11998918

Source:http://linkedlifedata.com/resource/pubmed/id/11998918

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0005575, umls-concept:C0008059, umls-concept:C0017431, umls-concept:C0220754, umls-concept:C0243102, umls-concept:C0332293, umls-concept:C1609982
pubmed:issue	3
pubmed:dateCreated	2002-5-9
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/11998918-11388594
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7603873
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Amidohydrolases, http://linkedlifedata.com/resource/pubmed/chemical/Biotin, http://linkedlifedata.com/resource/pubmed/chemical/Biotinidase
pubmed:status	MEDLINE
pubmed:month	Mar
pubmed:issn	0340-6199
pubmed:author	pubmed-author:WolfBarryB
pubmed:issnType	Print
pubmed:volume	161
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	167-8; author reply 169
pubmed:dateRevised	2006-11-15
pubmed:meshHeading	pubmed-meshheading:11998918-Amidohydrolases, pubmed-meshheading:11998918-Austria, pubmed-meshheading:11998918-Biotin, pubmed-meshheading:11998918-Biotinidase, pubmed-meshheading:11998918-Genotype, pubmed-meshheading:11998918-Humans, pubmed-meshheading:11998918-Infant, Newborn, pubmed-meshheading:11998918-Mass Screening, pubmed-meshheading:11998918-Multiple Carboxylase Deficiency
pubmed:year	2002
pubmed:articleTitle	Children with profound biotinidase deficiency should be treated with biotin regardless of their residual enzyme activity or genotype.
pubmed:publicationType	Letter, Comment