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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
10
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pubmed:dateCreated |
2000-9-27
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pubmed:abstractText |
Familial primary pulmonary hypertension (PPH) is an autosomal-dominant inherited disease with incomplete penetrance and poor prognosis. This study was performed to examine whether asymptomatic carriers of a mutated PPH gene can be identified at an early stage by their pulmonary artery systolic pressure (PASP) response to exercise.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
1524-4539
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:day |
5
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pubmed:volume |
102
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1145-50
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:10973844-Adolescent,
pubmed-meshheading:10973844-Adult,
pubmed-meshheading:10973844-Aged,
pubmed-meshheading:10973844-Child,
pubmed-meshheading:10973844-Echocardiography, Doppler,
pubmed-meshheading:10973844-Exercise,
pubmed-meshheading:10973844-Female,
pubmed-meshheading:10973844-Haplotypes,
pubmed-meshheading:10973844-Heterozygote,
pubmed-meshheading:10973844-Humans,
pubmed-meshheading:10973844-Hypertension, Pulmonary,
pubmed-meshheading:10973844-Male,
pubmed-meshheading:10973844-Middle Aged,
pubmed-meshheading:10973844-Pedigree,
pubmed-meshheading:10973844-Pulmonary Wedge Pressure
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pubmed:year |
2000
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pubmed:articleTitle |
Abnormal pulmonary artery pressure response in asymptomatic carriers of primary pulmonary hypertension gene.
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pubmed:affiliation |
Department of Cardiology, and the Institute of Human Genetics, University of Heidelberg, Heidelberg, Germany.
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pubmed:publicationType |
Journal Article
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