. Appleton and Lange Stamford 1997.
3. Pheochromocytoma in the adult and in the child
4. Pheochromocytoma
5. Phaeochromocytomas in 72 patients: Clinical and diagnostic features, treatment and long term results
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1. Pheochromocytoma;The Endocrinologist;2009-01
2. Childhood Sporadic Pheochromocytoma: Clinical Profile and Outcome in 19 Patients;Journal of Pediatric Endocrinology and Metabolism;2006-01
3. The importance of the interpretation of urine catecholamines is essential for the diagnosis and management of patient with dopamine-secreting paraganglioma;Annals of Clinical Biochemistry: International Journal of Laboratory Medicine;2005-01-01
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