Thyroperoxidase
Author:
Publisher
Springer International Publishing
Link
http://link.springer.com/content/pdf/10.1007/978-3-319-28845-1_5291-1
Reference34 articles.
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2. Baker, J. R., Jr., Saunders, N. B., Wartofsky, L., Tseng, Y. C., & Burman, K. D. (1988). Seronegative Hashimoto thyroiditis with thyroid autoantibody production localized to the thyroid. Annals of Internal Medicine, 108(1), 26–30. https://doi.org/10.7326/0003-4819-108-1-26.
3. Bakker, B., Bikker, H., Vulsma, T., de Randamie, J. S., Wiedijk, B. M., & De Vijlder, J. J. (2000). Two decades of screening for congenital hypothyroidism in The Netherlands: TPO gene mutations in total iodide organification defects (an update). The Journal of Clinical Endocrinology and Metabolism, 85(10), 3708–3712. https://doi.org/10.1210/jcem.85.10.6878.
4. Biondi, B., & Cooper, D. S. (2008). The clinical significance of subclinical thyroid dysfunction. Endocrine Reviews, 29(1), 76–131. https://doi.org/10.1210/er.2006-0043.
5. Chertok Shacham, E., Ishay, A., Irit, E., Pohlenz, J., & Tenenbaum-Rakover, Y. (2012). Minimally invasive follicular thyroid carcinoma developed in dyshormonogenetic multinodular goiter due to thyroid peroxidase gene mutation. Thyroid, 22(5), 542–546. https://doi.org/10.1089/thy.2011.0478.
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