| pubmed-article:6375356 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:6375356 | lifeskim:mentions | umls-concept:C0162569 | lld:lifeskim |
| pubmed-article:6375356 | lifeskim:mentions | umls-concept:C0042085 | lld:lifeskim |
| pubmed-article:6375356 | lifeskim:mentions | umls-concept:C0268323 | lld:lifeskim |
| pubmed-article:6375356 | lifeskim:mentions | umls-concept:C0205470 | lld:lifeskim |
| pubmed-article:6375356 | lifeskim:mentions | umls-concept:C2603343 | lld:lifeskim |
| pubmed-article:6375356 | pubmed:issue | 3 | lld:pubmed |
| pubmed-article:6375356 | pubmed:dateCreated | 1984-7-19 | lld:pubmed |
| pubmed-article:6375356 | pubmed:abstractText | Uroporphyrinogen decarboxylase activity was measured in hemoglobin-free lysates from two patients with hepatoerythropoietic porphyria (HEP) and from 12 unrelated patients with familial porphyria cutanea tarda (PCT). In HEP patients, enzyme activities were 5% of normal, and familial studies clearly confirmed that patients with HEP are cases of homozygous PCT. Immunoreactive uroporphyrinogen decarboxylase was measured by developing a direct and noncompetitive enzyme immunoassay (EIA). For the 12 familial PCT patients, we found an immunoreactive protein decreased (51%) to the same extent as the catalytic activity (48%) [cross-reactive immunological material ( CRIM ) negative]. The children from the HEP family were also CRIM negative, contrasting with another HEP family previously described as CRIM positive; our data support the hypothesis of a heterogeneity in familial uroporphyrinogen decarboxylase deficiency. | lld:pubmed |
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| pubmed-article:6375356 | pubmed:language | eng | lld:pubmed |
| pubmed-article:6375356 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:6375356 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:6375356 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:6375356 | pubmed:month | May | lld:pubmed |
| pubmed-article:6375356 | pubmed:issn | 0002-9297 | lld:pubmed |
| pubmed-article:6375356 | pubmed:author | pubmed-author:NordmannYY | lld:pubmed |
| pubmed-article:6375356 | pubmed:author | pubmed-author:de VerneuilHH | lld:pubmed |
| pubmed-article:6375356 | pubmed:author | pubmed-author:BeaumontCC | lld:pubmed |
| pubmed-article:6375356 | pubmed:author | pubmed-author:SfarZZ | lld:pubmed |
| pubmed-article:6375356 | pubmed:author | pubmed-author:KastallyRR | lld:pubmed |
| pubmed-article:6375356 | pubmed:author | pubmed-author:DeybachJ CJC | lld:pubmed |
| pubmed-article:6375356 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:6375356 | pubmed:volume | 36 | lld:pubmed |
| pubmed-article:6375356 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:6375356 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:6375356 | pubmed:pagination | 613-22 | lld:pubmed |
| pubmed-article:6375356 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:6375356 | pubmed:meshHeading | pubmed-meshheading:6375356-... | lld:pubmed |
| pubmed-article:6375356 | pubmed:year | 1984 | lld:pubmed |
| pubmed-article:6375356 | pubmed:articleTitle | Enzymatic and immunological studies of uroporphyrinogen decarboxylase in familial porphyria cutanea tarda and hepatoerythropoietic porphyria. | lld:pubmed |
| pubmed-article:6375356 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:6375356 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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