Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
12
pubmed:dateCreated
2008-12-29
pubmed:databankReference
pubmed:abstractText
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common inherited human enzyme defect. This deficiency provides some protection from clinical malaria, but it can also cause haemolysis after administration of drugs with oxidant properties.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/19112496-11423617, http://linkedlifedata.com/resource/pubmed/commentcorrection/19112496-12165212, http://linkedlifedata.com/resource/pubmed/commentcorrection/19112496-12387962, http://linkedlifedata.com/resource/pubmed/commentcorrection/19112496-14720085, http://linkedlifedata.com/resource/pubmed/commentcorrection/19112496-15183620, http://linkedlifedata.com/resource/pubmed/commentcorrection/19112496-15230645, http://linkedlifedata.com/resource/pubmed/commentcorrection/19112496-17007653, http://linkedlifedata.com/resource/pubmed/commentcorrection/19112496-17978087, http://linkedlifedata.com/resource/pubmed/commentcorrection/19112496-18320064, http://linkedlifedata.com/resource/pubmed/commentcorrection/19112496-18328518, http://linkedlifedata.com/resource/pubmed/commentcorrection/19112496-1867860, http://linkedlifedata.com/resource/pubmed/commentcorrection/19112496-5297001, http://linkedlifedata.com/resource/pubmed/commentcorrection/19112496-7617034, http://linkedlifedata.com/resource/pubmed/commentcorrection/19112496-835573
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
1932-6203
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
3
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
e4031
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:19112496-Amodiaquine, pubmed-meshheading:19112496-Antimalarials, pubmed-meshheading:19112496-Artemisinins, pubmed-meshheading:19112496-Child, pubmed-meshheading:19112496-Child, Preschool, pubmed-meshheading:19112496-Dapsone, pubmed-meshheading:19112496-Drug Combinations, pubmed-meshheading:19112496-Drug Therapy, Combination, pubmed-meshheading:19112496-Female, pubmed-meshheading:19112496-Glucosephosphate Dehydrogenase Deficiency, pubmed-meshheading:19112496-Humans, pubmed-meshheading:19112496-Infant, pubmed-meshheading:19112496-Malaria, Falciparum, pubmed-meshheading:19112496-Male, pubmed-meshheading:19112496-Oxidants, pubmed-meshheading:19112496-Polymorphism, Genetic, pubmed-meshheading:19112496-Proguanil, pubmed-meshheading:19112496-Pyrimethamine, pubmed-meshheading:19112496-Sulfadoxine
pubmed:year
2008
pubmed:articleTitle
High risk of severe anaemia after chlorproguanil-dapsone+artesunate antimalarial treatment in patients with G6PD (A-) deficiency.
pubmed:affiliation
Centre for Vaccinology and Tropical Medicine, Nuffield Department of Medicine, Oxford University, Oxford, United Kingdom. Caterina.Fanello@ndm.ox.ac.uk
pubmed:publicationType
Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't