Congenital Hypothyroidism
Reference38 articles.
1. Abramowicz, M. J., Duprez, L., Parma, J., et al. (1997). Familial congenital hypothyroidism due to inactivating mutation of the thyrotropin receptor causing profound hypoplasia of the thyroid gland. Journal of Clinical Investigation, 99, 3018–3024. 2. Abramowicz, M. J., Vassart, G., & Refetoff, S. (1997). Probing the cause of thyroid dysgenesis. Thyroid, 7, 325–336. 3. Abuhamad, A. Z., Fisher, D. A., Worsof, S. L., et al. (1995). Antenatal diagnosis and treatment of fetal goitrous hypothyroidism: Case report and review of the literature. Ultrasound in Obstetrics & Gynecology, 6, 368–371. 4. Agrawal, P., Ogilvy-Stuart, A., & Lees, C. (2002). Intrauterine diagnosis and management of congenital goitrous hypothyroidism. Ultrasound in Obstetrics & Gynecology, 19, 501–505. 5. Ambrugger, P., Stoeva, I., Biebermann, H., et al. (2001). Novel mutations of the thyroid peroxidase gene in patients with permanent congenital hypothyroidism. European Journal of Endocrinology, 145, 19–24.
|
|