Clinical Practice: Experience with newborn screening for congenital hypothyroidism in the Republic of Macedonia—a multiethnic country

Author:

Kocova Mirjana,Anastasovska Violeta,Sukarova-Angelovska Elena,Tanaskoska Milica,Taseva Elizabeta

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Reference18 articles.

1. Abduljabbar MA, Afifi AM (2012) Congenital hypothyroidism. J Pediatr Endocrinol Metab 25(1–2):13–29

2. Bongers-Schokking JJ, Koot HM, Wiersma D, Verkerk PH, de Muinck Keizer-Schrama SM (2000) Influence of timing and dose of thyroid hormone replacement on development in infants with congenital hypothyroidism. J Pediatr 136(292–7):183

3. Burgard P, Rupp K, Linder M, Haege G, Rigter T, Weinreich SS, Loeber JG, Taruscio D, Vittozzi L, Cornel MC, Hoffmann GF (2012) Newborn screening programmes in Europe; arguments and efforts regarding harmonization. Part 2—from screening laboratory results to treatment, follow-up and quality assurance. J Inherit Metab Dis 35(4):613–625

4. Dubuis JM, Glorieux J, Richer F, Deal CL, Dussault JH, Van Vliet G (1996) Outcome of severe congenital hypothyroidism: closing the developmental gap with early high dose levothyroxine treatment. J ClinEndocrinol Metab 81:222–7

5. Foley T, Kaplowitz PB, Kaye CL, Sundararjan S, Varma SK (2006) Update of newborn screening and therapy for congenital hypothyroidism, American Academy of Pediatrics, Rose SR, Section on Endocrinology and Committee on Genetics, American Thyroid Association, Brown RS, Public Health Committee, Lawson Wilkins Pediatric Endocrine Society. Pediatrics 117:2290–2303

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