Diabetes News

Endocrinology

sponsor
Become a Member Today!
Register
Email:


Password:

Remember me
Forgot your Password?
Invite Code?
Article ID

Your Article Summary

(Click the title below to leave the MDLinx Network and go to the Journal's Website)

Gaal J et al. – IDH mutations are very rare in paragangliomas and pheochromocytomas and do not appear to play an important role in oncogenic HIF activation known to be present in these tumors.


Related Articles

Clinical Predictors and Algorithm for the Genetic Diagnosis of Pheochromocytoma Patients
Clinical Cancer Research, 10/19/09    Relevance Score: 87%

Low Sensitivity of Glucagon Provocative Testing for Diagnosis of Pheochromocytoma
Journal of Clinical Endocrinology and Metabolism, 11/24/09    Relevance Score: 85%

ACTH-producing pheochromocytoma: Clinical considerations and concise review of the literature
European Journal of Internal Medicine, 10/12/09    Relevance Score: 85%

Radiofrequency Ablation of Metastatic Pheochromocytoma
Journal of Vascular and Interventional Radiology, 11/13/09    Relevance Score: 83%

Unusual Presentation of Pheochromocytoma with Ischemic Sigmoid Colitis and Stenosis
Southern Medical Journal, 10/08/09    Relevance Score: 82%

Today in Adrenal Glands...keeping you current

Partners in crime: deregulation of AR activity and androgen synthesis in prostate cancer
Trends in Endocrinology and Metabolism, 02/08/10

Improved Quality of Life, Blood Pressure, and Biochemical Status Following Laparoscopic Adrenalectomy for Unilateral Primary Aldosteronism
Journal of Clinical Endocrinology and Metabolism, 02/04/10

High Penetrance of Pheochromocytoma Associated with the Novel C634Y/Y791F Double Germline Mutation in the RET Protooncogene
Journal of Clinical Endocrinology and Metabolism, 02/04/10

Article Search

Keyword:

Search:

Published within

Sort By:
Date
Relevance


Sponsor

Sponsor

Send this Summary to a Colleague

Enter email address