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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
3
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pubmed:dateCreated |
2006-3-31
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pubmed:abstractText |
Central nervous system (CNS) hemangioblastomas are benign vascular tumors arising either sporadically or as a manifestation of von Hippel-Lindau (VHL) disease, a hereditary cancer syndrome. The authors studied a series of patients with CNS hemangioblastomas and their families to identify germline mutations in the VHL tumor suppressor gene and to establish a predictive testing and screening protocol.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0022-3085
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
104
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
389-94
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:16572651-Adolescent,
pubmed-meshheading:16572651-Adult,
pubmed-meshheading:16572651-Cerebellar Neoplasms,
pubmed-meshheading:16572651-Child,
pubmed-meshheading:16572651-Child, Preschool,
pubmed-meshheading:16572651-DNA Mutational Analysis,
pubmed-meshheading:16572651-Female,
pubmed-meshheading:16572651-Genetic Testing,
pubmed-meshheading:16572651-Germ-Line Mutation,
pubmed-meshheading:16572651-Hemangioblastoma,
pubmed-meshheading:16572651-Humans,
pubmed-meshheading:16572651-Male,
pubmed-meshheading:16572651-Mexico,
pubmed-meshheading:16572651-Middle Aged,
pubmed-meshheading:16572651-Pedigree,
pubmed-meshheading:16572651-Prognosis,
pubmed-meshheading:16572651-von Hippel-Lindau Disease
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pubmed:year |
2006
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pubmed:articleTitle |
Von Hippel-Lindau disease germline mutations in Mexican patients with cerebellar hemangioblastoma.
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pubmed:affiliation |
Department of Neurogenetics and Molecular Biology, Instituto Nacional de Neurología y Neurocirugía Manuel Velasco Suárez, Mexico.
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pubmed:publicationType |
Journal Article
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