18325745

Source:http://linkedlifedata.com/resource/pubmed/id/18325745

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0016037, umls-concept:C0029355, umls-concept:C0680243
pubmed:issue	3
pubmed:dateCreated	2008-4-8
pubmed:abstractText	Fibrodysplasia ossificans progressiva (FOP) is a rare disorder of the connective tissue associating malformation of the great toes and progressive heterotopic ossifications. Diagnosis is mostly clinical and currently no treatment is available. We report on the case of an 8 year old boy having an unusual form of FOP. We discuss clinical aspects of the disease and insist on the importance of early diagnosis, avoiding harmful events and therapeutic pitfalls.
pubmed:language	fre
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9421356
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Mar
pubmed:issn	0929-693X
pubmed:author	pubmed-author:DagherFF, pubmed-author:GhanemII, pubmed-author:KharratKK, pubmed-author:RachkidiRR
pubmed:issnType	Print
pubmed:volume	15
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	286-90
pubmed:meshHeading	pubmed-meshheading:18325745-Calcinosis, pubmed-meshheading:18325745-Child, pubmed-meshheading:18325745-Diagnosis, Differential, pubmed-meshheading:18325745-Humans, pubmed-meshheading:18325745-Male, pubmed-meshheading:18325745-Myositis Ossificans
pubmed:year	2008
pubmed:articleTitle	[Fibrodysplasia ossificans progressiva: orthopedic pitfalls and controversies].
pubmed:affiliation	Service de chirurgie orthopédique, hôpital Hôtel-Dieu de France, université Saint-Joseph, boulevard Alfred-Naccache, Beyrouth, Liban. ramirachkidi@hotmail.com
pubmed:publicationType	Journal Article, English Abstract, Case Reports