Source:http://linkedlifedata.com/resource/pubmed/id/20215394
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
2010-5-6
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pubmed:abstractText |
Pheochromocytomas and paragangliomas (PHEO/PGL) are neuroendocrine tumors that arise from sympathetic and parasympathetic paraganglia. Diagnosed rarely during childhood, PHEO/PGL are nonetheless important clinical entities, particularly given our evolving understanding of their pathophysiology.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
1945-7197
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
95
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2023-37
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pubmed:meshHeading |
pubmed-meshheading:20215394-Child,
pubmed-meshheading:20215394-Dopamine,
pubmed-meshheading:20215394-Genetic Counseling,
pubmed-meshheading:20215394-Humans,
pubmed-meshheading:20215394-Mutation, Missense,
pubmed-meshheading:20215394-Paraganglioma,
pubmed-meshheading:20215394-Pheochromocytoma,
pubmed-meshheading:20215394-Von Hippel-Lindau Tumor Suppressor Protein
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pubmed:year |
2010
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pubmed:articleTitle |
A current review of the etiology, diagnosis, and treatment of pediatric pheochromocytoma and paraganglioma.
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pubmed:affiliation |
Department of Endocrine Neoplasia and Hormonal Disorders, The Children's Cancer Hospital, University of Texas M. D. Anderson Cancer Center, PO Box 301402, Unit 1461, Houston, Texas 77230-1402, USA. swagues@mdanderson.org
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pubmed:publicationType |
Journal Article,
Review
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