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| Nonautoimmune congenital hyperthyroidism due to p.Asp633Glu mutation in the TSHR gene | |
| Won Kyoung Cho, Moon-Bae Ahn, Woori Jang, Hyojin Chae, Myungshin Kim, Byung-Kyu Suh | |
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Ann Pediatr Endocrinol Metab. 2018;23(4):235-239. Published online December 31, 2018 DOI: https://doi.org/10.6065/apem.2018.23.4.235 |
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Nonautoimmune congenital hyperthyroidism due to p.Asp633Glu mutation in the TSHR gene Annals of Pediatric Endocrinology & Metabolism. 2018;23(4):235-239  Subclinical hyperthyroidism due to a thyrotropin receptor (TSHR) gene mutation (S505R) Acta Paediatrica. 2006;95(12):1685-1687 Sporadic Nonautoimmune Congenital Hyperthyroidism due to a Strong Activating Mutation of the Thyrotropin Receptor Gene Thyroid. 2000;10(10):859-863 A Japanese family with nonautoimmune hyperthyroidism caused by a novel heterozygous thyrotropin receptor gene mutation Pediatric Research. 2014;75(6):749-753 Congenital Nonautoimmune Hyperthyroidism in a Nonidentical Twin Caused by a Sporadic Germline Mutation in the Thyrotropin Receptor Gene Thyroid. 1997;7(5):765-770 Long-Term Carbimazole Treatment of Neonatal Nonautoimmune Hyperthyroidism due to a New Activating TSH Receptor Gene Mutation (Ala428Val) Hormone Research in Paediatrics. 2005;64(4):203-208 Premature birth and low birth weight associated with nonautoimmune hyperthyroidism due to an activating thyrotropin receptor gene mutation Clinical Endocrinology. 2004;60(6):711-718 A Japanese family with familial nonautoimmune hyperthyroidism with a novel mutation (Asn406Ser) in extracellular domain of thyrotrophin receptor Clinical Endocrinology. 2012;77(2):329-330 Lack of in vitro constitutive activity for four previously reported TSH receptor mutations identified in patients with nonautoimmune hyperthyroidism and hot thyroid carcinomas Clinical Endocrinology. 2010;73(6):815-820 Fusidic acid/rifampicin Reactions Weekly. 2016;1622(1):100-100 |
