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Список литературы

1. Дедов И.И., Петеркова В.А. Справочник детского эндокринолога - М: Литтерра, 2020.-с. 91-103

2. Вадина Т.А. Врожденный гипотиреоз: эпидемиология, структура и социальная адаптация. // автореф. канд. диссертации - М., 2011 - 26 с.

3. Синнаи Г. Детская тиреоидология. // перевод с англ, под редакцией Петерковой В.А. -М„ 2016.-304 с.

4. Lain SJ, Bentley JP, Wiley V, et al. Association between borderline neonatal thyroid-stimulating hormone concentrations and educational and developmental outcomes: a population-based record-linkage study. Lancet Diabetes and Endocrinology, 2016. 4, p. 756-765.

5. Zwaveling-Soonawala N, van Trotsenburg AS, Verkerk PH. The severity of congenital hypothyroidism of central origin should not be underestimated. Journal of Clinical Endocrinology and Metabolism 2015, 100, E297-E300.

6. Ro vet JF. The role of thyroid hormones for brain development and cognitive function. Endocrine Development 2014, 26, p. 26^13.

7. Дедов И.И., Безлепкина О.Б., Вадина Т.А., Байбарина Е.Н., Чумакова О.В., Караваева Л.В. Безлепкин А.С., Петеркова В.А. Скрининг на врожденный гипотиреоз в Российской Федерации. //Проблемы эндокринологии. — 2018. — Т. 64. — № 1. — С. 14-20.

8. Barry Y, Bonaldi С, Goulet V, et al. Increased incidence of congenital hypothyroidism in France from 1982 to 2012: a nationwide multicenter analysis. Annals of Epidemiology 2016, 26, 100. E 4-105.

9. Deladoey J, Ruel J, Giguere Y, et al. Is the incidence of congenital hypothyroid-ism really increasing? A 20-year retrospective population-based study in Quebec. J Clin En-docrinol Metab, 2011; 96, p. 2422-2429.

10. LaFranchi SH Approach to the diagnosis and treatment of neonatal hypothyroidism. J Clin Endocrinol Metab 2011, 96, p. 2959-2967.

11. Graters A, Krade H Detection and treatment of congenital hypothyroidism. Nat Rev Endocrinol, 2012, 8, p. 104—113.

12. Макрецкая H. А. Молекулярно-генетические основы врожденного гипотиреоза: анализ с применением методов высокоэффктивного параллельного секвенирования.// автореферат канд. диссертации - М., 2018 - 28 с.

13. Beck-Peccoz Р, Rodari G, Giavoli С, et al. Central hypothyroidism - a neglected thyroid disorder. Nature Reviews Endocrinology 2017, 13, p. 588-598.

14. Grasberger H, Refetoff S. Genetic causes of congenital hypothyroidism due to dyshormon-ogenesis. Current Opinion in Pediatrics 2011, 23, p. 421^428.

15. Fernandez LP, Lopez-Marquez A, Santisteban P. Thyroid transcription factors in development, differentiation and disease. Nature Reviews Endocrinology 2015, 11, p. 29^-2.

16. Peters C, van Trotsenburg ASP, Schoenmakers N. Congenital hypothyroidism: update and perspectives. European Journal of Endocrinology, 2018, 179, p. 297-317.

17. Szirtnai G. Clinical genetics of congenital hypothyroidism. Endocrine Development 2014, 26, p. 60-78.

18. Leger J, Olivieri A, Donaldson M, et al. European Society for Paediatric Endocrinology Consensus Guidelines on Screening, Diagnosis, and Management of Congenital Hypothyroidism. J. Clin. Endocrinol. Metab. - 2014,99, 2. p. 363-384.

19. Park, I. S., Yoon, J. S., So, С. H., Lee, H. S., & Hwang, J. S. (2017). Predictors of transient congenital hypothyroidism in children with eutopic thyroid gland. Annals of Pediatric Endocrinology & Metabolism, 22(2), p.l 15.

20. Nicholas AK, Jaleel S, Lyons G, et al. Molecular spectrum of TSH0 subunit gene defects in central hypothyroidism in the UK and Ireland. Clinical Endocrinology 2017, 86, p. 410418.

21. Hermanns P, Couch R, Leonard N, et al. A novel deletion in the thyrotropin Beta-subunit gene identified by array comparative genomic hybridization analysis causes central congenital hypothyroidism in a boy originating from Turkey. Hormone Research in Paediatrics 2014, 82, p 201-205.

22. Tenenbaum-Rakover Y, Almashanu S, Hess O, et al. Long-term outcome of loss-of-function mutations in thyrotropin receptor gene. Thyroid 2015, 25, p. 292-299.

23. Garcia M, Gonzalez de Buitrago J, Jimenez-Roses M, et al. Central hypothyroidism due to a TRHR mutation causing impaired ligand affinity and transactivation of Gq. Journal of Clinical Endocrinology and Metabolism 2017, 102, p. 2433-2442.

24. Zwaveling-Soonawala N, van Trotsenburg ASP, Verkerk PH. TSH and FT4 Concentrations in congenital central hypothyroidism and mild congenital thyroidal hypothyroidism. Journal of Clinical Endocrinology and Metabolism 2018, 103, p.l 342-1348.

25. Ahmad N, Irfan A, Al Saedi SA. Congenital hypothyroidism: Screening, diagnosis, management, and outcome. J Clin Neonatol. 2017, 6, p. 64-70.

26. Corbetta C, Weber G, Cortinovis F et al. A 7-year experience with low blood TSH cutoff levels for neonatal screening reveals an unsuspected frequency of congenital hypothyroidism (CH). Clinical Endocrinology, 2009, 71, p.739-745.

27. Langham S, Hindmarsh P, Krywawych S et al. Screening for congenital hypothyroidism: comparison of borderline screening cut-off points and the effect on the number of children treated with levothyroxine. European Thyroid Journal, 2013, 2, p. 180-186.

28. Peters C, Brooke I, Heales S et al. Defining the newborn blood spot screening reference interval for TSH: impact of ethnicity. Journal of Clinical Endocrinology and Metabolism 2016, 101, p. 3445-3449.

29. Ford G. LaFranchi SH. Screening for congenital hypothyroidism: a worldwide view of strategies. Best Practice and Research Clinical Endocrinology and Metabolism, 2014, 28, p. 175-187.

30. Kilberg MJ, Rasooly IR, LaFranchi SH et al. Newborn screening in the US may miss mild persistent hypothyroidism. Journal of Pediatrics, 2018, 192, p. 204-208.

31. Adachi M, Soneda A, Asakura Y, et al. Mass screening of newborns for congenital hypothyroidism of central origin by free thyroxine measurement of blood samples on filter paper. European Journal of Endocrinology, 2012 166, p. 829-838.

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