Heterogeneous phenotype in children affected by non-autoimmune hypothyroidism: an update
Author:
Publisher
Springer Science and Business Media LLC
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Link
http://link.springer.com/content/pdf/10.1007/s40618-015-0288-5.pdf
Reference53 articles.
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3. Tajima T, Nakamura A, Morikawa S et al (2014) Neonatal screening and a new cause of congenital central hypothyroidism. Ann Pediatr Endocrinol Metab 19:117–121
4. Zwaveling-Soonawala N, van Trotsenburg P, Verkerk H et al (2015) The severity of congenital hypothyroidism of central origin should not be underestimated. J Clin Endocrinol Metab 100(2):E297–E300
5. Tajima T, Ishizu K, Nakamura A (2013) Molecular and clinical findings in patients with LHX4 and OTX2 mutations. Clin Pediatr Endocrinol 22(2):15–23
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