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Transient congenital hypothyroidism due to maternal autoimmune thyroid disease.
Mengreli C, Maniati-Christidi M, Kanaka-Gantenbein C, Girginoudis P, Vagenakis AG, Dacou-Voutetakis C. Mengreli C, et al. Among authors: maniati christidi m. Hormones (Athens). 2003 Apr-Jun;2(2):113-9. doi: 10.14310/horm.2002.1190. Hormones (Athens). 2003. PMID: 17003010 Free article.
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. Among authors: maniati christidi m. Hum Genet. 2004 Jul;115(2):174. Hum Genet. 2004. PMID: 15300985 No abstract available.
Low TSH congenital hypothyroidism: identification of a novel mutation of the TSH beta-subunit gene in one sporadic case (C85R) and of mutation Q49stop in two siblings with congenital hypothyroidism.
Sertedaki A, Papadimitriou A, Voutetakis A, Dracopoulou M, Maniati-Christidi M, Dacou-Voutetakis C. Sertedaki A, et al. Among authors: maniati christidi m. Pediatr Res. 2002 Dec;52(6):935-41. doi: 10.1203/00006450-200212000-00020. Pediatr Res. 2002. PMID: 12438673
Genetic aspects of congenital adrenal hyperplasia.
Dacou-Voutetakis C, Maniati-Christidi M, Dracopoulou-Vabouli M. Dacou-Voutetakis C, et al. J Pediatr Endocrinol Metab. 2001;14 Suppl 5:1303-8; discussion 1317. J Pediatr Endocrinol Metab. 2001. PMID: 11964027 Review.
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: maniati christidi m. Clin Endocrinol (Oxf). 2015 Apr;82(4):543-9. doi: 10.1111/cen.12543. Epub 2014 Aug 3. Clin Endocrinol (Oxf). 2015. PMID: 25041270
16 results