Malignant Pheochromocytoma in a Population-Based Study: Survival and Clinical Results-Reference-Cited by-同舟云学术

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Malignant Pheochromocytoma in a Population-Based Study: Survival and Clinical Results

Published:2006-08-01 Issue:1 Volume:1073 Page:512-516
ISSN:0077-8923
Container-title:Annals of the New York Academy of Sciences
language:en
Short-container-title:Annals of the New York Academy of Sciences

Author:

WANGBERG B.,MUTH A.,KHORRAM-MANESH A.,JANSSON S.,NILSSON O.,FORSSELL-ARONSSON E.,TISELL L.,AHLMAN H.

Publisher

Wiley

Subject

History and Philosophy of Science,General Biochemistry, Genetics and Molecular Biology,General Neuroscience

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1196/annals.1353.054/fullpdf

Reference11 articles.

1. Germ-Line Mutations in Nonsyndromic Pheochromocytoma

2. Pheochromocytoma: The Expanding Genetic Differential Diagnosis

3. Clinical Experience Over 48 Years With Pheochromocytoma

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1. Primary tumour resection for synchronously metastatic phaeochromocytoma and paraganglioma: A population‐based study;Clinical Endocrinology;2020-12-17

2. MYO5B mutations in pheochromocytoma/paraganglioma promote cancer progression;PLOS Genetics;2020-06-08

3. Pheochromocytoma/Paragangliomas;Updates in Hypertension and Cardiovascular Protection;2016

4. Malignant pheochromocytomas/paragangliomas harbor mutations in transport and cell adhesion genes;International Journal of Cancer;2015-12-30

5. The Presence of SDHB Mutations Should Modify Surgical Indications for Carotid Body Paragangliomas;Annals of Surgery;2014-07

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