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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
3
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pubmed:dateCreated |
2003-3-14
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pubmed:abstractText |
Adult patients with sickle-cell disease are at risk for the development of osteonecrosis of the hip. However, there is little information in the literature about the rate of progression of osteonecrosis once symptoms begin. The purpose of this study was to evaluate the natural history of the symptomatic hip in adult patients with osteonecrosis and sickle-cell disease.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0021-9355
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
85-A
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
500-4
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pubmed:dateRevised |
2010-10-25
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pubmed:meshHeading |
pubmed-meshheading:12637438-Adolescent,
pubmed-meshheading:12637438-Adult,
pubmed-meshheading:12637438-Anemia, Sickle Cell,
pubmed-meshheading:12637438-Disease Progression,
pubmed-meshheading:12637438-Female,
pubmed-meshheading:12637438-Femur Head Necrosis,
pubmed-meshheading:12637438-Follow-Up Studies,
pubmed-meshheading:12637438-Hip Joint,
pubmed-meshheading:12637438-Humans,
pubmed-meshheading:12637438-Male,
pubmed-meshheading:12637438-Prognosis,
pubmed-meshheading:12637438-Risk Factors
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pubmed:year |
2003
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pubmed:articleTitle |
The natural history of symptomatic osteonecrosis in adults with sickle-cell disease.
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pubmed:affiliation |
Department of Orthopaedic Surgery and Traumatology, Hôpital Henri Mondor, Creteil, France.
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pubmed:publicationType |
Journal Article
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