pubmed-article:8201479 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:8201479 | lifeskim:mentions | umls-concept:C0035579 | lld:lifeskim |
pubmed-article:8201479 | lifeskim:mentions | umls-concept:C1457869 | lld:lifeskim |
pubmed-article:8201479 | lifeskim:mentions | umls-concept:C0314603 | lld:lifeskim |
pubmed-article:8201479 | lifeskim:mentions | umls-concept:C1524003 | lld:lifeskim |
pubmed-article:8201479 | pubmed:issue | 6 | lld:pubmed |
pubmed-article:8201479 | pubmed:dateCreated | 1994-7-6 | lld:pubmed |
pubmed-article:8201479 | pubmed:abstractText | We examined two siblings who had severe rickets at ages 2 and 7 years, respectively, despite a history of adequate vitamin D intake. The patients' sera had calcium concentrations at the lower limits of normal, low phosphate concentrations, elevated alkaline phosphatase activity, and low levels of 25-hydroxyvitamin D. Treatment with high doses of vitamin D2 resulted in resolution of the biochemical abnormalities and radiographic deformities; pharmacologic doses of vitamin D2 were required to maintain normal concentrations of 25-hydroxyvitamin D in the serum even though vitamin D absorption was normal. These children may have a genetic defect of the 25-hydroxylation step in vitamin D activation. | lld:pubmed |
pubmed-article:8201479 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8201479 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8201479 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8201479 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8201479 | pubmed:language | eng | lld:pubmed |
pubmed-article:8201479 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8201479 | pubmed:citationSubset | AIM | lld:pubmed |
pubmed-article:8201479 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8201479 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8201479 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:8201479 | pubmed:month | Jun | lld:pubmed |
pubmed-article:8201479 | pubmed:issn | 0022-3476 | lld:pubmed |
pubmed-article:8201479 | pubmed:author | pubmed-author:HarrisonH EHE | lld:pubmed |
pubmed-article:8201479 | pubmed:author | pubmed-author:HolickM FMF | lld:pubmed |
pubmed-article:8201479 | pubmed:author | pubmed-author:ChenT CTC | lld:pubmed |
pubmed-article:8201479 | pubmed:author | pubmed-author:CasellaS JSJ | lld:pubmed |
pubmed-article:8201479 | pubmed:author | pubmed-author:ReinerB JBJ | lld:pubmed |
pubmed-article:8201479 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:8201479 | pubmed:volume | 124 | lld:pubmed |
pubmed-article:8201479 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:8201479 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:8201479 | pubmed:pagination | 929-32 | lld:pubmed |
pubmed-article:8201479 | pubmed:dateRevised | 2007-11-14 | lld:pubmed |
pubmed-article:8201479 | pubmed:meshHeading | pubmed-meshheading:8201479-... | lld:pubmed |
pubmed-article:8201479 | pubmed:meshHeading | pubmed-meshheading:8201479-... | lld:pubmed |
pubmed-article:8201479 | pubmed:meshHeading | pubmed-meshheading:8201479-... | lld:pubmed |
pubmed-article:8201479 | pubmed:meshHeading | pubmed-meshheading:8201479-... | lld:pubmed |
pubmed-article:8201479 | pubmed:meshHeading | pubmed-meshheading:8201479-... | lld:pubmed |
pubmed-article:8201479 | pubmed:meshHeading | pubmed-meshheading:8201479-... | lld:pubmed |
pubmed-article:8201479 | pubmed:meshHeading | pubmed-meshheading:8201479-... | lld:pubmed |
pubmed-article:8201479 | pubmed:year | 1994 | lld:pubmed |
pubmed-article:8201479 | pubmed:articleTitle | A possible genetic defect in 25-hydroxylation as a cause of rickets. | lld:pubmed |
pubmed-article:8201479 | pubmed:affiliation | Division of Pediatric Endocrinology, Johns Hopkins University School of Medicine, Baltimore, Maryland. | lld:pubmed |
pubmed-article:8201479 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:8201479 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
pubmed-article:8201479 | pubmed:publicationType | Case Reports | lld:pubmed |
pubmed-article:8201479 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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