| pubmed-article:7588958 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:7588958 | lifeskim:mentions | umls-concept:C0041400 | lld:lifeskim |
| pubmed-article:7588958 | lifeskim:mentions | umls-concept:C0010308 | lld:lifeskim |
| pubmed-article:7588958 | lifeskim:mentions | umls-concept:C0220908 | lld:lifeskim |
| pubmed-article:7588958 | pubmed:issue | 8 | lld:pubmed |
| pubmed-article:7588958 | pubmed:dateCreated | 1995-12-15 | lld:pubmed |
| pubmed-article:7588958 | pubmed:abstractText | A pilot study was performed to determine the incidence of congenital hypothyroidism (CH) in Turkey and to build a model for nationwide screening. From December 1991 to December 1992, 30,097 newborns were screened for CH using a primary measurement of thyroid stimulating hormone in capillary blood on days 3-5 of life. Samples were obtained in collaboration with the ongoing nationwide phenylketonuria screening programme. Eleven cases of primary CH were detected giving the incidence of 1:2736. Recall rate was 2.3%. Replacement therapy with L-thyroxine was started after the confirmation of diagnosis. The median age at the initiation of replacement therapy was 23 days (range 7-35 days). CONCLUSION: The incidence of CH is notably higher in Turkey than reported in most other countries. Iodine deficiency and/or dyshormonogenesis might contribute to this high incidence. This result emphasizes the necessity of a nationwide screening programme. | lld:pubmed |
| pubmed-article:7588958 | pubmed:language | eng | lld:pubmed |
| pubmed-article:7588958 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:7588958 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:7588958 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:7588958 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:7588958 | pubmed:month | Aug | lld:pubmed |
| pubmed-article:7588958 | pubmed:issn | 0340-6199 | lld:pubmed |
| pubmed-article:7588958 | pubmed:author | pubmed-author:OzalpII | lld:pubmed |
| pubmed-article:7588958 | pubmed:author | pubmed-author:YordamNN | lld:pubmed |
| pubmed-article:7588958 | pubmed:author | pubmed-author:TeziçTT | lld:pubmed |
| pubmed-article:7588958 | pubmed:author | pubmed-author:O?uzHH | lld:pubmed |
| pubmed-article:7588958 | pubmed:author | pubmed-author:HatunSS | lld:pubmed |
| pubmed-article:7588958 | pubmed:author | pubmed-author:Caliko?luA... | lld:pubmed |
| pubmed-article:7588958 | pubmed:author | pubmed-author:KandemirNN | lld:pubmed |
| pubmed-article:7588958 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:7588958 | pubmed:volume | 154 | lld:pubmed |
| pubmed-article:7588958 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:7588958 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:7588958 | pubmed:pagination | 614-6 | lld:pubmed |
| pubmed-article:7588958 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
| pubmed-article:7588958 | pubmed:meshHeading | pubmed-meshheading:7588958-... | lld:pubmed |
| pubmed-article:7588958 | pubmed:meshHeading | pubmed-meshheading:7588958-... | lld:pubmed |
| pubmed-article:7588958 | pubmed:meshHeading | pubmed-meshheading:7588958-... | lld:pubmed |
| pubmed-article:7588958 | pubmed:meshHeading | pubmed-meshheading:7588958-... | lld:pubmed |
| pubmed-article:7588958 | pubmed:meshHeading | pubmed-meshheading:7588958-... | lld:pubmed |
| pubmed-article:7588958 | pubmed:meshHeading | pubmed-meshheading:7588958-... | lld:pubmed |
| pubmed-article:7588958 | pubmed:meshHeading | pubmed-meshheading:7588958-... | lld:pubmed |
| pubmed-article:7588958 | pubmed:meshHeading | pubmed-meshheading:7588958-... | lld:pubmed |
| pubmed-article:7588958 | pubmed:meshHeading | pubmed-meshheading:7588958-... | lld:pubmed |
| pubmed-article:7588958 | pubmed:meshHeading | pubmed-meshheading:7588958-... | lld:pubmed |
| pubmed-article:7588958 | pubmed:meshHeading | pubmed-meshheading:7588958-... | lld:pubmed |
| pubmed-article:7588958 | pubmed:meshHeading | pubmed-meshheading:7588958-... | lld:pubmed |
| pubmed-article:7588958 | pubmed:meshHeading | pubmed-meshheading:7588958-... | lld:pubmed |
| pubmed-article:7588958 | pubmed:year | 1995 | lld:pubmed |
| pubmed-article:7588958 | pubmed:articleTitle | Screening for congenital hypothyroidism in Turkey. | lld:pubmed |
| pubmed-article:7588958 | pubmed:affiliation | Hacettepe University, Department of Paediatric Endocrinology, Ankara, Turkey. | lld:pubmed |
| pubmed-article:7588958 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:7588958 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
