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The spectrum of clinical, hormonal and molecular findings in 280 individuals with nonclassical congenital adrenal hyperplasia caused by mutations of the CYP21A2 gene.
Livadas S, Dracopoulou M, Dastamani A, Sertedaki A, Maniati-Christidi M, Magiakou AM, Kanaka-Gantenbein C, Chrousos GP, Dacou-Voutetakis C. Livadas S, et al. Among authors: sertedaki a. Clin Endocrinol (Oxf). 2015 Apr;82(4):543-9. doi: 10.1111/cen.12543. Epub 2014 Aug 3. Clin Endocrinol (Oxf). 2015. PMID: 25041270
Pituitary magnetic resonance imaging in 15 patients with Prop1 gene mutations: pituitary enlargement may originate from the intermediate lobe.
Voutetakis A, Argyropoulou M, Sertedaki A, Livadas S, Xekouki P, Maniati-Christidi M, Bossis I, Thalassinos N, Patronas N, Dacou-Voutetakis C. Voutetakis A, et al. Among authors: sertedaki a. J Clin Endocrinol Metab. 2004 May;89(5):2200-6. doi: 10.1210/jc.2003-031765. J Clin Endocrinol Metab. 2004. PMID: 15126542
Gene symbol: TSH B. Disease: congenital hypothyroidism.
Sertedaki A, Papadimitriou A, Voutetakis A, Dracopoulou A, Maniati-Christidi M, Dacou-Voutetakis C. Sertedaki A, et al. Hum Genet. 2004 Jul;115(2):174. Hum Genet. 2004. PMID: 15300985 No abstract available.
Gene symbol: PROP1. Disease: multiple pituitary hormone deficiency.
Sertedaki A, Voutetakis A, Maniati-Christidi A, Kanaka-Gantenbein Ch, Dracopoulou M, Argyropoulou M, Livadas S, Dacou-Voutetakis A, Sertedaki A. Sertedaki A, et al. Hum Genet. 2004 Jul;115(2):174. Hum Genet. 2004. PMID: 15300986 No abstract available.
60 results