GENERIC 11907857

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0015230, umls-concept:C0019621, umls-concept:C0021289, umls-concept:C0449450, umls-concept:C1744681
pubmed:issue	6
pubmed:dateCreated	2002-3-21
pubmed:abstractText	Congenital self-healing Langerhans cell histiocytosis (CSHLCH) is a rare condition which may present at birth or during the neonatal period. It is usually characterized by the eruption of multiple, disseminated, red-brown papules and nodules which may increase in size and number during the first few weeks of life. Systemic signs are usually absent except for occasional mild hepatomegaly.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9614685
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:issn	1203-4754
pubmed:author	pubmed-author:CallenJ PJP, pubmed-author:MorganK WKW
pubmed:issnType	Print
pubmed:volume	5
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	486-9
pubmed:dateRevised	2007-7-4
pubmed:meshHeading	pubmed-meshheading:11907857-Histiocytosis, Langerhans-Cell, pubmed-meshheading:11907857-Humans, pubmed-meshheading:11907857-Infant, Newborn, pubmed-meshheading:11907857-Male, pubmed-meshheading:11907857-Remission, Spontaneous, pubmed-meshheading:11907857-Skin Diseases, Vesiculobullous
pubmed:articleTitle	Self-healing congenital Langerhans cell histiocytosis presenting as neonatal papulovesicular eruption.
pubmed:affiliation	Department of Medicine, Division of Dermatology, University of Louisville, 310 East Broadway Avenue, Louisville, KY 40202, USA.
pubmed:publicationType	Journal Article, Case Reports