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Hereditary Paraganglioma

Known as: Familial Paraganglioma 
An inherited neoplasm arising from paraganglia. The majority of cases (up to 80%) are multifocal.
National Institutes of Health

Papers overview

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Highly Cited
2015
Highly Cited
2015
Disruption of the Krebs cycle is a hallmark of cancer. IDH1 and IDH2 mutations are found in many neoplasms, and germline… Expand
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Highly Cited
2008
Highly Cited
2008
OBJECTIVE Phaeochromocytomas and paragangliomas are familial in up to 25% of cases and can result from succinate dehydrogenase… Expand
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Review
2008
Review
2008
Hereditary paraganglioma (PGL) is characterised by genetic predisposition to the development of highly vascular tumours of the… Expand
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Highly Cited
2007
Highly Cited
2007
The tricarboxylic acid (TCA) cycle enzyme succinate dehydrogenase (SDH) is a tumor suppressor. Heterozygosity for defective SDH… Expand
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Highly Cited
2005
Highly Cited
2005
BackgroundGermline mutations of the SDHD, SDHB and SDHC genes, encoding three of the four subunits of succinate dehydrogenase… Expand
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Review
2003
Review
2003
  • Bora E. Baysal
  • Trends in Endocrinology & Metabolism
  • 2003
  • Corpus ID: 1175872
Hereditary paraganglioma (PGL) is characterized by the development of slow-growing, highly vascularized tumors that can present… Expand
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Highly Cited
2002
Highly Cited
2002
Background: Paragangliomas are rare and highly heritable tumours of neuroectodermal origin that often develop in the head and… 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
2001
Highly Cited
2001
Hereditary paragangliomas are usually benign tumors of the autonomic nervous system that are composed of cells derived from the… Expand
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Highly Cited
2000
Highly Cited
2000
Hereditary paraganglioma (PGL) is characterized by the development of benign, vascularized tumors in the head and neck. The most… Expand
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