19350124

Source:http://linkedlifedata.com/resource/pubmed/id/19350124

Download in:

Switch to

Custom View

Named Graph Language Inference

Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0009566, umls-concept:C0019080, umls-concept:C0019425, umls-concept:C0026882, umls-concept:C0087086, umls-concept:C0205198, umls-concept:C0547040, umls-concept:C0678227, umls-concept:C1706395
pubmed:issue	4
pubmed:dateCreated	2009-4-7
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/HL31048, http://linkedlifedata.com/resource/pubmed/grant/R01 HL031048-18, http://linkedlifedata.com/resource/pubmed/grant/R01 HL031048-19, http://linkedlifedata.com/resource/pubmed/grant/R01 HL031048-20, http://linkedlifedata.com/resource/pubmed/grant/R01 HL031048-21
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7608063
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Fibrinogen, http://linkedlifedata.com/resource/pubmed/chemical/Fibrinogens, Abnormal, http://linkedlifedata.com/resource/pubmed/chemical/fibrinogen Aalpha, http://linkedlifedata.com/resource/pubmed/chemical/fibrinogen Perth
pubmed:status	MEDLINE
pubmed:month	Apr
pubmed:issn	0340-6245
pubmed:author	pubmed-author:ArnoldErinE, pubmed-author:González-ManchónConsueloC, pubmed-author:GreenDavidD, pubmed-author:JayoAsierA, pubmed-author:LordSusan TST
pubmed:issnType	Print
pubmed:volume	101
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	770-2
pubmed:dateRevised	2010-12-3
pubmed:meshHeading	pubmed-meshheading:19350124-Arterial Occlusive Diseases, pubmed-meshheading:19350124-Blood Coagulation Disorders, Inherited, pubmed-meshheading:19350124-Blood Coagulation Tests, pubmed-meshheading:19350124-Female, pubmed-meshheading:19350124-Fibrinogen, pubmed-meshheading:19350124-Fibrinogens, Abnormal, pubmed-meshheading:19350124-Genetic Testing, pubmed-meshheading:19350124-Hand Injuries, pubmed-meshheading:19350124-Hemorrhage, pubmed-meshheading:19350124-Heterozygote, pubmed-meshheading:19350124-Humans, pubmed-meshheading:19350124-Menorrhagia, pubmed-meshheading:19350124-Middle Aged, pubmed-meshheading:19350124-Molecular Weight, pubmed-meshheading:19350124-Mutation, pubmed-meshheading:19350124-Pedigree, pubmed-meshheading:19350124-Phenotype, pubmed-meshheading:19350124-Postpartum Hemorrhage, pubmed-meshheading:19350124-Thrombosis
pubmed:year	2009
pubmed:articleTitle	Hypodysfibrinogenemia causing mild bleeding and thrombotic complications in a compound heterozygote of AalphaIVS4+1G>T mutation and Aalpha4841delC truncation (Aalpha(Perth)).
pubmed:affiliation	Departmento of Cellular and Molecular Physiopathology, Centro de Inverstigaciones Biológicas (CIB-CSIC), Madrid, Spain.
pubmed:publicationType	Journal Article, Case Reports, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural