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Title: | 18Fluoro-dihydroxy phenylalanine positron emission tomography/computed tomography scanning for congenital hyperinsulinism of infancy | Authors: | Fiumara, F. Conwell, L. S. Greer, R. M. Neville, K. A. Amato, L. A. Campbell, L. |
Issue Date: | 2015 | Source: | 51, (8), 2015, p. 826-829 | Pages: | 826-829 | Journal: | Journal of Paediatrics and Child Health | Abstract: | L6024298382015-02-25 | DOI: | 10.1111/jpc.12827 | Resources: | https://www.embase.com/search/results?subaction=viewrecord&id=L602429838&from=exporthttp://dx.doi.org/10.1111/jpc.12827 | | Keywords: | heterozygosity;hospital discharge;human;human cell;human tissue;hydrocortisone blood level;image analysis;immunohistochemistry;infant;infant feeding;insulin blood level;laboratory test;laparoscopic surgery;male;missense mutation;monozygotic twins;nose feeding;pancreas islet cell hyperplasia;patient transport;priority journal;persistent hyperinsulinemic hypoglycemia of infancy;3 hydroxybutyric acid6 fluorodopa f 18;diazoxide;fatty acid;glucagon;glucose;hydrochlorothiazide;hydrocortisone;insulin;octreotide;article;birth weight;blood glucose monitoring;case report;computer assisted emission tomography;continuous infusion;fatty acid blood level;genetic screening;glucose blood level | Type: | Article |
Appears in Sites: | Children's Health Queensland Publications |
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