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Pheochromocytoma

Known as: CHROMAFFINOMA, MEDULLARY, Pheochromocytoma, adrenal, pheochromocytoma syndrome 
A usually benign, well-encapsulated, lobular, vascular tumor of chromaffin tissue of the ADRENAL MEDULLA or sympathetic paraganglia. The cardinal… Expand
National Institutes of Health

Papers overview

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Review
2015
Review
2015
OBJECTIVE Pheochromocytomas (PHEOs) and paragangliomas (PGLs) are neural crest cell tumors associated with catecholamine… Expand
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Highly Cited
2007
Highly Cited
2007
The First International Symposium on Pheochromocytoma, held in October 2005, included discussions about developments concerning… Expand
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Highly Cited
2005
Highly Cited
2005
PURPOSE To assess the yield and the clinical value of systematic screening of susceptibility genes for patients with… Expand
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Highly Cited
2002
Highly Cited
2002
BACKGROUND The group of susceptibility genes for pheochromocytoma that included the proto-oncogene RET (associated with multiple… Expand
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Highly Cited
2002
Highly Cited
2002
CONTEXT Diagnosis of pheochromocytoma depends on biochemical evidence of catecholamine production by the tumor. However, the best… Expand
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Highly Cited
2001
Highly Cited
2001
The pheochromocytomas are an important cause of secondary hypertension. Although pheochromocytoma susceptibility may be… Expand
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Highly Cited
1995
Highly Cited
1995
Apoptosis plays an important role during neuronal development, and defects in apoptosis may underlie various neurodegenerative… Expand
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Highly Cited
1993
Highly Cited
1993
A novel hypotensive peptide was discovered in human pheochromocytoma by monitoring the elevating activity of platelet cAMP. Since… Expand
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Highly Cited
1992
Highly Cited
1992
 
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Highly Cited
1976
Highly Cited
1976
A single cell clonal line which responds reversibly to nerve growth factor (NGF) has been established from a transplantable rat… Expand
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